CHDD Publications 2018

IDDRC PUBLICATIONS

BY RESEARCH AFFILIATES

2014 - 2019

2014

Susan Astley

Astley, S. J. (2014). Invited commentary on Australian fetal alcohol spectrum disorder diagnostic guidelines. BMC Pediatrics, 14, 85. PMCID: PMC3994222. doi: 10.1186/1471-2431-14-85.

Astley, S. J. (2014). The value of a FASD diagnosis (2013). Journal of Population Therapeutics and Clinical Pharmacology, 21, e81-e105.

Elizabeth Aylward

Aylward, E. H. (2014). Magnetic resonance imaging striatal volumes: A biomarker for clinical trials in Huntington's disease. Movement Disorders, 29, 1429-33. PMCID: PMC4479278. doi: 10.1002/mds.26013.

Harrington, D. L., Liu, D., Smith, M. M., Mills, J. A., Long, J. D., Aylward, E. H., Paulsen, J. S. (2014). Neuroanatomical correlates of cognitive functioning in prodromal Huntington disease. Brain and Behavior, 4, 29-40. PMCID: PMC3937704. doi: 10.1002/brb3.185.

Padowski, J. M., Weaver, K. E., Richards, T. L., Laurino, M. Y., Samii, A., Aylward, E. H., Conley, K. E. (2014). Neurochemical correlates of caudate atrophy in Huntington's disease. Movement Disorders, 29, 327-35. PMCID: PMC3960319. doi: 10.1002/mds.25801.

Paulsen, J. S., Long, J. D., Johnson, H. J., Aylward, E. H., Ross, C. A., Williams, J. K., … Coordinators of the Huntington Study, Group (2014). Clinical and biomarker changes in premanifest Huntington disease show trial feasibility: A decade of the PREDICT-HD Study. Frontiers in Aging Neuroscience, 6, 78. PMCID: PMC4000999. doi: 10.3389/fnagi.2014.00078.

Ross, C. A., Aylward, E. H., Wild, E. J., Langbehn, D. R., Long, J. D., Warner, J. H., … Tabrizi, S. J. (2014). Huntington disease: Natural history, biomarkers and prospects for therapeutics. Nature Reviews Neurology, 10, 204-16. doi: 10.1038/nrneurol.2014.24.

Younes, L., Ratnanather, J. T., Brown, T., Aylward, E. H., Nopoulos, P., Johnson, H., … Coordinators of the Huntington Study, Group (2014). Regionally selective atrophy of subcortical structures in prodromal HD as revealed by statistical shape analysis. Human Brain Mapping, 35, 792-809. PMCID: PMC3715588. doi: 10.1002/hbm.22214.

Raphael Bernier

Ackerman, S., Wenegrat, J., Rettew, D., Althoff, R., Bernier, R. A. (2014). No increase in autism-associated genetic events in children conceived by assisted reproduction. Fertility and Sterility, 102, 388-93. PMCID: PMC5808861. doi: 10.1016/j.fertnstert.2014.04.020.

Bernier, R. A., Golzio, C., Xiong, B., Stessman, H. A., Coe, B. P., Penn, O., … Mefford, H. C., … Eichler, E. E. (2014). Disruptive CHD8 mutations define a subtype of autism early in development. Cell, 158, 263-276. PMCID: PMC4136921. doi: 10.1016/j.cell.2014.06.017.

Bernier, R. A., Aaronson, B., Kresse, A. (2014). EEG mu rhythm in typical and atypical development. Journal of Visualized Experiments, 86, e51412. PMCID: PMC4165377. doi: 10.3791/51412.

Buxbaum, J. D., Bolshakova, N., Brownfeld, J. M., Anney, R. J., Bender, P., Bernier, R. A., … Gallagher, L. (2014). The Autism Simplex Collection: An international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism, 5, 34. PMCID: PMC4228819. doi: 10.1186/2040-2392-5-34.

Deriziotis, P., O'Roak, B. J., Graham, S. A., Estruch, S. B., Dimitropoulou, D., Bernier, R. A., … Eichler, E. E., Fisher, S. E. (2014). De novo TBR1 mutations in sporadic autism disrupt protein functions. Nature Communications, 5, 4954. PMCID: PMC4212638. doi: 10.1038/ncomms5954.

King, B. H., Navot, N., Bernier, R. A., Webb, S. J. (2014). Update on diagnostic classification in autism. Current Opinion in Psychiatry, 27, 105-9. PMCID: PMC4929984. doi: 10.1097/YCO.0000000000000040.

Pinto, D., Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., … Bernier, R. A., … Wijsman, E. M., … Scherer, S. W. (2014). Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics, 94, 677-94. PMCID: PMC4067558. doi: 10.1016/j.ajhg.2014.03.018.

Vandeweyer, G., Helsmoortel, C., Van Dijck, A., Vulto-van Silfhout, A. T., Coe, B. P., Bernier, R. A., … Eichler, E. E., … Kooy, R. F. (2014). The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 166, 315-26. PMCID: PMC4195434. doi: 10.1002/ajmg.c.31413.

Virginia Berninger Jones, J. N., Abbott, R. D., Berninger, V. W. (2014). Predicting levels of reading and writing achievement in typically developing, English-speaking 2 and 5 graders. Learning and Individual Differences, 32, 54-68. PMCID: PMC4058427. doi: 10.1016/j.lindif.2014.03.013.

Niedo, J., Lee, Y. L., Breznitz, Z., Berninger, V. W. (2014). Computerized silent reading rate and strategy instruction for fourth graders at risk in silent reading rate. Learning Disability Quarterly, 37, 100-110. PMCID: PMC4047714. doi: 10.1177/0731948713507263.

Rubenstein, K. B., Raskind, W. H., Berninger, V. W., Matsushita, M. M., Wijsman, E. M. (2014). Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors. American Journal of Medical Genetics B: Neuropsychiatric Genetics, 165, 345-56. PMCID: PMC4053475. doi: 10.1002/ajmg.b.32237.

Kristie F. Bjornson

Bjornson, K. F., Zhou, C., Stevenson, R., Christakis, D. A., Song, K. (2014). Walking activity patterns in youth with cerebral palsy and youth developing typically. Disability and Rehabilitation, 36, 1279-84. PMCID: PMC4295907. doi: 10.3109/09638288.2013.845254.

Kang, M., Bjornson, K. F., Barreira, T. V., Ragan, B. G., Song, K. (2014). The minimum number of days required to establish reliable physical activity estimates in children aged 2-15 years. Physiological Measurement, 35, 2229-37. doi: 10.1088/0967-3334/35/11/2229.

Cathryn Booth-LaForce Booth-LaForce, C., Roisman, G. I. (2014). I. Introduction. Monographs of the Society for Research in Child Development, 79, 1-14. doi: 10.1111/mono.12110.

Booth-LaForce, C., Groh, A. M., Burchinal, M. R., Roisman, G. I., Owen, M. T., Cox, M. J. (2014). V. Caregiving and contextual sources of continuity and change in attachment security from infancy to late adolescence. Monographs of the Society for Research in Child Development, 79, 67-84. doi: 10.1111/mono.12114.

Groh, A. M., Roisman, G. I., Booth-LaForce, C., Fraley, R. C., Owen, M. T., Cox, M. J., Burchinal, M. R. (2014). IV. Stability of attachment security from infancy to late adolescence. Monographs of the Society for Research in Child Development, 79, 51-66. doi: 10.1111/mono.12113.

Haydon, K. C., Roisman, G. I., Owen, M. T., Booth-LaForce, C., Cox, M. J. (2014). VII. Shared and distinctive antecedents of Adult Attachment Interview state-of-mind and inferred-experience dimensions. Monographs of the Society for Research in Child Development, 79, 108-25. doi: 10.1111/mono.12116.

Murray, K. W., Dwyer, K. M., Rubin, K. H., Knighton-Wisor, S., Booth-LaForce, C. (2014). Parent-child relationships, parental psychological control, and aggression: Maternal and paternal relationships. Journal of Youth and Adolescence, 43, 1361-73. doi: 10.1007/s10964-013-0019-1.

Roisman, G. I., Fraley, R. C., Booth-LaForce, C. (2014). Pulling ourselves up by our bootstraps: A rejoinder to van IJzendoorn and Bakermans-Kranenburg (2014). Monographs of the Society for Research in Child Development, 79, 168-73. doi: 10.1111/mono.12121.

Roisman, G. I., Haltigan, J. D., Haydon, K. C., Booth-LaForce, C. (2014). VI. Earned-security in retrospect: Depressive symptoms, family stress, and maternal and paternal sensitivity from early childhood to mid-adolescence. Monographs of the Society for Research in Child Development, 79, 85-107. doi: 10.1111/mono.12115.

Roisman, G. I., Booth-LaForce, C. (2014). VIII. General discussion. Monographs of the Society for Research in Child Development, 79, 126-37. doi: 10.1111/mono.12117.

Steele, R. D., Waters, T. E., Bost, K. K., Vaughn, B. E., Truitt, W., Waters, H. S., Booth-LaForce, C., Roisman, G. I. (2014). Caregiving antecedents of secure base script knowledge: A comparative analysis of young adult attachment representations. Developmental Psychology, 50, 2526-2538. PMCID: PMC4562386. doi: 10.1037/a0037992.

Mark Bothwell Bothwell, M. (2014). NGF, BDNF, NT3, and NT4. Handbook of Experimental Pharmacology, 220, 3-15. doi: 10.1007/978-3-642-45106-5_1.

Wang, Y., Sakano, H., Beebe, K., Brown, M. R., de Laat, R., Bothwell, M., … Rubel, E. W. (2014). Intense and specialized dendritic localization of the fragile X mental retardation protein in binaural brainstem neurons: A comparative study in the alligator, chicken, gerbil, and human. The Journal of Comparative Neurology, 522, 2107-28. PMCID: PMC5564206. doi: 10.1002/cne.23520.

Eliot Brenowitz Larson, T. A., Thatra, N. M., Lee, B. H., Brenowitz, E. A. (2014). Reactive neurogenesis in response to naturally occurring apoptosis in an adult brain. The Journal of Neuroscience, 34, 13066-76. PMCID: PMC4172801. doi: 10.1523/JNEUROSCI.3316-13.2014.

William Catterall Catterall, W. A. (2014). Sodium channels, inherited epilepsy, and antiepileptic drugs. Annual Review of Pharmacology and Toxicology, 54, 317-38. doi: 10.1146/annurev-pharmtox-011112-140232.

Catterall, W. A. (2014). Structure and function of voltage-gated sodium channels at atomic resolution. Experimental Physiology, 99, 35-51. PMCID: PMC3885250. doi: 10.1113/expphysiol.2013.071969.

Christopoulos, A., Changeux, J. P., Catterall, W. A., Fabbro, D., Burris, T. P., Cidlowski, J. A., … Langmead, C. J. (2014). International union of basic and clinical pharmacology. XC. multisite pharmacology: Recommendations for the nomenclature of receptor allosterism and allosteric ligands. Pharmacological Reviews, 66, 918-47. doi: 10.1124/pr.114.008862.

Fu, Y., Westenbroek, R. E., Scheuer, T., Catterall, W. A. (2014). Basal and beta-adrenergic regulation of the cardiac calcium channel CaV1.2 requires phosphorylation of serine 1700. Proceedings of the National Academy of Sciences of the United States of America, 111, 16598-603. PMCID: PMC4246329. doi: 10.1073/pnas.1419129111.

Gamal El-Din, T. M., Scheuer, T., Catterall, W. A. (2014). Tracking S4 movement by gating pore currents in the bacterial sodium channel NaChBac. The Journal of General Physiology, 144, 147-57. PMCID: PMC4113903. doi: 10.1085/jgp.201411210.

Han, S., Tai, C., Jones, C. J., Scheuer, T., Catterall, W. A. (2014). Enhancement of inhibitory neurotransmission by GABAA receptors having alpha2, 3-subunits ameliorates behavioral deficits in a mouse model of autism. Neuron, 81, 1282-1289. PMCID: PMC4079471. doi: 10.1016/j.neuron.2014.01.016.

Murphy, J. G., Sanderson, J. L., Gorski, J. A., Scott, J. D., Catterall, W. A., Sather, W. A., Dell'Acqua, M. L. (2014). AKAP-anchored PKA maintains neuronal L-type calcium channel activity and NFAT transcriptional signaling. Cell Reports, 7, 1577-1588. PMCID: PMC4136445. doi: 10.1016/j.celrep.2014.04.027.

Shi, Y., Yang, G., Yu, J., Yu, L., Westenbroek, R., Catterall, W. A., … Yang, S. N. (2014). Apolipoprotein CIII hyperactivates beta cell CaV1 channels through SR-BI/beta1 integrin-dependent coactivation of PKA and Src. Cellular and Molecular Life Sciences, 71, 1289-303. PMCID: PMC3925466. doi: 10.1007/s00018-013-1442-x.

Tai, C., Abe, Y., Westenbroek, R. E., Scheuer, T., Catterall, W. A. (2014). Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome. Proceedings of the National Academy of Sciences of the United States of America, 111, E3139-48. PMCID: PMC4121787. doi: 10.1073/pnas.1411131111.

Jeffrey Chamberlain Banks, G. B., Combs, A. C., Odom, G. L., Bloch, R. J., Chamberlain, J. S. (2014). Muscle structure influences utrophin expression in mdx mice. PLoS Genetics, 10, e1004431. PMCID: PMC4055409. doi: 10.1371/journal.pgen.1004431.

Faber, R. M., Hall, J. K., Chamberlain, J. S., Banks, G. B. (2014). Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice. Skeletal Muscle, 4, 10. PMCID: PMC4047439. doi: 10.1186/2044-5040-4-10.

Pearson, T., Kabayo, T., Ng, R., Chamberlain, J. S., McArdle, A., Jackson, M. J. (2014). Skeletal muscle contractions induce acute changes in cytosolic superoxide, but slower responses in mitochondrial superoxide and cellular hydrogen peroxide. PLoS One, 9, e96378. PMCID: PMC4038480. doi: 10.1371/journal.pone.0096378.

Seto, J. T., Bengtsson, N. E., Chamberlain, J. S. (2014). Therapy of genetic disorders-novel therapies for Duchenne muscular dystrophy. Current Pediatrics Reports, 2, 102-112. PMCID: PMC4036820. doi: 10.1007/s40124-014-0044-x.

Swiderski, K., Shaffer, S. A., Gallis, B., Odom, G. L., Arnett, A. L., Scott Edgar, J., … Chamberlain, J. S. (2014). Phosphorylation within the cysteine-rich region of dystrophin enhances its association with beta-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting. Human Molecular Genetics, 23, 6697-711. PMCID: PMC4245040. doi: 10.1093/hmg/ddu388.

Dimitri Christakis

Christakis, D. A. (2014). Infants and interactive media use-reply. JAMA Pediatrics, 168, 969-70. doi: 10.1001/jamapediatrics.2014.748.

Christakis, D. A. (2014). Interactive media use at younger than the age of 2 years: Time to rethink the American Academy of Pediatrics guideline? JAMA Pediatrics, 168, 399-400. doi: 10.1001/jamapediatrics.2013.5081.

Jelenchick, L. A., Eickhoff, J., Christakis, D. A., Brown, R. L., Zhang, C., Benson, M., Moreno, M. A. (2014). The problematic and risky internet use screening scale (priuss) for adolescents and young adults: Scale development and refinement. Computers in Human Behavior, 35,171-178. PMCID: PMC4035908. doi: 10.1016/j.chb.2014.01.035.

McCormick, E., Kerns, S. E., McPhillips, H., Wright, J., Christakis, D. A., Rivara, F. P. (2014). Training pediatric residents to provide parent education: A randomized controlled trial. Academic Pediatrics, 14, 353-60. doi: 10.1016/j.acap.2014.03.009.

Radesky, J. S., Silverstein, M., Zuckerman, B., Christakis, D. A. (2014). Infant self-regulation and early childhood media exposure. Pediatrics, 133, e1172-8. PMCID: PMC4006432. doi: 10.1542/peds.2013-2367.

Truman Coggins Greenslade, K. J., Coggins, T. E. (2014). Assessing young children's intention-reading in authentic communicative contexts: Preliminary evidence and clinical utility. International Journal of Language & Communication Disorders, 49, 463-77. doi: 10.1111/1460-6984.12076.

Lucio Costa Cole, T. B., Li, W. F., Co, A. L., Hay, A. M., MacDonald, J. W., Bammler, T. K., … Costa, L. G., Furlong, C. E. (2014). Repeated gestational exposure of mice to chlorpyrifos oxon is associated with paraoxonase 1 (PON1) modulated effects in maternal and fetal tissues. Toxicological Sciences, 141, 409-22. PMCID: PMC4271046. doi: 10.1093/toxsci/kfu144.

Costa, L. G., de Laat, R., Dao, K., Pellacani, C., Cole, T. B., Furlong, C. E. (2014). Paraoxonase-2 (PON2) in brain and its potential role in neuroprotection. Neurotoxicology, 43, 3-9. PMCID: PMC3942372. doi: 10.1016/j.neuro.2013.08.011.

Costa, L. G., de Laat, R., Tagliaferri, S., Pellacani, C. (2014). A mechanistic view of polybrominated diphenyl ether (PBDE) developmental neurotoxicity. Toxicology Letters, 230, 282-94. PMCID: PMC4028440. doi: 10.1016/j.toxlet.2013.11.011.

Pellacani, C., Tagliaferri, S., Caglieri, A., Goldoni, M., Giordano, G., Mutti, A., Costa, L. G. (2014). Synergistic interactions between PBDEs and PCBs in human neuroblastoma cells. Environmental Toxicology, 29, 418-27. doi: 10.1002/tox.21768.

Roque, P. J., Guizzetti, M., Costa, L. G. (2014). Synaptic structure quantification in cultured neurons. Current Protocols in Toxicology, 60, 12 22 1-32. PMCID: PMC4318557. doi: 10.1002/0471140856.tx1222s60.

Zhou, C., Chen, J., Zhang, X., Costa, L. G., Guizzetti, M. (2014). Prenatal ethanol exposure up-regulates the cholesterol transporters ATP-binding cassette A1 and G1 and reduces cholesterol levels in the developing rat brain. Alcohol and Alcoholism, 49, 626-34. PMCID: PMC4834908. doi: 10.1093/alcalc/agu049.

Timothy Cox Cox, T. C., Camci, E. D., Vora, S., Luquetti, D. V., Turner, E. E. (2014). The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research. European Journal of Medical Genetics, 57, 394-401. PMCID: PMC4143470. doi: 10.1016/j.ejmg.2014.05.003.

Turner, E. E., Cox, T. C. (2014). Genetic evidence for conserved non-coding element function across species-the ears have it. Frontiers in Physiology, 5, 7. PMCID: PMC3896894. doi: 10.3389/fphys.2014.00007.

Wang, K. H., Heike, C. L., Clarkson, M. D., Mejino, J. L., Brinkley, J. F., Tse, R. W., … Cox, T. C. (2014). Evaluation and integration of disparate classification systems for clefts of the lip. Frontiers in Physiology, 5, 163. PMCID: PMC4030199. doi: 10.3389/fphys.2014.00163.

Michael Cunningham Corton, J. C., Cunningham, M. L., Hummer, B. T., Lau, C., Meek, B., Peters, J. M., … Klaunig, J. E. (2014). Mode of action framework analysis for receptor-mediated toxicity: The peroxisome proliferator-activated receptor alpha (PPARalpha) as a case study. Critical Reviews in Toxicology, 44, 1-49. doi: 10.3109/10408444.2013.835784.

Eisenberg, R. L., Cunningham, M. L., Siewert, B., Kruskal, J. B. (2014). Survey of faculty perceptions regarding a peer review system. Journal of the American College of Radiology: JACR, 11, 397-401. doi: 10.1016/j.jacr.2013.08.011.

Keppler-Noreuil, K. M., Sapp, J. C., Lindhurst, M. J., Parker, V. E., Blumhorst, C., Darling, T., … Cunningham, M. L., … Biesecker, L. G. (2014). Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. American Journal of Medical Genetics. Part A, 164, 1713-33. PMCID: PMC4320693. doi: 10.1002/ajmg.a.36552.

Kim, S. D., Yagnik, G., Cunningham, M. L., Kim, J., Boyadjiev, S. A. (2014). MAPK/ERK signaling pathway analysis in primary osteoblasts from patients with nonsyndromic sagittal craniosynostosis. The Cleft Palate-Craniofacial Journal, 51, 115-9. PMCID: PMC3708983. doi: 10.1597/12-136.

Lam, I., Cunningham, M. L., Speltz, M. L., Shapiro, L. (2014). Classifying craniosynostosis with a 3D projection-based feature extraction system. Proceedings / IEEE International Symposium on Computer-Based Medical Systems, 2014, 215-220. PMCID: PMC4205084. doi: 10.1109/CBMS.2014.63.

Smith, J. D., Hing, A. V., Clarke, C. M., Johnson, N. M., Perez, F. A., Park, S. S., … Cunningham, M. L. (2014). Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis. American Journal of Human Genetics, 95, 235-40. PMCID: PMC4129399. doi: 10.1016/j.ajhg.2014.07.008.

Raimondo D'Ambrosio Gupta, P. K., Sayed, N., Ding, K., Agostini, M. A., Van Ness, P. C., Yablon, S., … D'Ambrosio, R., Diaz-Arrastia, R. (2014). Subtypes of post-traumatic epilepsy: clinical, electrophysiological, and imaging features. Journal of Neurotrauma, 31, 1439-43. PMCID: PMC4132580. doi: 10.1089/neu.2013.3221.

Stephen Dager Lewis, J. D., Evans, A. C., Pruett, J. R., Botteron, K., Zwaigenbaum, L., Estes, A. M., … Dager, S. R., … Piven, J. (2014). Network inefficiencies in autism spectrum disorder at 24 months. Translational Psychiatry, 4, e388. PMCID: PMC4035719. doi: 10.1038/tp.2014.24.

Sureyya Dikmen Dikmen, S. S., Bauer, P. J., Weintraub, S., Mungas, D., Slotkin, J., Beaumont, J. L., … Heaton, R. K. (2014). Measuring episodic memory across the lifespan: NIH Toolbox Picture Sequence Memory Test. Journal of the International Neuropsychological Society, 20, 611-9. PMCID: PMC4254833. doi: 10.1017/S1355617714000460.

DiTommaso, C., Hoffman, J. M., Lucas, S., Dikmen, S. S., Temkin, N., Bell, K. R. (2014). Medication usage patterns for headache treatment after mild traumatic brain injury. Headache, 54, 511-9.

Hart, T., Benn, E. K., Bagiella, E., Arenth, P., Dikmen, S. S., Hesdorffer, D. C., … Zafonte, R. (2014). Early trajectory of psychiatric symptoms after traumatic brain injury: Relationship to patient and injury characteristics. Journal of Neurotrauma, 31, 610-7. PMCID: PMC3961785. doi: 10.1089/neu.2013.3041.

Mackelprang, J. L., Bombardier, C. H., Fann, J. R., Temkin, N. R., Barber, J. K., Dikmen, S. S. (2014). Rates and predictors of suicidal ideation during the first year after traumatic brain injury. American Journal of Public Health, 104, e100-7. PMCID: PMC4056207. doi: 10.2105/AJPH.2013.301794.

Christine Disteche Deng, X., Berletch, J. B., Nguyen, D. K., Disteche, C. M. (2014). X chromosome regulation: Diverse patterns in development, tissues and disease. Nature Reviews. Genetics, 15, 367-78. PMCID: PMC4117651. doi: 10.1038/nrg3687.

William B. Dobyns Cacciagli, P., Desvignes, J. P., Girard, N., Delepine, M., Zelenika, D., Lathrop, M., … Dobyns, W. B., Villard, L. (2014). AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). European Journal of Human Genetics, 22, 363-8. PMCID: PMC3925263. doi: 10.1038/ejhg.2013.135.

Cushion, T. D., Paciorkowski, A. R., Pilz, D. T., Mullins, J. G., Seltzer, L. E., Marion, R. W., … Dobyns, W. B. (2014). De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsy. American Journal of Human Genetics, 94, 634-41. PMCID: PMC3980418. doi: 10.1016/j.ajhg.2014.03.009.

French, C. R., Seshadri, S., Destefano, A. L., Fornage, M., Arnold, C. R., Gage, P. J., … Dobyns, W. B., Millen, K. J., … Lehmann, O. J. (2014). Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease. The Journal of Clinical Investigation, 124, 4877-81. PMCID: PMC4347243. doi: 10.1172/JCI75109.

Guerrini, R., Dobyns, W. B. (2014). Malformations of cortical development: Clinical features and genetic causes. The Lancet Neurology, 13, 710-26. PMCID: PMC5548104. doi: 10.1016/S1474-4422(14)70040-7.

Mirzaa, G. M., Millen, K. J., Barkovich, A. J., Dobyns, W. B., Paciorkowski, A. R. (2014). The Developmental Brain Disorders Database (DBDB): A curated neurogenetics knowledge base with clinical and research applications. American Journal of Medical Genetics. Part A, 164, 1503-11. PMCID: PMC4279915. doi: 10.1002/ajmg.a.36517.

Mirzaa, G. M., Vitre, B., Carpenter, G., Abramowicz, I., Gleeson, J. G., Paciorkowski, A. R., … Dobyns, W. B., O'Driscoll, M. (2014). Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism. Human Genetics, 133, 1023-39. PMCID: PMC4415612. doi: 10.1007/s00439-014-1443-3.

Mirzaa, G. M., Parry, D. A., Fry, A. E., Giamanco, K. A., Schwartzentruber, J., Vanstone, M., … Hevner, R. F., … Dobyns, W. B., Sheridan, E. G. (2014). De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. Nature Genetics, 46, 510-515. PMCID: PMC4004933. doi: 10.1038/ng.2948.

Mirzaa, G. M., Enyedi, L., Parsons, G., Collins, S., Medne, L., Adams, C., … Dobyns, W. B., Christian, S. (2014). Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: Five novel mutations and review of the literature. American Journal of Medical Genetics. Part A, 164, 2879-86. PMCID: PMC4205200. doi: 10.1002/ajmg.a.36707.

Paciorkowski, A. R., Weisenberg, J., Kelley, J. B., Spencer, A., Tuttle, E., Ghoneim, D., … Dobyns, W. B., Paschal, B. M. (2014). Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation. European Journal of Human Genetics, 22, 587-93. PMCID: PMC3992559. doi: 10.1038/ejhg.2013.196.

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Elaine Faustman Smith, M. N., Griffith, W. C., Beresford, S. A., Vredevoogd, M., Vigoren, E. M., Faustman, E. M. (2014). Using a biokinetic model to quantify and optimize cortisol measurements for acute and chronic environmental stress exposure during pregnancy. Journal of Exposure Science and Environmental Epidemiology, 24, 510-6. doi: 10.1038/jes.2013.86.

Thompson, B., Griffith, W. C., Barr, D. B., Coronado, G. D., Vigoren, E. M., Faustman, E. M. (2014). Variability in the take-home pathway: Farmworkers and non-farmworkers and their children. Journal of Exposure Science and Environmental Epidemiology, 24, 522-31. PMCID: PMC4141015. doi: 10.1038/jes.2014.12.

Clement Furlong Cole, T. B., Li, W. F., Co, A. L., Hay, A. M., MacDonald, J. W., Bammler, T. K., … Costa, L. G., Furlong, C. E. (2014). Repeated gestational exposure of mice to chlorpyrifos oxon is associated with paraoxonase 1 (PON1) modulated effects in maternal and fetal tissues. Toxicological Sciences, 141, 409-22. PMCID: PMC4271046. doi: 10.1093/toxsci/kfu144.

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Gwenn Garden Cortes, C. J., Miranda, H. C., Frankowski, H., Batlevi, Y., Young, J. E., Le, A., … Garden, G. A., La Spada, A. R. (2014). Polyglutamine-expanded androgen receptor interferes with TFEB to elicit autophagy defects in SBMA. Nature Neuroscience, 17, 1180-9. PMCID: PMC4180729. doi: 10.1038/nn.3787.

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Adam Geballe

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Ian Glass Miller, J. A., Ding, S. L., Sunkin, S. M., Smith, K. A., Ng, L., Szafer, A., … Glass, I. A., … Hevner, R. F., … Lein, E. S. (2014). Transcriptional landscape of the prenatal human brain. Nature, 508, 199-206. PMCID: PMC4105188. doi: 10.1038/nature13185.

Sidney Gospe, Jr. Beatty, C. W., Ko, P. R., Nixon, J., Gospe, S. M., Jr. (2014). Delayed-onset movement disorder and encephalopathy after oxycodone ingestion. Seminars in Pediatric Neurology, 21, 160-5. doi: 10.1016/j.spen.2014.06.009.

Friedman, S. D., Ishak, G. E., Poliachik, S. L., Poliakov, A. V., Otto, R. K., Shaw, D. W. W., … Gospe, S. M., Jr. (2014). Callosal alterations in pyridoxine-dependent epilepsy. Developmental Medicine and Child Neurology, 56, 1106-10. doi: 10.1111/dmcn.12511.

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Joan M. Goverman

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Madhyastha, T. M., Grabowski, T. J. (2014). Age-related differences in the dynamic architecture of intrinsic networks. Brain Connectivity, 4, 231-41. PMCID: PMC4028165. doi: 10.1089/brain.2013.0205.

Smith, M. M., Weaver, K. E., Grabowski, T. J., Rao, R. P., Darvas, F. (2014). Non-invasive detection of high gamma band activity during motor imagery. Frontiers in Human Neuroscience, 8, 817. PMCID: PMC4199322. doi: 10.3389/fnhum.2014.00817.

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Kahoud, R. J., Elsen, G. E., Hevner, R. F., Hodge, R. D. (2014). Conditional ablation of Tbr2 results in abnormal development of the olfactory bulbs and subventricular zone-rostral migratory stream. Developmental Dynamics, 243, 440-50. PMCID: PMC3992892. doi: 10.1002/dvdy.24090.

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Anne Hing Smith, J. D., Hing, A. V., Clarke, C. M., Johnson, N. M., Perez, F. A., Park, S. S., … Cunningham, M. L. (2014). Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis. American Journal of Human Genetics, 95, 235-40. PMCID: PMC4129399. doi: 10.1016/j.ajhg.2014.07.008.

Rodney Ho Duan, J., Freeling, J. P., Koehn, J., Shu, C., Ho, R. J. (2014). Evaluation of atazanavir and darunavir interactions with lipids for developing pH-responsive anti-HIV drug combination nanoparticles. Journal of Pharmaceutical Sciences, 103, 2520-9. PMCID: PMC4349556. doi: 10.1002/jps.24046.

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Kraft, J. C., Freeling, J. P., Wang, Z., Ho, R. J. (2014). Emerging research and clinical development trends of liposome and lipid nanoparticle drug delivery systems. Journal of Pharmaceutical Sciences, 103, 29-52. PMCID: PMC4074410. doi: 10.1002/jps.23773.

Philip Horner Mondello, S. E., Kasten, M. R., Horner, P. J., Moritz, C. T. (2014). Therapeutic intraspinal stimulation to generate activity and promote long-term recovery. Frontiers in Neuroscience, 8, 21. PMCID: PMC3936503. doi: 10.3389/fnins.2014.00021.

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Roxanne Hudson Fleury, V. P., Miramontez, S. H., Hudson, R. F., Schwartz, I. S. (2014). Promoting active participation in book reading for preschoolers with Autism Spectrum Disorder: A preliminary study. Child Language Teaching and Therapy, 30, 273-288. doi: 10.1177/0265659013514069.

Colleen Huebner Campanaro, M., Huebner, C. E., Davis, B. E. (2014). Facilitators and barriers to twice daily tooth brushing among children with special health care needs. Special Care in Dentistry, 34, 185-92. PMCID: PMC4495036. doi: 10.1111/scd.12057.

Melbye, M. L., Chi, D. L., Milgrom, P., Huebner, C. E., Grembowski, D. (2014). Washington state foster care: Dental utilization and expenditures. Journal of Public Health Dentistry, 74, 93-101. doi: 10.1111/jphd.12027.

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Suman Jayadev Su, W., Hopkins, S., Nesser, N. K., Sopher, B., Silvestroni, A., Ammanuel, S., Jayadev, S., … Weinstein, J. R., Garden, G. A. (2014). The p53 transcription factor modulates microglia behavior through microRNA-dependent regulation of c-Maf. Journal of Immunology, 192, 358-66. PMCID: PMC4195583. doi: 10.4049/jimmunol.1301397.

Sandra Juul Galinsky, R., Bennet, L., Groenendaal, F., Lear, C. A., Tan, S., van Bel, F., Juul, S. E., … Gunn, A. J. (2014). Magnesium is not consistently neuroprotective for perinatal hypoxia-ischemia in term-equivalent models in preclinical studies: A systematic review. Developmental Neuroscience, 36, 73-82. doi: 10.1159/000362206.

Rangarajan, V., Juul, S. E. (2014). Erythropoietin: Emerging role of erythropoietin in neonatal neuroprotection. Pediatric Neurology, 51, 481-8. PMCID: PMC4180944. doi: 10.1016/j.pediatrneurol.2014.06.008.

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Schober, M. E., Requena, D. F., Block, B., Davis, L. J., Rodesch, C., Casper, T. C., Juul, S. E., … Lane, R. H. (2014). Erythropoietin improved cognitive function and decreased hippocampal caspase activity in rat pups after traumatic brain injury. Journal of Neurotrauma, 31, 358-69. PMCID: PMC3922399. doi: 10.1089/neu.2013.2922.

David Kimelman Bouldin, C. M., Kimelman, D. (2014). Dual fucci: A new transgenic line for studying the cell cycle from embryos to adults. Zebrafish, 11, 182-3. PMCID: PMC4518878. doi: 10.1089/zeb.2014.0986.

Bouldin, C. M., Kimelman, D. (2014). Cdc25 and the importance of G2 control: Insights from developmental biology. Cell Cycle, 13, 2165-71. PMCID: PMC4111672. doi: 10.4161/cc.29537.

Suli, A., Guler, A. D., Raible, D. W., Kimelman, D. (2014). A targeted gene expression system using the tryptophan repressor in zebrafish shows no silencing in subsequent generations. Development, 141, 1167-74. PMCID: PMC3929415. doi: 10.1242/dev.100057.

Bryan King Erickson, C. A., Veenstra-Vanderweele, J. M., Melmed, R. D., McCracken, J. T., Ginsberg, L. D., Sikich, L., … King, B. H. (2014). STX209 (arbaclofen) for autism spectrum disorders: An 8-week open-label study. Journal of Autism and Developmental Disorders, 44, 958-64. doi: 10.1007/s10803-013-1963-z.

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King, B. H. (2014). Sunsetting DSM-IV's pervasive developmental disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 53, 494-6. doi: 10.1016/j.jaac.2014.01.013.

King, B. H., de Lacy, N., Siegel, M. (2014). Psychiatric assessment of severe presentations in autism spectrum disorders and intellectual disability. Child and Adolescent Psychiatric Clinics of North America, 23, 1-14. doi: 10.1016/j.chc.2013.07.001.

Lecavalier, L., Wood, J. J., Halladay, A. K., Jones, N. E., Aman, M. G., Cook, E. H., … King, B. H., … Scahill, L. (2014). Measuring anxiety as a treatment endpoint in youth with autism spectrum disorder. Journal of Autism and Developmental Disorders, 44, 1128-43. PMCID: PMC3981870. doi: 10.1007/s10803-013-1974-9.

Marrus, N., Veenstra-Vanderweele, J., Hellings, J. A., Stigler, K. A., Szymanski, L., King, B. H., … Pruett, J. R., Jr. (2014). Training of child and adolescent psychiatry fellows in autism and intellectual disability. Autism, 18, 471-5. PMCID: PMC5506488. doi: 10.1177/1362361313477247.

McClintic, A. M., King, B. H., Webb, S. J., Mourad, P. D. (2014). Mice exposed to diagnostic ultrasound in utero are less social and more active in social situations relative to controls. Autism Research, 7, 295-304. PMCID: PMC4025980. doi: 10.1002/aur.1349.

Siegel, M., King, B. H. (2014). Autism and developmental disorders: Management of serious behavioral disturbance. Child and Adolescent Psychiatric Clinics of North America, 23, xiii-xv. doi: 10.1016/j.chc.2013.08.007.

Patricia Kuhl Kuhl, P. K., Ramirez, R. R., Bosseler, A., Lin, J. F., Imada, T. (2014). Infants' brain responses to speech suggest analysis by synthesis. Proceedings of the National Academy of Sciences of the United States of America, 111, 11238-45. PMCID: PMC4128155. doi: 10.1073/pnas.1410963111.

Ramirez-Esparza, N., Garcia-Sierra, A., Kuhl, P. K. (2014). Look who's talking: Speech style and social context in language input to infants are linked to concurrent and future speech development. Developmental Science, 17, 880-91. PMCID: PMC4188803. doi: 10.1111/desc.12172.

Donghoon Lee Wang, Z., Halbert, C. L., Lee, D., Butts, T., Tapscott, S. J., Storb, R., Miller, A. D. (2014). Elimination of contaminating cap genes in AAV vector virions reduces immune responses and improves transgene expression in a canine gene therapy model. Gene Therapy, 21, 363-70. PMCID: PMC3976967. doi: 10.1038/gt.2014.4.

Heather Mefford Bernier, R. A., Golzio, C., Xiong, B., Stessman, H. A., Coe, B. P., Penn, O., … Mefford, H. C., … Eichler, E. E. (2014). Disruptive CHD8 mutations define a subtype of autism early in development. Cell, 158, 263-276. PMCID: PMC4136921. doi: 10.1016/j.cell.2014.06.017.

Carvill, G. L., Weckhuysen, S., McMahon, J. M., Hartmann, C., Moller, R. S., Hjalgrim, H., … Mefford, H. C. (2014). GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome. Neurology, 82, 1245-53. PMCID: PMC4001207. doi: 10.1212/WNL.0000000000000291.

Jahn, J. A., von Spiczak, S., Muhle, H., Obermeier, T., Franke, A., Mefford, H. C., … Helbig, I. (2014). Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies. Epilepsy Research, 108, 109-16. doi: 10.1016/j.eplepsyres.2013.10.001.

Mefford, H. C. (2014). CNVs in Epilepsy. Current Genetic Medicine Reports, 2, 162-167. PMCID: PMC4129225. doi: 10.1007/s40142-014-0046-6.

Mefford, H. C. (2014). Thinking about cognition and epilepsy. Epilepsy & Behavior, 41, 276. doi: 10.1016/j.yebeh.2014.09.007.

Michaud, J. L., Lachance, M., Hamdan, F. F., Carmant, L., Lortie, A., Diadori, P., … Mefford, H. C., … Rossignol, E. (2014). The genetic landscape of infantile spasms. Human Molecular Genetics, 23, 4846-58. doi: 10.1093/hmg/ddu199.

Reinthaler, E. M., Lal, D., Lebon, S., Hildebrand, M. S., Dahl, H. H., Regan, B. M., … Mefford, H. C., … Neubauer, B. A. (2014). 16p11.2 600 kb duplications confer risk for typical and atypical Rolandic epilepsy. Human Molecular Genetics, 23, 6069-80. doi: 10.1093/hmg/ddu306.

Scheffer, I. E., Mefford, H. C. (2014). Epilepsy: Beyond the single nucleotide variant in epilepsy genetics. Nature Reviews Neurology, 10, 490-1. doi: 10.1038/nrneurol.2014.146.

Watson, C. T., Marques-Bonet, T., Sharp, A. J., Mefford, H. C. (2014). The genetics of microdeletion and microduplication syndromes: An update. Annual Review of Genomics and Human Genetics, 15, 215-244. PMCID: PMC4476258. doi: 10.1146/annurev-genom-091212-153408.

Andrew Meltzoff Harms, M. B., Zayas, V., Meltzoff, A. N., Carlson, S. M. (2014). Stability of executive function and predictions to adaptive behavior from middle childhood to pre-adolescence. Frontiers in Psychology, 5, 331. PMCID: PMC4001056. doi: 10.3389/fpsyg.2014.00331.

Marshall, P. J., Meltzoff, A. N. (2014). Neural mirroring mechanisms and imitation in human infants. Philosophical Transactions of the Royal Society of London, B, Biological Sciences, 369, 20130620. PMCID: PMC4006193. doi: 10.1098/rstb.2013.0620.

Taylor, A. H., Cheke, L. G., Waismeyer, A., Meltzoff, A. N., Miller, R., Gopnik, A., … Gray, R. D. (2014). Of babies and birds: Complex tool behaviours are not sufficient for the evolution of the ability to create a novel causal intervention. Proceedings of the Royal Society B: Biological Sciences, 281, 20140837. PMCID: PMC4071556. doi: 10.1098/rspb.2014.0837.

Kathleen J. Millen

Chervenak, A. P., Bank, L. M., Thomsen, N., Glanville-Jones, H. C., Jonathan, S., Millen, K. J., … Barald, K. F. (2014). The role of Zic genes in inner ear development in the mouse: Exploring mutant mouse phenotypes. Developmental Dynamics, 243, 1487-98. PMCID: PMC4206579. doi: 10.1002/dvdy.24186.

Millen, K. J., Steshina, E. Y., Iskusnykh, I. Y., Chizhikov, V. V. (2014). Transformation of the cerebellum into more ventral brainstem fates causes cerebellar agenesis in the absence of Ptf1a function. Proceedings of the National Academy of Sciences of the United States of America, 111, E1777-86. PMCID: PMC4035921. doi: 10.1073/pnas.1315024111.

Cecilia B. Moens Blasky, A. J., Pan, L., Moens, C. B., Appel, B. (2014). Pard3 regulates contact between neural crest cells and the timing of Schwann cell differentiation but is not essential for neural crest migration or myelination. Developmental Dynamics, 243, 1511-23. PMCID: PMC4237626. doi: 10.1002/dvdy.24172.

DeLaurier, A., Huycke, T. R., Nichols, J. T., Swartz, M. E., Larsen, A., Walker, C., … Moens, C. B., Kimmel, C. B. (2014). Role of mef2ca in developmental buffering of the zebrafish larval hyoid dermal skeleton. Developmental Biology, 385, 189-99. PMCID: PMC3892954. doi: 10.1016/j.ydbio.2013.11.016.

Martiny, D., Bart, A., Vandenberg, O., Verhaar, N., Wentink-Bonnema, E., Moens, C. B., van Gool, T. (2014). Subtype determination of Blastocystis isolates by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS). European Journal of Clinical Microbiology & Infectious Diseases, 33, 529-36. doi: 10.1007/s10096-013-1980-z.

Quillien, A., Moore, J. C., Shin, M., Siekmann, A. F., Smith, T., Pan, L., Moens, C. B., … Lawson, N. D. (2014). Distinct Notch signaling outputs pattern the developing arterial system. Development, 141, 1544-52. PMCID: PMC4074308. doi: 10.1242/dev.099986.

Su, C. Y., Kemp, H. A., Moens, C. B. (2014). Cerebellar development in the absence of Gbx function in zebrafish. Developmental Biology, 386, 181-90. PMCID: PMC3935510. doi: 10.1016/j.ydbio.2013.10.026.

Wang, Y., Pan, L., Moens, C. B., Appel, B. (2014). Notch3 establishes brain vascular integrity by regulating pericyte number. Development, 141, 307-17. PMCID: PMC3879812. doi: 10.1242/dev.096107.

Zigman, M., Laumann-Lipp, N., Titus, T., Postlethwait, J., Moens, C. B. (2014). Hoxb1b controls oriented cell division, cell shape and microtubule dynamics in neural tube morphogenesis. Development, 141, 639-49. PMCID: PMC3899817. doi: 10.1242/dev.098731.

David Morris

Saraf, A., Luo, J., Morris, D. R., Storm, D. R. (2014). Phosphorylation of eukaryotic translation initiation factor 4E and eukaryotic translation initiation factor 4E-binding protein (4EBP) and their upstream signaling components undergo diurnal oscillation in the mouse hippocampus: Implications for memory persistence. The Journal of Biological Chemistry, 289, 20129-38. PMCID: PMC4106328. doi: 10.1074/jbc.M114.552638.

Richard Morrison Murphy, S. P., Lee, R. J., McClean, M. E., Pemberton, H. E., Uo, T., Morrison, R. S., … Baltan, S. (2014). MS-275, a class I histone deacetylase inhibitor, protects the p53-deficient mouse against ischemic injury. Journal of Neurochemistry, 129, 509-15. doi: 10.1111/jnc.12498.

Pierre D. Mourad Levitt, M. R., McGah, P. M., Aliseda, A., Mourad, P. D., Nerva, J. D., Vaidya, S. S., … Kim, L. J. (2014). Cerebral aneurysms treated with flow-diverting stents: Computational models with intravascular blood flow measurements. American Journal of Neuroradiology, 35, 143-8. PMCID: PMC3858573. doi: 10.3174/ajnr.A3624.

Mehic, E., Xu, J. M., Caler, C. J., Coulson, N. K., Moritz, C. T., Mourad, P. D. (2014). Increased anatomical specificity of neuromodulation via modulated focused ultrasound. PLoS One, 9, e86939. PMCID: PMC3913583. doi: 10.1371/journal.pone.0086939.

Xu, Z. S., Yao, A., Chu, S. S., Paun, M. K., McClintic, A. M., Murphy, S. P., Mourad, P. D. (2014). Detection of mild traumatic brain injury in rodent models using shear wave elastography: Preliminary studies. Journal of Ultrasound in Medicine, 33, 1763-71. doi: 10.7863/ultra.33.10.1763.

Sean Murphy Murphy, S. P., Lee, R. J., McClean, M. E., Pemberton, H. E., Uo, T., Morrison, R. S., … Baltan, S. (2014). MS-275, a class I histone deacetylase inhibitor, protects the p53-deficient mouse against ischemic injury. Journal of Neurochemistry, 129, 509-15. doi: 10.1111/jnc.12498.

Michael Mustari Walton, M., Mustari, M. J., Willoughby, C. L., McLoon, L. K. (2014). Abnormal activity of neurons in abducens nucleus of strabismic monkeys. Investigative Ophthalmology & Visual Science, 56, 10-9. PMCID: PMC4283474. doi: 10.1167/iovs.14-15360.

Walton, M. M., Ono, S., Mustari, M. J. (2014). Vertical and oblique saccade disconjugacy in strabismus. Investigative Ophthalmology & Visual Science, 55, 275-90. PMCID: PMC3891270. doi: 10.1167/iovs.13-13473.

Jeffrey Ojemann Blakely, T., Ojemann, J. G., Rao, R. P. (2014). Short-time windowed covariance: A metric for identifying non-stationary, event-related covariant cortical sites. Journal of Neuroscience Methods, 222, 24-33. PMCID: PMC3951335. doi: 10.1016/j.jneumeth.2013.10.005.

Loring, D. W., Gaillard, W. D., Bookheimer, S. Y., Meador, K. J., Ojemann, J. G. (2014). Cortical cartography reveals political and physical maps. Epilepsia, 55, 633-7. PMCID: PMC4197796. doi: 10.1111/epi.12553.

Miller, K. J., Honey, C. J., Hermes, D., Rao, R. P., denNijs, M., Ojemann, J. G. (2014). Broadband changes in the cortical surface potential track activation of functionally diverse neuronal populations. Neuroimage, 85, 711-20. PMCID: PMC4347924. doi: 10.1016/j.neuroimage.2013.08.070.

Monica Oxford Spieker, S. J., Oxford, M. L., Fleming, C. B. (2014). Permanency outcomes for toddlers in child welfare two years after a randomized trial of a parenting intervention. Children and Youth Services Review, 44, 201-206. PMCID: PMC4128499. doi: 10.1016/j.childyouth.2014.06.017.

Leo Pallanck Burman, J. L., Itsara, L. S., Kayser, E. B., Suthammarak, W., Wang, A. M., Kaeberlein, M., … Pallanck, L. J. (2014). A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer. Disease Models & Mechanisms, 7, 1165-74. PMCID: PMC4174527. doi: 10.1242/dmm.015321.

Itsara, L. S., Kennedy, S. R., Fox, E. J., Yu, S., Hewitt, J. J., Sanchez-Contreras, M., … Pallanck, L. J. (2014). Oxidative stress is not a major contributor to somatic mitochondrial DNA mutations. PLoS Genetics, 10, e1003974. PMCID: PMC3916223. doi: 10.1371/journal.pgen.1003974.

Thomas, R. E., Andrews, L. A., Burman, J. L., Lin, W. Y., Pallanck, L. J. (2014). PINK1-Parkin pathway activity is regulated by degradation of PINK1 in the mitochondrial matrix. PLoS Genetics, 10, e1004279. PMCID: PMC4038460. doi: 10.1371/journal.pgen.1004279.

Jay Parrish Jiang, N., Soba, P., Parker, E., Kim, C. C., Parrish, J. Z. (2014). The microRNA bantam regulates a developmental transition in epithelial cells that restricts sensory dendrite growth. Development, 141, 2657-68. PMCID: PMC4067962. doi: 10.1242/dev.107573.

David J. Perkel Portfors, C. V., Perkel, D. J. (2014). The role of ultrasonic vocalizations in mouse communication. Current Opinion in Neurobiology, 28, 115-20. PMCID: PMC4177333. doi: 10.1016/j.conb.2014.07.002.

James Phillips

Golub, J. S., Ling, L., Nie, K., Nowack, A., Shepherd, S. J., Bierer, S. M., … Phillips, J. O., Rubinstein, J. T. (2014). Prosthetic implantation of the human vestibular system. Otology & Neurotology, 35, 136-47. PMCID: PMC4369342. doi: 10.1097/MAO.0000000000000003.

Nicholas Poolos Poolos, N. P. (2014). Stopping epileptogenesis dead in its tracks. Epilepsy Currents, 14, 163-4. PMCID: PMC4038288. doi: 10.5698/1535-7597-14.3.163.

Bensheng Qiu Long, Q., Fan, C., Kai, W., Luo, Q., Xin, W., Wang, P., … Qiu, B., Liu, W. (2014). Hypoxia inducible factor-1alpha expression is associated with hippocampal apoptosis during epileptogenesis. Brain Research, 1590, 20-30. doi: 10.1016/j.brainres.2014.09.028.

Jan-Marino (Nino) Ramirez Czech-Damal, N. U., Geiseler, S. J., Hoff, M. L., Schliep, R., Ramirez, J. M., Folkow, L. P., Burmester, T. (2014). The role of glycogen, glucose and lactate in neuronal activity during hypoxia in the hooded seal (Cystophora cristata) brain. Neuroscience, 275, 374-83. doi: 10.1016/j.neuroscience.2014.06.024.

Raghuraman, S., Garcia, A. J., Anderson, T. M., Twede, V. D., Curtice, K. J., Chase, K., Ramirez, J. M., … Teichert, R. W. (2014). Defining modulatory inputs into CNS neuronal subclasses by functional pharmacological profiling. Proceedings of the National Academy of Sciences of the United States of America, 111, 6449-54. PMCID: PMC4035978. doi: 10.1073/pnas.1404421111.

Zanella, S., Doi, A., Garcia, A. J., 3rd, Elsen, F., Kirsch, S., Wei, A. D., Ramirez, J. M. (2014). When norepinephrine becomes a driver of breathing irregularities: How intermittent hypoxia fundamentally alters the modulatory response of the respiratory network. The Journal of Neuroscience, 34, 36-50. PMCID: PMC3866492. doi: 10.1523/JNEUROSCI.3644-12.2014.

Bruce Ransom Hansen, D. B., Ye, Z. C., Calloe, K., Braunstein, T. H., Hofgaard, J. P., Ransom, B. R., … MacAulay, N. (2014). Activation, permeability, and inhibition of astrocytic and neuronal large pore (hemi)channels. The Journal of Biological Chemistry, 289, 26058-73. PMCID: PMC4176216. doi: 10.1074/jbc.M114.582155.

Yang, X., Hamner, M. A., Brown, A. M., Evans, R. D., Ye, Z. C., Chen, S., Ransom, B. R. (2014). Novel hypoglycemic injury mechanism: N-methyl-D-aspartate receptor-mediated white matter damage. Annals of Neurology, 75, 492-507. doi: 10.1002/ana.24050.

Wendy Raskind Chen, Y. Z., Friedman, J. R., Chen, D. H., Chan, G. C., Bloss, C. S., Hisama, F. M., … Raskind, W. H., Torkamani, A. (2014). Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia. Annals of Neurology, 75, 542-9. PMCID: PMC4457323. doi: 10.1002/ana.24119.

Thomas A. Reh Hyde, D. R., Reh, T. A. (2014). The past, present, and future of retinal regeneration. Experimental Eye Research, 123, 105-6. doi: 10.1016/j.exer.2014.03.003.

Stergachis, A. B., Neph, S., Sandstrom, R., Haugen, E., Reynolds, A. P., Zhang, M., … Hansen, R. S., … Reh, T. A., … Stamatoyannopoulos, J. A. (2014). Conservation of trans-acting circuitry during mammalian regulatory evolution. Nature, 515, 365-70. PMCID: PMC4405208. doi: 10.1038/nature13972.

Todd Richards

Robert Rostomily Baldock, A. L., Ahn, S., Rockne, R., Johnston, S., Neal, M., Corwin, D., … Rostomily, R. C., … Swanson, K. R. (2014). Patient-specific metrics of invasiveness reveal significant prognostic benefit of resection in a predictable subset of gliomas. PLoS One, 9, e99057. PMCID: PMC4211670. doi: 10.1371/journal.pone.0099057.

Edwin Rubel Cox, B. C., Chai, R., Lenoir, A., Liu, Z., Zhang, L., Nguyen, D. H., … Rubel, E. W., … Zuo, J. (2014). Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo. Development, 141, 816-29. PMCID: PMC3912828. doi: 10.1242/dev.103036.

Esterberg, R., Hailey, D. W., Rubel, E. W., Raible, D. W. (2014). ER-mitochondrial calcium flow underlies vulnerability of mechanosensory hair cells to damage. The Journal of Neuroscience, 34, 9703-19. PMCID: PMC4099547. doi: 10.1523/JNEUROSCI.0281-14.2014.

Seidl, A. H., Rubel, E. W., Barria, A. (2014). Differential conduction velocity regulation in ipsilateral and contralateral collaterals innervating brainstem coincidence detector neurons. The Journal of Neuroscience, 34, 4914-9. PMCID: PMC3972718. doi: 10.1523/JNEUROSCI.5460-13.2014.

Stawicki, T. M., Owens, K. N., Linbo, T., Reinhart, K. E., Rubel, E. W., Raible, D. W. (2014). The zebrafish merovingian mutant reveals a role for pH regulation in hair cell toxicity and function. Disease Models & Mechanisms, 7, 847-56. PMCID: PMC4073274. doi: 10.1242/dmm.016576.

Craig Rubens Rubens, C. E., Sadovsky, Y., Muglia, L., Gravett, M. G., Lackritz, E., Gravett, C. (2014). Prevention of preterm birth: Harnessing science to address the global epidemic. Science Translational Medicine, 6, 262sr5. doi: 10.1126/scitranslmed.3009871.

Jay Rubinstein Golub, J. S., Ling, L., Nie, K., Nowack, A., Shepherd, S. J., Bierer, S. M., … Phillips, J. O., Rubinstein, J. T. (2014). Prosthetic implantation of the human vestibular system. Otology & Neurotology, 35, 136-47. PMCID: PMC4369342. doi: 10.1097/MAO.0000000000000003.

Hannele Ruohola-Baker Mathieu, J., Zhou, W., Xing, Y., Sperber, H., Ferreccio, A., Agoston, Z., … Ruohola-Baker, H. (2014). Hypoxia-inducible factors have distinct and stage-specific roles during reprogramming of human cells to pluripotency. Cell Stem Cell, 14, 592-605. PMCID: PMC4028142. doi: 10.1016/j.stem.2014.02.012.

Ware, C. B., Nelson, A. M., Mecham, B., Hesson, J., Zhou, W., Jonlin, E. C., … Ruohola-Baker, H. (2014). Derivation of naive human embryonic stem cells. Proceedings of the National Academy of Sciences of the United States of America, 111, 4484-9. PMCID: PMC3970494. doi: 10.1073/pnas.1319738111.

Ilene Schwartz Fleury, V. P., Miramontez, S. H., Hudson, R. F., Schwartz, I. S. (2014). Promoting active participation in book reading for preschoolers with autism spectrum disorder: A preliminary study. Child Language Teaching and Therapy, 30, 273-288. doi: 10.1177/0265659013514069.

C. Ronald Scott Barcenas, M., Suhr, T. R., Scott, C. R., Turecek, F., Gelb, M. H. (2014). Quantification of sulfatides in dried blood and urine spots from metachromatic leukodystrophy patients by liquid chromatography/electrospray tandem mass spectrometry. Clinica Chimica Acta, 433, 39-43. PMCID: PMC4039571. doi: 10.1016/j.cca.2013.12.016.

Barcenas, M., Xue, C., Marushchak-Vlaskin, T, Scott, C. R., Gelb, M. H., Turecek, F. (2014). Tandem mass spectrometry assays of palmitoyl protein thioesterase 1 and tripeptidyl peptidase activity in dried blood spots for the detection of neuronal ceroid lipofuscinoses in newborns. Analytical Chemistry, 86, 7962-7968. doi: 10.1021/ac501994b.

Chennamaneni, N. K., Kumar, A. B., Barcenas, M., Spacil, Z., Scott, C. R., Turecek, F., Gelb, M. H. (2014). Improved reagents for newborn screening of mucopolysaccharidosis types I, II, and VI by tandem mass spectrometry. Analytical Chemistry, 86, 4508-14. PMCID: PMC4014144. doi: 10.1021/ac5004135.

Dennis Shaw Friedman, S. D., Ishak, G. E., Poliachik, S. L., Poliakov, A. V., Otto, R. K., Shaw, D. W. W., … Gospe, S. M., Jr. (2014). Callosal alterations in pyridoxine-dependent epilepsy. Developmental Medicine and Child Neurology, 56, 1106-10. doi: 10.1111/dmcn.12511.

Tawil, R., Shaw, D. W. W., van der Maarel, S. M., Tapscott, S. J. (2014). Clinical trial preparedness in facioscapulohumeral dystrophy: Outcome measures and patient access: 8-9 April 2013, Leiden, The Netherlands. Neuromuscular Disorders, 24, 79-85. doi: 10.1016/j.nmd.2013.07.009.

Matthew Speltz Collett, B. R., Wehby, G. L., Barron, S., Romitti, P. A., Ansley, T. N., Speltz, M. L. (2014). Academic achievement in children with oral clefts versus unaffected siblings. Journal of Pediatric Psychology, 39, 743-51. PMCID: PMC4107579. doi: 10.1093/jpepsy/jsu049.

Wehby, G. L., Collet, B., Barron, S., Romitti, P. A., Ansley, T. N., Speltz, M. L. (2014). Academic achievement of children and adolescents with oral clefts. Pediatrics, 133, 785-92. PMCID: PMC4006437. doi: 10.1542/peds.2013-3072.

Susan Spieker Cyr, M., Pasalich, D. S., McMahon, R. J., Spieker, S. J. (2014). The longitudinal link between parenting and child aggression: The moderating effect of attachment security. Child Psychiatry and Human Development, 45, 555-64. doi: 10.1007/s10578-013-0424-4.

Spieker, S. J., Oxford, M. L., Fleming, C. B. (2014). Permanency outcomes for toddlers in child welfare two years after a randomized trial of a parenting intervention. Children and Youth Services Review, 44, 201-206. PMCID: PMC4128499. doi: 10.1016/j.childyouth.2014.06.017.

Thomas, K. A., Burr, R. L., Spieker, S. J., Lee, J., Chen, J. (2014). Mother-infant circadian rhythm: Development of individual patterns and dyadic synchrony. Early Human Development, 90, 885-90. PMCID: PMC4312214. doi: 10.1016/j.earlhumdev.2014.09.005.

Mark Stein Santisteban, J. A., Stein, M. A., Bergmame, L., Gruber, R. (2014). Effect of extended-release dexmethylphenidate and mixed amphetamine salts on sleep: A double-blind, randomized, crossover study in youth with attention-deficit hyperactivity disorder. CNS Drugs, 28, 825-33. PMCID: PMC4362706. doi: 10.1007/s40263-014-0181-3.

Stein, M. A., Waldman, I., Newcorn, J., Bishop, J., Kittles, R., Cook, E. H., Jr. (2014). Dopamine transporter genotype and stimulant dose-response in youth with attention-deficit/hyperactivity disorder. Journal of Child and Adolescent Psychopharmacology, 24, 238-44. PMCID: PMC4064733. doi: 10.1089/cap.2013.0102.

Nephi Stella Cherry, A. E., Stella, N. (2014). G protein-coupled receptors as oncogenic signals in glioma: Emerging therapeutic avenues. Neuroscience, 278, 222-36. PMCID: PMC4180709. doi: 10.1016/j.neuroscience.2014.08.015.

Kow, R. L., Jiang, K., Naydenov, A. V., Le, J. H., Stella, N., Nathanson, N. M. (2014). Modulation of pilocarpine-induced seizures by cannabinoid receptor 1. PLoS One, 9, e95922. PMCID: PMC3994118. doi: 10.1371/journal.pone.0095922.

Naydenov, A. V., Sepers, M. D., Swinney, K., Raymond, L. A., Palmiter, R. D., Stella, N. (2014). Genetic rescue of CB1 receptors on medium spiny neurons prevents loss of excitatory striatal synapses but not motor impairment in HD mice. Neurobiology of Disease, 71, 140-50. PMCID: PMC4180675. doi: 10.1016/j.nbd.2014.08.009.

Naydenov, A. V., Horne, E. A., Cheah, C. S., Swinney, K., Hsu, K. L., Cao, J. K., … Stella, N. (2014). ABHD6 blockade exerts antiepileptic activity in PTZ-induced seizures and in spontaneous seizures in R6/2 mice. Neuron, 83, 361-371. PMCID: PMC4136499. doi: 10.1016/j.neuron.2014.06.030.

Jennifer Stone Pujol, R., Pickett, S. B., Nguyen, T. B., Stone, J. S. (2014). Large basolateral processes on type II hair cells are novel processing units in mammalian vestibular organs. The Journal of Comparative Neurology, 522, 3141-59. PMCID: PMC4107051. doi: 10.1002/cne.23625.

Wendy Stone Lieberman-Betz, R. G., Yoder, P., Stone, W. L., Nahmias, A. S., Carter, A. S., Celimli-Aksoy, S., Messinger, D. S. (2014). An illustration of using multiple imputation versus listwise deletion analyses: The effect of Hanen's "More than words" on parenting stress. American Journal on Intellectual and Developmental Disabilities, 119, 472-86. doi: 10.1352/1944-7558-119.5.472.

Nichols, C. M., Ibanez, L. V., Foss-Feig, J. H., Stone, W. L. (2014). Social smiling and its components in high-risk infant siblings without later ASD symptomatology. Journal of Autism and Developmental Disorders, 44, 894-902. PMCID: PMC3949178. doi: 10.1007/s10803-013-1944-2.

Sullivan, K., Stone, W. L., Dawson, G. (2014). Potential neural mechanisms underlying the effectiveness of early intervention for children with autism spectrum disorder. Research in Developmental Disabilities, 35, 2921-32. PMCID: PMC4163495. doi: 10.1016/j.ridd.2014.07.027.

Zwaigenbaum, L., Young, G. S., Stone, W. L., Dobkins, K., Ozonoff, S., Brian, J., … Messinger, D. (2014). Early head growth in infants at risk of autism: A baby siblings research consortium study. Journal of the American Academy of Child and Adolescent Psychiatry, 53, 1053-62. PMCID: PMC4173119. doi: 10.1016/j.jaac.2014.07.007.

Colin Studholme Fogtmann, M., Seshamani, S., Kroenke, C., Xi, Cheng, Chapman, T., Wilm, J., … Studholme, C. (2014). A unified approach to diffusion direction sensitive slice registration and 3-D DTI reconstruction from moving fetal brain anatomy. IEEE Transactions on Medical Imaging, 33, 272-89. PMCID: PMC4271809. doi: 10.1109/TMI.2013.2284014.

Stephen Tapscott Tawil, R., van der Maarel, S. M., Tapscott, S. J. (2014). Facioscapulohumeral dystrophy: The path to consensus on pathophysiology. Skeletal Muscle, 4, 12. PMCID: PMC4060068. doi: 10.1186/2044-5040-4-12.

Wang, Z., Halbert, C. L., Lee, D., Butts, T., Tapscott, S. J., Storb, R., Miller, A. D. (2014). Elimination of contaminating cap genes in AAV vector virions reduces immune responses and improves transgene expression in a canine gene therapy model. Gene Therapy, 21, 363-70. PMCID: PMC3976967. doi: 10.1038/gt.2014.4.

Yao, Z., Snider, L., Balog, J., Lemmers, R. J., Van Der Maarel, S. M., Tawil, R., Tapscott, S. J. (2014). DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle. Human Molecular Genetics, 23, 5342-52. PMCID: PMC4168822. doi: 10.1093/hmg/ddu251.

Bruce Tempel Street, V. A., Kujawa, S. G., Manichaikul, A., Broman, K. W., Kallman, J. C., Shilling, D. J., … Tempel, B. L. (2014). Resistance to noise-induced hearing loss in 129S6 and MOLF mice: Identification of independent, overlapping, and interacting chromosomal regions. Journal of the Association for Research in Otolaryngology, 15, 721-38. PMCID: PMC4164691. doi: 10.1007/s10162-014-0472-x.

Watson, C. J., Lies, S. M., Minich, R. R., Tempel, B. L. (2014). Changes in cochlear PMCA2 expression correlate with the maturation of auditory sensitivity. Journal of the Association for Research in Otolaryngology, 15, 543-54. PMCID: PMC4141437. doi: 10.1007/s10162-014-0454-z.

Eric Turner Cox, T. C., Camci, E. D., Vora, S., Luquetti, D. V., Turner, E. E. (2014). The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research. European Journal of Medical Genetics, 57, 394-401. PMCID: PMC4143470. doi: 10.1016/j.ejmg.2014.05.003.

Han, V. Z., Magnus, G., Zhang, Y., Wei, A. D., Turner, E. E. (2014). Bidirectional modulation of deep cerebellar nuclear cells revealed by optogenetic manipulation of inhibitory inputs from Purkinje cells. Neuroscience, 277, 250-66. PMCID: PMC5862060. doi: 10.1016/j.neuroscience.2014.07.006.

Hsu, Y. W., Wang, S. D., Wang, S., Morton, G., Zariwala, H. A., de la Iglesia, H. O., Turner, E. E. (2014). Role of the dorsal medial habenula in the regulation of voluntary activity, motor function, hedonic state, and primary reinforcement. The Journal of Neuroscience, 34, 11366-84. PMCID: PMC4138345. doi: 10.1523/JNEUROSCI.1861-14.2014.

Jashvant Unadkat Ke, A. B., Rostami-Hodjegan, A., Zhao, P., Unadkat, J. D. (2014). Pharmacometrics in pregnancy: An unmet need. Annual Review of Pharmacology and Toxicology, 54, 53-69. doi: 10.1146/annurev-pharmtox-011613-140009.

Prasad, B., Unadkat, J. D. (2014). Optimized approaches for quantification of drug transporters in tissues and cells by MRM proteomics. The AAPS Journal, 16, 634-48. PMCID: PMC4070263. doi: 10.1208/s12248-014-9602-y.

Prasad, B., Unadkat, J. D. (2014). Comparison of heavy labeled (SIL) peptide versus SILAC proteiniInternal standards for LC-MS/MS quantification of hepatic drug transporters. International Journal of Proteomics, 2014, 451510. PMCID: PMC3955635. doi: 10.1155/2014/451510.

Sara Jane Webb

Kodish, I., Rockhill, C. M., Webb, S. J. (2014). ASD: Psychopharmacologic treatments and neurophysiologic underpinnings. Current Topics in Behavioral Neurosciences, 21, 257-75. PMCID: PMC4180816. doi: 10.1007/7854_2014_298.

Webb, S. J. (2014). Neonatal factors associated with autism spectrum disorders in infants. Evidence-Based Mental Health, 17, 106. PMCID: PMC4844341. doi: 10.1136/eb-2014-101763.

Jonathan Weinstein

Becker, K. J., Dankwa, D., Lee, R. J., Schulze, J., Zierath, D., Tanzi, P., … Weinstein, J. R. (2014). Stroke, IL-1ra, IL1RN, infection and outcome. Neurocritical Care, 21, 140-6. PMCID: PMC4161032. doi: 10.1007/s12028-013-9899-x.

Weinstein, J. R., Schulze, J., Lee, R. V., Phillips, H., Zierath, D., Tanzi, P., … Becker, K. J. (2014). Functional polymorphisms in toll-like receptor 4 are associated with worse outcome in acute ischemic stroke patients. Neuroreport, 25, 580-4. PMCID: PMC4009512. doi: 10.1097/WNR.0000000000000140.

John P. Welsh

Turecek, J., Yuen, G. S., Han, V. Z., Zeng, X. H., Bayer, K. U., Welsh, J. P. (2014). NMDA receptor activation strengthens weak electrical coupling in mammalian brain. Neuron, 81, 1375-1388. PMCID: PMC4266555. doi: 10.1016/j.neuron.2014.01.024.

Ellen M. Wijsman Blue, E. M., Sun, L., Tintle, N. L., Wijsman, E. M. (2014). Value of Mendelian laws of segregation in families: Data quality control, imputation, and beyond. Genetic Epidemiology, 38, S21-8. PMCID: PMC4135526. doi: 10.1002/gepi.21821.

Blue, E. M., Cheung, C. Y., Glazner, C. G., Conomos, M. P., Lewis, S. M., Sverdlov, S., … Wijsman, E. M. (2014). Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analyses. BMC Proceedings, 8, S19. PMCID: PMC4143703. doi: 10.1186/1753-6561-8-S1-S19.

Cheung, C. Y., Thompson, E. A., Wijsman, E. M. (2014). Detection of Mendelian consistent genotyping errors in pedigrees. Genetic Epidemiology, 38, 291-9. PMCID: PMC4081466. doi: 10.1002/gepi.21806.

Kim, S., Saad, M., Tsuang, D. W., Wijsman, E. M. (2014). Visualization of haplotype sharing patterns in pedigree samples. Human Heredity, 78, 1-8. PMCID: PMC4112026. doi: 10.1159/000358171.

Saad, M., Wijsman, E. M. (2014). Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees. Genetic Epidemiology, 38, 579-90. PMCID: PMC4190076. doi: 10.1002/gepi.21844.

Thornton, T., Conomos, M. P., Sverdlov, S., Blue, E. M., Cheung, C. Y., Glazner, C. G., … Wijsman, E. M. (2014). Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. BMC Proceedings, 8, S5. PMCID: PMC4143704. doi: 10.1186/1753-6561-8-S1-S5.

Zhengui Xia Choi, W. S., Xia, Z. (2014). Maneb-induced dopaminergic neuronal death is not affected by loss of mitochondrial complex I activity: Results from primary mesencephalic dopaminergic neurons cultured from individual Ndufs4+/+ and Ndufs4-/- mouse embryos. Neuroreport, 25, 1350-5. PMCID: PMC4213303. doi: 10.1097/WNR.0000000000000271.

2015

Kristina Adams Waldorf

Adams Waldorf, K. M., Singh, N., Mohan, A. R., Young, R. C., Ngo, L., Das, A., Tsai, J. J., … Johnson, M. R. (2015). Uterine overdistention induces preterm labor mediated by inflammation: Observations in pregnant women and nonhuman primates. American Journal of Obstetrics and Gynecology, 213, 830 e1-830 e19. PMCID: PMC4679421. doi: 10.1016/j.ajog.2015.08.028.

Gendrin, C., Vornhagen, J., Ngo, L., Whidbey, C., Boldenow, E., Santana-Ufret, V., … Adams Waldorf, K. M., … Rajagopal, L. (2015). Mast cell degranulation by a hemolytic lipid toxin decreases GBS colonization and infection. Science Advances, 1, e1400225. PMCID: PMC4584422. doi: 10.1126/sciadv.1400225.

McAdams, R. M., Bierle, C. J., Boldenow, E., Weed, S., Tsai, J. J., Beyer, R. P., … Adams Waldorf, K. M. (2015). Choriodecidual group B streptococcal infection induces miR-155-5p in the fetal lung in Macaca nemestrina. Infection and Immunity, 83, 3909-17. PMCID: PMC4567641. doi: 10.1128/IAI.00695-15.

Whidbey, C., Vornhagen, J., Gendrin, C., Boldenow, E., Samson, J. M., Doering, K., … Adams Waldorf, K. M., Rajagopal, L. (2015). A streptococcal lipid toxin induces membrane permeabilization and pyroptosis leading to fetal injury. EMBO Molecular Medicine, 7, 488-505. PMCID: PMC4403049. doi: 10.15252/emmm.201404883.

Susan Astley Astley, S. J. (2015). Palpebral fissure length measurement: Accuracy of the FAS facial photographic analysis software and inaccuracy of the ruler. Journal of Population Therapeutics and Clinical Pharmacology, 22, e9-e26.

Elizabeth Aylward D'Angelo, D., Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. G., Hippolyte, L., … Bernier, R. A., … Aylward, E. H., … Chung, W. K. (2015). Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities. JAMA Psychiatry, 1-11. doi: 10.1001/jamapsychiatry.2015.2123.

Weaver, K. E., Richards, T. L., Logsdon, R. G., McGough, E. L., Minoshima, S., Aylward, E. H., Kleinhans, N. M., Grabowski, T. J., … Teri, L. (2015). Posterior cingulate lactate as a metabolic biomarker in amnestic mild cognitive impairment. BioMed Research International, 2015, 610605. PMCID: PMC4568343. doi: 10.1155/2015/610605.

Olivia Bermingham-McDonogh Ueki, Y., Wilken, M. S., Cox, K. E., Chipman, L. B., Bermingham-McDonogh, O., Reh, T. A. (2015). A transient wave of BMP signaling in the retina is necessary for Muller glial differentiation. Development, 142, 533-43. PMCID: PMC4302996. doi: 10.1242/dev.118745.

Raphael Bernier Chapman, N. H., Nato, A. Q., Jr., Bernier, R. A., Ankenman, K., Sohi, H., Munson, J., … Webb, S. J., … Raskind, W. H., Brkanac, Z., Wijsman, E. M. (2015). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics, 134, 1055-68. PMCID: PMC4578871. doi: 10.1007/s00439-015-1585-y.

D'Angelo, D., Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. G., Hippolyte, L., … Bernier, R. A., … Aylward, E. H., … Chung, W. K. (2015). Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities. JAMA Psychiatry, 1-11. doi: 10.1001/jamapsychiatry.2015.2123.

Hanson, E., Bernier, R. A., Porche, K., Jackson, F. I., Goin-Kochel, R. P., Snyder, L. G., … Chung, W. K. (2015). The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population. Biological Psychiatry, 77, 785-93. PMCID: PMC5410712. doi: 10.1016/j.biopsych.2014.04.021.

Hudac, C. M., Kresse, A., Aaronson, B., DesChamps, T. D., Webb, S. J., Bernier, R. A. (2015). Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications. Journal of Neurodevelopmental Disorders, 7, 25. PMCID: PMC4514956. doi: 10.1186/s11689-015-9118-5.

Krumm, N., Turner, T. N., Baker, C., Vives, L., Mohajeri, K., Witherspoon, K., … Bernier, R. A., Eichler, E. E. (2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics, 47, 582-8. PMCID: PMC4449286. doi: 10.1038/ng.3303.

Mazina, V., Gerdts, J., Trinh, S., Ankenman, K., Ward, T., Dennis, M. Y., … Eichler, E. E., Bernier, R. A. (2015). Epigenetics of autism-related impairment: Copy number variation and maternal infection. Journal of Developmental and Behavioral Pediatrics, 36, 61-7. PMCID: PMC4318761. doi: 10.1097/DBP.0000000000000126.

Moreno-De-Luca, A., Evans, D. W., Boomer, K. B., Hanson, E., Bernier, R. A., Goin-Kochel, R. P., … Ledbetter, D. H. (2015). The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. JAMA Psychiatry, 72, 119-26. doi: 10.1001/jamapsychiatry.2014.2147.

Naples, A., Nguyen-Phuc, A., Coffman, M., Kresse, A., Faja, S., Bernier, R. A., McPartland, J. C. (2015). A computer-generated animated face stimulus set for psychophysiological research. Behavior Research Methods, 47, 562-70. PMCID: PMC4297263. doi: 10.3758/s13428-014-0491-x.

Naples, A., Nguyen-Phuc, A., Coffman, M., Kresse, A., Faja, S., Bernier, R. A., McPartland, J. C. (2015). Erratum to: A computer-generated animated face stimulus set for psychophysiological research. Behavior Research Methods, 47, 571. doi: 10.3758/s13428-014-0518-3.

Nelson, T. M., Sheller, B., Friedman, C. S., Bernier, R. A. (2015). Educational and therapeutic behavioral approaches to providing dental care for patients with autism spectrum disorder. Special Care in Dentistry, 35, 105-13. doi: 10.1111/scd.12101.

Neuhaus, E., Kresse, A., Faja, S., Bernier, R. A., Webb, S. J. (2015). Face processing among twins with and without autism: Social correlates and twin concordance. Social Cognitive and Affective Neuroscience, 11, 44-54. PMCID: PMC4692310. doi: 10.1093/scan/nsv085.

Neuhaus, E., Bernier, R. A., Beauchaine, T. P. (2015). Electrodermal response to reward and non-reward among children with autism. Autism Research, 8, 357-70. doi: 10.1002/aur.1451.

Neuhaus, E., Bernier, R. A., Beauchaine, T. P. (2015). Children with autism show altered autonomic adaptation to novel and familiar social partners. Autism Research, 9, 579-591. doi: 10.1002/aur.1543.

Upshaw, M. B., Bernier, R. A., Sommerville, J. A. (2015). Infants' grip strength predicts mu rhythm attenuation during observation of lifting actions with weighted blocks. Developmental Science, 19, 195-207. PMCID: PMC5839743. doi: 10.1111/desc.12308.

van Bon, B. W., Coe, B. P., Bernier, R. A., Green, C., Gerdts, J., Witherspoon, K., … Mefford, H. C., … Eichler, E. E. (2015). Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular Psychiatry, 21, 126-132. PMCID: PMC4547916. doi: 10.1038/mp.2015.5.

Webb, S. J., Bernier, R. A., Henderson, H. A., Johnson, M. H., Jones, E. J., Lerner, M. D., … Westerfield, M. (2015). Guidelines and best practices for electrophysiological data collection, analysis and reporting in autism. Journal of Autism and Developmental Disorders, 45, 425-43. PMCID: PMC4141903. doi: 10.1007/s10803-013-1916-6.

Virginia Berninger Alstad, Z., Sanders, E., Abbott, R. D., Barnett, A. L., Henderson, S. E., Connelly, V., Berninger, V. W. (2015). Modes of alphabet letter production during middle childhood and adolescence: Interrelationships with each other and other writing skills. Journal of Writing Research, 6, 199-231. PMCID: PMC4433034. doi: 10.17239/jowr-2015.06.03.1.

Berninger, V. W., Nagy, W., Tanimoto, S., Thompson, R., Abbott, R. D. (2015). Computer instruction in handwriting, spelling, and composing for students with specific learning disabilities in grades 4 to 9. Computers & Education, 81, 154-168. PMCID: PMC4217090. doi: 10.1016/j.compedu.2014.10.005.

Berninger, V. W., Richards, T. L., Abbott, R. D. (2015). Differential diagnosis of dysgraphia, dyslexia, and OWL LD: Behavioral and neuroimaging evidence. Reading and Writing, 28, 1119-1153. PMCID: PMC4553247. doi: 10.1007/s11145-015-9565-0.

Del Campo, R., Buchanan, W. R., Abbott, R. D., Berninger, V. W. (2015). Levels of phonology related to reading and writing in middle childhood. Reading and Writing, 28, 183-198. PMCID: PMC4313929. doi: 10.1007/s11145-014-9520-5.

Richards, T. L., Grabowski, T. J., Boord, P., Yagle, K., Askren, M., Mestre, Z., … Berninger, V. W. (2015). Contrasting brain patterns of writing-related DTI parameters, fMRI connectivity, and DTI-fMRI connectivity correlations in children with and without dysgraphia or dyslexia. NeuroImage: Clinical, 8, 408-21. PMCID: PMC4473717. doi: 10.1016/j.nicl.2015.03.018.

Kristie F. Bjornson

Bjornson, K. F. (2015). Time to take notice: What about fatigue? Developmental Medicine and Child Neurology, 57, 700-1. doi: 10.1111/dmcn.12767.

Churchill, S. S., Kieckhefer, G. M., Bjornson, K. F., Herting, J. R. (2015). Relationship between sleep disturbance and functional outcomes in daily life habits of children with Down syndrome. Sleep, 38, 61-71. PMCID: PMC4262957. doi: 10.5665/sleep.4326.

Dodds, C. B., Bjornson, K. F., Sweeney, J. K., Narayanan, U. G. (2015). The effect of supported physical activity on parental-reported health-related quality of life in children with medical complexity. Journal of Pediatric Rehabilitation Medicine, 8, 83-95. doi: 10.3233/PRM-150322.

Lennon, N., Thorpe, D., Balemans, A. C., Fragala-Pinkham, M., O'Neil, M., Bjornson, K. F., … Dallmeijer, A. J. (2015). The clinimetric properties of aerobic and anaerobic fitness measures in adults with cerebral palsy: A systematic review of the literature. Research in Developmental Disabilities, 45, 316-28. doi: 10.1016/j.ridd.2015.08.002.

Myers, E., Davis, B. E., Stobbe, G., Bjornson, K. F. (2015). Community and social participation among individuals with autism spectrum disorder transitioning to adulthood. Journal of Autism and Developmental Disorders, 45, 2373-81. doi: 10.1007/s10803-015-2403-z.

Tsao, E., Bjornson, K. F., Christensen, A., Apkon, S. (2015). Functional outcomes and unplanned transfers of pediatric patients with central neurological impairments receiving inpatient rehabilitation care with cancer and noncancer diagnoses. PM&R, 8, 529-535. doi: 10.1016/j.pmrj.2015.10.007.

Cathryn Booth-LaForce Raby, K. L., Roisman, G. I., Booth-LaForce, C. (2015). Genetic moderation of stability in attachment security from early childhood to age 18 years: A replication study. Developmental Psychology, 51, 1645-1649. PMCID: PMC4624037. doi: 10.1037/dev0000053.

Shepherd-Banigan, M., Bell, J. F., Basu, A., Booth-LaForce, C., Harris, J. R. (2015). Workplace stress and working from home influence depressive symptoms among employed women with young children. International Journal of Behavioral Medicine, 23, 102-111. doi: 10.1007/s12529-015-9482-2.

Mark Bothwell de Laat, R., Meabon, J. S., Wiley, J. C., Hudson, M. P., Montine, T. J., Bothwell, M. (2015). LINGO-1 promotes lysosomal degradation of amyloid-beta protein precursor. Pathobiology of Aging & Age Related Diseases, 5, 25796. PMCID: PMC4355507. doi: 10.3402/pba.v5.25796.

Hatzi, K., Nance, J. P., Kroenke, M. A., Bothwell, M., Haddad, E. K., Melnick, A., Crotty, S. (2015). BCL6 orchestrates Tfh cell differentiation via multiple distinct mechanisms. The Journal of Experimental Medicine, 212, 539-53. PMCID: PMC4387288. doi: 10.1084/jem.20141380.

Meabon, J. S., de Laat, R., Ieguchi, K., Serbzhinsky, D., Hudson, M. P., Huber, B. R., … Bothwell, M. (2015). Intracellular LINGO-1 negatively regulates Trk neurotrophin receptor signaling. Molecular and Cellular Neurosciences, 70, 1-10. doi: 10.1016/j.mcn.2015.11.002.

Meabon, J. S., De Laat, R., Ieguchi, K., Wiley, J. C., Hudson, M. P., Bothwell, M. (2015). LINGO-1 protein interacts with the p75 neurotrophin receptor in intracellular membrane compartments. The Journal of Biological Chemistry, 290, 9511-20. PMCID: PMC4392256. doi: 10.1074/jbc.M114.608018.

Eliot Brenowitz Brenowitz, E. A., Larson, T. A. (2015). Neurogenesis in the adult avian song-control system. Cold Spring Harbor Perspectives in Biology, 7, PMCID: PMC4448602. doi: 10.1101/cshperspect.a019000.

Brenowitz, E. A. (2015). Transsynaptic trophic effects of steroid hormones in an avian model of adult brain plasticity. Frontiers in Neuroendocrinology, 37, 119-28. PMCID: PMC4385747. doi: 10.1016/j.yfrne.2014.09.003.

Brenowitz, E. A., Zakon, H. H. (2015). Emerging from the bottleneck: Benefits of the comparative approach to modern neuroscience. Trends in Neurosciences, 38, 273-8. PMCID: PMC4417368. doi: 10.1016/j.tins.2015.02.008.

Caras, M. L., Sen, K., Rubel, E. W., Brenowitz, E. A. (2015). Seasonal plasticity of precise spike timing in the avian auditory system. The Journal of Neuroscience, 35, 3431-45.PMCID: PMC4339354. doi: 10.1523/JNEUROSCI.3407-14.2015.

Larson, T. A., Lent, K. L., Bammler, T. K., MacDonald, J. W., Wood, W. E., Caras, M. L., … Perkel, D. J., Brenowitz, E. A. (2015). Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit. BMC Genomics, 16, 905. PMCID: PMC4636775. doi: 10.1186/s12864-015-2175-z.

Zoran Brkanac

Chapman, N. H., Nato, A. Q., Jr., Bernier, R. A., Ankenman, K., Sohi, H., Munson, J., … Webb, S. J., … Raskind, W. H., Brkanac, Z., Wijsman, E. M. (2015). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics, 134, 1055-68. PMCID: PMC4578871. doi: 10.1007/s00439-015-1585-y.

Nato, A. Q., Jr., Chapman, N. H., Sohi, H. K., Nguyen, H. D., Brkanac, Z., Wijsman, E. M. (2015). PBAP: A pipeline for file processing and quality control of pedigree data with dense genetic markers. Bioinformatics, 31, 3790-8. PMCID: PMC4668752. doi: 10.1093/bioinformatics/btv444.

Thomas Burbacher Curtis, B., Liberato, N., Rulien, M., Morrisroe, K., Kenney, C., Yutuc, V., … Burbacher, T. M., Sackett, G. P., Hewitson, L. (2015). Examination of the safety of pediatric vaccine schedules in a non-human primate model: Assessments of neurodevelopment, learning, and social behavior. Environmental Health Perspectives, 123, 579-89. PMCID: PMC4455585. doi: 10.1289/ehp.1408257.

Meyer, J., Grant, K., Burbacher, T. M., Worlein, J., Kenney, C., Dettmer, A., … Novak, M. (2015). Relationship between prenatal cortisol exposure and behavioral development in Macaque monkeys. Psychoneuroendocrinology, 61, 30-31. doi: 10.1016/j.psyneuen.2015.07.473.

Mohanty, A. F., Farin, F. M., Bammler, T. K., MacDonald, J. W., Afsharinejad, Z., Burbacher, T. M., … Enquobahrie, D. A. (2015). Infant sex-specific placental cadmium and DNA methylation associations. Environmental Research, 138, 74-81. PMCID: PMC4385453. doi: 10.1016/j.envres.2015.02.004.

Mohanty, A. F., Thompson, M. L., Burbacher, T. M., Siscovick, D. S., Williams, M. A., Enquobahrie, D. A. (2015). Periconceptional seafood intake and fetal growth. Paediatric and Perinatal Epidemiology, 29, 376-87. PMCID: PMC4536156. doi: 10.1111/ppe.12205.

Mohanty, A. F., Siscovick, D. S., Williams, M. A., Thompson, M. L., Burbacher, T. M., Enquobahrie, D. A. (2015). Periconceptional seafood intake and pregnancy complications. Public Health Nutrition, 1-9. doi: 10.1017/S136898001500316X.

Heather Carmichael Olson

Fitzpatrick, J. P., Latimer, J., Carter, M., Oscar, J., Ferreira, M. L., Carmichael Olson, H., … Elliott, E. J. (2015). Prevalence of Fetal Alcohol syndrome in a population-based sample of children living in remote Australia: The Lililwan Project. Journal of Paediatrics and Child Health, 51, 450-7. doi: 10.1111/jpc.12814.

Howell, K. B., McMahon, J. M., Carvill, G. L., Tambunan, D., Mackay, M. T., Rodriguez-Casero, V., … Carmichael Olson, H., … Mefford, H. C., … Scheffer, I. E. (2015). SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures. Neurology, 85, 958-66. PMCID: PMC4567464. doi: 10.1212/WNL.0000000000001926.

William Catterall Brunet, S., Emrick, M. A., Sadilek, M., Scheuer, T., Catterall, W. A. (2015). Phosphorylation sites in the Hook domain of CaVbeta subunits differentially modulate CaV1.2 channel function. Journal of Molecular and Cellular Cardiology, 87, 248-56. PMCID: PMC4637217. doi: 10.1016/j.yjmcc.2015.08.006.

Catterall, W. A. (2015). Regulation of cardiac calcium channels in the fight-or-flight response. Current Molecular Pharmacology, 8, 12-21. PMCID: PMC4664455.

Catterall, W. A. (2015). Finding channels. The Journal of Biological Chemistry, 290, 28357-73. PMCID: PMC4653694. doi: 10.1074/jbc.X115.683383.

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Michael Cunningham Goss, M. A., Lievano, F., Buchanan, K. M., Seminack, M. M., Cunningham, M. L., Dana, A. (2015). Final report on exposure during pregnancy from a pregnancy registry for quadrivalent human papillomavirus vaccine. Vaccine, 33, 3422-8. doi: 10.1016/j.vaccine.2015.04.014.

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Christine Disteche Berletch, J. B., Ma, W., Yang, F., Shendure, J., Noble, W. S., Disteche, C. M., Deng, X. (2015). Escape from X inactivation varies in mouse tissues. PLoS Genetics, 11, e1005079. PMCID: PMC4364777. doi: 10.1371/journal.pgen.1005079.

Deng, X., Ma, W., Ramani, V., Hill, A., Yang, F., Ay, F., … Disteche, C. M. (2015). Bipartite structure of the inactive mouse X chromosome. Genome Biology, 16, 152. PMCID: PMC4539712. doi: 10.1186/s13059-015-0728-8.

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William B. Dobyns Barkovich, A. J., Dobyns, W. B., Guerrini, R. (2015). Malformations of cortical development and epilepsy. Cold Spring Harbor Perspectives in Medicine, 5, a022392. PMCID: PMC4448581. doi: 10.1101/cshperspect.a022392.

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Kakar, N., Ahmad, J., Morris-Rosendahl, D. J., Altmuller, J., Friedrich, K., Barbi, G., … Dobyns, W. B., Borck, G. (2015). STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly. Human Genetics, 134, 45-51. doi: 10.1007/s00439-014-1487-4.

Luks, V. L., Kamitaki, N., Vivero, M. P., Uller, W., Rab, R., Bovee, J. V., … Dobyns, W. B., … Murillo, R. (2015). Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. The Journal of Pediatrics, 166, 1048-54 e1. PMCID: PMC4498659. doi: 10.1016/j.jpeds.2014.12.069.

McMahon, K. Q., Papandreou, A., Ma, M., Barry, B. J., Mirzaa, G. M., Dobyns, W. B., … Paciorkowski, A. R. (2015). Familial recurrences of FOXG1-related disorder: Evidence for mosaicism. American Journal of Medical Genetics. Part A, 167, 3096-102. PMCID: PMC4715619. doi: 10.1002/ajmg.a.37353.

Mirzaa, G. M., Conti, V., Timms, A. E., Smyser, C. D., Ahmed, S., Carter, M., … Dobyns, W. B., Guerrini, R. (2015). Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: A next-generation sequencing study. The Lancet Neurology, 14, 1182-95. PMCID: PMC4672724. doi: 10.1016/S1474-4422(15)00278-1.

Mirzaa, G. M., Collins, S., Dobyns, W. B. (2015). Corrigendum to "Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: Five novel mutations and review of the literature. Am J Med Genet Part A 2014 164A:2879-86". American Journal of Medical Genetics. Part A, 14 Nov 2015. doi: 10.1002/ajmg.a.37449.

Oegema, R., Cushion, T. D., Phelps, I. G., Chung, S. K., Dempsey, J. C., Collins, S., … Dobyns, W. B., … Doherty, D. A. (2015). Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes. Human Molecular Genetics, 24, 5313-25. PMCID: PMC4550818. doi: 10.1093/hmg/ddv250.

Paciorkowski, A. R., McDaniel, S. S., Jansen, L. A., Tully, H. M., Tuttle, E., Ghoneim, D. H., … Dobyns, W. B., Hahn, S. (2015). Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia, 56, 422-30. PMCID: PMC4363281. doi: 10.1111/epi.12914.

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Verloes, A., Di Donato, N., Masliah-Planchon, J., Jongmans, M., Abdul-Raman, O. A., Albrecht, B., … Dobyns, W. B., Pilz, D. T. (2015). Baraitser-Winter cerebrofrontofacial syndrome: Delineation of the spectrum in 42 cases. European Journal of Human Genetics, 23, 292-301. PMCID: PMC4326722. doi: 10.1038/ejhg.2014.95.

Daniel Doherty Bachmann-Gagescu, R., Phelps, I. G., Dempsey, J. C., Sharma, V. A., Ishak, G. E., Boyle, E. A., … Doherty, D. A. (2015). KIAA0586 is mutated in Joubert syndrome. Human Mutation, 36, 831-5. PMCID: PMC4537327. doi: 10.1002/humu.22821.

Bachmann-Gagescu, R., Dona, M., Hetterschijt, L., Tonnaer, E., Peters, T., de Vrieze, E., … Doherty, D. A., Moens, C. B., … van Wijk, E. (2015). The ciliopathy protein CC2D2A associates with NINL and functions in EAB8-MICAL3-regulated vesicle trafficking. PLoS Genetics, 11, e1005575. PMCID: PMC4617701. doi: 10.1371/journal.pgen.1005575.

Bachmann-Gagescu, R., Dempsey, J. C., Phelps, I. G., O'Roak, B. J., Knutzen, D. M., Rue, T. C., … Glass, I. A., … Doherty, D. A. (2015). Joubert syndrome: A model for untangling recessive disorders with extreme genetic heterogeneity. Journal of Medical Genetics, 52, 514-22. PMCID: PMC5082428. doi: 10.1136/jmedgenet-2015-103087.

Pan, L., Shah, A. N., Phelps, I. G., Doherty, D. A., Johnson, E. A., Moens, C. B. (2015). Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis. BMC Genomics, 16, 83. PMCID: PMC4457992. doi: 10.1186/s12864-015-1263-4.

Poretti, A., Denecke, J., Miller, D. C., Schiffmann, H., Buhk, J. H., Grange, D. K., Doherty, D. A., Boltshauser, E. (2015). Brainstem disconnection: Two additional patients and expansion of the phenotype. Neuropediatrics, 46, 139-44. doi: 10.1055/s-0034-1544127.

Slaats, G. G., Isabella, C. R., Kroes, H. Y., Dempsey, J. C., Gremmels, H., Monroe, G. R., … Glass, I. A., … Doherty, D. A. (2015). MKS1 regulates ciliary INPP5E levels in Joubert syndrome. Journal of Medical Genetics, 21 Oct 2015. doi: 10.1136/jmedgenet-2015-103250.

Vernon, M. M., Powell, D., Schultz, A. H., Simon, T. D., Doherty, D. A. (2015). Is routine preoperative transthoracic echocardiography necessary in newborns with myelomeningocele? Journal of Perinatology, 35, 842-5. PMCID: PMC5115780. doi: 10.1038/jp.2015.74.

Wheway, G., Schmidts, M., Mans, D. A., Szymanska, K., Nguyen, T. M., Racher, H., … Doherty, D. A., … Johnson, C. A. (2015). An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. Nature Cell Biology, 17, 1074-1087. PMCID: PMC4536769. doi: 10.1038/ncb3201.

Evan Eichler Carlson, K. D., Sudmant, P. H., Press, M. O., Eichler, E. E., Shendure, J., Queitsch, C. (2015). Corrigendum: MIPSTR: a method for multiplex genotyping of germline and somatic STR variation across many individuals. Genome Research, 25, 1244. PMCID: PMC4510007.

Carlson, K. D., Sudmant, P. H., Press, M. O., Eichler, E. E., Shendure, J., Queitsch, C. (2015). MIPSTR: a method for multiplex genotyping of germline and somatic STR variation across many individuals. Genome Research, 25, 750-61. PMCID: PMC4417122. doi: 10.1101/gr.182212.114.

Chaisson, M. J., Huddleston, J., Dennis, M. Y., Sudmant, P. H., Malig, M., Hormozdiari, F., … Eichler, E. E. (2015). Resolving the complexity of the human genome using single-molecule sequencing. Nature, 517, 608-11. PMCID: PMC4317254. doi: 10.1038/nature13907.

Chaisson, M. J., Wilson, R. K., Eichler, E. E. (2015). Genetic variation and the de novo assembly of human genomes. Nature Reviews. Genetics, 16, 627-40. PMCID: PMC4745987. doi: 10.1038/nrg3933.

Chen, D. H., Meneret, A., Friedman, J. R., Korvatska, O., Gad, A., Bonkowski, E. S., … Eichler, E. E., … Raskind, W. H. (2015). ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations. Neurology, 85, 2026-35. PMCID: PMC4676753. doi: 10.1212/WNL.0000000000002058.

De Rocker, N., Vergult, S., Koolen, D., Jacobs, E., Hoischen, A., Zeesman, S., … Eichler, E. E., … Menten, B. (2015). Refinement of the critical 2p25.3 deletion region: The role of MYT1L in intellectual disability and obesity. Genetics in Medicine, 17, 460-6. doi: 10.1038/gim.2014.124.

Duyzend, M. H., Eichler, E. E. (2015). Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism". Biological Psychiatry, 77, 769-71. PMCID: PMC4657856. doi: 10.1016/j.biopsych.2015.02.032.

Hormozdiari, F., Penn, O., Borenstein, E., Eichler, E. E. (2015). The discovery of integrated gene networks for autism and related disorders. Genome Research, 25, 142-54. PMCID: PMC4317170. doi: 10.1101/gr.178855.114.

Houge, G., Haesen, D., Vissers, L. E., Mehta, S., Parker, M. J., Wright, M., … Eichler, E. E., … Janssens, V. (2015). B56delta-related protein phosphatase 2A dysfunction identified in patients with intellectual disability. The Journal of Clinical Investigation, 125, 3051-62. PMCID: PMC4623570. doi: 10.1172/JCI79860.

Kloosterman, W. P., Francioli, L. C., Hormozdiari, F., Marschall, T., Hehir-Kwa, J. Y., Abdellaoui, A., … Eichler, E. E., … Guryev, V. (2015). Characteristics of de novo structural changes in the human genome. Genome Research, 25, 792-801. PMCID: PMC4448676. doi: 10.1101/gr.185041.114.

Mitchell, E., Douglas, A., Kjaegaard, S., Callewaert, B., Vanlander, A., Janssens, S., … Eichler, E. E., … Mefford, H. C. (2015). Recurrent duplications of 17q12 associated with variable phenotypes. American Journal of Medical Genetics. Part A, 167, 3038-45. doi: 10.1002/ajmg.a.37351.

Pino-Yanes, M., Gignoux, C. R., Galanter, J. M., Levin, A. M., Campbell, C. D., Eng, C., … Eichler, E. E., … Burchard, E. G. (2015). Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos. The Journal of Allergy and Clinical Immunology, 135, 1502-10. PMCID: PMC4458233. doi: 10.1016/j.jaci.2014.10.033.

Snijders Blok, L., Madsen, E., Juusola, J., Gilissen, C., Baralle, D., Reijnders, M. R., … Eichler, E. E., … Kleefstra, T. (2015). Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt Signaling. American Journal of Human Genetics, 97, 343-52. PMCID: PMC4573244. doi: 10.1016/j.ajhg.2015.07.004.

Snyder, M. W., Simmons, L. E., Kitzman, J. O., Coe, B. P., Henson, J. M., Daza, R. M., Eichler, E. E., … Gammill, H. S. (2015). Copy-number variation and false positive prenatal aneuploidy screening results. The New England Journal of Medicine, 372, 1639-45. PMCID: PMC4411081. doi: 10.1056/NEJMoa1408408.

Sudmant, P. H., Rausch, T., Gardner, E. J., Handsaker, R. E., Abyzov, A., Huddleston, J., … Zhang, J., … Eichler, E. E., Korbel, J. O. (2015). An integrated map of structural variation in 2,504 human genomes. Nature, 526, 75-81. PMCID: PMC4617611. doi: 10.1038/nature15394.

Sudmant, P. H., Mallick, S., Nelson, B. J., Hormozdiari, F., Krumm, N., Huddleston, J., … Eichler, E. E. (2015). Global diversity, population stratification, and selection of human copy-number variation. Science, 349, aab3761. PMCID: PMC4568308. doi: 10.1126/science.aab3761. van Bon, B. W., Coe, B. P., Bernier, R. A., Green, C., Gerdts, J., Witherspoon, K., … Mefford, H. C., … Eichler, E. E. (2015). Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular Psychiatry, 21, 126-132. PMCID: PMC4547916. doi: 10.1038/mp.2015.5.

Watson, C. T., Steinberg, K. M., Graves, T. A., Warren, R. L., Malig, M., Schein, J., … Eichler, E. E., Breden, F. (2015). Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity. Genes and Immunity, 16, 24-34. PMCID: PMC4304971. doi: 10.1038/gene.2014.56.

Annette Mercer Estes Estes, A. M., Munson, J., Rogers, S. J., Greenson, J., Winter, J., Dawson, G. (2015). Long-term outcomes of early intervention in 6-year-old children with autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 54, 580-7. PMCID: PMC4475272. doi: 10.1016/j.jaac.2015.04.005.

Swanson, M. R., Wolff, J. J., Elison, J. T., Gu, H., Hazlett, H. C., Botteron, K., … Dager, S. R., Estes, A. M., … Piven, J. (2015). Splenium development and early spoken language in human infants. Developmental Science, 21 Oct 2015. doi: 10.1111/desc.12360.

Zwaigenbaum, L., Bauman, M. L., Choueiri, R., Fein, D., Kasari, C., Pierce, K., Stone, W. L., … Estes, A. M., … Wetherby, A. (2015). Early identification and interventions for autism spectrum disorder: Executive summary. Pediatrics, 136, S1-9. doi: 10.1542/peds.2014-3667B.

Zwaigenbaum, L., Bauman, M. L., Stone, W. L., Yirmiya, N., Estes, A. M., Hansen, R. L., … Wetherby, A. (2015). Early identification of autism spectrum disorder: Recommendations for practice and research. Pediatrics, 136, S10-40. doi: 10.1542/peds.2014-3667C.

Zwaigenbaum, L., Bauman, M. L., Choueiri, R., Kasari, C., Carter, A., Granpeesheh, D., … Stone, W. L., … Estes, A. M., … Natowicz, M. R. (2015). Early intervention for children with autism spectrum disorder under 3 years of age: Recommendations for practice and research. Pediatrics, 136, S60-81. doi: 10.1542/peds.2014-3667E.

Zwaigenbaum, L., Bauman, M. L., Fein, D., Pierce, K., Buie, T., Davis, P. A., … Stone, W. L., … Estes, A. M., … Wagner, S. (2015). Early screening of autism spectrum disorder: Recommendations for practice and research. Pediatrics, 136, S41-59. doi: 10.1542/peds.2014-3667D.

Elaine Faustman Arbuckle, T. E., Marro, L., Davis, K., Fisher, M., Ayotte, P., Belanger, P., … Faustman, E. M., … Fraser, W. D. (2015). Exposure to free and conjugated forms of bisphenol A and triclosan among pregnant women in the MIREC cohort. Environmental Health Perspectives, 123, 277-84. PMCID: PMC4384201. doi: 10.1289/ehp.1408187.

Harris, S., Hermsen, S. A., Yu, X., Hong, S. W., Faustman, E. M. (2015). Comparison of toxicogenomic responses to phthalate ester exposure in an organotypic testis co-culture model and responses observed in vivo. Reproductive Toxicology, 58, 149-59. PMCID: PMC5166712. doi: 10.1016/j.reprotox.2015.10.002.

Lee, V., McMahan, R. S., Hu, X., Gao, X., Faustman, E. M., Griffith, W. C., … Parks, W. C. (2015). Amphiphilic polymer-coated CdSe/ZnS quantum dots induce pro-inflammatory cytokine expression in mouse lung epithelial cells and macrophages. Nanotoxicology, 9, 336-43. PMCID: PMC4669048. doi: 10.3109/17435390.2014.930532.

Scoville, D. K., White, C. C., Botta, D., McConnachie, L. A., Zadworny, M. E., Schmuck, S. C., … Faustman, E. M., Kavanagh, T. J. (2015). Susceptibility to quantum dot induced lung inflammation differs widely among the Collaborative Cross founder mouse strains. Toxicology and Applied Pharmacology, 289, 240-50. PMCID: PMC4651801. doi: 10.1016/j.taap.2015.09.019.

Smith, M. N., Wilder, C. S., Griffith, W. C., Workman, T., Thompson, B., Dills, R., … Faustman, E. M. (2015). Seasonal variation in cortisol biomarkers in Hispanic mothers living in an agricultural region. Biomarkers, 20, 299-305. PMCID: PMC4850059. doi: 10.3109/1354750X.2015.1068863.

Wegner, S. H., Yu, X., Pacheco Shubin, S., Griffith, W. C., Faustman, E. M. (2015). Stage-specific signaling pathways during murine testis development and spermatogenesis: A pathway-based analysis to quantify developmental dynamics. Reproductive Toxicology, 51, 31-9. PMCID: PMC4425996. doi: 10.1016/j.reprotox.2014.11.008.

Gwenn Garden Jebelli, J., Su, W., Hopkins, S., Pocock, J., Garden, G. A. (2015). Glia: Guardians, gluttons, or guides for the maintenance of neuronal connectivity? Annals of the New York Academy of Sciences, 1351, 1-10. PMCID: PMC4564356. doi: 10.1111/nyas.12711.

Su, W., Aloi, M. S., Garden, G. A. (2015). MicroRNAs mediating CNS inflammation: Small regulators with powerful potential. Brain, Behavior, and Immunity, 52, 1-8. PMCID: PMC5030842. doi: 10.1016/j.bbi.2015.07.003.

Adam Geballe

Brennan, G., Kitzman, J. O., Shendure, J., Geballe, A. P. (2015). Experimental evolution identifies vaccinia virus mutations in A24R and A35R that antagonize the protein kinase R pathway and accompany collapse of an extragenic gene amplification. Journal of Virology, 89, 9986-97. PMCID: PMC4577882. doi: 10.1128/JVI.01233-15.

Schleiss, M. R., Bierle, C. J., Swanson, E. C., McVoy, M. A., Wang, J. B., Al-Mahdi, Z., Geballe, A. P. (2015). Vaccination with a live attenuated cytomegalovirus devoid of a protein kinase R inhibitory gene results in reduced maternal viremia and improved pregnancy outcome in a guinea pig congenital infection model. Journal of Virology, 89, 9727-38. PMCID: PMC4577886. doi: 10.1128/JVI.01419-15.

Ian Glass Bachmann-Gagescu, R., Dempsey, J. C., Phelps, I. G., O'Roak, B. J., Knutzen, D. M., Rue, T. C., … Glass, I. A., … Doherty, D. A. (2015). Joubert syndrome: A model for untangling recessive disorders with extreme genetic heterogeneity. Journal of Medical Genetics, 52, 514-22. PMCID: PMC5082428. doi: 10.1136/jmedgenet-2015-103087.

Christine Gleason Fleishman, R., Zhou, C., Gleason, C., Larison, C., Myaing, M. T., Mangione-Smith, R. (2015). Standardizing morphine use for ventilated preterm neonates with a nursing-driven comfort protocol. Journal of Perinatology, 35, 46-51. doi: 10.1038/jp.2014.131.

Sidney Gospe, Jr. Arredondo, J., Lara, M., Gospe, S. M., Jr., Mazia, C. G., Vaccarezza, M., Garcia-Erro, M., … Maselli, R. A. (2015). Choline acetyltransferase mutations causing congenital myasthenic syndrome: Molecular findings and genotype-phenotype correlations. Human Mutation, 36, 881-93. PMCID: PMC4537391. doi: 10.1002/humu.22823.

Mefford, H. C., Zemel, M., Geraghty, E., Cook, J., Clayton, P. T., Paul, K., … Gospe, S. M., Jr. (2015). Intragenic deletions of ALDH7A1 in pyridoxine-dependent epilepsy caused by Alu-Alu recombination. Neurology, 85, 756-62. PMCID: PMC4553021. doi: 10.1212/WNL.0000000000001883.

Ng, Y. T., Gospe, S. M., Jr., Sahin, M. (2015). Pediatric neurology 2014 trainee publication award winner: Dr. Mitchel T. Williams. Pediatric Neurology, 53, 103-4. doi: 10.1016/j.pediatrneurol.2015.04.010.

Poliachik, S. L., Friedman, S. D., Poliakov, A. V., Budech, C. B., Ishak, G. E., Shaw, D. W. W., Gospe, S. M., Jr. (2015). Corpus callosum diffusion and connectivity features in high functioning subjects with pyridoxine-dependent epilepsy. Pediatric Neurology, 25 Sept 2015. doi: 10.1016/j.pediatrneurol.2015.09.012.

Joan M. Goverman Wagner, C. A., Goverman, J. M. (2015). Novel insights and therapeutics in multiple sclerosis. F1000Research, 4, 517. PMCID: PMC4544373. doi: 10.12688/f1000research.6378.1.

Thomas J. Grabowski, Jr. Madhyastha, T. M., Askren, M. K., Boord, P., Grabowski, T. J. (2015). Dynamic connectivity at rest predicts attention task performance. Brain Connectivity, 5, 45-59. PMCID: PMC4313397. doi: 10.1089/brain.2014.0248.

Tungaraza, R. L., Mehta, S. H., Haynor, D. R., Grabowski, T. J. (2015). Anatomically informed metrics for connectivity-based cortical parcellation from diffusion MRI. IEEE Journal of Biomedical and Health Informatics, 19, 1375-83. PMCID: PMC4561620. doi: 10.1109/JBHI.2015.2444917.

Therese Grant Shaw, M. R., Grant, T., Barbosa-Leiker, C., Fleming, S. E., Henley, S., Graham, J. C. (2015). Intervention with substance-abusing mothers: Are there rural-urban differences? The American Journal on Addictions, 24, 144-152. doi: 10.1111/ajad.12155.

R. Scott Hansen Kundaje, A., Meuleman, W., Ernst, J., Bilenky, M., Yen, A., Heravi-Moussavi, A., … Hansen, R. S., … Kellis, M. (2015). Integrative analysis of 111 reference human epigenomes. Nature, 518, 317-30. PMCID: PMC4530010. doi: 10.1038/nature14248.

Wilken, M. S., Brzezinski, J. A., La Torre, A., Siebenthall, K., Thurman, R., Sabo, P., … Hansen, R. S., … Reh, T. A. (2015). DNase I hypersensitivity analysis of the mouse brain and retina identifies region-specific regulatory elements. Epigenetics & Chromatin, 8, 8. PMCID: PMC4429822. doi: 10.1186/1756-8935-8-8.

Robert Hevner Easton, C. R., Dickey, C. W., Moen, S. P., Neuzil, K. E., Barger, Z., Anderson, T. M., … Hevner, R. F. (2015). Distinct calcium signals in developing cortical interneurons persist despite disorganization of cortex by Tbr1 KO. Developmental Neurobiology, 03 Nov 2015. doi: 1002/dneu.22354.

Hevner, R. F. (2015). Evolution of the mammalian dentate gyrus. The Journal of Comparative Neurology, 14 Jul 2015. doi: 10.1002/cne.23851.

Hevner, R. F. (2015). Brain overgrowth in disorders of RTK-PI3K-AKT signaling: A mosaic of malformations. Seminars in Perinatology, 39, 36-43. PMCID: PMC4268391. doi: 10.1053/j.semperi.2014.10.006.

Studer, M., Magrinelli, E., Harb, K., Hevner, R. F., Alfano, C. (2015). Post-mitotic control of sensory area specification during neocortical development. International Journal of Developmental Neuroscience, 47, 39-39. doi: 10.1016/j.ijdevneu.2015.04.111.

Tronnes, A. A., Koschnitzky, J., Daza, R., Hitti, J., Ramirez, J. M., Hevner, R. F. (2015). Effects of lipopolysaccharide and progesterone exposures on embryonic cerebral cortex development in mice. Reproductive Sciences, doi: 10.1177/1933719115618273.

Rodney Ho Freeling, J. P., Koehn, J., Shu, C., Sun, J., Ho, R. J. (2015). Anti-HIV drug-combination nanoparticles enhance plasma drug exposure duration as well as triple-drug combination levels in cells within lymph nodes and blood in primates. AIDS Research and Human Retroviruses, 31, 107-14. PMCID: PMC4287118. doi: 10.1089/aid.2014.0210.

David Horn Mitchell, R. M., Horn, D. L. (2015). Migration of a cochlear implant ground electrode through the calvarium of a pediatric patient. International Journal of Pediatric Otorhinolaryngology, 79, 278-80. doi: 10.1016/j.ijporl.2014.11.031.

Park, M. H., Won, J. H., Horn, D. L., Rubinstein, J. T. (2015). Acoustic temporal modulation detection in normal-hearing and cochlear implanted listeners: Effects of hearing mechanism and development. Journal of the Association for Research in Otolaryngology, 16, 389-99. PMCID: PMC4417089. doi: 10.1007/s10162-014-0499-z.

Purcell, P. L., Iwata, A. J., Phillips, G. S., Paladin, A. M., Sie, K. C., Horn, D. L. (2015). Bony cochlear nerve canal stenosis and speech discrimination in pediatric unilateral hearing loss. The Laryngoscope, 125, 1691-6. doi: 10.1002/lary.25087.

Shinn, J. R., Purcell, P. L., Horn, D. L., Sie, K. C., Manning, S. C. (2015). First branchial cleft anomalies: Otologic manifestations and treatment outcomes. Otolaryngology--Head and Neck Surgery, 152, 506-12. doi: 10.1177/0194599814562773.

Philip Horner Choi, J. L., Tan, J. K., Sellers, D. L., Wei, H., Horner, P. J., Pun, S. H. (2015). Guanidinylated block copolymers for gene transfer: A comparison with amine-based materials for in vitro and in vivo gene transfer efficiency. Biomaterials, 54, 87-96. PMCID: PMC4409668. doi: 10.1016/j.biomaterials.2015.03.008.

Coughlin, L., Morrison, R. S., Horner, P. J., Inman, D. M. (2015). Mitochondrial morphology differences and mitophagy deficit in murine glaucomatous optic nerve. Investigative Ophthalmology & Visual Science, 56, 1437-46. PMCID: PMC4347310. doi: 10.1167/iovs.14-16126.

Elias, P. Z., Liu, G. W., Wei, H., Jensen, M. C., Horner, P. J., Pun, S. H. (2015). A functionalized, injectable hydrogel for localized drug delivery with tunable thermosensitivity: Synthesis and characterization of physical and toxicological properties. Journal of Controlled Release, 208, 76-84. doi: 10.1016/j.jconrel.2015.03.003.

Marshall S. Horwitz Nayak, R. C., Trump, L. R., Aronow, B. J., Myers, K., Mehta, P., Kalfa, T., … Horwitz, M. S., … Cancelas, J. A. (2015). Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cells. The Journal of Clinical Investigation, 125, 3103-16. PMCID: PMC4563755. doi: 10.1172/JCI80924.

Colleen Huebner Collett, B. R., Huebner, C. E., Seminario, A. L., Wallace, E., Gray, K. E., Speltz, M. L. (2015). Observed child and parent toothbrushing behaviors and child oral health. International Journal of Paediatric Dentistry, 04 Jul 2015. doi: 10.1111/ipd.12175.

Huebner, C. E., Chi, D. L., Masterson, E., Milgrom, P. (2015). Preventive dental health care experiences of preschool-age children with special health care needs. Special Care in Dentistry, 35, 68-77. PMCID: PMC4312543. doi: 10.1111/scd.12084.

Huebner, C. E., Milgrom, P. (2015). Evaluation of a parent-designed programme to support tooth brushing of infants and young children. International Journal of Dental Hygiene, 13, 65-73. PMCID: PMC4486350. doi: 10.1111/idh.12100.

Nelson, T. M., Huebner, C. E., Kim, A., Scott, J. M., Pickrell, J. E. (2015). Parent-reported distress in children under 3 years old during preventive medical and dental care. European Archives of Paediatric Dentistry, 16, 283-90. PMCID: PMC4470890. doi: 10.1007/s40368-014-0161-9.

Riedy, C. A., Weinstein, P., Mancl, L., Garson, G., Huebner, C. E., Milgrom, P., … Sutherland, M. (2015). Dental attendance among low-income women and their children following a brief motivational counseling intervention: A community randomized trial. Social Science & Medicine, 144, 9-18. PMCID: PMC4610142. doi: 10.1016/j.socscimed.2015.09.005.

Clifford Hume

Luo, C., Omelchenko, I., Manson, R., Robbins, C., Oesterle, E. C., Cao, G. Z., … Hume, C. R. (2015). Direct intracochlear acoustic stimulation using a PZT microactuator. Trends in Hearing, 19, PMCID: PMC4771031. doi: 10.1177/2331216515616942.

Tong, L., Strong, M. K., Kaur, T., Juiz, J. M., Oesterle, E. C., Hume, C. R., … Rubel, E. W. (2015). Selective deletion of cochlear hair cells causes rapid age-dependent changes in spiral ganglion and cochlear nucleus neurons. The Journal of Neuroscience, 35, 7878-91. PMCID: PMC4438131. doi: 10.1523/JNEUROSCI.2179-14.2015.

Tracy Jirikowic McCoy, S. W., Jirikowic, T. L., Price, R., Ciol, M. A., Hsu, L. Y., Dellon, B., Kartin, D. (2015). Virtual sensorimotor balance training for children with fetal alcohol spectrum disorders: Feasibility study. Physical Therapy, 95, 1569-81. PMCID: PMC4625061. doi: 10.2522/ptj.20150124.

Sandra Juul Baserga, M. C., Beachy, J. C., Roberts, J. K., Ward, R. M., DiGeronimo, R. J., Walsh, W. F., … Juul, S. E., … Yoder, B. A. (2015). Darbepoetin administration to neonates undergoing cooling for encephalopathy: A safety and pharmacokinetic trial. Pediatric Research, 78, 315-22. PMCID: PMC5564328. doi: 10.1038/pr.2015.101.

Christensen, R. D., Juul, S. E., Del Vecchio, A. (2015). The expanding evidence base to guide neonatal hematology and transfusion medicine practice. preface. Clinics in Perinatology, 42, xix-xx. doi: 10.1016/j.clp.2015.05.002.

Chun, P. T., McPherson, R. J., Marney, L. C., Zangeneh, S. Z., Parsons, B. A., Shojaie, A., … Juul, S. E. (2015). Serial plasma metabolites following hypoxic-ischemic encephalopathy in a nonhuman primate model. Developmental Neuroscience, 37, 161-71. PMCID: PMC4406798. doi: 10.1159/000370147.

Empie, K., Rangarajan, V., Juul, S. E. (2015). Is the ferret a suitable species for studying perinatal brain injury? International Journal of Developmental Neuroscience, 45, 2-10. PMCID: PMC4793918. doi: 10.1016/j.ijdevneu.2015.06.005.

Juul, S. E., Pet, G. C. (2015). Erythropoietin and Neonatal Neuroprotection. Clinics in Perinatology, 42, 469-81. PMCID: PMC4529536. doi: 10.1016/j.clp.2015.04.004.

McAdams, R. M., McPherson, R. J., Beyer, R. P., Bammler, T. K., Farin, F. M., Juul, S. E. (2015). Dose-dependent effects of morphine exposure on mRNA and microRNA (miR) expression in hippocampus of stressed neonatal mice. PLoS One, 10, e0123047. PMCID: PMC4386824. doi: 10.1371/journal.pone.0123047.

McAdams, R. M., McPherson, R. J., Kapur, R. P., Phillips, B., Shen, D. D., Juul, S. E. (2015). Dexmedetomidine reduces cranial temperature in hypothermic neonatal rats. Pediatric Research, 77, 772-8. doi: 10.1038/pr.2015.45.

Ohls, R. K., Christensen, R. D., Widness, J. A., Juul, S. E. (2015). Erythropoiesis stimulating agents demonstrate safety and show promise as neuroprotective agents in neonates. The Journal of Pediatrics, 167, 10-2. PMCID: PMC4795451. doi: 10.1016/j.jpeds.2015.03.054.

Peeples, E. S., Mehic, E., Mourad, P. D., Juul, S. E. (2015). Fast Doppler as a novel bedside measure of cerebral perfusion in preterm infants. Pediatric Research, 05 Nov 2015. doi: 10.1038/pr.2015.227.

Shah, A., Porter, K., Juul, S. E., Wilfond, B. S. (2015). Precluding consent by clinicians who are both the attending and the investigator: An outdated shibboleth? American Journal of Bioethics, 15, 80-2. PMCID: PMC4593708. doi: 10.1080/15265161.2015.1011007.

Raj P. Kapur McAdams, R. M., McPherson, R. J., Kapur, R. P., Phillips, B., Shen, D. D., Juul, S. E. (2015). Dexmedetomidine reduces cranial temperature in hypothermic neonatal rats. Pediatric Research, 77, 772-8. doi: 10.1038/pr.2015.45.

David Kimelman Bouldin, C. M., Manning, A. J., Peng, Y. H., Farr, G. H., 3rd, Hung, K. L., Dong, A., Kimelman, D. (2015). Wnt signaling and tbx16 form a bistable switch to commit bipotential progenitors to mesoderm. Development, 142, 2499-507. PMCID: PMC4510867. doi: 10.1242/dev.124024.

Manning, A. J., Kimelman, D. (2015). Tbx16 and Msgn1 are required to establish directional cell migration of zebrafish mesodermal progenitors. Developmental Biology, 406, 172-85. PMCID: PMC4639448. doi: 10.1016/j.ydbio.2015.09.001.

Bryan King Carr, T., Shih, W., Lawton, K., Lord, C., King, B. H., Kasari, C. (2015). The relationship between treatment attendance, adherence, and outcome in a caregiver-mediated intervention for low-resourced families of young children with autism spectrum disorder. Autism, 19 Aug 2015. doi: 10.1177/1362361315598634.

Chowdhury, M., Aman, M. G., Lecavalier, L., Smith, T., Johnson, C., Swiezy, N., … King, B. H., … Scahill, L. (2015). Factor structure and psychometric properties of the revised Home Situations Questionnaire for autism spectrum disorder: The Home Situations Questionnaire-Autism Spectrum Disorder. Autism, 17 Jul 2015. doi: 10.1177/1362361315593941.

de Vries, P. J., Whittemore, V. H., Leclezio, L., Byars, A. W., Dunn, D., Ess, K. C., … King, B. H., … Jansen, A. (2015). Tuberous sclerosis associated neuropsychiatric disorders (TAND) and the TAND Checklist. Pediatric Neurology, 52, 25-35. PMCID: PMC4427347. doi: 10.1016/j.pediatrneurol.2014.10.004.

King, B. H. (2015). Promising forecast for autism spectrum disorders. JAMA, 313, 1518-9. doi: 10.1001/jama.2015.2628.

King, B. H. (2015). Assessing risk of autism spectrum disorder in children after antidepressant use during pregnancy. JAMA Pediatrics, 1-2. doi: 10.1001/jamapediatrics.2015.3493.

Scahill, L., Aman, M. G., Lecavalier, L., Halladay, A. K., Bishop, S. L., Bodfish, J. W., … King, B. H., … Dawson, G. (2015). Measuring repetitive behaviors as a treatment endpoint in youth with autism spectrum disorder. Autism, 19, 38-52. doi: 10.1177/1362361313510069.

Natalia Kleinhans Weaver, K. E., Richards, T. L., Logsdon, R. G., McGough, E. L., Minoshima, S., Aylward, E. H., Kleinhans, N. M., Grabowski, T. J., … Teri, L. (2015). Posterior cingulate lactate as a metabolic biomarker in amnestic mild cognitive impairment. BioMed Research International, 2015, 610605. PMCID: PMC4568343. doi: 10.1155/2015/610605.

Sara T. Kover Benjamin, D. P., McDuffie, A. S., Thurman, A. J., Kover, S. T., Mastergeorge, A. M., Hagerman, R. J., Abbeduto, L. (2015). Effect of speaker gaze on word learning in fragile X syndrome: A comparison with nonsyndromic autism spectrum disorder. Journal of Speech, Language, and Hearing Research, 58, 383-95. PMCID: PMC4675125. doi: 10.1044/2015_JSLHR-L-14-0136.

Ellis Weismer, S., Kover, S. T. (2015). Preschool language variation, growth, and predictors in children on the autism spectrum. Journal of Child Psychology and Psychiatry and Allied Disciplines, 56, 1327-37. PMCID: PMC4565784. doi: 10.1111/jcpp.12406.

Kover, S. T., McCary, L. M., Ingram, A. M., Hatton, D. D., Roberts, J. E. (2015). Language development in infants and toddlers with fragile X syndrome: Change over time and the role of attention. American Journal on Intellectual and Developmental Disabilities, 120, 125-44. PMCID: PMC5656241. doi: 10.1352/1944-7558-120.2.125.

Thurman, A. J., McDuffie, A., Kover, S. T., Hagerman, R., Channell, M. M., Mastergeorge, A., Abbeduto, L. (2015). Use of emotional cues for lexical learning: A comparison of autism spectrum disorder and fragile X syndrome. Journal of Autism and Developmental Disorders, 45, 1042-61. PMCID: PMC4369166. doi: 10.1007/s10803-014-2260-1.

Thurman, A. J., McDuffie, A., Kover, S. T., Hagerman, R. J., Abbeduto, L. (2015). Autism symptomatology in boys with fragile X syndrome: A cross sectional developmental trajectories comparison with nonsyndromic autism spectrum disorder. Journal of Autism and Developmental Disorders, 45, 2816-32. PMCID: PMC4554893. doi: 10.1007/s10803-015-2443-4.

Venker, C. E., Kover, S. T. (2015). An open conversation on using eye-gaze methods in studies of neurodevelopmental disorders. Journal of Speech, Language, and Hearing Research, 58, 1719-32. PMCID: PMC4987028. doi: 10.1044/2015_JSLHR-L-14-0304.

Patricia Kuhl Conboy, B. T., Brooks, R., Meltzoff, A. N., Kuhl, P. K. (2015). Social interaction in infants' learning of second-language phonetics: An exploration of brain-behavior relations. Developmental Neuropsychology, 40, 216-29. PMCID: PMC4824050. doi: 10.1080/87565641.2015.1014487.

Kuhl, P. K. (2015). Baby talk. Scientific American, 313, 64-9.

Moon, C., Zernzach, R. C., Kuhl, P. K. (2015). Mothers say "baby" and their newborns do not choose to listen: A behavioral preference study to compare with ERP results. Frontiers in Human Neuroscience, 9, 153. PMCID: PMC4373280. doi: 10.3389/fnhum.2015.00153.

Zhao, T. C., Kuhl, P. K. (2015). Higher-level linguistic categories dominate lower-level acoustics in lexical tone processing. Journal of the Acoustical Society of America, 138, EL133-7. doi: 10.1121/1.4927632.

Donghoon Lee Girard, E., Ditzler, S., Lee, D., Richards, A., Yagle, K., Park, J., … Olson, J. (2015). Efficacy of cabazitaxel in mouse models of pediatric brain tumors. Neuro-Oncology, 17, 107-15. PMCID: PMC4483053. doi: 10.1093/neuonc/nou163.

Qiu, L., Zhang, F., Shi, Y., Bai, Z., Wang, J., Li, Y., Lee, D., … Yang, X. (2015). Gliomas: Motexafin gadolinium-enhanced molecular mr imaging and optical imaging for potential intraoperative delineation of tumor margins. Radiology, 150895. doi: 10.1148/radiol.2015150895.

Ali Murat Maga Anderson, R., Maga, A. M. (2015). A novel procedure for rapid imaging of adult mouse brains with microct using iodine-based contrast. PLoS One, 10, e0142974. PMCID: PMC4646620. doi: 10.1371/journal.pone.0142974.

Young, R., Maga, A. M. (2015). Performance of single and multi-atlas based automated landmarking methods compared to expert annotations in volumetric microCT datasets of mouse mandibles. Frontiers in Zoology, 12, 33. PMCID: PMC4666065. doi: 10.1186/s12983-015-0127-8.

Kenneth Maravilla

Maravilla, K. R., Smith, M. P., Vymazal, J., Goyal, M., Herman, M., Baima, J. J., … Pirovano, G. (2015). Are there differences between macrocyclic gadolinium contrast agents for brain tumor imaging? Results of a multicenter intraindividual crossover comparison of gadobutrol with gadoteridol (the TRUTH Study). American Journal of Neuroradiology, 36, 14-23. doi: 10.3174/ajnr.A4154.

Schur, E. A., Melhorn, S. J., Oh, S. K., Lacy, J. M., Berkseth, K. E., Guyenet, S. J., … Maravilla, K. R. (2015). Radiologic evidence that hypothalamic gliosis is associated with obesity and insulin resistance in humans. Obesity (Silver Spring), 23, 2142-8. PMCID: PMC4634110. doi: 10.1002/oby.21248.

Yarnykh, V. L., Bowen, J. D., Samsonov, A., Repovic, P., Mayadev, A., Qian, P., … Maravilla, K. R., Jung Henson, L. K. (2015). Fast whole-brain three-dimensional macromolecular proton fraction mapping in multiple sclerosis. Radiology, 274, 210-20. PMCID: PMC4314118. doi: 10.1148/radiol.14140528.

Ryan McAdams McAdams, R. M., Bierle, C. J., Boldenow, E., Weed, S., Tsai, J. J., Beyer, R. P., … Adams Waldorf, K. M. (2015). Choriodecidual group B streptococcal infection induces miR-155-5p in the fetal lung in Macaca nemestrina. Infection and Immunity, 83, 3909-17. PMCID: PMC4567641. doi: 10.1128/IAI.00695-15.

McAdams, R. M., Hedstrom, A. B., DiBlasi, R. M., Mant, J. E., Nyonyintono, J., Otai, C. D., … Batra, M. (2015). Implementation of Bubble CPAP in a Rural Ugandan Neonatal ICU. Respiratory Care, 60, 437-45. doi: 10.4187/respcare.03438.

McAdams, R. M. (2015). Bubble CPAP may be safe and efficacious for neonates in low and middle income countries, but more evidence is needed. Evidence-based Medicine, 20, 62. doi: 10.1136/ebmed-2014-110135.

Katie A. McLaughlin Atwoli, L., Stein, D. J., Koenen, K. C., McLaughlin, K. A. (2015). Epidemiology of posttraumatic stress disorder: Prevalence, correlates and consequences. Current Opinion in Psychiatry, 28, 307-11. PMCID: PMC4452282. doi: 10.1097/YCO.0000000000000167.

Germine, L., Dunn, E. C., McLaughlin, K. A., Smoller, J. W. (2015). Childhood adversity is associated with adult theory of mind and social affiliation, but not face processing. PLoS One, 10, e0129612. PMCID: PMC4466913. doi: 10.1371/journal.pone.0129612.

Gooding, H. C., Milliren, C. E., Austin, S. B., Sheridan, M. A., McLaughlin, K. A. (2015). Child abuse, resting blood pressure, and blood pressure reactivity to psychosocial stress. Journal of Pediatric Psychology, 14 May 2015. doi: 10.1093/jpepsy/jsv040.

Gooding, H. C., Milliren, C., Austin, S. B., Sheridan, M. A., McLaughlin, K. A. (2015). Exposure to violence in childhood is associated with higher body mass index in adolescence. Child Abuse & Neglect, 50, 151-8. PMCID: PMC4688211. doi: 10.1016/j.chiabu.2015.08.005.

Humphreys, K. L., McGoron, L., Sheridan, M. A., McLaughlin, K. A., Fox, N. A., Nelson, C. A., 3rd, Zeanah, C. H. (2015). High-quality foster care mitigates callous-unemotional traits following early deprivation in boys: A randomized controlled trial. Journal of the American Academy of Child and Adolescent Psychiatry, 54, 977-83. PMCID: PMC4660264. doi: 10.1016/j.jaac.2015.09.010.

McLaughlin, K. A., Rith-Najarian, L., Dirks, M. A., Sheridan, M. A. (2015). Low vagal tone magnifies the association between psychosocial stress exposure and internalizing psychopathology in adolescents. Journal of Clinical Child and Adolescent Psychology, 44, 314-28. PMCID: PMC4076387. doi: 10.1080/15374416.2013.843464.

McLaughlin, K. A., Peverill, M., Gold, A. L., Alves, S., Sheridan, M. A. (2015). Child maltreatment and neural systems underlying emotion regulation. Journal of the American Academy of Child and Adolescent Psychiatry, 54, 753-62. PMCID: PMC4548288. doi: 10.1016/j.jaac.2015.06.010.

McLaughlin, K. A., Koenen, K. C., Friedman, M. J., Ruscio, A. M., Karam, E. G., Shahly, V., … Kessler, R. C. (2015). Subthreshold posttraumatic stress disorder in the world health organization world mental health surveys. Biological Psychiatry, 77, 375-84. PMCID: PMC4194258. doi: 10.1016/j.biopsych.2014.03.028.

McLaughlin, K. A., Sheridan, M. A., Tibu, F., Fox, N. A., Zeanah, C. H., Nelson, C. A., 3rd (2015). Causal effects of the early caregiving environment on development of stress response systems in children. Proceedings of the National Academy of Sciences of the United States of America, 112, 5637-42. PMCID: PMC4426436. doi: 10.1073/pnas.1423363112.

McLaughlin, K. A., King, K. (2015). Developmental trajectories of anxiety and depression in early adolescence. Journal of Abnormal Child Psychology, 43, 311-23. PMCID: PMC4286282. doi: 10.1007/s10802-014-9898-1.

Sumner, J. A., Sheridan, M. A., Drury, S. S., Esteves, K. C., Walsh, K., Koenen, K. C., McLaughlin, K. A. (2015). Variation in CACNA1C is associated with amygdala structure and function in adolescents. Journal of Child and Adolescent Psychopharmacology, 25, 701-10. PMCID: PMC4653820. doi: 10.1089/cap.2015.0047.

Heather Mefford Carvill, G. L., McMahon, J. M., Schneider, A., Zemel, M., Myers, C. T., Saykally, J., … Mefford, H. C. (2015). Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic-atonic seizures. American Journal of Human Genetics, 96, 808-15. PMCID: PMC4570550. doi: 10.1016/j.ajhg.2015.02.016.

Damiano, J. A., Mullen, S. A., Hildebrand, M. S., Bellows, S. T., Lawrence, K. M., Arsov, T., … Mefford, H. C., … Berkovic, S. F. (2015). Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy. Epilepsy Research, 117, 70-3. doi: 10.1016/j.eplepsyres.2015.09.007.

Galizia, E. C., Myers, C. T., Leu, C., de Kovel, C. G., Afrikanova, T., Cordero-Maldonado, M. L., … Mefford, H. C., … Sisodiya, S. M. (2015). CHD2 variants are a risk factor for photosensitivity in epilepsy. Brain, 138, 1198-207. PMCID: PMC4407192. doi: 10.1093/brain/awv052.

Hartmann, C., von Spiczak, S., Suls, A., Weckhuysen, S., Buyse, G., Vilain, C., … Mefford, H. C. (2015). Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis. Epilepsia, 56, e26-32. PMCID: PMC4363163. doi: 10.1111/epi.12920.

Jones, K. L., Schwarze, U., Adam, M. P., Byers, P. H., Mefford, H. C. (2015). A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes. American Journal of Medical Genetics. Part A, 167, 2691-6. PMCID: PMC4654953. doi: 10.1002/ajmg.a.37209.

Larsen, J., Carvill, G. L., Gardella, E., Kluger, G., Schmiedel, G., Barisic, N., … Mefford, H. C., … Euro, Epinomics R. E. S. Consortium C. R. P. (2015). The phenotypic spectrum of SCN8A encephalopathy. Neurology, 84, 480-9. PMCID: PMC4336074. doi: 10.1212/WNL.0000000000001211.

Mefford, H. C. (2015). Copy number matters in epilepsy. Epilepsy Currents, 15, 180-2. PMCID: PMC4532226. doi: 10.5698/1535-7511-15.4.180.

Mefford, H. C. (2015). Clinical genetic testing in epilepsy. Epilepsy Currents, 15, 197-201. PMCID: PMC4532232. doi: 10.5698/1535-7511-15.4.197.

Moller, R. S., Heron, S. E., Larsen, L. H., Lim, C. X., Ricos, M. G., Bayly, M. A., … Mefford, H. C., … Dibbens, L. M. (2015). Mutations in KCNT1 cause a spectrum of focal epilepsies. Epilepsia, 56, e114-20. PMCID: PMC5915334. doi: 10.1111/epi.13071.

Myers, C. T., Mefford, H. C. (2015). Advancing epilepsy genetics in the genomic era. Genome Medicine, 7, 91. PMCID: PMC4549122. doi: 10.1186/s13073-015-0214-7.

Paemka, L., Mahajan, V. B., Ehaideb, S. N., Skeie, J. M., Tan, M. C., Wu, S., … Mefford, H. C., … Bassuk, A. G. (2015). Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase. PLoS Genetics, 11, e1005022. PMCID: PMC4357451. doi: 10.1371/journal.pgen.1005022.

Thomas, R. H., Zhang, L. M., Carvill, G. L., Archer, J. S., Heavin, S. B., Mandelstam, S. A., … Mefford, H. C., Scheffer, I. E. (2015). CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures. Neurology, 84, 951-8. PMCID: PMC4351660. doi: 10.1212/WNL.0000000000001305. van Bon, B. W., Coe, B. P., Bernier, R. A., Green, C., Gerdts, J., Witherspoon, K., … Mefford, H. C., … Eichler, E. E. (2015). Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular Psychiatry, 21, 126-132. PMCID: PMC4547916. doi: 10.1038/mp.2015.5.

Van Dijck, A., van der Werf, I. M., Reyniers, E., Scheers, S., Azage, M., Siefkas, K., … Mefford, H. C., … Kooy, R. F. (2015). Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities. European Journal of Medical Genetics, 58, 503-8. doi: 10.1016/j.ejmg.2015.08.004.

Andrew Meltzoff Brooks, R., Meltzoff, A. N. (2015). Connecting the dots from infancy to childhood: A longitudinal study connecting gaze following, language, and explicit theory of mind. Journal of Experimental Child Psychology, 130, 67-78. doi: 10.1016/j.jecp.2014.09.010.

Conboy, B. T., Brooks, R., Meltzoff, A. N., Kuhl, P. K. (2015). Social interaction in infants' learning of second-language phonetics: An exploration of brain-behavior relations. Developmental Neuropsychology, 40, 216-29. PMCID: PMC4824050. doi: 10.1080/87565641.2015.1014487.

Marshall, P. J., Meltzoff, A. N. (2015). Body maps in the infant brain. Trends in Cognitive Sciences, 19, 499-505. PMCID: PMC4556559. doi: 10.1016/j.tics.2015.06.012.

Saby, J. N., Meltzoff, A. N., Marshall, P. J. (2015). Neural body maps in human infants: Somatotopic responses to tactile stimulation in 7-month-olds. Neuroimage, 118, 74-8. doi: 10.1016/j.neuroimage.2015.05.097.

Taylor, A. H., Cheke, L. G., Waismeyer, A., Meltzoff, A. N., Miller, R., Gopnik, A., … Gray, R. D. (2015). No conclusive evidence that corvids can create novel causal interventions. Proceedings of the Royal Society B: Biological Sciences, 282, 20150796. PMCID: PMC4632611. doi: 10.1098/rspb.2015.0796.

Waismeyer, A., Meltzoff, A. N., Gopnik, A. (2015). Causal learning from probabilistic events in 24-month-olds: An action measure. Developmental Science, 18, 175-82. doi: 10.1111/desc.12208.

Wang, Z., Williamson, R. A., Meltzoff, A. N. (2015). Imitation as a mechanism in cognitive development: A cross-cultural investigation of 4-year-old children's rule learning. Frontiers in Psychology, 6, 562. PMCID: PMC4429617. doi: 10.3389/fpsyg.2015.00562.

Wang, Z., Meltzoff, A. N., Williamson, R. A. (2015). Social learning promotes understanding of the physical world: Preschool children's imitation of weight sorting. Journal of Experimental Child Psychology, 136, 82-91. doi: 10.1016/j.jecp.2015.02.010.

Kathleen J. Millen

Comer, J. D., Pan, F. C., Willet, S. G., Haldipur, P., Millen, K. J., Wright, C. V., Kaltschmidt, J. A. (2015). Sensory and spinal inhibitory dorsal midline crossing is independent of Robo3. Frontiers in Neural Circuits, 9, 36. PMCID: PMC4511845. doi: 10.3389/fncir.2015.00036.

Haldipur, P., Gillies, G., Janson, O. K., Chizhikov, V. V., Millen, K. J. (2015). Mesenchymal Foxc1 non-autonomously controls cerebellar development through SDF1alpha-CXCR4 maintenance of radial glial cells. International Journal of Developmental Neuroscience, 47, 34. doi: 10.1016/j.ijdevneu.2015.04.097.

Sheri Mizumori

Baker, P. M., Oh, S. E., Kidder, K. S., Mizumori, S. J. (2015). Ongoing behavioral state information signaled in the lateral habenula guides choice flexibility in freely moving rats. Frontiers in Behavioral Neuroscience, 9, 295. PMCID: PMC4631824. doi: 10.3389/fnbeh.2015.00295.

Mizumori, S. J., Tryon, V. L. (2015). Integrative hippocampal and decision-making neurocircuitry during goal-relevant predictions and encoding. Progress in Brain Research, 219, 217-42. doi: 10.1016/bs.pbr.2015.03.010.

Redila, V., Kinzel, C., Jo, Y. S., Puryear, C. B., Mizumori, S. J. (2015). A role for the lateral dorsal tegmentum in memory and decision neural circuitry. Neurobiology of Learning and Memory, 117, 93-108. PMCID: PMC5327698. doi: 10.1016/j.nlm.2014.05.009.

Redish, A. D., Mizumori, S. J. (2015). Memory and decision making. Neurobiology of Learning and Memory, 117, 1-3. PMCID: PMC4428655. doi: 10.1016/j.nlm.2014.08.014.

Cecilia B. Moens Bachmann-Gagescu, R., Dona, M., Hetterschijt, L., Tonnaer, E., Peters, T., de Vrieze, E., … Doherty, D. A., Moens, C. B., … van Wijk, E. (2015). The ciliopathy protein CC2D2A associates with NINL and functions in EAB8-MICAL3-regulated vesicle trafficking. PLoS Genetics, 11, e1005575. PMCID: PMC4617701. doi: 10.1371/journal.pgen.1005575.

Li-Villarreal, N., Forbes, M. M., Loza, A. J., Chen, J., Ma, T., Helde, K., Moens, C. B., … Solnica-Krezel, L. (2015). Dachsous1b cadherin regulates actin and microtubule cytoskeleton during early zebrafish embryogenesis. Development, 142, 2704-18. PMCID: PMC4529026. doi: 10.1242/dev.119800.

Miller, A. C., Voelker, L. H., Shah, A. N., Moens, C. B. (2015). Neurobeachin is required postsynaptically for electrical and chemical synapse formation. Current Biology, 25, 16-28. PMCID: PMC4329981. doi: 10.1016/j.cub.2014.10.071.

Richard Morrison Coughlin, L., Morrison, R. S., Horner, P. J., Inman, D. M. (2015). Mitochondrial morphology differences and mitophagy deficit in murine glaucomatous optic nerve. Investigative Ophthalmology & Visual Science, 56, 1437-46. PMCID: PMC4347310. doi: 10.1167/iovs.14-16126.

Young, J. M., Nelson, J. W., Cheng, J., Zhang, W., Mader, S., Davis, C. M., Morrison, R. S., Alkayed, N. J. (2015). Peroxisomal biogenesis in ischemic brain. Antioxidants & Redox Signaling, 22, 109-20. PMCID: PMC4281844. doi: 10.1089/ars.2014.5833.

Pierre Mourad Peeples, E. S., Mehic, E., Mourad, P. D., Juul, S. E. (2015). Fast Doppler as a novel bedside measure of cerebral perfusion in preterm infants. Pediatric Research, 05 Nov 2015. doi: 10.1038/pr.2015.227.

Suarez, M. W., Dever, D. D., Gu, X., Ray Illian, P., McClintic, A. M., Mehic, E., Mourad, P. D. (2015). Transcranial vibro-acoustography can detect traumatic brain injury, in-vivo: Preliminary studies. Ultrasonics, 61, 151-6. doi: 10.1016/j.ultras.2015.04.014.

Jeffrey Munson Chapman, N. H., Nato, A. Q., Jr., Bernier, R. A., Ankenman, K., Sohi, H., Munson, J., … Webb, S. J., … Raskind, W. H., Brkanac, Z., Wijsman, E. M. (2015). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics, 134, 1055-68. PMCID: PMC4578871. doi: 10.1007/s00439-015-1585-y.

Estes, A. M., Munson, J., Rogers, S. J., Greenson, J., Winter, J., Dawson, G. (2015). Long-term outcomes of early intervention in 6-year-old children with autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 54, 580-7. PMCID: PMC4475272. doi: 10.1016/j.jaac.2015.04.005.

Michael Mustari Brostek, L., Buttner, U., Mustari, M. J., Glasauer, S. (2015). Eye velocity gain fields in mstd during optokinetic stimulation. Cerebral Cortex, 25, 2181-90. PMCID: PMC4494029. doi: 10.1093/cercor/bhu024.

Tang, X., Buttner-Ennever, J. A., Mustari, M. J., Horn, A. K. (2015). Internal organization of medial rectus and inferior rectus muscle neurons in the C group of the oculomotor nucleus in monkey. The Journal of Comparative Neurology, 523, 1809-23. PMCID: PMC4472491. doi: 10.1002/cne.23760.

Walton, M. M., Mustari, M. J. (2015). Abnormal tuning of saccade-related cells in pontine reticular formation of strabismic monkeys. Journal of Neurophysiology, 114, 857-68. PMCID: PMC4533063. doi: 10.1152/jn.00238.2015.

Willoughby, C. L., Fleuriet, J., Walton, M. M., Mustari, M. J., McLoon, L. K. (2015). Adaptability of the immature ocular motor control system: Unilateral IGF-1 medial rectus treatment. Investigative Ophthalmology & Visual Science, 56, 3484-96. PMCID: PMC4463801. doi: 10.1167/iovs.15-16761.

Willoughby, C. L., Fleuriet, J., Walton, M. M., Mustari, M. J., McLoon, L. K. (2015). Adaptation of slow myofibers: The effect of sustained BDNF treatment of extraocular muscles in infant nonhuman primates. Investigative Ophthalmology & Visual Science, 56, 3467-83. PMCID: PMC4464045. doi: 10.1167/iovs.15-16852.

Zeeh, C., Mustari, M. J., Hess, B. J., Horn, A. K. (2015). Transmitter inputs to different motoneuron subgroups in the oculomotor and trochlear nucleus in monkey. Frontiers in Neuroanatomy, 9, 95. PMCID: PMC4513436. doi: 10.3389/fnana.2015.00095.

Edward J. Novotny, Jr. Lerche, H., Novotny, E. J., Jr. (2015). Microscopic brain structure revisited in genetic epilepsy. Neurology, 84, 1290-1. doi: 10.1212/WNL.0000000000001427.

Olson, J. D., Wander, J. D., Johnson, L., Sarma, D., Weaver, K., Novotny, E. J., Jr., Ojemann, J. G., Darvas, F. (2015). Comparison of subdural and subgaleal recordings of cortical high-gamma activity in humans. Clinical Neurophysiology, 127, 277-284. PMCID: PMC4600028. doi: 10.1016/j.clinph.2015.03.014.

Shurtleff, H. A., Barry, D., Firman, T., Warner, M. H., Aguilar-Estrada, R. L., Saneto, R. P., … Novotny, E. J., Jr., Ojemann, J. G. (2015). Impact of epilepsy surgery on development of preschool children: Identification of a cohort likely to benefit from early intervention. Journal of Neurosurgery. Pediatrics, 16, 383-92. doi: 10.3171/2015.3.PEDS14359.

Elizabeth Oesterle Luo, C., Omelchenko, I., Manson, R., Robbins, C., Oesterle, E. C., Cao, G. Z., … Hume, C. R. (2015). Direct intracochlear acoustic stimulation using a PZT microactuator. Trends in Hearing, 19, PMCID: PMC4771031. doi: 10.1177/2331216515616942.

Jeffrey Ojemann Brunton, B. W., Johnson, L. A., Ojemann, J. G., Kutz, J. N. (2015). Extracting spatial-temporal coherent patterns in large-scale neural recordings using dynamic mode decomposition. Journal of Neuroscience Methods, 258, 1-15. doi: 10.1016/j.jneumeth.2015.10.010.

Drane, D. L., Loring, D. W., Voets, N. L., Price, M., Ojemann, J. G., Willie, J. T., … Gross, R. E. (2015). In response: Naming and recognition after laser amygdalohippocampotomy: Is the hippocampus involved? Epilepsia, 56, 1318-9. PMCID: PMC4523895. doi: 10.1111/epi.13065.

Drane, D. L., Loring, D. W., Voets, N. L., Price, M., Ojemann, J. G., Willie, J. T., … Gross, R. E. (2015). Better object recognition and naming outcome with MRI-guided stereotactic laser amygdalohippocampotomy for temporal lobe epilepsy. Epilepsia, 56, 101-13. PMCID: PMC4446987. doi: 10.1111/epi.12860.

Miller, K. J., Hermes, D., Witthoft, N., Rao, R. P., Ojemann, J. G. (2015). The physiology of perception in human temporal lobe is specialized for contextual novelty. Journal of Neurophysiology, 114, 256-63. PMCID: PMC4507949. doi: 10.1152/jn.00131.2015.

Jaime Olavarria Andelin, A. K., Bruning, D. J., Felleman, D. J., Olavarria, J. F. (2015). Visual interhemispheric and striate-extrastriate cortical connections in the rabbit: A multiple tracer study. Neurology Research International, 2015, 591245. PMCID: PMC4578745. doi: 10.1155/2015/591245.

Laing, R. J., Turecek, J., Takahata, T., Olavarria, J. F. (2015). Identification of eye-specific domains and their relation to callosal connections in primary visual cortex of Long Evans rats. Cerebral Cortex, 25, 3314-29. PMCID: PMC4585489. doi: 10.1093/cercor/bhu128.

Jay Parrish Jiang, N., Parrish, J. Z. (2015). Muscles get dendrites into shape. Developmental Cell, 33, 369-70. doi: 10.1016/j.devcel.2015.05.006.

Lee, J., Peng, Y., Lin, W. Y., Parrish, J. Z. (2015). Coordinate control of terminal dendrite patterning and dynamics by the membrane protein Raw. Development, 142, 162-73. PMCID: PMC4299136. doi: 10.1242/dev.113423.

Lin, W. Y., Williams, C., Yan, C., Koledachkina, T., Luedke, K., Dalton, J., … Parrish, J. Z. (2015). The SLC36 transporter Pathetic is required for extreme dendrite growth in Drosophila sensory neurons. Genes & Development, 29, 1120-35. PMCID: PMC4470281. doi: 10.1101/gad.259119.115.

Peng, Y., Lee, J., Rowland, K., Wen, Y., Hua, H., Carlson, N., … Parrish, J. Z., Kim, M. D. (2015). Regulation of dendrite growth and maintenance by exocytosis. Journal of Cell Science, 128, 4279-92. PMCID: PMC4712815. doi: 10.1242/jcs.174771.

David J. Perkel Larson, T. A., Lent, K. L., Bammler, T. K., MacDonald, J. W., Wood, W. E., Caras, M. L., … Perkel, D. J., Brenowitz, E. A. (2015). Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit. BMC Genomics, 16, 905. PMCID: PMC4636775. doi: 10.1186/s12864-015-2175-z.

James Phillips Phillips, C., Ling, L., Oxford, T., Nowack, A., Nie, K., Rubinstein, J. T., Phillips, J. O. (2015). Longitudinal performance of an implantable vestibular prosthesis. Hearing Research, 322, 200-11. PMCID: PMC4369472. doi: 10.1016/j.heares.2014.09.003.

Weiss, A. H., Kelly, J. P., Hopper, R. A., Phillips, J. O. (2015). Crouzon syndrome: Relationship of eye movements to pattern strabismus. Investigative Ophthalmology & Visual Science, 56, 4394-402. doi: 10.1167/iovs.14-15645.

Nicholas Poolos Williams, A. D., Jung, S., Poolos, N. P. (2015). Protein kinase C bidirectionally modulates Ih and hyperpolarization-activated cyclic nucleotide-gated (HCN) channel surface expression in hippocampal pyramidal neurons. The Journal of Physiology, 593, 2779-92. PMCID: PMC4506181. doi: 10.1113/JP270453.

Suzie Pun Choi, J. L., Tan, J. K., Sellers, D. L., Wei, H., Horner, P. J., Pun, S. H. (2015). Guanidinylated block copolymers for gene transfer: A comparison with amine-based materials for in vitro and in vivo gene transfer efficiency. Biomaterials, 54, 87-96. PMCID: PMC4409668. doi: 10.1016/j.biomaterials.2015.03.008.

Tan, J. K., Choi, J. L., Wei, H., Schellinger, J. G., Pun, S. H. (2015). Reducible, dibromomaleimide-linked polymers for gene delivery. Biomaterials Science, 3, 112-20. PMCID: PMC4255961. doi: 10.1039/c4bm00240g.

Wang, C. E., Stayton, P. S., Pun, S. H., Convertine, A. J. (2015). Polymer nanostructures synthesized by controlled living polymerization for tumor-targeted drug delivery. Journal of Controlled Release, 219, 345-354. PMCID: PMC4656053. doi: 10.1016/j.jconrel.2015.08.054.

Bensheng Qiu Long, Q., Li, J., Luo, Q., Hei, Y., Wang, K., Tian, Y., … Qiu, B., Liu, W. (2015). MRI tracking of bone marrow mesenchymal stem cells labeled with ultra-small superparamagnetic iron oxide nanoparticles in a rat model of temporal lobe epilepsy. Neuroscience Letters, 606, 30-5. doi: 10.1016/j.neulet.2015.08.040.

Jan-Marino (Nino) Ramirez Dick, T. E., Dutschmann, M., Feldman, J. L., Fong, A. Y., Hulsmann, S., Morris, K. M., Ramirez, J. M., … Respiratory Neurobiology, Consortium (2015). Facts and challenges in respiratory neurobiology. Respiratory Physiology & Neurobiology, 31 Jan 2015. doi: 10.1016/j.resp.2015.01.014.

Koch, H., Caughie, C., Elsen, F. P., Doi, A., Garcia, A. J., 3rd, Zanella, S., Ramirez, J. M. (2015). Prostaglandin E2 differentially modulates the central control of eupnoea, sighs and gasping in mice. The Journal of Physiology, 593, 305-19. PMCID: PMC4293069. doi: 10.1113/jphysiol.2014.279794.

Bruce Ransom Brown, A. M., Ransom, B. R. (2015). Astrocyte glycogen as an emergency fuel under conditions of glucose deprivation or intense neural activity. Metabolic Brain Disease, 30, 233-9. doi: 10.1007/s11011-014-9588-2.

Hamner, M. A., Ye, Z., Lee, R. V., Colman, J. R., Le, T., Gong, D. C., Ransom, B. R., Weinstein, J. R. (2015). Ischemic preconditioning in white matter: Magnitude and mechanism. The Journal of Neuroscience, 35, 15599-611. PMCID: PMC4659824. doi: 10.1523/JNEUROSCI.2544-15.2015.

Ye, B., Shen, H., Zhang, J., Zhu, Y. G., Ransom, B. R., Chen, X. C., Ye, Z. C. (2015). Dual pathways mediate beta-amyloid stimulated glutathione release from astrocytes. Glia, 63, 2208-19. doi: 10.1002/glia.22886.

Wendy Raskind

Amendola, L. M., Dorschner, M. O., Robertson, P. D., Salama, J. S., Hart, R., Shirts, B. H., … Scott, C. R., … Raskind, W. H., … Jarvik, G. P. (2015). Actionable exomic incidental findings in 6503 participants: Challenges of variant classification. Genome Research, 25, 305-15. PMCID: PMC4352885. doi: 10.1101/gr.183483.114.

Thomas A. Reh Brzezinski, J. A., Reh, T. A. (2015). Photoreceptor cell fate specification in vertebrates. Development, 142, 3263-73. PMCID: PMC4631758. doi: 10.1242/dev.127043.

La Torre, A., Hoshino, A., Cavanaugh, C., Ware, C. B., Reh, T. A. (2015). The GIPC1-Akt1 pathway is required for the specification of the eye field in mouse embryonic stem cells. Stem Cells, 33, 2674-85. PMCID: PMC4549161. doi: 10.1002/stem.2062.

Thompson, D. A., Ali, R. R., Banin, E., Branham, K. E., Flannery, J. G., Gamm, D. M., … Reh, T. A., … Monaciano, Consortium (2015). Advancing therapeutic strategies for inherited retinal degeneration: Recommendations from the Monaciano Symposium. Investigative Ophthalmology & Visual Science, 56, 918-31. PMCID: PMC4554258. doi: 10.1167/iovs.14-16049.

Ueki, Y., Wilken, M. S., Cox, K. E., Chipman, L. B., Bermingham-McDonogh, O., Reh, T. A. (2015). A transient wave of BMP signaling in the retina is necessary for Muller glial differentiation. Development, 142, 533-43. PMCID: PMC4302996. doi: 10.1242/dev.118745.

Ueki, Y., Wilken, M. S., Cox, K. E., Chipman, L., Jorstad, N., Sternhagen, K., … Reh, T. A. (2015). Transgenic expression of the proneural transcription factor Ascl1 in Muller glia stimulates retinal regeneration in young mice. Proceedings of the National Academy of Sciences of the United States of America, 112, 13717-22. PMCID: PMC4640735. doi: 10.1073/pnas.1510595112.

Zhang, J., Taylor, R. J., La Torre, A., Wilken, M. S., Cox, K. E., Reh, T. A., Vetter, M. L. (2015). Ezh2 maintains retinal progenitor proliferation, transcriptional integrity, and the timing of late differentiation. Developmental Biology, 403, 128-38. PMCID: PMC4469612. doi: 10.1016/j.ydbio.2015.05.010.

Todd Richards

Ishiyama, M., Richards, T. L., Parvathaneni, U., Anzai, Y. (2015). Dynamic contrast-enhanced magnetic resonance imaging in head and neck cancer: Differentiation of new H&N cancer, recurrent disease, and benign post-treatment changes. Clinical Imaging, 39, 566-70. doi: 10.1016/j.clinimag.2015.01.016.

Robert Rostomily

Bobola, M. S., Alnoor, M., Chen, J. Y., Kolstoe, D. D., Silbergeld, D. L., Rostomily, R. C., … Silber, J. R. (2015). O-methylguanine-DNA methyltransferase activity is associated with response to alkylating agent therapy and with promoter methylation in glioblastoma and anaplastic glioma. BBA Clinical, 3, 1-10. PMCID: PMC4280839. doi: 10.1016/j.bbacli.2014.11.003.

Ly, K. I., Hamilton, S. R., Rostomily, R. C., Rockhill, J. K., Mrugala, M. M. (2015). Improvement in visual fields after treatment of intracranial meningioma with Bevacizumab. Journal of Neuro-Ophthalmology, 35, 382-6. doi: 10.1097/WNO.0000000000000253.

Mikheev, A. M., Mikheeva, S. A., Trister, A. D., Tokita, M. J., Emerson, S. N., Parada, C. A., … Rostomily, R. C. (2015). Periostin is a novel therapeutic target that predicts and regulates glioma malignancy. Neuro-Oncology, 17, 372-82. PMCID: PMC4483094. doi: 10.1093/neuonc/nou161.

Ramakrishna, R., Hebb, A., Barber, J., Rostomily, R. C., Silbergeld, D. (2015). Outcomes in reoperated low-grade gliomas. Neurosurgery, 77, 175-84; discussion 184. doi: 10.1227/NEU.0000000000000753.

Edwin Rubel Caras, M. L., Sen, K., Rubel, E. W., Brenowitz, E. A. (2015). Seasonal plasticity of precise spike timing in the avian auditory system. The Journal of Neuroscience, 35, 3431-45. PMCID: PMC4339354. doi: 10.1523/JNEUROSCI.3407-14.2015.

Kaur, T., Zamani, D., Tong, L., Rubel, E. W., Ohlemiller, K. K., Hirose, K., Warchol, M. E. (2015). Fractalkine signaling regulates macrophage recruitment into the cochlea and promotes the survival of spiral ganglion neurons after selective hair cell lesion. The Journal of Neuroscience, 35, 15050-61. PMCID: PMC4642237. doi: 10.1523/JNEUROSCI.2325-15.2015.

Kaur, T., Hirose, K., Rubel, E. W., Warchol, M. E. (2015). Macrophage recruitment and epithelial repair following hair cell injury in the mouse utricle. Frontiers in Cellular Neuroscience, 9, 150. PMCID: PMC4406144. doi: 10.3389/fncel.2015.00150.

Stawicki, T. M., Esterberg, R., Hailey, D. W., Raible, D. W., Rubel, E. W. (2015). Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death. Frontiers in Cellular Neuroscience, 9, 46. PMCID: PMC4332341. doi: 10.3389/fncel.2015.00046.

Thomas, A. J., Wu, P., Raible, D. W., Rubel, E. W., Simon, J. A., Ou, H. C. (2015). Identification of small molecule inhibitors of cisplatin-induced hair cell death: Results of a 10,000 compound screen in the zebrafish lateral line. Otology & Neurotology, 36, 519-25. PMCID: PMC4332566. doi: 10.1097/MAO.0000000000000487.

Craig Rubens Cowgill, K. D., Bishop, J., Norgaard, A. K., Rubens, C. E., Gravett, M. G. (2015). Obstetric fistula in low-resource countries: an under-valued and under-studied problem--systematic review of its incidence, prevalence, and association with stillbirth. BMC Pregnancy and Childbirth, 15, 193. PMCID: PMC4550077. doi: 10.1186/s12884-015-0592-2.

Jay Rubinstein Drennan, W. R., Oleson, J. J., Gfeller, K., Crosson, J., Driscoll, V. D., Won, J. H., … Rubinstein, J. T. (2015). Clinical evaluation of music perception, appraisal and experience in cochlear implant users. International Journal of Audiology, 54, 114-23. PMCID: PMC4297259. doi: 10.3109/14992027.2014.948219.

Phillips, C., Ling, L., Oxford, T., Nowack, A., Nie, K., Rubinstein, J. T., Phillips, J. O. (2015). Longitudinal performance of an implantable vestibular prosthesis. Hearing Research, 322, 200-11. PMCID: PMC4369472. doi: 10.1016/j.heares.2014.09.003.

Won, J. H., Jones, G. L., Moon, I. J., Rubinstein, J. T. (2015). Spectral and temporal analysis of simulated dead regions in cochlear implants. Journal of the Association for Research in Otolaryngology, 16, 285-307. PMCID: PMC4368650. doi: 10.1007/s10162-014-0502-8.

Hannele Ruohola-Baker Kuppusamy, K. T., Jones, D. C., Sperber, H., Madan, A., Fischer, K. A., Rodriguez, M. L., … Ruohola- Baker, H. (2015). Let-7 family of microRNA is required for maturation and adult-like metabolism in stem cell-derived cardiomyocytes. Proceedings of the National Academy of Sciences of the United States of America, 112, E2785-94. PMCID: PMC4450404. doi: 10.1073/pnas.1424042112.

Sperber, H., Mathieu, J., Wang, Y., Ferreccio, A., Hesson, J., Xu, Z., … Ruohola-Baker, H. (2015). The metabolome regulates the epigenetic landscape during naive-to-primed human embryonic stem cell transition. Nature Cell Biology, 17, 1523-35. PMCID: PMC4662931. doi: 10.1038/ncb3264.

Xing, Y., Su, T. T., Ruohola-Baker, H. (2015). Tie-mediated signal from apoptotic cells protects stem cells in Drosophila melanogaster. Nature Communications, 6, 7058. PMCID: PMC4451836. doi: 10.1038/ncomms8058.

Gene Sackett Curtis, B., Liberato, N., Rulien, M., Morrisroe, K., Kenney, C., Yutuc, V., … Burbacher, T. M., Sackett, G. P., Hewitson, L. (2015). Examination of the safety of pediatric vaccine schedules in a non-human primate model: Assessments of neurodevelopment, learning, and social behavior. Environmental Health Perspectives, 123, 579-89. PMCID: PMC4455585. doi: 10.1289/ehp.1408257.

Gadad, B. S., Li, W., Yazdani, U., Grady, S., Johnson, T., Hammond, J., … Sackett, G. P., … German, D. C. (2015). Administration of thimerosal-containing vaccines to infant rhesus Macaques does not result in autism-like behavior or neuropathology. Proceedings of the National Academy of Sciences of the United States of America, 112, 12498-503. PMCID: PMC4603476. doi: 10.1073/pnas.1500968112.

C. Ronald Scott Amendola, L. M., Dorschner, M. O., Robertson, P. D., Salama, J. S., Hart, R., Shirts, B. H., … Scott, C. R., … Raskind, W. H., … Jarvik, G. P. (2015). Actionable exomic incidental findings in 6503 participants: Challenges of variant classification. Genome Research, 25, 305-15. PMCID: PMC4352885. doi: 10.1101/gr.183483.114.

Charrow, J., Scott, C. R. (2015). Long-term treatment outcomes in Gaucher disease. American Journal of Hematology, 90, S19-24. doi: 10.1002/ajh.24056.

Gelb, M. H., Scott, C. R., Turecek, F. (2015). Newborn screening for lysosomal storage diseases. Clinical Chemistry, 61, 335-46. PMCID: PMC4345406. doi: 10.1373/clinchem.2014.225771.

Germain, D. P., Charrow, J., Desnick, R. J., Guffon, N., Kempf, J., Lachmann, R. H., … Scott, C. R., … Wilcox, W. R. (2015). Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease. Journal of Medical Genetics, 52, 353-8. PMCID: PMC4413801. doi: 10.1136/jmedgenet-2014-102797.

Ghomashchi, F., Barcenas, M., Turecek, F., Scott, C. R., Gelb, M. H. (2015). Reliable assay of acid sphingomyelinase deficiency with the mutation q292k by tandem mass spectrometry. Clinical Chemistry, 61, 771-2. PMCID: PMC4733389. doi: 10.1373/clinchem.2014.236448.

Kumar, A. B., Masi, S., Ghomashchi, F., Chennamaneni, N. K., Ito, M., Scott, C. R., … Spacil, Z. (2015). Tandem mass spectrometry has a larger analytical range than fluorescence assays of lysosomal enzymes: Application to newborn screening and diagnosis of mucopolysaccharidoses types ii, iva, and vi. Clinical Chemistry, 61, 1363-71. PMCID: PMC4737431. doi: 10.1373/clinchem.2015.242560.

Kumar, A. B., Spacil, Z., Ghomashchi, F., Masi, S., Sumida, T., Ito, M., … Scott, C. R., Gelb, M. H. (2015). Fluorimetric assays for N-acetylgalactosamine-6-sulfatase and arylsulfatase B based on the natural substrates for confirmation of mucopolysaccharidoses types IVA and VI. Clinica Chimica Acta, 451, 125-8. PMCID: PMC4656091. doi: 10.1016/j.cca.2015.08.010.

Marcadier, J. L., Boland, M., Scott, C. R., Issa, K., Wu, Z., McIntyre, A. D., … Lines, M. A. (2015). Congenital sucrase-isomaltase deficiency: Identification of a common Inuit founder mutation. CMAJ, 187, 102-7. PMCID: PMC4312148. doi: 10.1503/cmaj.140657.

Spacil, Z., Babu Kumar, A., Liao, H. C., Auray-Blais, C., Stark, S., Suhr, T. R., Scott, C. R., … Gelb, M. H. (2015). Sulfatide analysis by mass spectrometry for screening of metachromatic leukodystrophy in dried blood and urine samples. Clinical Chemistry, Dec 2015. doi: 10.1373/clinchem.2015.245159.

Underhill, H. R., Golden-Grant, K., Garrett, L. T., Uhrich, S., Zielinski, B. A., Scott, C. R. (2015). Detecting the effects of Fabry disease in the adult human brain with diffusion tensor imaging and fast bound-pool fraction imaging. Journal of Magnetic Resonance Imaging, 42, 1611-22. PMCID: PMC4662657. doi: 10.1002/jmri.24952.

Wijburg, F. A., Benichou, B., Bichet, D. G., Clarke, L. A., Dostalova, G., Fainboim, A., … Scott, C. R., … Ramaswami, U. (2015). Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial. PLoS One, 10, e0124987. PMCID: PMC4425695. doi: 10.1371/journal.pone.0124987.

Dennis Shaw Dager, S. R., Corrigan, N. M., Shaw, D. W. W. (2015). Brain lactate as a potential biomarker for comorbid anxiety disorder in autism spectrum disorder. JAMA Psychiatry, 72, 190. doi: 10.1001/jamapsychiatry.2014.2419.

Stephen E. P. Smith Gopal, A. K., Chen, R., Smith, S. E. P., Ansell, S. M., Rosenblatt, J. D., Savage, K. J., … Younes, A. (2015). Durable remissions in a pivotal phase 2 study of brentuximab vedotin in relapsed or refractory Hodgkin lymphoma. Blood, 125, 1236-43. PMCID: PMC4335079. doi: 10.1182/blood-2014-08-595801.

Donald Sodora Kilgore, K. M., Murphy, M. K., Burton, S. L., Wetzel, K. S., Smith, S. A., Xiao, P., … Sodora, D. L., … Derdeyn, C. A. (2015). Characterization and implementation of a diverse simian immunodeficiency virus SIVsm envelope panel in the assessment of neutralizing antibody breadth elicited in rhesus Macaques by multimodal vaccines expressing the SIVmac239 envelope. Journal of Virology, 89, 8130-51. PMCID: PMC4524250. doi: 10.1128/JVI.01221-14.

Mir, K. D., Mavigner, M., Wang, C., Paiardini, M., Sodora, D. L., Chahroudi, A. M., … Silvestri, G. (2015). Reduced simian immunodeficiency virus replication in macrophages of sooty mangabeys is associated with increased expression of host restriction factors. Journal of Virology, 89, 10136-44. PMCID: PMC4580171. doi: 10.1128/JVI.00710-15.

Tchakoute, C. T., Hesseling, A. C., Kidzeru, E. B., Gamieldien, H., Passmore, J. A., Jones, C. E., … Sodora, D. L., Jaspan, H. B. (2015). Delaying BCG vaccination until 8 weeks of age results in robust BCG-specific T-cell responses in HIV-exposed infants. The Journal of Infectious Diseases, 211, 338-46. PMCID: PMC4318913. doi: 10.1093/infdis/jiu434.

Matthew Speltz Collett, B. R., Huebner, C. E., Seminario, A. L., Wallace, E., Gray, K. E., Speltz, M. L. (2015). Observed child and parent toothbrushing behaviors and child oral health. International Journal of Paediatric Dentistry, 04 Jul 2015. doi: 10.1111/ipd.12175.

Cradock, M. M., Gray, K. E., Kapp-Simon, K. A., Collett, B. R., Buono, L. A., Speltz, M. L. (2015). Sex differences in the neurodevelopment of school-age children with and without single-suture craniosynostosis. Child's Nervous System, 31, 1103-11. doi: 10.1007/s00381-015-2671-0.

Gray, K. E., Cradock, M. M., Kapp-Simon, K. A., Collett, B. R., Pullmann, L. D., Speltz, M. L. (2015). Longitudinal analysis of parenting stress in mothers and fathers of infants with and without single-suture craniosynostosis. The Cleft Palate-Craniofacial Journal, 52, 3-11. doi: 10.1597/13-239.

Gray, K. E., Kapp-Simon, K. A., Starr, J. R., Collett, B. R., Wallace, E. R., Speltz, M. L. (2015). Predicting developmental delay in a longitudinal cohort of preschool children with single-suture craniosynostosis: Is neurobehavioral assessment important? Developmental Medicine and Child Neurology, 57, 456-62. PMCID: PMC4397127. doi: 10.1111/dmcn.12643.

Speltz, M. L., Birgfeld, C., Starr, J. R., Collett, B., Kapp-Simon, K. (2015). The effects of whole-vault cranioplasty versus strip craniectomy on long-term neuropsychological outcomes in sagittal craniosynostosis. Plastic and Reconstructive Surgery, 135, 646e-647e. doi: 10.1097/PRS.0000000000001067.

Susan Spieker Thomas, K. A., Burr, R. L., Spieker, S. J. (2015). Maternal and infant activity: Analytic approaches for the study of circadian rhythm. Infant Behavior & Development, 41, 80-7. PMCID: PMC4644484. doi: 10.1016/j.infbeh.2015.08.002.

Mark Stein Bedard, A. C., Stein, M. A., Halperin, J. M., Krone, B., Rajwan, E., Newcorn, J. H. (2015). Differential impact of methylphenidate and atomoxetine on sustained attention in youth with attention-deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry and Allied Disciplines, 56, 40-8. PMCID: PMC4272337. doi: 10.1111/jcpp.12272.

Gaedigk, A., Freeman, N., Hartshorne, T., Riffel, A. K., Irwin, D., Bishop, J. R., Stein, M. A., … Leeder, J. S. (2015). SNP genotyping using TaqMan technology: the CYP2D6*17 assay conundrum. Scientific Reports, 5, 9257. PMCID: PMC4365394. doi: 10.1038/srep09257.

Hammer, R., Cooke, G. E., Stein, M. A., Booth, J. R. (2015). Functional neuroimaging of visuospatial working memory tasks enables accurate detection of attention deficit and hyperactivity disorder. NeuroImage: Clinical, 9, 244-52. PMCID: PMC4576365. doi: 10.1016/j.nicl.2015.08.015.

Hammer, R., Tennekoon, M., Cooke, G. E., Gayda, J., Stein, M. A., Booth, J. R. (2015). Feedback associated with expectation for larger-reward improves visuospatial working memory performances in children with ADHD. Developmental Cognitive Neuroscience, 14, 38-49. PMCID: PMC4536089. doi: 10.1016/j.dcn.2015.06.002.

Snyder, S. M., Rugino, T. A., Hornig, M., Stein, M. A. (2015). Integration of an EEG biomarker with a clinician's ADHD evaluation. Brain and Behavior, 5, e00330. PMCID: PMC4356845. doi: 10.1002/brb3.330.

Stein, M. A., Sikirica, V., Weiss, M. D., Robertson, B., Lyne, A., Newcorn, J. H. (2015). Does guanfacine extended release impact functional impairment in children with attention-deficit/hyperactivity disorder? Results from a randomized controlled trial. CNS Drugs, 29, 953-62. PMCID: PMC4653245. doi: 10.1007/s40263-015-0291-6.

Stein, M. A., Shaffer, M., Echo-Hawk, A., Smith, J., Stapleton, A., Melvin, A. (2015). Research start: A multimethod study of barriers and accelerators of recruiting research participants. Clinical and Translational Science, 8, 647-54. PMCID: PMC4753776. doi: 10.1111/cts.12351.

Nephi Stella Di Marzo, V., Stella, N., Zimmer, A. (2015). Endocannabinoid signalling and the deteriorating brain. Nature Reviews. Neuroscience, 16, 30-42. PMCID: PMC4471876. doi: 10.1038/nrn3876.

Fung, S., Cherry, A. E., Xu, C., Stella, N. (2015). Alkylindole-sensitive receptors modulate microglial cell migration and proliferation. Glia, 63, 1797-808. PMCID: PMC4418235. doi: 10.1002/glia.22845.

Kow, R. L., Cheng, E. M., Jiang, K., Le, J. H., Stella, N., Nathanson, N. M. (2015). Muscarinic M1 receptor and cannabinoid CB1 receptor do not modulate paraoxon-induced seizures. Pharmacology Research & Perspectives, 3, e00100. PMCID: PMC4317231. doi: 10.1002/prp2.100.

Ling, X., Zhang, S., Shao, P., Li, W., Yang, L., Ding, Y., … Stella, N., Bai, M. (2015). A novel near-infrared fluorescence imaging probe that preferentially binds to cannabinoid receptors CB2R over CB1R. Biomaterials, 57, 169-78. PMCID: PMC4426855. doi: 10.1016/j.biomaterials.2015.04.018.

Wendy Stone Durkin, M. S., Elsabbagh, M., Barbaro, J., Gladstone, M., Happe, F., Hoekstra, R. A., … Stone, W. L., … Shih, A. (2015). Autism screening and diagnosis in low resource settings: Challenges and opportunities to enhance research and services worldwide. Autism Research, 8, 473-6. PMCID: PMC4901137. doi: 10.1002/aur.1575.

Key, A. P., Ibanez, L. V., Henderson, H. A., Warren, Z., Messinger, D. S., Stone, W. L. (2015). Positive affect processing and joint attention in infants at high risk for autism: An exploratory study. Journal of Autism and Developmental Disorders, 45, 4051-62. PMCID: PMC4305358. doi: 10.1007/s10803-014-2191-x.

Key, A. P., Ibanez, L. V., Henderson, H. A., Warren, Z., Messinger, D. S., Stone, W. L. (2015). Erratum to: Positive affect processing and joint attention in infants at high risk for autism: An exploratory study. Journal of Autism and Developmental Disorders, 45, 4063. doi: 10.1007/s10803-014-2213-8.

Lambert-Brown, B. L., McDonald, N. M., Mattson, W. I., Martin, K. B., Ibanez, L. V., Stone, W. L., Messinger, D. S. (2015). Positive emotional engagement and autism risk. Developmental Psychology, 51, 848-55. PMCID: PMC4446222. doi: 10.1037/a0039182.

Messinger, D. S., Young, G. S., Webb, S. J., Ozonoff, S., Bryson, S. E., Carter, A., … Stone, W. L., … Zwaigenbaum, L. (2015). Early sex differences are not autism-specific: A Baby Siblings Research Consortium (BSRC) study. Molecular Autism, 6, 32. PMCID: PMC4455973. doi: 10.1186/s13229-015-0027-y.

Ozonoff, S., Young, G. S., Landa, R. J., Brian, J., Bryson, S., Charman, T., … Stone, W. L., … Iosif, A. M. (2015). Diagnostic stability in young children at risk for autism spectrum disorder: A Baby Siblings Research Consortium Study. Journal of Child Psychology and Psychiatry and Allied Disciplines, 56, 988-98. PMCID: PMC4532646. doi: 10.1111/jcpp.12421.

Weitlauf, A. S., Vehorn, A. C., Stone, W. L., Fein, D., Warren, Z. E. (2015). Using the M-CHAT-R/F to identify developmental concerns in a high-risk 18-month-old sibling sample. Journal of Developmental and Behavioral Pediatrics, 36, 497-502. PMCID: PMC4564349. doi: 10.1097/DBP.0000000000000194.

Colin Studholme

Studholme, C. (2015). Mapping the developing human brain in utero using quantitative MR imaging techniques. Seminars in Perinatology, 39, 105-12. PMCID: PMC4383603. doi: 10.1053/j.semperi.2015.01.003.

Wang, X., Pettersson, D. R., Studholme, C., Kroenke, C. D. (2015). Characterization of laminar zones in the mid-gestation primate brain with magnetic resonance imaging and histological methods. Frontiers in Neuroanatomy, 9, 147. PMCID: PMC4656822. doi: 10.3389/fnana.2015.00147.

Stephen Tapscott Balog, J., Thijssen, P. E., Shadle, S., Straasheijm, K. R., van der Vliet, P. J., Krom, Y. D., … Tapscott, S. J., van der Maarel, S. M. (2015). Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4. Epigenetics, 10, 1133-42. PMCID: PMC4844215. doi: 10.1080/15592294.2015.1113798.

Daxinger, L., Tapscott, S. J., van der Maarel, S. M. (2015). Genetic and epigenetic contributors to FSHD. Current Opinion in Genetics & Development, 33, 56-61. PMCID: PMC4674299. doi: 10.1016/j.gde.2015.08.007.

Feng, Q., Snider, L., Jagannathan, S., Tawil, R., van der Maarel, S. M., Tapscott, S. J.,Bradley, R. K. (2015). A feedback loop between nonsense-mediated decay and the retrogene DUX4 in Facioscapulohumeral muscular dystrophy. eLife, 4, PMCID: PMC4383350. doi: 10.7554/eLife.04996.

Fong, A. P., Yao, Z., Zhong, J. W., Johnson, N. M., Farr, G. H., 3rd, Maves, L., Tapscott, S. J. (2015). Conversion of MyoD to a neurogenic factor: Binding site specificity determines lineage. Cell Reports, 10, 1937-46. PMCID: PMC4683018. doi: 10.1016/j.celrep.2015.02.055.

Lemmers, R. J., Goeman, J. J., van der Vliet, P. J., van Nieuwenhuizen, M. P., Balog, J., Vos-Versteeg, M., … Tapscott, S. J., … van der Maarel, S. M. (2015). Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2. Human Molecular Genetics, 24, 659-69. PMCID: PMC4291246. doi: 10.1093/hmg/ddu486.

Lemmers, R. J., van den Boogaard, M. L., van der Vliet, P. J., Donlin-Smith, C. M., Nations, S. P., Ruivenkamp, C. A., … Tapscott, S. J., … van der Maarel, S. M. (2015). Hemizygosity for SMCHD1 in Facioscapulohumeral muscular dystrophy type 2: Consequences for 18p deletion syndrome. Human Mutation, 36, 679-83. PMCID: PMC4475473. doi: 10.1002/humu.22792.

Lim, J. W., Snider, L., Yao, Z., Tawil, R., Van Der Maarel, S. M., Rigo, F., … Tapscott, S. J. (2015). DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD. Human Molecular Genetics, 24, 4817-28. PMCID: PMC4527486. doi: 10.1093/hmg/ddv206.

Statland, J. M., Shah, B., Henderson, D., Van Der Maarel, S., Tapscott, S. J., Tawil, R. (2015). Muscle pathology grade for Facioscapulohumeral muscular dystrophy biopsies. Muscle & Nerve, 52, 521-6. PMCID: PMC4546927. doi: 10.1002/mus.24621.

Statland, J. M., Odrzywolski, K. J., Shah, B., Henderson, D., Fricke, A. F., van der Maarel, S. M., Tapscott, S. J., Tawil, R. (2015). Immunohistochemical characterization of Facioscapulohumeral muscular dystrophy muscle biopsies. Journal of Neuromuscular Diseases, 2, 291-299. PMCID: PMC4560242. doi: 10.3233/JND-150077.

Statland, J. M., Donlin-Smith, C. M., Tapscott, S. J., Lemmers, R. J., van der Maarel, S. M., Tawil, R. (2015). Milder phenotype in Facioscapulohumeral dystrophy with 7-10 residual D4Z4 repeats. Neurology, 85, 2147-50. PMCID: PMC4691686. doi: 10.1212/WNL.0000000000002217.

Yang, Z. J., Broz, D. K., Noderer, W. L., Ferreira, J. P., Overton, K. W., Spencer, S. L., … Tapscott, S. J., … Wang, C. L. (2015). p53 suppresses muscle differentiation at the myogenin step in response to genotoxic stress. Cell Death and Differentiation, 22, 560-73. PMCID: PMC4356341. doi: 10.1038/cdd.2014.189.

Bruce Tempel Kopp-Scheinpflug, C., Tempel, B. L. (2015). Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder. Hearing Research, 330, 213-20. PMCID: PMC4689642. doi: 10.1016/j.heares.2015.06.014.

Peguero, B., Tempel, B. L. (2015). A chromosome 17 locus engenders frequency-specific non-progressive hearing loss that contributes to age-related hearing loss in mice. Journal of the Association for Research in Otolaryngology, 16, 459-71. PMCID: PMC4488168. doi: 10.1007/s10162-015-0519-7.

Jeffrey Tsai Adams Waldorf, K. M., Singh, N., Mohan, A. R., Young, R. C., Ngo, L., Das, A., Tsai, J. J., … Johnson, M. R. (2015). Uterine overdistention induces preterm labor mediated by inflammation: Observations in pregnant women and nonhuman primates. American Journal of Obstetrics and Gynecology, 213, 830 e1-830 e19. PMCID: PMC4679421. doi: 10.1016/j.ajog.2015.08.028.

Hannah Tully Paciorkowski, A. R., McDaniel, S. S., Jansen, L. A., Tully, H. M., Tuttle, E., Ghoneim, D. H., … Dobyns, W. B., Hahn, S. (2015). Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia, 56, 422-30. PMCID: PMC4363281. doi: 10.1111/epi.12914.

Tully, H. M., Capote, R. T., Saltzman, B. S. (2015). Maternal and infant factors associated with infancy-onset hydrocephalus in Washington State. Pediatric Neurology, 52, 320-5. PMCID: PMC4365975. doi: 10.1016/j.pediatrneurol.2014.10.030.

Eric Turner Fortney, J. C., Pyne, J. M., Turner, E. E., Farris, K. M., Normoyle, T. M., Avery, M. D., … Unutzer, J. (2015). Telepsychiatry integration of mental health services into rural primary care settings. International Review of Psychiatry, 27, 525-39. doi: 10.3109/09540261.2015.1085838.

Huang, S., O'Donovan, K. J., Turner, E. E., Zhong, J., Ginty, D. D. (2015). Extrinsic and intrinsic signals converge on the Runx1/CBFbeta transcription factor for nonpeptidergic nociceptor maturation. eLife, 4, e10874. PMCID: PMC4657622. doi: 10.7554/eLife.10874.

Quina, L. A., Tempest, L., Ng, L., Harris, J. A., Ferguson, S., Jhou, T. C., Turner, E. E. (2015). Efferent pathways of the mouse lateral habenula. The Journal of Comparative Neurology, 523, 32-60. PMCID: PMC4232452. doi: 10.1002/cne.23662.

Jashvant Unadkat Kumar, V., Prasad, B., Patilea, G., Gupta, A., Salphati, L., Evers, R., … Unadkat, J. D. (2015). Quantitative transporter proteomics by liquid chromatography with tandem mass spectrometry: Addressing methodologic issues of plasma membrane isolation and expression-activity relationship. Drug Metabolism and Disposition, 43, 284-8. doi: 10.1124/dmd.114.061614.

Liu, H., Yu, N., Lu, S., Ito, S., Zhang, X., Prasad, B., … Unadkat, J. D., … Sahi, J. (2015). Solute carrier family of the organic anion-transporting polypeptides 1A2-Madin-Darby canine kidney II: A promising in vitro system to understand the role of organic anion-transporting polypeptide 1A2 in blood-brain barrier drug penetration. Drug Metabolism and Disposition, 43, 1008-18. doi: 10.1124/dmd.115.064170.

Liu, L., Collier, A. C., Link, J. M., Domino, K. B., Mankoff, D. A., Eary, J. F., … Unadkat, J. D. (2015). Modulation of P-glycoprotein at the human blood-brain barrier by Quinidine or Rifampin Treatment: A positron emission tomography imaging study. Drug Metabolism and Disposition, 43, 1795-804. PMCID: PMC4613948. doi: 10.1124/dmd.114.058685.

Prasad, B., Unadkat, J. D. (2015). The concept of fraction of drug transported (ft) with special emphasis on BBB efflux of CNS and antiretroviral drugs. Clinical Pharmacology and Therapeutics, 97, 320-3. doi: 10.1002/cpt.72.

Shirasaka, Y., Chaudhry, A. S., McDonald, M., Prasad, B., Wong, T., Calamia, J. C., … Unadkat, J. D., … Thummel, K. E. (2015). Interindividual variability of CYP2C19-catalyzed drug metabolism due to differences in gene diplotypes and cytochrome P450 oxidoreductase content. The Pharmacogenomics Journal, 1 Sept 2015. doi: 10.1038/tpj.2015.58.

Zhang, Z., Farooq, M., Prasad, B., Grepper, S., Unadkat, J. D. (2015). Prediction of gestational age-dependent induction of in vivo hepatic CYP3A activity based on HepaRG cells and human hepatocytes. Drug Metabolism and Disposition, 43, 836-42. PMCID: PMC4429679. doi: 10.1124/dmd.114.062984.

Sara Jane Webb

Baldarcara, L., Currie, S., Hadjivassiliou, M., Hoggard, N., Jack, A., Jackowski, A. P., … Webb, S. J., Habas, C. (2015). Consensus paper: Radiological biomarkers of cerebellar diseases. Cerebellum (London, England), 14, 175-96. PMCID: PMC4929983. doi: 10.1007/s12311-014-0610-3.

Jones, E. J., Venema, K., Lowy, R., Earl, R. K., Webb, S. J. (2015). Developmental changes in infant brain activity during naturalistic social experiences. Developmental Psychobiology, 57, 842-53. PMCID: PMC4615531. doi: 10.1002/dev.21336.

Navot, N., Jorgenson, A. G., Vander Stoep, A., Toth, K., Webb, S. J. (2015). Family planning and family vision in mothers after diagnosis of a child with autism spectrum disorder. Autism, 22 Sept 2015. doi: 10.1177/1362361315602134.

Jonathan Weinstein Becker, K., Kohen, R., Lee, R., Tanzi, P., Zierath, D., Cain, K., … Weinstein, J. R. (2015). Poststroke fatigue: Hints to a biological mechanism. Journal of Stroke & Cerebrovascular Diseases, 24, 618-21. PMCID: PMC4359660. doi: 10.1016/j.jstrokecerebrovasdis.2014.10.008.

Santiago-Ortiz, J., Ojala, D. S., Westesson, O., Weinstein, J. R., Wong, S. Y., Steinsapir, A., … Schaffer, D. V. (2015). AAV ancestral reconstruction library enables selection of broadly infectious viral variants. Gene Therapy, 22, 934-46. PMCID: PMC4509550. doi: 10.1038/gt.2015.74.

Weinstein, J. R., Quan, Y., Hanson, J. F., Colonna, L., Iorga, M., Honda, S., … Moller, T. (2015). IgM-dependent phagocytosis in microglia is mediated by complement receptor 3, not Fcalpha/mu receptor. Journal of Immunology, 195, 5309-17. PMCID: PMC4655136. doi: 10.4049/jimmunol.1401195.

John P. Welsh Zhu, Z., Zeng, X. H., Turecek, J., Han, V. Z., Welsh, J. P. (2015). RNA interference of GluN1 inhibits neuronal rhythmogenesis in the adult inferior olive. Journal of Molecular Neuroscience, 55, 416-29. doi: 10.1007/s12031-014-0353-0.

Ellen M. Wijsman Chapman, N. H., Nato, A. Q., Jr., Bernier, R. A., Ankenman, K., Sohi, H., Munson, J., … Webb, S. J., … Raskind, W. H., Brkanac, Z., Wijsman, E. M. (2015). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics, 134, 1055-68. PMCID: PMC4578871. doi: 10.1007/s00439-015-1585-y.

Zhengui Xia Choi, W. S., Kim, H. W., Xia, Z. (2015). JNK inhibition of VMAT2 contributes to rotenone-induced oxidative stress and dopamine neuron death. Toxicology, 328, 75-81. PMCID: PMC4308505. doi: 10.1016/j.tox.2014.12.005.

Engstrom, A., Wang, H., Xia, Z. (2015). Lead decreases cell survival, proliferation, and neuronal differentiation of primary cultured adult neural precursor cells through activation of the JNK and p38 MAP kinases. Toxicology in Vitro, 29, 1146-55. PMCID: PMC4457670. doi: 10.1016/j.tiv.2015.05.001.

Kim, H. W., Choi, W. S., Sorscher, N., Park, H. J., Tronche, F., Palmiter, R. D., Xia, Z. (2015). Genetic reduction of mitochondrial complex I function does not lead to loss of dopamine neurons in vivo. Neurobiology of Aging, 36, 2617-27. PMCID: PMC4523431. doi: 10.1016/j.neurobiolaging.2015.05.008.

Luo, J., Chen, X., Pan, Y. W., Lu, S., Xia, Z., Storm, D. R. (2015). The type 3 adenylyl cyclase is required for the survival and maturation of newly generated granule cells in the olfactory bulb. PLoS One, 10, e0122057. PMCID: PMC4373939. doi: 10.1371/journal.pone.0122057.

Wang, W., Lu, S., Li, T., Pan, Y. W., Zou, J., Abel, G. M., Xu, L., … Xia, Z. (2015). Inducible activation of ERK5 MAP kinase enhances adult neurogenesis in the olfactory bulb and improves olfactory function. The Journal of Neuroscience, 35, 7833-49. PMCID: PMC4438129. doi: 10.1523/JNEUROSCI.3745-14.2015.

Yu, A. K., Song, L., Murray, K. D., van der List, D., Sun, C., Shen, Y., Xia, Z., Cortopassi, G. A. (2015). Mitochondrial complex I deficiency leads to inflammation and retinal ganglion cell death in the Ndufs4 mouse. Human Molecular Genetics, 24, 2848-60. PMCID: PMC4406296. doi: 10.1093/hmg/ddv045.

Zou, J., Wang, W., Pan, Y. W., Abel, G. M., Storm, D. R., Xia, Z. (2015). Conditional inhibition of adult neurogenesis by inducible and targeted deletion of ERK5 MAP kinase is not associated with anxiety/depression-like behaviors(1,2). eNeuro, 2, PMCID: PMC4596085. doi: 10.1523/ENEURO.0014-14.2015.

Zou, J., Wang, W., Pan, Y. W., Lu, S., Xia, Z. (2015). Methods to measure olfactory behavior in mice. Current Protocols in Toxicology, 63, 11 18 1-21. PMCID: PMC4339283. doi: 10.1002/0471140856.tx1118s63.

Libin Xu Wang, W., Lu, S., Li, T., Pan, Y. W., Zou, J., Abel, G. M., Xu, L., … Xia, Z. (2015). Inducible activation of ERK5 MAP kinase enhances adult neurogenesis in the olfactory bulb and improves olfactory function. The Journal of Neuroscience, 35, 7833-49. PMCID: PMC4438129. doi: 10.1523/JNEUROSCI.3745-14.2015.

Jing Zhang

de Cabo, R., Liu, L., Ali, A., Price, N., Zhang, J., Wang, M., … Irusta, P. M. (2015). Serum from calorie-restricted animals delays senescence and extends the lifespan of normal human fibroblasts in vitro. Aging (Albany NY), 7, 152-66. PMCID: PMC4394727. doi: 10.18632/aging.100719.

Jing, H., Ozdemir, S. K., Geng, Z., Zhang, J., Lu, X. Y., Peng, B., … Nori, F. (2015). Optomechanically-induced transparency in parity-time-symmetric microresonators. Scientific Reports, 5, 9663. PMCID: PMC4500988. doi: 10.1038/srep09663.

Lou, Y., Han, Y., Yang, L., Wu, M., Zhang, J., Cheng, J., … Li, G. (2015). CmpacC regulates mycoparasitism, oxalate degradation and antifungal activity in the mycoparasitic fungus Coniothyrium minitans. Environmental Microbiology, 17, 4711-29. doi: 10.1111/1462-2920.13018.

Peskind, E. R., Kraemer, B., Zhang, J. (2015). Biofluid biomarkers of mild traumatic brain injury: Whither plasma tau. JAMA Neurology, 72, 1103-5. doi: 10.1001/jamaneurol.2015.1789.

Wang, Z., Zhou, Y., Luo, Y., Zhang, J., Zhai, Y., Yang, D., … Ma, R. Z. (2015). Gene expression profiles of main olfactory epithelium in adenylyl cyclase 3 knockout mice. International Journal of Molecular Sciences, 16, 28320-33. PMCID: PMC4691054. doi: 10.3390/ijms161226107.

Yu, L., Sang, W., Wu, M. D., Zhang, J., Yang, L., Zhou, Y. J., … Li, G. Q. (2015). Novel hypovirulence-associated RNA mycovirus in the plant-pathogenic fungus Botrytis cinerea: Molecular and biological characterization. Applied and Environmental Microbiology, 81, 2299-310. PMCID: PMC4357927. doi: 10.1128/AEM.03992-14.

Zhang, J., Jiao, J., Cermelli, S., Muir, K., Jung, K. H., Zou, R., … Beretta, L. (2015). miR-21 inhibition reduces liver fibrosis and prevents tumor development by inducing apoptosis of CD24+ progenitor cells. Cancer Research, 75, 1859-67. PMCID: PMC4603420. doi: 10.1158/0008-5472.CAN-14-1254.

Zhang, T., Tian, X., Wang, Q., Tong, Y., Wang, H., Li, Z., … Zhang, J., … Chui, D. (2015). Surgical stress induced depressive and anxiety like behavior are improved by dapsone via modulating NADPH oxidase level. Neuroscience Letters, 585, 103-8. doi: 10.1016/j.neulet.2014.11.045.

2016

Kristina Adams Waldorf

Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Hughes, S. M., Shu, Z., Levy, C. N., Ferre, A. L., Hartig, H., Fang, C., … Adams Waldorf, K. M., … Hladik, F. (2016). Cryopreservation of human mucosal leukocytes. PLoS One, 11, e0156293. PMCID: PMC4883784. doi: 10.1371/journal.pone.0156293.

Vornhagen, J., Quach, P., Boldenow, E., Merillat, S., Whidbey, C., Ngo, L. Y., Adams Waldorf, K. M., Rajagopal, L. (2016). Bacterial hyaluronidase promotes ascending GBS infection and preterm birth. mBio, 7, PMCID: PMC4937215. doi: 10.1128/mBio.00781-16.

Elizabeth Aylward Faja, S., Dawson, G., Aylward, E. H., Wijsman, E. M., Webb, S. J. (2016). Early event-related potentials to emotional faces differ for adults with autism spectrum disorder and by serotonin transporter genotype. Clinical Neurophysiology, 127, 2436-47. PMCID: PMC5279301. doi: 10.1016/j.clinph.2016.02.022.

Kleinhans, N. M., Richards, T. L., Greenson, J., Dawson, G., Aylward, E. H. (2016). Altered dynamics of the fMRI response to faces in individuals with autism. Journal of Autism and Developmental Disorders, doi: 10.1007/s10803-015-2565-8.

Forrest Bennett Chesley, P., Sanchez, S. E., Melzer, L., Oron, A., Horslen, S., Bennett, C. F., Javid, P. J. (2016). Neurodevelopmental and cognitive outcomes in children with intestinal failure. Journal of Pediatric Gastroenterology and Nutrition, 63, 41-45. doi: 10.1097/mpg.0000000000001067.

Olivia Bermingham-McDonogh Slowik, Amber D., Bermingham-McDonogh, O. (2016). A central to peripheral progression of cell cycle exit and hair cell differentiation in the developing mouse cristae. Developmental Biology, 411, 1-14. PMCID: PMC4769996. doi: 10.1016/j.ydbio.2016.01.033.

Raphael Bernier Bernier, R. A., Steinman, K. J., Reilly, B., Wallace, A. S., Sherr, E. H., Pojman, N., Mefford, H. C., … Simons, V. I. P. Consortium (2016). Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genetics in Medicine, 18, 341-9. doi: 10.1038/gim.2015.78.

Duyzend, M. H., Nuttle, X., Coe, B. P., Baker, C., Nickerson, D. A., Bernier, R. A., Eichler, E. E. (2016). Maternal modifiers and Parent-of-Origin bias of the autism-associated 16p11.2 CNV. American Journal of Human Genetics, 98, 45-57. PMCID: PMC4716684. doi: 10.1016/j.ajhg.2015.11.017.

Faja, S., Dawson, G., Sullivan, K., Meltzoff, A. N., Estes, A. M., Bernier, R. A. (2016). Executive function predicts the development of play skills for verbal preschoolers with autism spectrum disorders. Autism Research, 9, 1274-1284. PMCID: PMC4990498. doi: 10.1002/aur.1608.

Green Snyder, L., D'Angelo, D., Chen, Q., Bernier, R. A., Goin-Kochel, R. P., Wallace, A. S., … Simons, V. I. P. consortium (2016). Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication. Journal of Autism and Developmental Disorders, 46, 2734-48. doi: 10.1007/s10803-016-2807-4.

Hippolyte, L., Maillard, A. M., Rodriguez-Herreros, B., Pain, A., Martin-Brevet, S., Ferrari, C., … Bernier, R. A., … Jacquemont, S. (2016). The number of genomic copies at the 16p11.2 locus modulates language, verbal memory, and inhibition. Biological Psychiatry, 80, 129-139. doi: 10.1016/j.biopsych.2015.10.021.

Lugtenberg, D., Reijnders, M. R., Fenckova, M., Bijlsma, E. K., Bernier, R. A., van Bon, B. W., … Eichler, E. E., Mefford, H. C., … Vissers, L. E. (2016). De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila. European Journal of Human Genetics, 24, 1145-53. PMCID: PMC4970694. doi: 10.1038/ejhg.2015.282.

Stessman, H. A., Willemsen, M. H., Fenckova, M., Penn, O., Hoischen, A., Xiong, B., … Bernier, R. A., … Eichler, E. E., Kleefstra, T. (2016). Disruption of POGZ is associated with intellectual disability and autism spectrum disorders. American Journal of Human Genetics, 98, 541-552. PMCID: PMC4890241. doi: 10.1016/j.ajhg.2016.02.004.

Virginia Berninger Longcamp, M., Richards, T. L., Velay, J. L., Berninger, V. W. (2016). Neuroanatomy of handwriting and related reading and writing skills in adults and children with and without learning disabilities: French-American connections. Pratiques, 171, PMCID: PMC5297261.

Nielsen, K., Abbott, R., Griffin, W., Lott, J., Raskind, W. H., Berninger, V. W. (2016). Evidence-based reading and writing assessment for dyslexia in adolescents and young adults. Learning Disabilities (Pittsburgh), 21, 38-56. PMCID: PMC4739804. doi: 10.18666/LDMJ-2016-V21-I1-6971.

Kristie F. Bjornson

Bjornson, K. F., Zhou, C., Fatone, S., Orendurff, M., Stevenson, R., Rashid, S. (2016). The effect of ankle-foot orthoses on community-based walking in cerebral palsy: A clinical pilot study. Pediatric Physical Therapy, 28, 179-86. PMCID: PMC4811757. doi: 10.1097/PEP.0000000000000242.

Dodds, C. B., Bjornson, K. F., Sweeney, J. K., Narayanan, U. G. (2016). The effect of supported physical activity on parental-reported sleep qualities and pain severity in children with medical complexity. Journal of Pediatric Rehabilitation Medicine, 9, 195-206. doi: 10.3233/PRM-160388.

Moreau, N. G., Bodkin, A. W., Bjornson, K. F., Hobbs, A., Soileau, M., Lahasky, K. (2016). Effectiveness of rehabilitation interventions to improve gait speed in children with Cerebral Palsy: Systematic review and meta-analysis. Physical Therapy, 96, 1938-1954. PMCID: PMC5131187. doi: 10.2522/ptj.20150401.

Russell, J. C., Bjornson, K. F. (2016). Participation in daily life: Influence on quality of life in ambulatory children with Cerebral Palsy. PM&R, 8, S151. doi: 10.1016/j.pmrj.2016.07.019.

Cathryn Booth-LaForce

Hiratsuka, V. Y., Suchy-Dicey, A. M., Garroutte, E. M., Booth-LaForce, C. (2016). Patient and provider factors associated with American Indian and Alaska Native adolescent tobacco use screening. Journal of Primary Care & Community Health, 7, 2-9. PMCID: PMC4670602. doi: 10.1177/2150131915602469.

Roisman, G. I., Fraley, R. C., Haltigan, J. D., Cauffman, E., Booth-LaForce, C. (2016). Strategic considerations in the search for transactional processes: Methods for detecting and quantifying transactional signals in longitudinal data. Developmental Psychopathology, 28, 791-800. doi: 10.1017/S0954579416000316.

Mark Bothwell Bothwell, M. (2016). Recent advances in understanding neurotrophin signaling. F1000Research, 5, PMCID: PMC4965695. doi: 10.12688/f1000research.8434.1.

Heather Carmichael Olson Jirikowic, T. L., Chen, M., Nash, J., Gendler, B., Carmichael Olson, H. (2016). Regulatory behaviors and stress reactivity among infants at high risk for fetal alcohol spectrum disorders: An exploratory study. Journal of Mental Health Research in Intellectual Disabilities, 9, 171-188. doi: 10.1080/19315864.2016.1183246.

Lucas, B. R., Latimer, J., Fitzpatrick, J. P., Doney, R., Watkins, R. E., Tsang, T. W., Jirikowic, T. L., Carmichael Olson, H., … Elliott, E. J. (2016). Soft neurological signs and prenatal alcohol exposure: A population-based study in remote Australia. Developmental Medicine and Child Neurology, 58, 861-7. doi: 10.1111/dmcn.13071.

William Catterall Levin, M. D., Singh, G. K., Zhang, H. X., Uchida, K., Kozel, B. A., Stein, P. K., … Catterall, W. A., … Nichols, C. G. (2016). KATP channel gain-of-function leads to increased myocardial L-type Ca2+ current and contractility in Cantu syndrome. Proceedings of the National Academy of Sciences of the United States of America, 113, 6773-8. PMCID: PMC4914204. doi: 10.1073/pnas.1606465113.

Nanou, E., Scheuer, T., Catterall, W. A. (2016). Calcium sensor regulation of the CaV2.1 Ca2+ channel contributes to long-term potentiation and spatial learning. Proceedings of the National Academy of Sciences of the United States of America, 113, 13209-13214. PMCID: PMC5135313. doi: 10.1073/pnas.1616206113.

Nanou, E., Yan, J., Whitehead, N. P., Kim, M. J., Froehner, S. C., Scheuer, T., Catterall, W. A. (2016). Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channels. Proceedings of the National Academy of Sciences of the United States of America, 113, 1068-73. PMCID: PMC4743804. doi: 10.1073/pnas.1524650113.

Nanou, E., Sullivan, J. M., Scheuer, T., Catterall, W. A. (2016). Calcium sensor regulation of the CaV2.1 Ca2+ channel contributes to short-term synaptic plasticity in hippocampal neurons. Proceedings of the National Academy of Sciences of the United States of America, 113, 1062-7. PMCID: PMC4743814. doi: 10.1073/pnas.1524636113.

Patriarchi, T., Qian, H., Di Biase, V., Malik, Z. A., Chowdhury, D., Price, J. L., … Catterall, W. A., … Hell, J. W. (2016). Phosphorylation of Cav1.2 on S1928 uncouples the L-type Ca2+ channel from the beta2 adrenergic receptor. The EMBO Journal, 35, 1330-45. PMCID: PMC4910527. doi: 10.15252/embj.201593409.

Southan, C., Sharman, J. L., Benson, H. E., Faccenda, E., Pawson, A. J., Alexander, S. P., … Catterall, W. A., … NC-IUPHAR). The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: Towards curated quantitative interactions between 1300 protein targets and 6000 ligands. Nucleic Acids Research, 44, D1054-68. PMCID: PMC4702778. doi: 10.1093/nar/gkv1037.

Jeffrey Chamberlain Bengtsson, N. E., Seto, J. T., Hall, J. K., Chamberlain, J. S., Odom, G. L. (2016). Progress and prospects of gene therapy clinical trials for the muscular dystrophies. Human Molecular Genetics, 25, R9-17. doi: 10.1093/hmg/ddv420.

Muir, L. A., Murry, C. E., Chamberlain, J. S. (2016). Prosurvival factors improve functional engraftment of myogenically converted dermal cells into dystrophic skeletal muscle. Stem Cells and Development, 25,1559-1569. PMCID: PMC5035915. doi: 10.1089/scd.2016.0136.

Pisconti, A., Banks, G. B., Babaeijandaghi, F., Betta, N. D., Rossi, F. M., Chamberlain, J. S., Olwin, B. B. (2016). Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration. Skeletal Muscle, 6, 34. PMCID: PMC5064903. doi: 10.1186/s13395-016-0104-8.

Dimitri Christakis Ravinder, S., Donckels, E. A., Ramirez, J. S., Christakis, D. A., Ramirez, J. M., Ferguson, S. M. (2016). Excessive sensory stimulation during development alters neural plasticity and vulnerability to cocaine in mice. eNeuro, 3, PMCID: PMC4994069. doi: 10.1523/ENEURO.0199-16.2016.

Lucio Costa

Cole, T. B., Coburn, J., Dao, K., Roque, P., Chang, Y. C., Kalia, V., … Costa, L. G. (2016). Sex and genetic differences in the effects of acute diesel exhaust exposure on inflammation and oxidative stress in mouse brain. Toxicology, 374, 1-9. PMCID: PMC5154914. doi: 10.1016/j.tox.2016.11.010.

Furlong, C. E., Marsillach, J., Jarvik, G. P., Costa, L. G. (2016). Paraoxonases-1, -2 and -3: What are their functions? Chemico-Biological Interactions, 259, 51-62. PMCID: PMC5391248. doi: 10.1016/j.cbi.2016.05.036.

Garrick, J. M., Dao, K., de Laat, R., Elsworth, J., Cole, T. B., Marsillach, J., Furlong, C. E., Costa, L. G. (2016). Developmental expression of paraoxonase 2. Chemico-Biological Interactions, 259, 168-174. PMCID: PMC5055469. doi: 10.1016/j.cbi.2016.04.001.

Marsillach, J., Costa, L. G., Furlong, C. E. (2016). Paraoxonase-1 and early-life environmental exposures. Annals of Global Health, 82, 100-10. PMCID: PMC4916371. doi: 10.1016/j.aogh.2016.01.009.

Roque, P. J., Dao, K., Costa, L. G. (2016). Microglia mediate diesel exhaust particle-induced cerebellar neuronal toxicity through neuroinflammatory mechanisms. Neurotoxicology, 56, 204-214. PMCID: PMC5048600. doi: 10.1016/j.neuro.2016.08.006.

Wallace, R. J., Gropp, J., Dierick, N., Costa, L. G., Martelli, G., Brantom, P. G., … Leng, L. (2016). Risks associated with endotoxins in feed additives produced by fermentation. Environmental Health, 15, 5. PMCID: PMC4714429. doi: 10.1186/s12940-016-0087-2.

Timothy Cox Rosin, J. M., Li, W., Cox, L. L., Rolfe, S. M., Latorre, V., Akiyama, J. A., … Turner, E. E., Cox, T. C. (2016). A distal 594 bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complex. Development, 143, 2582-92. PMCID: PMC4958336. doi: 10.1242/dev.133736.

Michael Cunningham

Al-Rekabi, Z., Wheeler, M. M., Leonard, A., Fura, A. M., Juhlin, I., Frazar, C., … Cunningham, M. L., Sniadecki, N. J. (2016). Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosis. Journal of Cell Science, 129, 483-491. doi: 10.1242/jcs.175976.

Shaffer, J. R., Orlova, E., Lee, M. K., Leslie, E. J., Raffensperger, Z. D., Heike, C. L., Cunningham, M. L., … Weinberg, S. M. (2016). Genome-wide association study reveals multiple loci influencing normal human facial morphology. PLoS Genetics, 12, e1006149. PMCID: PMC4999139. doi: 10.1371/journal.pgen.1006149.

Stephen Dager Kim, S. H., Lyu, I., Fonov, V. S., Vachet, C., Hazlett, H. C., Smith, R. G., … Dager, S. R., … IBIS Network. (2016). Development of cortical shape in the human brain from 6 to 24 months of age via a novel measure of shape complexity. Neuroimage, 135, 163-76. PMCID: PMC4915970. doi: 10.1016/j.neuroimage.2016.04.053.

Kleinhans, N. M., Reiter, Maya A., Neuhaus, Emily, Pauley, Greg, Martin, Nathalie, Dager, S. R., Estes, A. M. (2016). Subregional differences in intrinsic amygdala hyperconnectivity and hypoconnectivity in autism spectrum disorder. Autism Research, 9, 760-72. PMCID: PMC4909596. doi: 10.1002/aur.1589.

St. John, T., Estes, A. M., Dager, S. R., Kostopoulos, P., Wolff, J. J., Pandey, J., … Piven, J. (2016). Emerging executive functioning and motor development in infants at high and low risk for autism spectrum disorder. Frontiers in Psychology, 7, 1016. PMCID: PMC4932099. doi: 10.3389/fpsyg.2016.01016

Christine Disteche Ramani, V., Cusanovich, D. A., Hause, R. J., Ma, W., Qiu, R., Deng, X., … Disteche, C. M., … Duan, Z. (2016). Mapping 3D genome architecture through in situ DNase Hi-C. Nature Protocols, 11, 2104-21. PMCID: PMC5547819. doi: 10.1038/nprot.2016.126.

Wei, G., Deng, X., Agarwal, S., Iwase, S., Disteche, C. M., Xu, J. (2016). Patient mutations of the intellectual disability gene KDM5C downregulate netrin G2 and suppress neurite growth in Neuro2a cells. Journal of Molecular Neuroscience, 60, 33-45. PMCID: PMC5412133. doi: 10.1007/s12031-016-0770-3.

William B. Dobyns Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Bennett, J. T., Tan, T. Y., Alcantara, D., Tetrault, M., Timms, A. E., Jensen, D., … Dobyns, W. B., … McDonell, L. M. (2016). Mosaic activating mutations in FGFR1cause encephalocraniocutaneous lipomatosis. American Journal of Human Genetics, 98, 579-587. PMCID: PMC4800051. doi: 10.1016/j.ajhg.2016.02.006.

Di Donato, N., Jean, Y. Y., Maga, A. M., Krewson, B. D., Shupp, A. B., Avrutsky, M. I., … Millen, K. J., … Dobyns, W. B., … Jinks, R. N. (2016). Mutations in CRADD result in reduced caspase-2-mediated neuronal apoptosis and cause megalencephaly with a rare lissencephaly variant. American Journal of Human Genetics, 99, 1117-1129. PMCID: PMC5097945. doi: 10.1016/j.ajhg.2016.09.010.

Di Donato, N., Neuhann, T., Kahlert, A. K., Klink, B., Hackmann, K., Neuhann, I., … Glass, I. A., … Dobyns, W. B., … Rump, A. (2016). Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. Journal of Medical Genetics, 53, 419-25. doi: 10.1136/jmedgenet-2015-103511.

Di Donato, N., Kuechler, A., Vergano, S., Heinritz, W., Bodurtha, J., Merchant, S. R., … Dobyns, W. B. (2016). Update on the ACTG1-associated Baraitser-Winter cerebrofrontofacial syndrome. American Journal of Medical Genetics. Part A, 170, 2644-51.doi: 10.1002/ajmg.a.37771.

Gobius, I., Morcom, L., Suarez, R., Bunt, J., Bukshpun, P., Reardon, W., Dobyns, W. B., … Richards, L. J. (2016). Astroglial-mediated remodeling of the interhemispheric midline is required for the formation of the corpus callosum. Cell Reports, 17, 735-747. PMCID: PMC5094913. doi: 10.1016/j.celrep.2016.09.033.

Gripp, K. W., Aldinger, K. A., Bennett, J. T., Baker, L., Tusi, J., Powell-Hamilton, N., … Dobyns, W. B. (2016). A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair. American Journal of Medical Genetics. Part A, 170, 2237-47. PMCID: PMC5134331. doi: 10.1002/ajmg.a.37781.

Huang, L., Vanstone, M. R., Hartley, T., Osmond, M., Barrowman, N., Allanson, J., … Dobyns, W. B., … Lines, M. A. (2016). Mandibulofacial dysostosis with microcephaly: Mutation and database update. Human Mutation, 37, 148-54.doi: 10.1002/humu.22924

Leto, K., Arancillo, M., Becker, E. B., Buffo, A., Chiang, C., Ding, B., Dobyns, W. B., … Millen, K. J., … Hawkes, R. (2016). Consensus paper: Cerebellar development. Cerebellum (London, England),15, 789-828. doi: 10.1007/s12311-015-0724-2.

Ma, M., Adams, H. R., Seltzer, L. E., Dobyns, W. B., Paciorkowski, A. R. (2016). Phenotype differentiation of FOXG1 and MECP2 disorders: A new method for characterization of developmental encephalopathies. The Journal of Pediatrics, 178, 233-240 e10. PMCID: PMC5873956. doi: 10.1016/j.jpeds.2016.08.032.

Mirzaa, G. M., Campbell, C. D., Solovieff, N., Goold, C. P., Jansen, L. A., Menon, S., … Novotny, E. J., Jr., … Hevner, R. F., Ojemann, J. G., … Dobyns, W. B. (2016). Association of MTOR mutations with developmental brain disorders, including megalencephaly, focal cortical dysplasia, and pigmentary mosaicism. JAMA Neurology, 73, 836-845. PMCID: PMC4979321. doi: 10.1001/jamaneurol.2016.0363.

Mirzaa, G. M., Timms, A. E., Conti, V., Boyle, E. A., Girisha, K. M., Martin, B., … Glass, I. A., … Dobyns, W. B. (2016). PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution. JCI Insight, 1, PMCID: PMC5019182. doi: 10.1172/jci.insight.87623.

Parrini, E., Conti, V., Dobyns, W. B., Guerrini, R. (2016). Genetic basis of brain malformations. Molecular Syndromology, 7, 220-233. PMCID: PMC5073505. doi: 10.1159/000448639.

Tully, H. M., Wenger, T. L., Kukull, W. A., Doherty, D. A., Dobyns, W. B. (2016). Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage. Neurosurgical Focus, 41, E5. PMCID: PMC5510987. doi: 10.3171/2016.8.FOCUS16241.

Yang, J., Bassuk, A. G., Merl-Pham, J., Hsu, C. W., Colgan, D. F., Li, X., … Dobyns, W. B., … Tsang, S. H. (2016). Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors. Human Molecular Genetics, 25, 4201-4210. PMCID: PMC5291196. doi: 10.1093/hmg/ddw253.

Daniel Doherty Aldinger, K. A., Doherty, D. A. (2016). The genetics of cerebellar malformations. Seminars in Fetal & Neonatal Medicine, 21, 321-32. PMCID: PMC5035570. doi: 10.1016/j.siny.2016.04.008.

Chapman, T., Perez, F. A., Ishak, G. E., Doherty, D. A. (2016). Prenatal diagnosis of Chudley-McCullough syndrome. American Journal of Medical Genetics. Part A, 170, 2426-30. doi: 10.1002/ajmg.a.37806.

Chong, J. X., Caputo, V., Phelps, I. G., Stella, L., Worgan, L., Dempsey, J. C., … Doherty, D. A. (2016). Recessive inactivating mutations in TBCK, encoding a Rab GTPase-activating protein, cause severe infantile syndromic encephalopathy. American Journal of Human Genetics, 98, 772-81. PMCID: PMC4833196. doi: 10.1016/j.ajhg.2016.01.016.

Nixon, J. N., Dempsey, J. C., Doherty, D. A., Ishak, G. E. (2016). Temporal bone and cranial nerve findings in pontine tegmental cap dysplasia. Neuroradiology, 58, 179-87. doi: 10.1007/s00234-015-1604-7.

Evan Eichler Ba, W., Yan, Y., Reijnders, M. R., Schuurs-Hoeijmakers, J. H., Feenstra, I., Bongers, E. M., … Mefford, H. C., Eichler, E. E., … De Vries, B. B. (2016). TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function. Human Molecular Genetics, 25, 892-902. PMCID: PMC4754042. doi: 10.1093/hmg/ddv618.

Dennis, M. Y., Eichler, E. E. (2016). Human adaptation and evolution by segmental duplication. Current Opinion in Genetics & Development, 41, 44-52. PMCID: PMC5161654. doi: 10.1016/j.gde.2016.08.001.

Fox, K., Johnsen, J. M., Coe, B. P., Frazar, C. D., Reiner, A. P.,Nhlbi Exome Sequencing Project, Minority Health-Grid Network, Eichler, E. E., Nickerson, D. A. (2016). Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry. Transfusion, 56, 2744-2749. doi: 10.1111/trf.13797.

Hehir-Kwa, J. Y., Marschall, T., Kloosterman, W. P., Francioli, L. C., Baaijens, J. A., Dijkstra, L. J., … Eichler, E. E., … Guryev, V. (2016). A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nature Communications, 7, 12989. PMCID: PMC5059695. doi: 10.1038/ncomms12989.

Huddleston, J., Eichler, E. E. (2016). An incomplete understanding of human genetic variation. Genetics, 202, 1251-4. PMCID: PMC4905539. doi: 10.1534/genetics.115.180539.

Koolen, D. A., Pfundt, R., Linda, K., Beunders, G., Veenstra-Knol, H. E., Conta, J. H., … Eichler, E. E., de Vries, B. B. (2016). The Koolen-de Vries syndrome: A phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant. European Journal of Human Genetics, 24, 652-9. PMCID: PMC4930086. doi: 10.1038/ejhg.2015.178.

Mamiya, P. C., Richards, T. L., Coe, B. P., Eichler, E. E., Kuhl, P. K. (2016). Brain white matter structure and COMT gene are linked to second-language learning in adults. Proceedings of the National Academy of Sciences of the United States of America, 113, 7249-54. PMCID: PMC4932981. doi: 10.1073/pnas.1606602113.

Mohajeri, K., Cantsilieris, S., Huddleston, J., Nelson, B. J., Coe, B. P., Campbell, C. D., … Eichler, E. E. (2016). Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region. Genome Research, 26, 1453-1467. PMCID: PMC5088589. doi: 10.1101/gr.211284.116.

Priest, J. R., Osoegawa, K., Mohammed, N., Nanda, V., Kundu, R., Schultz, K., … Eichler, E. E., … Ashley, E. A. (2016). De novo and rare variants at multiple loci support the oligogenic origins of atrioventricular septal heart defects. PLoS Genetics, 12, e1005963. PMCID: PMC4825975. doi: 10.1371/journal.pgen.1005963.

Rafati, N., Andersson, L. S., Mikko, S., Feng, C., Raudsepp, T., Pettersson, J., … Eichler, E. E., … Rubin, C. J. (2016). Large deletions at the SHOX locus in the pseudoautosomal region are associated with skeletal atavism in Shetland ponies. G3 (Bethesda), 6, 2213-23. PMCID: PMC4938674. doi: 10.1534/g3.116.029645.

Stessman, H. A., Turner, T. N., Eichler, E. E. (2016). Molecular subtyping and improved treatment of neurodevelopmental disease. Genome Medicine, 8, 22. PMCID: PMC4766622. doi: 10.1186/s13073-016-0278-z.

Turner, T. N., Hormozdiari, F., Duyzend, M. H., McClymont, S. A., Hook, P. W., Iossifov, I., … Faustman, E. M., … Eichler, E. E. (2016). Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA. American Journal of Human Genetics, 98, 58-74. PMCID: PMC4716689. doi: 10.1016/j.ajhg.2015.11.023.

Wang, T., Guo, H., Xiong, B., Stessman, H. A., Wu, H., Coe, B. P., … Eichler, E. E. (2016). De novo genic mutations among a Chinese autism spectrum disorder cohort. Nature Communications, 7, 13316. PMCID: PMC5105161. doi: 10.1038/ncomms13316.

Annette Mercer Estes Faja, S., Dawson, G., Sullivan, K., Meltzoff, A. N., Estes, A. M., Bernier, R. A. (2016). Executive function predicts the development of play skills for verbal preschoolers with autism spectrum disorders. Autism Research, 9, 1274-1284. PMCID: PMC4990498. doi: 10.1002/aur.1608.

Jones, E. J., Venema, K., Earl, R., Lowy, R., Barnes, K., Estes, A. M., … Webb, S. J. (2016). Reduced engagement with social stimuli in 6-month-old infants with later autism spectrum disorder: A longitudinal prospective study of infants at high familial risk. Journal of Neurodevelopmental Disorders, 8, 7. PMCID: PMC4791854. doi: 10.1186/s11689-016-9139-8.

Kleinhans, N. M., Reiter, M. A., Neuhaus, E., Pauley, G., Martin, N., Dager, S. R., Estes, A. M. (2016). Subregional differences in intrinsic amygdala hyperconnectivity and hypoconnectivity in autism spectrum disorder. Autism Research, 9, 760-72. PMCID: PMC4909596. doi: 10.1002/aur.1589.

Neuhaus, E., Jones, E. J., Barnes, K., Sterling, L., Estes, A. M., Munson, J., … Webb, S. J. (2016). The relationship between early neural responses to emotional faces at age 3 and later autism and anxiety symptoms in adolescents with autism. Journal of Autism and Developmental Disorders, 46, 2450-63. PMCID: PMC5305034. doi: 10.1007/s10803-016-2780-y.

Elaine Faustman

Harris, S., Shubin, S. P., Wegner, S., Van Ness, K., Green, F., Hong, S. W., Faustman, E. M. (2016). The presence of macrophages and inflammatory responses in an in vitro testicular co-culture model of male reproductive development enhance relevance to in vivo conditions. Toxicology in Vitro, 36, 210-215. PMCID: PMC5026229. doi: 10.1016/j.tiv.2016.08.003.

Holme, F., Thompson, B., Holte, S., Vigoren, E. M., Espinoza, N., Ulrich, A., … Faustman, E. M. (2016). The role of diet in children's exposure to organophosphate pesticides. Environmental Research, 147, 133-40. PMCID: PMC4821762. doi: 10.1016/j.envres.2016.02.003.

Juberg, D. R., Knudsen, T. B., Sander, M., Beck, N. B., Faustman, E. M., Mendrick, D. L., … Crofton, K. M. (2016). Future Tox III: Bridges for translation. Toxicological Sciences, doi: 10.1093/toxsci/kfw194.

Kim, H. Y., Wegner, S. H., Van Ness, K. P., Park, J. J., Pacheco, S. E., Workman, T., … Faustman, E. M. (2016). Differential epigenetic effects of chlorpyrifos and arsenic in proliferating and differentiating human neural progenitor cells. Reproductive Toxicology, 65, 212-223. PMCID: PMC5067221. doi: 10.1016/j.reprotox.2016.08.005.

Lee, J. H., Han, J. H., Kim, J. H., Kim, B., Bello, D., Kim, J. K., … Faustman, E. M., Yu, I. J. (2016). Exposure monitoring of graphene nanoplatelets manufacturing workpaces. Inhalation Toxicology, 28, 281-91. doi: 10.3109/08958378.2016.1163442.

Smith, M. N., Grice, J., Cullen, A., Faustman, E. M. (2016). A toxicological framework for the prioritization of children's Safe Product Act data. International Journal of Environmental Research and Public Health, 13, 431. PMCID: PMC4847093. doi: 10.3390/ijerph13040431.

Turner, T. N., Hormozdiari, F., Duyzend, M. H., McClymont, S. A., Hook, P. W., Iossifov, I., … Faustman, E. M., … Eichler, E. E. (2016). Genomesequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA. American Journal of Human Genetics, 98, 58-74. PMCID: PMC4716689. doi: 10.1016/j.ajhg.2015.11.023.

Weldon, B. A., Shubin, S. P., Smith, M. N., Workman, T., Artemenko, A., Griffith, W. C., … Faustman, E. M. (2016). Urinary microRNAs as potential biomarkers of pesticide exposure. Toxicology and Applied Pharmacology, 312, 19-25. PMCID: PMC4963307. doi: 10.1016/j.taap.2016.01.018.

Martin Frasch Anegroaie, P., Frasch, M. G., Rupprecht, S., Antonow-Schlorke, I., Muller, T., Schubert, H., … Schwab, M. (2016). Development of somatosensory-evoked potentials in foetal sheep: Effects of betamethasone. Acta Physiologica (Oxf), 4 Oct 2016. doi: 10.1111/apha.12795.

Frasch, M. G., Szynkaruk, M., Prout, A. P., Nygard, K., Cao, M., Veldhuizen, R., … Richardson, B. S. (2016). Decreased neuroinflammation correlates to higher vagus nerve activity fluctuations in near-term ovine fetuses: A case for the afferent cholinergic anti-inflammatory pathway? Journal of Neuroinflammation, 13, 103. PMCID: PMC4894374. doi: 10.1186/s12974-016-0567-x.

Clement Furlong Furlong, C. E., Marsillach, J., Jarvik, G. P., Costa, L. G. (2016). Paraoxonases-1, -2 and -3: What are their functions? Chemico-Biological Interactions, 259, 51-62. PMCID: PMC5391248. doi: 10.1016/j.cbi.2016.05.036.

Marsillach, J., Costa, L. G., Furlong, C. E. (2016). Paraoxonase-1 and early-life environmental exposures. Annals of Global Health, 82, 100-10. PMCID: PMC4916371. doi: 10.1016/j.aogh.2016.01.009.

Gwenn Garden Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Garden, G. A., Campbell, B. M. (2016). Glial biomarkers in human central nervous system disease. Glia, 64, 1755-71. PMCID: PMC5575821. doi: 10.1002/glia.22998.

Moller, T., Bard, F., Bhattacharya, A., Biber, K., Campbell, B., Dale, E., … Garden, G. A., … Boddeke, H. W. (2016). Critical data-based re-evaluation of minocycline as a putative specific microglia inhibitor. Glia, 64, 1788-94. doi: 10.1002/glia.23007.

Adam Geballe Mouna, L., Hernandez, E., Bonte, D., Brost, R., Amazit, L., Delgui, L. R., … Geballe, A. P., … Esclatine, A. (2016). Analysis of the role of autophagy inhibition by two complementary human cytomegalovirus BECN1/Beclin 1-binding proteins. Autophagy, 12, 327-42. PMCID: PMC4836022. doi: 10.1080/15548627.2015.1125071.

Ian Glass Bi, W., Glass, I. A., Muzny, D. M., Gibbs, R. A., Eng, C. M., Yang, Y., Sun, A. (2016). Whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE). American Journal of Medical Genetics. Part A, 170, 2181-5. doi: 10.1002/ajmg.a.37727.

Bowdin, S., Gilbert, A., Bedoukian, E., Carew, C., Adam, M. P., Belmont, J., … Glass, I. A., … Krantz, I. D. (2016). Recommendations for the integration of genomics into clinical practice. Genetics in Medicine, 18, 1075-1084. PMCID: PMC5557020. doi: 10.1038/gim.2016.17.

Sidney Gospe, Jr. Byers, H. M., Beatty, C. W., Hahn, S. H., Gospe, S. M., Jr. (2016). Dramatic response after lamotrigine in a patient with epileptic encephalopathy and a de novo CACNA1A variant. Pediatric Neurology, 60, 79-82. PMCID: PMC4987102. doi: 10.1016/j.pediatrneurol.2016.03.012.

Joan M. Goverman Johnson, M. C., Pierson, E. R., Spieker, A. J., Nielsen, A. S., Posso, S., Kita, M., … Goverman, J. M. (2016). Distinct T cell signatures define subsets of patients with multiple sclerosis. Neurology: Neuroimmunology & Neuroinflammation, 3, e278. PMCID: PMC4996538. doi: 10.1212/NXI.0000000000000278.

Thomas J. Grabowski, Jr. Askren, M. K., McAllister-Day, T. K., Koh, N., Mestre, Z., Dines, J. N., Korman, B. A., … Grabowski, T. J., Madhyastha, T. M. (2016). Using “Make” for reproducible and parallel neuroimaging workflow and quality-assurance. Frontiers in Neuroinformatics, 10, 2. PMCID: PMC4735413. doi: 10.3389/fninf.2016.00002.

Bledsoe, J. C., Xiao, D., Chaovalitwongse, A., Mehta, S., Grabowski, T. J., Semrud-Clikeman, M., … Breiger, D. (2016). Diagnostic classification of ADHD versus control: Support vector machine classification using brief neuropsychological assessment. Journal of Attention Disorders, 26 May 2016. doi: 10.1177/1087054716649666.

Casimo, K., Darvas, F., Wander, J., Ko, A., Grabowski, T. J., Novotny, E. J., Jr., … Ojemann, J. G., Weaver, K. E. (2016). Regional patterns of cortical phase synchrony in the resting state. Brain Connectivity, 6, 470-81. PMCID: PMC4976227. doi: 10.1089/brain.2015.0362.

Emmorey, K., Mehta, S., McCullough, S., Grabowski, T. J. (2016). The neural circuits recruited for the production of signs and fingerspelled words. Brain and Language, 160, 30-41. PMCID: PMC5002375. doi: 10.1016/j.bandl.2016.07.003.

Xiao, C., Bledsoe, J., Wang, S., Chaovalitwongse, W. A., Mehta, S., Semrud-Clikeman, M., Grabowski, T. J. (2016). An integrated feature ranking and selection framework for ADHD characterization. Brain Informatics, 3, 145-155. PMCID: PMC4999568. doi: 10.1007/s40708-016-0047-1.

Robert Hevner

Bakken, T. E., Miller, J. A., Ding, S. L., Sunkin, S. M., Smith, K. A., Ng, L., … Hevner, R. F., … Lein, E. S. (2016). A comprehensive transcriptional map of primate brain development. Nature, 535, 367-75. PMCID: PMC5325728. doi: 10.1038/nature18637.

Mihalas, A. B., Elsen, G. E., Bedogni, F., Daza, R. A., Ramos-Laguna, K. A., Arnold, S. J., Hevner, R. F. (2016). Intermediate progenitor cohorts differentially generate cortical layers and require Tbr2 for timely acquisition of neuronal subtype identity. Cell Reports, 16, 92-105. PMCID: PMC4927342. doi: 10.1016/j.celrep.2016.05.072.

Anne Hing

Heike, C. L., Wallace, E., Speltz, M. L., Siebold, B., Werler, M. M., Hing, A. V., … Luquetti, D. V. (2016). Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical research. Birth Defects Research Part A: Clinical and Molecular Teratology, 106, 915-926. doi: 10.1002/bdra.23560.

Rodney Ho Cherry, A. E., Haas, B. R., Naydenov, A. V., Fung, S., Xu, C., Swinney, K., … Ho, R. J., … Stella, N. (2016). St-11: A new brain-penetrant microtubule-destabilizing agent with therapeutic potential for glioblastoma multiforme. Molecular Cancer Therapeutics, 15, 2018-29. PMCID: PMC5010991. doi: 10.1158/1535-7163.MCT-15-0800.

Philip Horner Cheng, Y., Wei, H., Tan, J. K., Peeler, D. J., Maris, D. O., Sellers, D. L., Horner, P. J., Pun, S. H. (2016). Nano-sized sunflower polycations as effective gene transfer vehicles. Small, 12, 2750-8. PMCID: PMC5052141. doi: 10.1002/smll.201502930.

Tan, J. Y., Sellers, D. L., Pham, B., Pun, S. H., Horner, P. J. (2016). Non-viral nucleic acid delivery strategies to the central nervous system. Frontiers in Molecular Neuroscience, 9, 108. PMCID: PMC5088201. doi: 10.3389/fnmol.2016.00108.

Marshall S. Horwitz McKenna, A., Findlay, G. M., Gagnon, J. A., Horwitz, M. S., Schier, A. F., Shendure, J. (2016). Whole-organism lineage tracing by combinatorial and cumulative genome editing. Science, 353, aaf7907. PMCID: PMC4967023. doi: 10.1126/science.aaf7907.

Roxanne Hudson Hackett, J.D., Hudson, R. F., West, E.A., Brown, S E. (2016). Cambodian inclusive education for vulnerable populations: Toward an ecological perspective policy. Journal of International Special Needs Education, 19, 3-14. doi: 10.9782/JISNE-D-15-00004.1.

Colleen Huebner Cruz, S., Chi, D. L., Huebner, C. E. (2016). Oral health services within community-based organizations for young children with special health care needs. Special Care in Dentistry, 36, 243-53. PMCID: PMC5010451. doi: 10.1111/scd.12174.

Tracy Jirikowic Jirikowic, T. L., Chen, M., Nash, J., Gendler, B., Carmichael Olson, H. (2016). Regulatory behaviors and stress reactivity among infants at high risk for fetal alcohol spectrum disorders: An exploratory study. Journal of Mental Health Research in Intellectual Disabilities, 9, 171-188. doi: 10.1080/19315864.2016.1183246.

Jirikowic, T. L., Kerfeld, C. I. (2016). Health-promoting physical activity of children who use assistive mobility devices: A scoping review. American Journal of Occupational Therapy, 70, 7005180050p1-7005180050p11. doi: 10.5014/ajot.2016.021543.

Jirikowic, T. L., Westcott McCoy, S., Price, R., Ciol, M. A., Hsu, L. Y., Kartin, D. (2016). Virtual sensorimotor training for balance: Pilot study results for children with fetal alcohol spectrum disorders. Pediatric Physical Therapy, 28, 460-8. doi: 10.1097/PEP.0000000000000300.

Lucas, B. R., Elliott, E. J., Coggan, S., Pinto, R. Z., Jirikowic, T. L., McCoy, S. W., Latimer, J. (2016). Interventions to improve gross motor performance in children with neurodevelopmental disorders: A meta-analysis. BMC Pediatrics, 16, 193. PMCID: PMC5129231. doi: 10.1186/s12887-016-0731-6.

Sandra Juul Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

McAdams, R. M., Juul, S. E. (2016). Neonatal encephalopathy: Update on therapeutic hypothermia and other novel therapeutics. Clinics in Perinatology, 43, 485-500. PMCID: PMC4987711. doi: 10.1016/j.clp.2016.04.007.

Peeples, E. S., Strandjord, T. P., Juul, S. E. (2016). Evaluating an association between ampicillin and intraventricular hemorrhage in preterm infants. Neuropediatrics, 47, 221-5. doi: 10.1055/s-0036-1583182.

Wu, Y. W., Mathur, A. M., Chang, T., McKinstry, R. C., Mulkey, S. B., Mayock, D. E., … Juul, S. E., … Ballard, R. A. (2016). High-dose erythropoietin and hypothermia for hypoxic-ischemic encephalopathy: A phase II trial. Pediatrics, 137, doi: 10.1542/peds.2016-0191.

Raj P. Kapur Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

David Kimelman Kimelman, D. (2016). A novel cold-sensitive mutant of NTLA reveals temporal roles of brachyury in zebrafish. Developmental Dynamics, 245, 874-80. PMCID: PMC4947019. doi: 10.1002/dvdy.24417.

Kimelman, D. (2016). Tales of tails (and trunks): Forming the posterior body in vertebrate embryos. Current Topics in Developmental Biology, 116, 517-36. PMCID: PMC4883064. doi: 10.1016/bs.ctdb.2015.12.008.

Yoshimatsu, T., D'Orazi, F. D., Gamlin, C. R., Suzuki, S. C., Suli, A., Kimelman, D., … Wong, R. O. (2016). Presynaptic partner selection during retinal circuit reassembly varies with timing of neuronal regeneration in vivo. Nature Communications, 7, 10590. PMCID: PMC4742908. doi: 10.1038/ncomms10590.

Bryan King Kasari, C., Dean, M., Kretzmann, M., Shih, W., Orlich, F., Whitney, R., … King, B. H. (2016). Children with autism spectrum disorder and social skills groups at school: A randomized trial comparing intervention approach and peer composition. Journal of Child Psychology and Psychiatry and Allied Disciplines, 57, 171-9. doi: 10.1111/jcpp.12460.

Stein, M. A., King, B. H. (2016). Unequal individual risk and potential benefit balanced by benefits to the population at large in autism clinical trials? American Journal of Bioethics, 16, 72-4. doi: 10.1080/15265161.2016.1145298.

Natalia Kleinhans Kleinhans, N. M., Reiter, Maya A., Neuhaus, Emily, Pauley, Greg, Martin, Nathalie, Dager, S. R., Estes, A. M. (2016). Subregional differences in intrinsic amygdala hyperconnectivity and hypoconnectivity in autism spectrum disorder. Autism Research, 9, 760-72. PMCID: PMC4909596. doi: 10.1002/aur.1589.

Prat, C. S., Stocco, A., Neuhaus, E., Kleinhans, N. M. (2016). Basal ganglia impairments in autism spectrum disorder are related to abnormal signal gating to prefrontal cortex. Neuropsychologia, 91, 268-281. doi: 10.1016/j.neuropsychologia.2016.08.007.

Sara T. Kover Kover, S. T., Edmunds, S. R., Ellis Weismer, S. (2016). Brief report: Ages of language milestones as predictors of developmental trajectories in young children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 46, 2501-7. PMCID: PMC4903886. doi: 10.1007/s10803-016-2756-y.

Venker, C. E., Kover, S. T., Weismer, S. E. (2016). Brief report: Fast mapping predicts differences in concurrent and later language abilities among children with ASD. Journal of Autism and Developmental Disorders, 46, 1118-23. PMCID: PMC4747812. doi: 10.1007/s10803-015-2644-x.

Patricia Kuhl Garcia-Sierra, A., Ramirez-Esparza, N., Kuhl, P. K. (2016). Relationships between quantity of language input and brain responses in bilingual and monolingual infants. International Journal of Psychophysiology, 110, 1-17. doi: 10.1016/j.ijpsycho.2016.10.004.

Kuhl, P. K., Stevenson, J., Corrigan, N. M., van den Bosch, J. J., Can, D. D., Richards, T. L. (2016). Neuroimaging of the bilingual brain: Structural brain correlates of listening and speaking in a second language. Brain and Language, 162, 1-9. doi: 10.1016/j.bandl.2016.07.004.

Kuhl, P. K. (2016). Predicting the integration of overlapping memories by decoding mnemonic processing states during learning. Neuroimage, 124, 323-335. PMCID: PMC4651766. doi: 10.1016/j.neuroimage.2015.08.051.

Zhao, T. Christina, Kuhl, P. K. (2016). Musical intervention enhances infants' neural processing of temporal structure in music and speech. Proceedings of the National Academy of Sciences of the United States of America, 113, 5212-7. PMCID: PMC4868410. doi: 10.1073/pnas.1603984113.

Adrian K.C. Lee Bizley, J. K., Maddox, R. K., Lee, A. K. C. (2016). Defining auditory-visual objects: Behavioral tests and physiological mechanisms. Trends in Neurosciences, 39, 74-85. PMCID: PMC4738154. doi: 10.1016/j.tins.2015.12.007.

McCloy, D. R., Larson, E. D., Lau, B., Lee, A. K. C. (2016). Temporal alignment of pupillary response with stimulus events via deconvolution. Journal of the Acoustical Society of America, 139, EL57-62. PMCID: PMC5392052. doi: 10.1121/1.4943787.

McEvoy, S. D., Lee, A. K. C., Poliakov, A., Friedman, S., Shaw, D. W. W., Browd, S. R., … Ojemann, J. G., Mac Donald, C. L. (2016). Longitudinal cerebellar diffusion tensor imaging changes in posterior fossa syndrome. NeuroImage: Clinical, 12, 582-590. PMCID: PMC5031477. doi: 10.1016/j.nicl.2016.09.007.

Wronkiewicz, M., Larson, E., Lee, A. K. C. (2016). Incorporating modern neuroscience findings to improve brain-computer interfaces: Tracking auditory attention. Journal of Neural Engineering, 13, 056017. doi: 10.1088/1741-2560/13/5/056017.

Donghoon Lee Finno, C. J., Bordbari, M. H., Valberg, S. J., Lee, D., Herron, J., Hines, K., … Xu, L. (2016). Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genes. Free Radical Biology and Medicine, 101, 261-271. PMCID: PMC5154892. doi: 10.1016/j.freeradbiomed.2016.10.009.

Ali Murat Maga Di Donato, N., Jean, Y. Y., Maga, A. M., Krewson, B. D., Shupp, A. B., Avrutsky, M. I., … Millen, K. J., … Dobyns, W. B., … Jinks, R. N. (2016). Mutations in CRADD result in reduced caspase-2-mediated neuronal apoptosis and cause megalencephaly with a rare lissencephaly variant. American Journal of Human Genetics, 99, 1117-1129. PMCID: PMC5097945. doi: 10.1016/j.ajhg.2016.09.010.

Maga, A. M. (2016). Postnatal development of the craniofacial skeleton in male C57BL/6J mice. The Journal of the American Association for Laboratory Animal Science, 55, 131-6. PMCID: PMC4783629.

Kenneth Maravilla Murata, N., Gonzalez-Cuyar, L. F., Murata, K., Fligner, C., Dills, R., Hippe, D., Maravilla, K. R. (2016). Macrocyclic and other non-Group 1 Gadolinium contrast agents deposit low levels of Gadolinium in brain and bone tissue: preliminary results from 9 patients with normal renal function. Investigative Radiology, 51, 447-53. doi: 10.1097/RLI.0000000000000252.

Sundarakumar, D. K., Smith, C. M., Hwang, W. D., Mossa-Basha, M., Maravilla, K. R. (2016). Evaluation of focal cervical spinal cord lesions in Multiple Sclerosis: Comparison of white matter-suppressed T1 inversion recovery sequence versus conventional STIR and proton density-weighted turbo spin-echo sequences. American Journal of Neuroradiology, 37, 1561-6. doi: 10.3174/ajnr.A4761.

Ryan McAdams McAdams, R. M., Juul, S. E. (2016). Neonatal encephalopathy: Update on therapeutic hypothermia and other novel therapeutics. Clinics in Perinatology, 43, 485-500. PMCID: PMC4987711. doi: 10.1016/j.clp.2016.04.007.

McAdams, R. M., Chabra, S. (2016). Umbilical cord haematoma and adrenal haemorrhage in a macrosomic neonate with anaemia. BMJ Case Reports, 2016, PMCID: PMC4746510. doi: 10.1136/bcr-2015-214140.

Katie A. McLaughlin Bush, N. R., Lane, R. D., McLaughlin, K. A. (2016). Mechanisms underlying the association between early-life adversity and physical health: Charting a course for the future. Psychosomatic Medicine, 78, 1114-1119. PMCID: PMC5111624. doi: 10.1097/PSY.0000000000000421.

Carliner, H., Keyes, K. M., McLaughlin, K. A., Meyers, J. L., Dunn, E. C., Martins, S. S. (2016). Childhood trauma and illicit drug use in adolescence: A population-based national comorbidity survey replication-adolescent supplement study. Journal of the American Academy of Child and Adolescent Psychiatry, 55, 701-8. PMCID: PMC4964281. doi: 10.1016/j.jaac.2016.05.010.

Gold, A. L., Sheridan, M. A., Peverill, M., Busso, D. S., Lambert, H. K., Alves, S., … McLaughlin, K. A. (2016). Childhood abuse and reduced cortical thickness in brain regions involved in emotional processing. Journal of Child Psychology and Psychiatry and Allied Disciplines, 57, 1154-64. PMCID: PMC5031358. doi: 10.1111/jcpp.12630.

Keyes, K. M., McLaughlin, K. A., Vo, T., Galbraith, T., Heimberg, R. G. (2016). Anxious and aggressive: The co-occurrence of IED with anxiety disorders. Depression and Anxiety, 33, 101-111. PMCID: PMC4729594. doi: 10.1002/da.22428.

McLaughlin, K. A. (2016). Future directions in childhood adversity and youth psychopathology. Journal of Clinical Child and Adolescent Psychology, 45, 361-82. PMCID: PMC4837019. doi: 10.1080/15374416.2015.1110823.

McLaughlin, K. A., Sheridan, M. A. (2016). Beyond cumulative risk: A dimensional approach to childhood adversity. Current Directions in Psychological Science, 25, 239-245. PMCID: PMC5070918. doi: 10.1177/0963721416655883.

McLaughlin, K. A., Lane, R. D., Bush, N. R. (2016). Introduction to the special issue of Psychosomatic Medicine: Mechanisms linking early-life adversity to physical health. Psychosomatic Medicine, 78, 976-978. PMCID: PMC5123679.doi: 10.1097/PSY.0000000000000420.

McLaughlin, K. A., Basu, A., Walsh, K., Slopen, N., Sumner, J. A., Koenen, K. C., Keyes, K. M. (2016). Childhood exposure to violence and chronic physical conditions in a national sample of us adolescents. Psychosomatic Medicine, 78, 1072-1083. PMCID: PMC5096968. doi: 10.1097/PSY.0000000000000366.

Seeley, S. H., Mennin, D. S., Aldao, A., McLaughlin, K. A., Rottenberg, J., Fresco, D. M. (2016). Impact of comorbid depressive disorders on subjective and physiological responses to emotion in generalized anxiety disorder. Cognitive Therapy and Research, 40, 290-303. PMCID: PMC5029787. doi: 10.1007/s10608-015-9744-y.

Heather Mefford

Afawi, Z., Oliver, K. L., Kivity, S., Mazarib, A., Blatt, I., Neufeld, M. Y., … Mefford, H. C., … Berkovic, S. F. (2016). Multiplex families with epilepsy: Success of clinical and molecular genetic characterization. Neurology, 86, 713-22. PMCID: PMC4763801. doi: 10.1212/WNL.0000000000002404.

Ba, W., Yan, Y., Reijnders, M. R., Schuurs-Hoeijmakers, J. H., Feenstra, I., Bongers, E. M., … Mefford, H. C., Eichler, E. E., … De Vries, B. B. (2016). TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function. Human Molecular Genetics, 25, 892-902. PMCID: PMC4754042. doi: 10.1093/hmg/ddv618.

Bernier, R. A., Steinman, K. J., Reilly, B., Wallace, A. S., Sherr, E. H., Pojman, N., Mefford, H. C., … Simons, V. I. P. consortium (2016). Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genetics in Medicine, 18, 341-9. doi: 10.1038/gim.2015.78.

Caplan, R., Mefford, H. C., Berl, M., Chang, B., Lin, J., Mazarati, A., … Stroke Epilepsy Benchmark, Stewards (2016). 2014 Epilepsy benchmarks area I: Understanding the causes of the epilepsies and epilepsy-related neurologic, psychiatric, and somatic conditions. Epilepsy Currents, 16, 182-6. PMCID: PMC4913856. doi: 10.5698/1535-7511-16.3.182.

Corbett, M. A., Bellows, S. T., Li, M., Carroll, R., Micallef, S., Carvill, G. L., … Mefford, H. C., … Gecz, J. (2016). Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy. Neurology, 87, 1975-1984. PMCID: PMC5109949. doi: 10.1212/WNL.0000000000003309. de Lange, I. M., Helbig, K. L., Weckhuysen, S., Moller, R. S., Velinov, M., Dolzhanskaya, N., … Mefford, H. C., … Koeleman, B. P. (2016). De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy. Journal of Medical Genetics, 53, 850-858. PMCID: PMC5264224. doi: 10.1136/jmedgenet-2016-103909.

Djemie, T., Weckhuysen, S., von Spiczak, S., Carvill, G. L., Jaehn, J., Anttonen, A. K., … Mefford, H. C., … Euro, Epinomics-R. E. S. Dravet working group (2016). Pitfalls in genetic testing: The story of missed SCN1A mutations. Molecular Genetics & Genomic Medicine, 4, 457 -64. PMCID: PMC4947864. doi: 10.1002/mgg3.217.

Helbig, I., Heinzen, E. L., Mefford, H. C., Ilae Genetics Commission (2016). Primer part 1-the building blocks of epilepsy genetics. Epilepsia, 57, 861-8. doi: 10.1111/epi.13381.

Hildebrand, M. S., Myers, C. T., Carvill, G. L., Regan, B. M., Damiano, J. A., Mullen, S. A., … Mefford, H. C. (2016). A targeted resequencing gene panel for focal epilepsy. Neurology, 86, 1605-12. PMCID: PMC4844234. doi: 10.1212/WNL.0000000000002608.

Meisler, M. H., Helman, G., Hammer, M. F., Fureman, B. E., Gaillard, W. D., Goldin, A. L., … Mefford, H. C., … Scheffer, I. E. (2016). SCN8A encephalopathy: Research progress and prospects. Epilepsia, 57, 1027-35. PMCID: PMC5495462. doi: 10.1111/epi.13422.

Mignot, C., von Stulpnagel, C., Nava, C., Ville, D., Sanlaville, D., Lesca, G., … Mefford, H. C., … Depienne, C. (2016). Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy. Journal of Medical Genetics, 53, 511-22. doi: 10.1136/jmedgenet-2015-103451.

Myers, C. T., Mefford, H. C. (2016). Genetic investigations of the epileptic encephalopathies: Recent advances. Progress in Brain Research, 226, 35-60. doi: 10.1016/bs.pbr.2016.04.006.

Petrovski, S., Kury, S., Myers, C. T., Anyane-Yeboa, K., Cogne, B., Bialer, M., … Mefford, H. C., … Goldstein, D. B. (2016). Germline de novo mutations in GNB1 cause severe neurodevelopmental disability, hypotonia, and seizures. American Journal of Human Genetics, 98, 1001-1010. PMCID: PMC4863562. doi: 10.1016/j.ajhg.2016.03.011.

Rudolf, G., Lesca, G., Mehrjouy, M. M., Labalme, A., Salmi, M., Bache, I., … Mefford, H. C., … Szepetowski, P. (2016). Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy. European Journal of Human Genetics, 24, 1761-1770. PMCID: PMC5117930. doi: 10.1038/ejhg.2016.80.

Tsai, M. H., Kuo, P. W., Myers, C. T., Li, S. W., Lin, W. C., Fu, T. Y., … Mefford, H. C., … Tsai, J. W. (2016). A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. European Journal of Paediatric Neurology, 20, 788-94. doi: 10.1016/j.ejpn.2016.05.010.

Andrew Meltzoff Boucenna, S., Cohen, D., Meltzoff, A. N., Gaussier, P., Chetouani, M. (2016). Robots learn to recognize individuals from imitative encounters with people and avatars. Scientific Reports, 6, 19908. PMCID: PMC4741103. doi: 10.1038/srep19908.

Cvencek, D., Greenwald, A. G., Meltzoff, A. N. (2016). Implicit measures for preschool children confirm self-esteem's role in maintaining a balanced identity. Journal of Experimental Social Psychology, 62, 50-57. doi: 10.1016/j.jesp.2015.09.015.

Master, A., Cheryan, S., Meltzoff, A. N. (2016). Computing whether she belongs: Sterotypes undermine girls' interest and sense of belonging in computer science. Journal of Educational Psychology, 108, 424-437. doi: 10.1037/edu0000061.

Repacholi, B. M., Meltzoff, A. N., Hennings, T. M., Ruba, Ashley L. (2016). Transfer of social learning across contexts: Exploring infants' attribution of trait-like emotions to adults. Infancy, 21, 785-806. doi: 10.1111/infa.12136.

Repacholi, B. M., Meltzoff, A. N., Toub, T. S., Ruba, A. L. (2016). Infants' generalizations about other people's emotions: Foundations for trait-like attributions. Developmental Psychology, 52, 364-78. doi: 10.1037/dev0000097.

Rogers, L. O., Meltzoff, A. N. (2016). Is gender more important and meaningful than race? An analysis of racial and gender identity among black, white, and mixed-race. Cultural Diversity and Ethnic Minority Psychology, 23, 323-334. 10.1037/cdp0000125.

Saby, J. N., Meltzoff, A. N., Marshall, P. J. (2016). Beyond the N1: A review of late somatosensory evoked responses in human infants. International Journal of Psychophysiology, 110, 146-152. PMCID: PMC5215472. doi: 10.1016/j.ijpsycho.2016.08.008.

Kathleen J. Millen

Sheri Mizumori

Baker, P. M., Jhou, T., Li, B., Matsumoto, M., Mizumori, S. J., Stephenson-Jones, M., Vicentic, A. (2016). The lateral habenula circuitry: Reward processing and cognitive control. The Journal of Neuroscience, 36, 11482-11488. PMCID: PMC5125215. doi: 10.1523/JNEUROSCI.2350-16.2016.

Jo, Y. S., Mizumori, S. J. (2016). Prefrontal regulation of neuronal activity in the ventral tegmental area. Cerebral Cortex, 26, 4057-4068. doi: 10.1093/cercor/bhv215.

Cecilia B. Moens Anderson, S., Poudel, K. R., Roh-Johnson, M., Brabletz, T., Yu, M., Borenstein-Auerbach, N., … Moens, C. B., … Conacci-Sorrell, M. (2016). MYC-nick promotes cell migration by inducing fascin expression and Cdc42 activation. Proceedings of the National Academy of Sciences of the United States of America, 113, E5481-90. PMCID: PMC5027433. doi: 10.1073/pnas.1610994113.

Davey, C. F., Mathewson, A. W., Moens, C. B. (2016). Pcp signaling between migrating neurons and their planar-polarized neuroepithelial environment controls filopodial dynamics and directional migration. PLoS Genetics, 12, e1005934. PMCID: PMC4798406. doi: 10.1371/journal.pgen.1005934.

Stawicki, T. M., Hernandez, L., Esterberg, R., Linbo, T., Owens, K. N., Shah, A. N., … Moens, C. B., Rubel, E. W., Raible, D. W. (2016). Cilia-associated genes play differing roles in aminoglycoside-induced hair cell death in zebrafish. G3 (Bethesda), 6, 2225-35. PMCID: PMC4938675. doi: 10.1534/g3.116.030080.

Pierre D. Mourad Bonow, R. H., Silber, J. R., Enzmann, D. R., Beauchamp, N. J., Ellenbogen, R. G., Mourad, P. D. (2016). Towards use of MRI-guided ultrasound for treating cerebral vasospasm. Journal of Therapeutic Ultrasound, 4, 6. PMCID: PMC4770693. doi: 10.1186/s40349-016-0050-2.

Darvas, F., Mehic, E., Caler, C. J., Ojemann, J. G., Mourad, P. D. (2016). Toward deep brain monitoring with superficial EEG sensors plus neuromodulatory focused ultrasound. Ultrasound in Medicine and Biology, 42, 1834-47. PMCID: PMC5768413. doi: 10.1016/j.ultrasmedbio.2016.02.020.

Jeffrey Munson Neuhaus, E., Jones, E. J., Barnes, K., Sterling, L., Estes, A. M., Munson, J., … Webb, S. J. (2016). The relationship between early neural responses to emotional faces at age 3 and later autism and anxiety symptoms in adolescents with autism. Journal of Autism and Developmental Disorders, 46, 2450-63. PMCID: PMC5305034. doi: 10.1007/s10803-016-2780-y.

Michael Mustari Fleuriet, J., Walton, M. M., Ono, S., Mustari, M. J. (2016). Electrical microstimulation of the superior colliculus in strabismic monkeys. Investigative Ophthalmology & Visual Science, 57, 3168-80. PMCID: PMC4928695. doi: 10.1167/iovs.16-19488.

Ono, S., Mustari, M. J. (2016). Response properties of MST parafoveal neurons during smooth pursuit adaptation. Journal of Neurophysiology, 116, 210-7. PMCID: PMC4961761. doi: 10.1152/jn.00203.2016.

Elizabeth A. Nance Zhang, F., Nance, E., Alnasser, Y., Kannan, R., Kannan, S. (2016). Microglial migration and interactions with dendrimer nanoparticles are altered in the presence of neuroinflammation. Journal of Neuroinflammation, 13, 65. PMCID: PMC4802843. doi: 10.1186/s12974-016-0529-3.

Edward J. Novotny, Jr.

Jeffrey Ojemann Buckley, R., Estronza-Ojeda, S., Ojemann, J. G. (2016). Laser ablation in pediatric epilepsy. Neurosurgery Clinics of North America, 27, 69-78. doi: 10.1016/j.nec.2015.08.006.

Kellis, S., Sorensen, L., Darvas, F., Sayres, C., O'Neill, K., 3rd, Brown, R. B., … Ojemann, J. G., Greger, B. (2016). Multi-scale analysis of neural activity in humans: Implications for micro-scale electrocorticography. Clinical Neurophysiology, 127, 591-601. doi: 10.1016/j.clinph.2015.06.002.

Klein, E., Ojemann, J. G. (2016). Informed consent in implantable BCI research: Identification of research risks and recommendations for development of best practices. Journal of Neural Engineering, 13, 043001. doi: 10.1088/1741-2560/13/4/043001.

Monica Oxford

Oxford, M. L., Spieker, S. J., Lohr, M. J., Fleming, C. B. (2016). Promoting First Relationships®: Randomized trial of a 10-week home visiting program with families referred to child protective services. Child Maltreatment, 21, 267-277. PMCID: PMC5357588. doi: 10.1177/1077559516668274.

Oxford, M. L., Marcenko, M., Fleming, C. B., Lohr, M. J., Spieker, S. J. (2016). Promoting birth parents' relationships with their toddlers upon reunification: Results from Promoting First Relationships® home visiting program. Children and Youth Services Review, 61, 109-116. PMCID: PMC4746016. doi: 10.1016/j.childyouth.2015.12.004.

Pasalich, D. S., Fleming, C. B., Oxford, M. L., Zheng, Y., Spieker, S. J. (2016). Can parenting intervention prevent cascading effects from placement instability to insecure attachment to externalizing problems in maltreated toddlers? Child Maltreatment, 21, 175-85. PMCID: PMC5131711. doi: 10.1177/1077559516656398.

Russell, B. S., Lee, J. O., Spieker, S. J., Oxford, M. L. (2016). Parenting and preschool self-regulation as predictors of social emotional competence in 1st grade. Journal of Research in Childhood Education, 30, 153-169. PMCID: PMC5015765. doi: 10.1080/02568543.2016.1143414.

Leo Pallanck

Davis, M. Y., Trinh, K., Thomas, R. E., Yu, S., Germanos, A. A., Whitley, B. N., … Pallanck, L. J. (2016). Glucocerebrosidase deficiency in Drosophila results in alpha-synuclein-independent protein aggregation and neurodegeneration. PLoS Genetics, 12, e1005944. PMCID: PMC4809718. doi: 10.1371/journal.pgen.1005944.

Jay Parrish Meltzer, S., Yadav, S., Lee, J., Soba, P., Younger, S. H., Jin, P., … Parrish, J. Z., … Jan, Y. N. (2016). Epidermis-derived semaphorin promotes dendrite self-avoidance by regulating dendrite-substrate adhesion in drosophila sensory neurons. Neuron, 89, 741-55. PMCID: PMC4760923. doi: 10.1016/j.neuron.2016.01.020.

Williams, C. R., Baccarella, A., Parrish, J. Z., Kim, C. C. (2016). Trimming of sequence reads alters RNA-Seq gene expression estimates. BMC Bioinformatics, 17, 103. PMCID: PMC4766705. doi: 10.1186/s12859-016-0956-2.

James Phillips Kelly, J. P., Phillips, J. O., Weiss, A. H. (2016). VEP analysis methods in children with optic nerve hypoplasia: Relationship to visual acuity and optic disc diameter. Documenta Ophthalmologica, 133, 159-169. doi: 10.1007/s10633-016-9566-6.

Kelly, J. P., Ishak, G. E., Phillips, J. O., Nguyen, H., Weiss, A. H. (2016). Visual sensory and ocular motor function in children with polymicrogyria: Relationship to magnetic resonance imaging. Journal of AAPOS, 20, 37-43. doi: 10.1016/j.jaapos.2015.10.016.

Weiss, A. H., Kelly, J. P., Phillips, J. O. (2016). Infantile nystagmus and abnormalities of conjugate eye movements in Down syndrome. Investigative Ophthalmology & Visual Science, 57, 1301-9. doi: 10.1167/iovs.15-18532.

Nicholas Poolos Brennan, G. P., Baram, T. Z., Poolos, N. P. (2016). Hyperpolarization-activated cyclic nucleotide-gated (hcn) channels in epilepsy. Cold Spring Harbor Perspectives in Medicine, 6, a022384. PMCID: PMC4772079. doi: 10.1101/cshperspect.a022384.

Suzie Pun Cheng, Y., Yumul, R. C., Pun, S. H. (2016). Virus-inspired polymer for efficient in vitro and in vivo gene delivery. Angewandte Chemie International Edition in English, 55, 12013-7. PMCID: PMC5034564. doi: 10.1002/anie.201605958.

Cheng, Y., Wei, H., Tan, J. K., Peeler, D. J., Maris, D. O., Sellers, D. L., Horner, P. J., Pun, S. H. (2016). Nano-sized sunflower polycations as effective gene transfer vehicles. Small, 12, 2750-8. PMCID: PMC5052141. doi: 10.1002/smll.201502930.

Ngambenjawong, C., Gustafson, H. H., Pineda, J. M., Kacherovsky, N. A., Cieslewicz, M., Pun, S. H. (2016). Serum stability and affinity optimization of an M2 macrophage-targeting peptide (M2pep). Theranostics, 6, 1403-14. PMCID: PMC4924508. doi: 10.7150/thno.15394.

Wu, J. P., Cheng, B., Roffler, S. R., Lundy, D. J., Yen, C. Y., Chen, P., … Pun, S. H., … Hsieh, P. C. (2016). Reloadable multidrug capturing delivery system for targeted ischemic disease treatment. Science Translational Medicine, 8, 365ra160. doi: 10.1126/scitranslmed.aah6228.

Jan-Marino (Nino) Ramirez Ravinder, S., Donckels, E. A., Ramirez, J. S., Christakis, D. A., Ramirez, J. M., Ferguson, S. M. (2016). Excessive sensory stimulation during development alters neural plasticity and vulnerability to cocaine in mice. eNeuro, 3, PMCID: PMC4994069. doi: 10.1523/ENEURO.0199-16.2016.

Wendy Raskind Chen, D. H., Below, J. E., Shimamura, A., Keel, S. B., Matsushita, M., Wolff, J., … Raskind, W. H. (2016). Ataxia-Pancytopenia syndrome is caused by missense mutations in SAMD9L. American Journal of Human Genetics, 98, 1146-1158. PMCID: PMC4908176. doi: 10.1016/j.ajhg.2016.04.009.

Peter, B., Wijsman, E. M., Nato, A. Q., Jr., University of Washington Center for Mendelian, Genomics, Matsushita, M. M., Chapman, K. L., … Raskind, W. H. (2016). Genetic candidate variants in two multigenerational families with childhood apraxia of speech. PLoS One, 11, e0153864. PMCID: PMC4847873. doi: 10.1371/journal.pone.0153864.

Raskind, W. H., Hisama, F. M., Bennett, R. L. (2016). Biochemical and imaging surveillance in Li-Fraumeni syndrome. The Lancet Oncology, 17, e472. doi: 10.1016/S1470-2045(16)30530-7.

Thomas A. Reh Wohl, S. G., Reh, T. A. (2016). miR-124-9-9* potentiates Ascl1-induced reprogramming of cultured Muller glia. Glia, 64, 743-62. PMCID: PMC5303620. doi: 10.1002/glia.22958.

Wohl, S. G., Reh, T. A. (2016). The microRNA expression profile of mouse Muller glia in vivo and in vitro. Scientific Reports, 6, 35423. PMCID: PMC5064377. doi: 10.1038/srep35423.

Todd Richards Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Longcamp, M., Richards, T. L., Velay, J. L., Berninger, V. W. (2016). Neuroanatomy of handwriting and related reading and writing skills in adults and children with and without learning disabilities: French-American connections. Pratiques, 171, PMCID: PMC5297261.

Edwin Rubel

Cramer, K. S., Rubel, E. W. (2016). Glial cell contributions to auditory brainstem development. Frontiers in Neural Circuits, 10, 83. PMCID: PMC5073128. doi: 10.3389/fncir.2016.00083.

Seidl, A. H., Rubel, E. W. (2016). Systematic and differential myelination of axon collaterals in the mammalian auditory brainstem. Glia, 64, 487-494. PMCID: PMC4752408. doi: 10.1002/glia.22941.

Suli, A., Pujol, R., Cunningham, D. E., Hailey, D. W., Prendergast, A., Rubel, E. W., Raible, D. W. (2016). Innervation regulates synaptic ribbons in lateral line mechanosensory hair cells. Journal of Cell Science, 129, 2250-60. PMCID: PMC4920245. doi: 10.1242/jcs.182592.

Jay Rubinstein Drennan, W. R., Won, J. H., Timme, A. O., Rubinstein, J. T. (2016). Nonlinguistic outcome measures in adult cochlear implant users over the first year of implantation. Ear and Hearing, 37, 354-364. doi: 10.1097/aud.0000000000000261.

O'Brien, G. E., Imennov, N. S., Rubinstein, J. T. (2016). Simulating electrical modulation detection thresholds using a biophysical model of the auditory nerve. Journal of the Acoustical Society of America, 139, 2448. doi: 10.1121/1.4947430.

Hannele Ruohola-Baker Ellen Kreipke, R., Wang, Y., Miklas, J. W., Mathieu, J., Ruohola-Baker, H. (2016). Metabolic remodeling in early development and cardiomyocyte maturation. Seminars in Cell and Developmental Biology, 52, 84-92. PMCID: PMC4820352. doi: 10.1016/j.semcdb.2016.02.004.

Mathieu, J., Ruohola-Baker, H. (2016). Metabolic remodelin of pluripotency. Cell Stem Cell, 19, 3-4. doi: 10.1016/j.stem.2016.06.016.

Rahkonen, N., Stubb, A., Malonzo, M., Edelman, S., Emani, M. R., Narva, E., … Ruohola-Baker, H., … Lund, R. (2016). Mature Let-7 miRNAs fine tune expression of LIN28B in pluripotent human embryonic stem cells. Stem Cell Research, 17, 498-503. doi: 10.1016/j.scr.2016.09.025.

Xu, Z., Robitaille, A. M., Berndt, J. D., Davidson, K. C., Fischer, K. A., Mathieu, J., … Ruohola-Baker, H., Moon, R. T. (2016). Wnt/beta-catenin signaling promotes self-renewal and inhibits the primed state transition in naive human embryonic stem cells. Proceedings of the National Academy of Sciences of the United States of America, 113, E6382-E6390. PMCID: PMC5081574. doi: 10.1073/pnas.1613849113.

Ilene Schwartz Kamps, Debra, Rosenberg, Nancy, Mason, Rose, Schwartz, I. S. (2016). Effects of reading mastery as a small group intervention for young children with ASD. Journal of Developmental and Physical Disabilities, 28, 703-722. doi: 10.1007/s10882-016-9503-3.

C. Ronald Scott Byers, H. M., Bennett, R. L., Malouf, E. A., Weiss, M. D., Feng, J., Scott, C. R., Jayadev, S. (2016). Erratum to: Novel report of phosphoserine phosphatase deficiency in an adult with myeloneuropathy and limb contractures. JMID Reports, 30, 109. PMCID: PMC5110440. doi: 10.1007/8904_2016_540.

Elliott, S., Buroker, N., Cournoyer, J. J., Potier, A. M., Trometer, J. D., Elbin, C., … Scott, C. R. (2016). Pilot study of newborn screening for six lysosomal storage diseases using Tandem Mass Spectrometry. Molecular Genetics and Metabolism, 118, 304-9. PMCID: PMC5318163. doi: 10.1016/j.ymgme.2016.05.015.

Elliott, S., Buroker, N., Cournoyer, J. J., Potier, A. M., Trometer, J. D., Elbin, C., … Scott, C. R. (2016). Dataset and standard operating procedure for newborn screening of six lysosomal storage diseases: By tandem mass spectrometry. Data Brief, 8, 915-24. PMCID: PMC4961295. doi: 10.1016/j.dib.2016.06.052.

Dennis Shaw Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Eilers, B., Albers, E., Law, Y., McMullan, D. M., Shaw, D. W. W., Kemna, M. (2016). Posterior reversible encephalopathy syndrome after pediatric heart transplantation: Increased risk for children with preexisting Glenn/Fontan physiology. Pediatric Transplantation, 20, 552-8. doi: 10.1111/petr.12702.

Petek, L. M., Rickard, A. M., Budech, C., Poliachik, S. L., Shaw, D. W. W., Ferguson, M. R., … Miller, D. G. (2016). A cross sectional study of two independent cohorts identifies serum biomarkers for facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders, 26, 405-13. PMCID: PMC4912392. doi: 10.1016/j.nmd.2016.04.012.

Donald Sodora Gasper, M. A., Biswas, S. P., Fisher, B. S., Ehnert, S. C., Sherman, D. R., Sodora, D. L. (2016). Nonpathogenic SIV and pathogenic HIV infections associate with disparate innate cytokine signatures in response to mycobacterium bovis BCG. PLoS One, 11, e0158149. PMCID: PMC4978473. doi: 10.1371/journal.pone.0158149.

Matthew Speltz

Kapp-Simon, K. A., Wallace, E., Collett, B. R., Cradock, M. M., Crerand, C. E., Speltz, M. L. (2016). Language, learning, and memory in children with and without single-suture craniosynostosis. Journal of Neurosurgery. Pediatrics, 17, 578-88. doi: 10.3171/2015.9.PEDS15238.

Parker, S. E., Lijewski, V. A., Janulewicz, P. A., Collett, B. R., Speltz, M. L., Werler, M. M. (2016). Upper respiratory infection during pregnancy and neurodevelopmental outcomes among offspring. Neurotoxicology and Teratology, 57, 54-59. PMCID: PMC5056812. doi: 10.1016/j.ntt.2016.06.007.

Speltz, M. L., Collett, B. R., Wallace, E. R., Kapp-Simon, K. (2016). Behavioral adjustment of school-age children with and without single-suture craniosynostosis. Plastic and Reconstructive Surgery, 138, 435-45. doi: 10.1097/PRS.0000000000002383.

Wallace, E. R., Collett, B. R., Kapp-Simon, K., Starr, J. R., Birgfeld, C., Speltz, M. L. (2016). Visuomotor function in school-age children with single-suture craniosynostosis. Journal of Developmental and Behavioral Pediatrics, 37, 483-90. PMCID: PMC4930420. doi: 10.1097/DBP.0000000000000319.

Susan Spieker Oxford, M. L., Spieker, S. J., Lohr, M. J., Fleming, C. B. (2016). Promoting First Relationships®: Randomized trial of a 10-week home visiting program with families referred to child protective services. Child Maltreatment, 21, 267-277. PMCID: PMC5357588. doi: 10.1177/1077559516668274.

Mark Stein Becker, S. P., Pfiffner, L. J., Stein, M. A., Burns, G. L., McBurnett, K. (2016). Sleep habits in children with attention-deficit/hyperactivity disorder predominantly inattentive type and associations with comorbid psychopathology symptoms. Sleep Medicine, 21, 151-9. PMCID: PMC4889552. doi: 10.1016/j.sleep.2015.11.011.

Chronis-Tuscano, A., Wang, C. H., Strickland, J., Almirall, D., Stein, M. A. (2016). Personalized treatment of mothers with ADHD and their young at-risk children: A smart pilot. Journal of Clinical Child and Adolescent Psychology, 45, 510-21. PMCID: PMC4930389. doi: 10.1080/15374416.2015.1102069.

Su, Y., Yang, L., Stein, M. A., Cao, Q., Wang, Y. (2016). Osmotic release oral system methylphenidate versus atomoxetine for the treatment of attention-deficit/hyperactivity disorder in Chinese youth: 8-week comparative efficacy and 1-year follow-up. Journal of Child and Adolescent Psychopharmacology, 26, 362-71. doi: 10.1089/cap.2015.0031.

Nephi Stella Cherry, A. E., Haas, B. R., Naydenov, A. V., Fung, S., Xu, C., Swinney, K., … Ho, R. J., … Stella, N. (2016). St-11: A new brain-penetrant microtubule-destabilizing agent with therapeutic potential for glioblastoma multiforme. Molecular Cancer Therapeutics, 15, 2018-29. PMCID: PMC5010991. doi: 10.1158/1535-7163.MCT-15-0800.

Wendy Stone Harker, C. M., Ibanez, L. V., Nguyen, T. P., Messinger, D. S., Stone, W. L. (2016). The effect of parenting style on social smiling in infants at high and low risk for ASD. Journal of Autism and Developmental Disorders, 46, 2399-407. PMCID: PMC4903899. doi: 10.1007/s10803-016-2772-y.

Key, A. P., Yoder, P. J., Stone, W. L. (2016). Consonant differentiation mediates the discrepancy between non-verbal and verbal abilities in children with ASD. Journal of Intellectual Disability Research, 60, 478-90. doi: 10.1111/jir.12286.

Messinger, D. S., Young, G. S., Webb, S. J., Ozonoff, S., Bryson, S. E., Carter, A., … Stone, W. L., … Zwaigenbaum, L. (2016). Commentary: Sex difference differences? A reply to Constantino. Molecular Autism, 7, 31. PMCID: PMC4926305. doi: 10.1186/s13229-016-0093-9.

Colin Studholme Adams Waldorf, K. M., Stencel-Baerenwald, J. E., Kapur, R. P., Studholme, C., Boldenow, E., Vornhagen, J., … Richards, T. L., Garden, G. A., … Juul, S. E., … Shaw, D. W. W., … Hevner, R. F., Dobyns, W. B., … Rajagopal, L. (2016). Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primate. Nature Medicine, 22, 1256-1259. PMCID: PMC5365281. doi: 10.1038/nm.4193.

Zwicker, J. G., Miller, S. P., Grunau, R. E., Chau, V., Brant, R., Studholme, C., … Tam, E. W. (2016). Smaller cerebellar growth and poorer neurodevelopmental outcomes in very preterm infants exposed to neonatal morphine. The Journal of Pediatrics, 172, 81-87 e2. PMCID: PMC5462546. doi: 10.1016/j.jpeds.2015.12.024.

Stephen Tapscott Conerly, M. L., Yao, Z., Zhong, J. W., Groudine, M., Tapscott, S. J. (2016). Distinct activities of Myf5 and Myod indicate separate roles in skeletal muscle lineage specification and differentiation. Developmental Cell, 36, 375-85. PMCID: PMC4769793. doi: 10.1016/j.devcel.2016.01.021.

Jagannathan, S., Shadle, S. C., Resnick, R., Snider, L., Tawil, R. N., van der Maarel, S. M., … Tapscott, S. J. (2016). Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells. Human Molecular Genetics, 25, 4419-4431. PMCID: PMC6078597. doi: 10.1093/hmg/ddw271. van den Boogaard, M. L., Lemmers, R. J., Camano, P., van der Vliet, P. J., Voermans, N., van Engelen, B. G., … Tapscott, S. J., … van der Maarel, S. M. (2016). Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2. European Journal of Human Genetics, 24, 78-85. PMCID: PMC4795239. doi: 10.1038/ejhg.2015.55.

Bruce Tempel Weatherstone, J. H., Kopp-Scheinpflug, C., Pilati, N., Wang, Y., Forsythe, I. D., Rubel, E. W., Tempel, B. L. (2016). Maintenance of neuronal size gradient in MNTB requires sound-evoked activity. Journal of Neurophysiology, jn 00528 2016. doi: 10.1152/jn.00528.2016.

Hannah Tully Natarajan, N., Tully, H. M., Chapman, T. (2016). Prenatal presentation of pyruvate dehydrogenase complex deficiency. Pediatric Radiology, 46, 1354-7. doi: 10.1007/s00247-016-3585-z.

Tully, H. M., Kukull, W. A., Mueller, B. A. (2016). Clinical and surgical factors associated with increased epilepsy risk in children with hydrocephalus. Pediatric Neurology, 59, 18-22. doi: 10.1016/j.pediatrneurol.2016.02.011.

Eric Turner Rosin, J. M., Li, W., Cox, L. L., Rolfe, S. M., Latorre, V., Akiyama, J. A., … Turner, E. E., Cox, T. C. (2016). A distal 594 bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by the Hox-Pbx-Meis complex. Development, 143, 2582-92. PMCID: PMC4958336. doi: 10.1242/dev.133736.

Jashvant Unadkat Farooq, M., Kelly, E. J., Unadkat, J. D. (2016). CYP2D6 is inducible by endogenous and exogenous corticosteroids. Drug Metabolism and Disposition, 44, 750-7. PMCID: PMC4851303. doi: 10.1124/dmd.115.069229.

Joshi, A. A., Vaidya, S. S., St-Pierre, M. V., Mikheev, A. M., Desino, K. E., Nyandege, A. N., … Unadkat, J. D., Gerk, P. M. (2016). Placental ABC transporters: Biological impact and pharmaceutical significance. Pharmaceutical Research, 33, 2847-2878. PMCID: PMC5384842. doi: 10.1007/s11095-016-2028-8.

Sara Jane Webb Charman, T., Young, G. S., Brian, J., Carter, A., Carver, L. J., Chawarska, K., … Stone, W. L., … Webb, S. J., … Zwaigenbaum, L. (2016). Non-ASD outcomes at 36 months in siblings at familial risk for autism spectrum disorder (ASD): A Baby Siblings Research Consortium (BSRC) study. Autism Research, 15 Jul 2016. doi: 10.1002/aur.1669.

Faja, S., Clarkson, T., Webb, S. J. (2016). Neural and behavioral suppression of interfering flankers by children with and without autism spectrum disorder. Neuropsychologia, 93, 251-261. PMCID: PMC5154614. doi: 10.1016/j.neuropsychologia.2016.10.017.

Faja, S., Dawson, G., Aylward, E. H., Wijsman, E. M., Webb, S. J. (2016). Early event-related potentials to emotional faces differ for adults with autism spectrum disorder and by serotonin transporter genotype. Clinical Neurophysiology, 127, 2436-47. PMCID: PMC5279301. doi: 10.1016/j.clinph.2016.02.022.

Garman, H. D., Spaulding, C. J., Webb, S. J., Mikami, A. Y., Morris, J. P., Lerner, M. D. (2016). Wanting it too much: An inverse relation between social motivation and facial emotion recognition in autism spectrum disorder. Child Psychiatry and Human Development, 47, 890-902. PMCID: PMC4936965. doi: 10.1007/s10578-015-0620-5.

Jonathan Weinstein McDonough, A., Weinstein, J. R. (2016). Neuroimmune response in ischemic preconditioning. Neurotherapeutics, 13, 748-761. PMCID: PMC5081114. doi: 10.1007/s13311-016-0465-z.

John P. Welsh Turecek, J., Han, V. Z., Cuzon Carlson, V. C., Grant, K. A., Welsh, J. P. (2016). Electrical coupling and synchronized subthreshold oscillations in the inferior olive of the Rhesus Macaque. The Journal of Neuroscience, 36, 6497-502. PMCID: PMC5015785. doi: 10.1523/JNEUROSCI.4495-15.2016. Welsh, J. P., Oristaglio, J. T. (2016). Autism and classical eyeblink conditioning: Performance changes of the conditioned response related to autism spectrum disorder diagnosis. Frontiers in Psychiatry, 7, 137. PMCID: PMC4980680. doi: 10.3389/fpsyt.2016.00137.

H. Steve White Barker-Haliski, M. L., Heck, T. D., Dahle, E. J., Vanegas, F., Pruess, T. H., Wilcox, K. S., White, H. S. (2016). Acute treatment with minocycline, but not valproic acid, improves long-term behavioral outcomes in the Theiler's virus model of temporal lobe epilepsy. Epilepsia, 57, 1958-1967. PMCID: PMC5154893. doi: 10.1111/epi.13577.

Gidal, B. E., Wechsler, R. T., Sankar, R., Montouris, G. D., White, H. S., Cloyd, J. C., … Isojarvi, J. (2016). Deconstructing tolerance with clobazam: Post hoc analyses from an open-label extension study. Neurology, 87, 1806-1812. PMCID: PMC5089527. doi: 10.1212/WNL.0000000000003253.

Umpierre, A. D., Bennett, I. V., Nebeker, L. D., Newell, T. G., Tian, B. B., Thomson, K. E., White, H. S., … Wilcox, K. S. (2016). Repeated low-dose kainate administration in C57BL/6J mice produces temporal lobe epilepsy pathology but infrequent spontaneous seizures. Experimental Neurology, 279, 116-126. PMCID: PMC5382800. doi: 10.1016/j.expneurol.2016.02.014.

Ellen M. Wijsman Faja, S., Dawson, G., Aylward, E. H., Wijsman, E. M., Webb, S. J. (2016). Early event-related potentials to emotional faces differ for adults with autism spectrum disorder and by serotonin transporter genotype. Clinical Neurophysiology, 127, 2436-47. PMCID: PMC5279301. doi: 10.1016/j.clinph.2016.02.022.

Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M., … Wijsman, E. M., … Gruen, J. R. (2016). Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. Human Genetics, 135, 1329-1341. PMCID: PMC5065602. doi: 10.1007/s00439-016-1717-z.

Wijsman, E. M. (2016). Family-based approaches: Design, imputation, analysis, and beyond. BMC Genetics, 17, 9. PMCID: PMC4895701. doi: 10.1186/s12863-015-0318-5.

Libin Xu Finno, C. J., Bordbari, M. H., Valberg, S. J., Lee, D., Herron, J., Hines, K., … Xu, L. (2016). Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genes. Free Radical Biology and Medicine, 101, 261-271. PMCID: PMC5154892. doi: 10.1016/j.freeradbiomed.2016.10.009.

Herron, J., Reese, R. C., Tallman, K. A., Narayanaswamy, R., Porter, N. A., Xu, L. (2016). Identification of environmental quaternary ammonium compounds as direct inhibitors of cholesterol biosynthesis. Toxicological Sciences, 151, 261-70. PMCID: PMC4880132. doi: 10.1093/toxsci/kfw041.

Hines, K. M., May, J. C., McLean, J. A., Xu, L. (2016). Evaluation of Collision Cross Section calibrants for structural analysis of lipids by traveling wave ion mobility-mass spectrometry. Analytical Chemistry, 88, 7329-36. PMCID: PMC4955523. doi: 10.1021/acs.analchem.6b01728.

Pfeffer, B. A., Xu, L., Porter, N. A., Rao, S. R., Fliesler, S. J. (2016). Differential cytotoxic effects of 7-dehydrocholesterol-derived oxysterols on cultured retina-derived cells: Dependence on sterol structure, cell type, and density. Experimental Eye Research, 145, 297-316. PMCID: PMC5024725. doi: 10.1016/j.exer.2016.01.016.

Jason Yeatman Teubner-Rhodes, S., Vaden, K. I., Jr., Cute, S. L., Yeatman, J. D., Dougherty, R. F., Eckert, M. A. (2016). Aging-resilient associations between the arcuate fasciculus and vocabulary knowledge: Microstructure or morphology? The Journal of Neuroscience, 36, 7210-22. PMCID: PMC4938863. doi: 10.1523/JNEUROSCI.4342-15.2016.

Yeatman, J. D., Norcia, A. M. (2016). Temporal tuning of word- and face-selective cortex. Journal of Cognitive Neuroscience, 28, 1820-1827. PMCID: PMC5045815. doi: 10.1162/jocn_a_01002.

Jing Zhang Shao, L. W., Pan, Y., Qi, X. L., Li, Y. X., Ma, X. L., Yi, W. N., Zhang, J., … Chang, Q. (2016). ATRX loss in adult supratentorial diffuse astrocytomas correlates with p53 over expression and IDH1 mutation and predicts better outcome in p53 accumulated patients. Histology and histopathology, 31, 103-114. doi: 10.14670/hh-11-664.

2017

Kristina Adams Waldorf

Harrell, M. I., Burnside, K., Whidbey, C., Vornhagen, J., Adams Waldorf, K. M., Rajagopal, L. (2017). Exploring the pregnant guinea pig as a model for group B Streptococcus intrauterine infection. Journal of Infectious Diseases and Medicine, 27 Jul 2017. PMCID: PMC5635843.

Li, J., Baird, M. A., Davis, M. A., Tai, W., Zweifel, L. S., Adams Waldorf, K. M., … Gao, X. (2017). Dramatic enhancement of the detection limits of bioassays via ultrafast deposition of polydopamine. Nature Biomedical Engineering, 1, PMCID: PMC5654575. doi: 10.1038/s41551-017-0082.

Elizabeth Aylward Aldridge, K., Collett, B. R., Wallace, E. R., Birgfeld, C., Austin, J. R., Yeh, R., … Aylward, E. H., Cunningham, M. L., Speltz, M. L. (2017). Structural brain differences in school-age children with and without single-suture craniosynostosis. Journal of Neurosurgery. Pediatrics, 19, 479-489. PMCID: PMC5642047. doi: 10.3171/2016.9.PEDS16107.

Frost, C., Mulick, A., Scahill, R. I., Owen, G., Aylward, E. H., Leavitt, B. R., … Track-HD Investigators (2017). Design optimization for clinical trials in early-stage manifest Huntington's disease. Movement Disorders, 32, 1610-1619. doi: 10.1002/mds.27122.

Scahill, R. I., Andre, R., Tabrizi, S. J., Aylward, E. H. (2017). Structural imaging in premanifest and manifest Huntington disease. Handbook of Clinical Neurology, 144, 247-261. doi: 10.1016/B978-0-12-801893-4.00020-1.

Velasquez, F., Qin, X. A., Reilly, M. A., Neuhaus, E., Estes, A. M., Aylward, E. H., Kleinhans, N. M. (2017). Neural correlates of emotional inhibitory control in autism spectrum disorders. Research in Developmental Disabilities, 64, 64-77. doi: 10.1016/j.ridd.2017.03.008.

Melissa Barker-Haliski Barker-Haliski, M. L., Loscher, W., White, H. S., Galanopoulou, A. S. (2017). Neuroinflammation in epileptogenesis: Insights and translational perspectives from new models of epilepsy. Epilepsia, 58, 39-47. PMCID: PMC5604891. doi: 10.1111/epi.13785.

Raphael Bernier Ackerman, S., Schoenbrun, S., Hudac, C., Bernier, R. A. (2017). Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 47, 3489-3496. doi: 10.1007/s10803-017-3246-6.

Ackerman, S., Schoenbrun, S., Hudac, C., Bernier, R. A. (2017). Erratum to: Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of Autism Spectrum Disorder. Journal of Autism and Developmental Disorders, 47, 3497. doi: 10.1007/s10803-017-3301-3.

Bernier, R. A., Hudac, C. M., Chen, Q., Zeng, C., Wallace, A. S., Gerdts, J., … Simons V. I. P. Consortium. (2017). Developmental trajectories for young children with 16p11.2 copy number variation. American Journal of Medical Genetics B: Neuropsychiatric Genetics, 174, 367-380. doi: 10.1002/ajmg.b.32525.

Bramswig, N. C., Ludecke, H. J., Pettersson, M., Albrecht, B., Bernier, R. A., Cremer, K., Eichler, E. E., … Wieczorek, D. (2017). Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism. Human Genetics, 136, 179-192. PMCID: PMC5821420. doi: 10.1007/s00439-016-1743-x.

Carvalho, J. O., Springate, B., Bernier, R. A., Davis, J. (2017). Psychometrics of the AAN Caregiver Driving Safety Questionnaire and contributors to caregiver concern about driving safety in older adults. International Psychogeriatrics, 1-10. doi: 10.1017/S1041610217001727.

Earl, R. K., Turner, T. N., Mefford, H. C., Hudac, C. M., Gerdts, J., Eichler, E. E., Bernier, R. A. (2017). Clinical phenotype of ASD-associated DYRK1A haploinsufficiency. Molecular Autism, 8, 54. PMCID: PMC5629761. doi: 10.1186/s13229-017-0173-5.

Geisheker, M. R., Heymann, G., Wang, T., Coe, B. P., Turner, T. N., Stessman, H. A. F., … Bernier, R. A., … Eichler, E. E. (2017). Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nature Neuroscience, 20, 1043-1051. PMCID: PMC5539915. doi: 10.1038/nn.4589.

Goin-Kochel, R. P., Trinh, S., Barber, S., Bernier, R. A. (2017). Gene disrupting mutations associated with regression in autism spectrum disorder. Journal of Autism and Developmental Disorders, 47, 3600-3607. PMCID: PMC5693665. doi: 10.1007/s10803-017-3256-4.

Hudac, C. M., Stessman, H. A. F., DesChamps, T. D., Kresse, A., Faja, S., Neuhaus, E., Webb, S. J., Eichler, E. E., Bernier, R. A. (2017). Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism. Journal of Neurodevelopmental Disorders, 9, 24. PMCID: PMC5446693. 26 May 2017. doi: 10.1186/s11689-017-9199-4.

Jansen, S., Hoischen, A., Coe, B. P., Carvill, G. L., Van Esch, H., Bosch, D. G. M., … Bernier, R. A., … Mefford, H. C., … Eichler, E. E., de Vries, B. B. A. (2017). A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics, 5 Dec 2017.doi: 10.1038/s41431-017-0039-5.

Jansen, S., Geuer, S., Pfundt, R., Brough, R., Ghongane, P., Herkert, J. C., … Bernier, R. A., … de Vries, B. B. (2017). De novo truncating mutations in the last and penultimate exons of PPM1D cause an intellectual disability syndrome. American Journal of Human Genetics, 100, 650-658. PMCID: PMC5384016. doi: 10.1016/j.ajhg.2017.02.005.

Krupp, D. R., Barnard, R. A., Duffourd, Y., Evans, S. A., Mulqueen, R. M., Bernier, R. A., … O'Roak, B. J. (2017). Exonic mosaic mutations contribute risk for autism spectrum disorder. American Journal of Human Genetics, 101, 369-390. PMCID: PMC5590950. doi: 10.1016/j.ajhg.2017.07.016.

Patowary, A., Nesbitt, R., Archer, M., Bernier, R. A., Brkanac, Z. (2017). Next generation sequencing mitochondrial DNA analysis in autism spectrum disorder. Autism Research, 10, 1338-1343. PMCID: PMC5573912. doi: 10.1002/aur.1792.

Siper, P. M., De Rubeis, S., Trelles, M. D. P., Durkin, A., Di Marino, D., Muratet, F., … Eichler, E. E., … Mefford, H. C., Bernier, R. A., … Buxbaum, J. D. (2017). Prospective investigation of FOXP1 syndrome. Molecular Autism, 8, 57. PMCID: PMC5655854. doi: 10.1186/s13229-017-0172-6.

Stessman, H. A., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., … Bernier, R. A., Eichler, E. E. (2017). Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nature Genetics, 49, 515-526. PMCID: PMC5374041. doi: 10.1038/ng.3792.

Turner, T. N., Yi, Q., Krumm, N., Huddleston, J., Hoekzema, K., F. Stessman HA, … Bernier, R. A., … Eichler, E. E. (2017). denovo-db: A compendium of human de novo variants. Nucleic Acids Research, 45, D804-D811. PMCID: PMC5210614. doi: 10.1093/nar/gkw865.

Webb, S. J., Garrison, M. M., Bernier, R. A., McClintic, A. M., King, B. H., Mourad, P. D. (2017). Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasound. Autism Research, 10, 472-484. PMCID: PMC5332517. doi: 10.1002/aur.1690.

Virginia Berninger

Berninger, V. W., Richards, T. L., Abbott, R. D. (2017). Brain and behavioral assessment of executive functions for self-regulating levels of language in reading brain. Journal of Nature and Science, 3, e464. PMCID: PMC5662027.

Berninger, V. W., Abbott, R., Cook, C. R. (2017). Relationships of attention and executive functions to oral language, reading, and writing skills and systems in middle childhood and early adolescence. Journal of Learning Disabilities, 50, 434-449. PMCID: PMC4938801. doi: 10.1177/0022219415617167.

Richards, T. L., Berninger, V. W., Yagle, K. J., Abbott, R. D., Peterson, D. J. (2017). Changes in DTI diffusivity and fMRI connectivity cluster coefficients for students with and without specific learning disabilities in written language: Brain's response to writing instruction. Journal of Nature and Science, 3, e350. PMCID: PMC5488805.

Wolf, B., Abbott, R. D., Berninger, V. W. (2017). Effective beginning handwriting instruction: Multi-modal, consistent format for 2 years, and linked to spelling and composing. Reading and Writing: An Interdisciplinary Journal, 30, 299-317. PMCID: PMC5300752. doi: 10.1007/s11145-016-9674-4.

Kristie F. Bjornson

Bjornson, K. F. (2017). Response to "Developing a clinical protocol for habitual physical activity monitoring in youth with cerebral palsy". Pediatric Physical Therapy, 29, 187-188. doi: 10.1097/PEP.0000000000000391.

Gannotti, M. E., Bailes, A., Bjornson, K. F., O'Neil, M., Grant-Buettler, M., Dusing, S. (2017). Pediatric rehabilitation services for children with Cerebral Palsy: What can existing data sources tell us? Pediatric Physical Therapy, 29, 179-186. doi: 10.1097/PEP.0000000000000377.

Cathryn Booth-LaForce Haltigan, J. D., Roisman, G. I., Cauffman, E., Booth-LaForce, C. (2017). Correlates of childhood vs. adolescence internalizing symptomatology from infancy to young adulthood. Journal of Youth and Adolescence, 46, 197-212. doi: 10.1007/s10964-016-0578-z.

Shepherd-Banigan, M., Bell, J. F., Basu, A., Booth-LaForce, C., Harris, J. R. (2017). Mothers' employment attributes and use of preventive child health services. Medical Care Research and Review, 74, 208-226. doi: 10.1177/1077558716634555.

Mark Bothwell Bothwell, M. (2017). Mechanisms and medicines for remyelination. Annual Review of Medicine, 68, 431-443. doi: 10.1146/annurev-med-050715-104400.

Zoran Brkanac Patowary, A., Nesbitt, R., Archer, M., Bernier, R. A., Brkanac, Z. (2017). Next generation sequencing mitochondrial DNA analysis in autism spectrum disorder. Autism Research, 10, 1338-1343. PMCID: PMC5573912. doi: 10.1002/aur.1792.

Thomas Burbacher

Grant, K. S., Worlein, J. M., Meyer, J. S., Novak, M. A., Kroeker, R., Rosenberg, K., … Burbacher, T. M. (2017). A longitudinal study of hair cortisol concentrations in Macaca nemestrina mothers and infants. American Journal of Primatology, 79, 1-9. PMCID: PMC6040647. doi: 10.1002/ajp.22591.

Shiotani, M., Cole, T. B., Hong, S., Park, J. J. Y., Griffith, W. C., Burbacher, T. M., … Costa, L. G., Faustman, E. M. (2017). Neurobehavioral assessment of mice following repeated oral exposures to Domoic acid during prenatal development. Neurotoxicology and Teratology, 64, 8-19. doi: 10.1016/j.ntt.2017.09.002.

Tigges, B. B., Kaar, J. L., Erbstein, N., Silberman, P., Winseck, K., Lopez-Class, M., Burbacher, T. M. (2017). Effectiveness of community outreach and engagement in recruitment success for a prebirth cohort. Journal of Clinical and Translational Science, 1, 184-191. PMCID: PMC5647659. doi: 10.1017/cts.2017.7.

Heather Carmichael Olson Hanlon-Dearman, A., Chen, M. L., Carmichael Olson, H. (2017). Understanding and managing sleep disruption in children with FASD. Biochemistry and Cell Biology, 4 Oct 2017. doi: 10.1139/bcb-2017-0064.

Petrenko, C. L. M., Pandolfino, M. E., Quamma, J., Carmichael Olson, H. (2017). Emotional understanding in school-aged children with fetal alcohol spectrum disorders: A promising target for intervention. Journal of Population Therapeutics and Clinical Pharmacology, 24, e21-e31. PMCID: PMC5627645. doi: 10.22374/1710-6222.24.2.5.

Tsang, T. W., Carmichael Olson, H., Latimer, J., Fitzpatrick, J., Hand, M., Oscar, J., … Elliott, E. J. (2017). Behavior in children with fetal alcohol spectrum disorders in remote Australia: A population-based study. Journal of Developmental and Behavioral Pediatrics, 38, 528-537. doi: 10.1097/DBP.0000000000000463.

William Catterall Catterall, W. A. (2017). Forty years of sodium channels: Structure, function, pharmacology, and epilepsy. Neurochemical Research, 42, 2495-2504. PMCID: PMC5693772. doi: 10.1007/s11064-017-2314-9.

Catterall, W. A., Wisedchaisri, G., Zheng, N. (2017). The chemical basis for electrical signaling. Nature Chemical Biology, 13, 455-463. PMCID: PMC5464002. doi: 10.1038/nchembio.2353.

Kaplan, J. S., Stella, N., Catterall, W. A., Westenbroek, R. E. (2017). Cannabidiol attenuates seizures and social deficits in a mouse model of Dravet syndrome. Proceedings of the National Academy of Sciences of the United States of America, 114, 11229-11234. PMCID: PMC5651774. doi: 10.1073/pnas.1711351114.

Lenaeus, M. J., Gamal El-Din, T. M., Ing, C., Ramanadane, K., Pomes, R., Zheng, N., Catterall, W. A. (2017). Structures of closed and open states of a voltage-gated sodium channel. Proceedings of the National Academy of Sciences of the United States of America, 114, E3051-E3060. PMCID: PMC5393245. doi: 10.1073/pnas.1700761114.

Jeffrey Chamberlain Bengtsson, N. E., Hall, J. K., Odom, G. L., Phelps, M. P., Andrus, C. R., Hawkins, R. D., … Chamberlain, J. S. (2017). Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy. Nature Communications, 8, 14454. PMCID: PMC5316861. doi: 10.1038/ncomms14454.

Bengtsson, N. E., Hall, J. K., Odom, G. L., Phelps, M. P., Andrus, C. R., Hawkins, R. D., … Chamberlain, J. S. (2017). Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy. Nature Communications, 8, 16007. PMCID: PMC5489999. doi: 10.1038/ncomms16007.

Chamberlain, J. R., Chamberlain, J. S. (2017). Progress toward gene therapy for Duchenne muscular dystrophy. Molecular Therapy, 25, 1125-1131. PMCID: PMC5417844. doi: 10.1016/j.ymthe.2017.02.019.

Hakim, C. H., Wasala, N. B., Pan, X., Kodippili, K., Yue, Y., Zhang, K., … Chamberlain, J. S., Duan, D. (2017). A five-repeat micro-dystrophin gene ameliorated dystrophic phenotype in the severe DBA/2J-mdx model of Duchenne muscular dystrophy. Molecular Therapy Methods & Clinical Development, 6, 216-230. PMCID: PMC5596503. doi: 10.1016/j.omtm.2017.06.006.

Dimitri Christakis Anderson, C. A., Bushman, B. J., Bartholow, B. D., Cantor, J., Christakis, D. A., Coyne, S. M., … Ybarra, M. (2017). Screen violence and youth behavior. Pediatrics, 140, S142-S147. doi: 10.1542/peds.2016-1758T.

Christakis, D. A., Rivara, F. P. (2017). Guns and violent media: A toxic mix with an available antidote. JAMA Pediatrics, 171, 1040-1041. doi: 10.1001/jamapediatrics.2017.2383.

Lucio Costa Chang, Y. C., Cole, T. B., Costa, L. G. (2017). Behavioral phenotyping for autism spectrum disorders in mice. Current Protocols in Toxicology, 72, 11 22 1-11 22 21. PMCID: PMC5494990. doi: 10.1002/cptx.19.

Costa, L. G., Cole, T. B., Coburn, J., Chang, Y. C., Dao, K., Roque, P. J. (2017). Neurotoxicity of traffic-related air pollution. Neurotoxicology, 59, 133-139. PMCID: PMC4875879. doi: 10.1016/j.neuro.2015.11.008.

Costa, L. G., Cole, T. B., Garrick, J. M., Marsillach, J., Furlong, C. E. (2017). Metals and paraoxonases. Advances in Neurobiology, 18, 85-111. doi: 10.1007/978-3-319-60189-2_5.

Costa, L. G., Chang, Y. C., Cole, T. B. (2017). Developmental neurotoxicity of traffic-related air pollution: Focus on Autism. Current Environmental Health Reports, 4, 156-165. doi: 10.1007/s40572-017-0135-2.

Costa, L. G. (2017). Overview of neurotoxicology. Current Protocols in Toxicology, 74, 11.1.1-11.1.11. doi: 10.1002/cptx.36.

Roque, P. J., Costa, L. G. (2017). Co-culture of neurons and microglia. Current Protocols in Toxicology, 74, 11 24 1-11 24 17. PMCID: PMC5774987. doi: 10.1002/cptx.32.

Timothy Cox

Lee, E., Le, T., Zhu, Y., Elakis, G., Turner, A., Lo, W., … Cox, T. C., … Roscioli, T. (2017). A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: Findings and recommendations. Genetics in Medicine, 7 Dec 2017. doi: 10.1038/gim.2017.214.

Parada-Sanchez, M. T., Chu, E. Y., Cox, L. L., Undurty, S. S., Standley, J. M., Murray, J. C., Cox, T. C. (2017). Disrupted IRF6-NME1/2 complexes as a cause of cleft lip/palate. Journal of Dental Research, 96, 1330-1338. PMCID: PMC5613882. doi: 10.1177/0022034517723615.

Tamasas, B., Cox, T. C. (2017). Massively increased caries susceptibility in an Irf6 cleft lip/palate model. Journal of Dental Research, 96, 315-322. doi: 10.1177/0022034516679376.

Yu, K., Deng, M., Naluai-Cecchini, T., Glass, I. A., Cox, T. C. (2017). Differences in oral structure and tissue interactions during mouse vs. human palatogenesis: Implications for the translation of findings from mice. Frontiers in Physiology, 8, 154. PMCID: PMC5350148. doi: 10.3389/fphys.2017.00154.

Michael Cunningham Aldridge, K., Collett, B. R., Wallace, E. R., Birgfeld, C., Austin, J. R., Yeh, R., … Aylward, E. H., Cunningham, M. L., Speltz, M. L. (2017). Structural brain differences in school-age children with and without single-suture craniosynostosis. Journal of Neurosurgery. Pediatrics, 19, 479-489. PMCID: PMC5642047. doi: 10.3171/2016.9.PEDS16107.

Gordon, C. T., Xue, S., Yigit, G., Filali, H., Chen, K., Rosin, N., … Cunningham, M. L., … Reversade, B. (2017). De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature Genetics, 49, 249-255. doi: 10.1038/ng.3765.

Wenger, T. L., Dahl, J., Bhoj, E. J., Rosen, A., McDonald-McGinn, D., Zackai, E., … Hing, A. V., … Cunningham, M. L., Perkins, J. (2017). Tracheal cartilaginous sleeves in children with syndromic craniosynostosis. Genetics in Medicine, 19, 62-68. PMCID: PMC5846326. doi: 10.1038/gim.2016.60.

Raimondo D'Ambrosio Kadam, S. D., D'Ambrosio, R., Duveau, V., Roucard, C., Garcia-Cairasco, N., Ikeda, A., … Kelly, K. M. (2017). Methodological standards and interpretation of video-electroencephalography in adult control rodents. A TASK1-WG1 report of the AES/ILAE Translational Task Force of the ILAE. Epilepsia, 58, 10-27. PMCID: PMC5679281. doi: 10.1111/epi.13903.

Tai, T. Y., Warner, L. N., Jones, T. D., Jung, S., Concepcion, F. A., Skyrud, D. W., … D'Ambrosio, R., Poolos, N. P. (2017). Antiepileptic action of c-Jun N-terminal kinase (JNK) inhibition in an animal model of temporal lobe epilepsy. Neuroscience, 349, 35-47. PMCID: PMC5386321. doi: 10.1016/j.neuroscience.2017.02.024.

Stephen Dager Dimian, A. F., Botteron, K. N., Dager, S. R., Elison, J. T., Estes, A. M., Pruett, J. R., Jr., … IBIS Network. (2017). Potential risk factors for the development of self-injurious behavior among infants at risk for autism spectrum disorder. Journal of Autism and Developmental Disorders, 47, 1403-1415. PMCID: PMC5385192. doi: 10.1007/s10803-017-3057-9.

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Peng, T., Chanthaphavong, R. S., Sun, S., Trigilio, J. A., Phasouk, K., Jin, L., … Glass, I. A., … Zhu, J. (2017). Keratinocytes produce IL-17c to protect peripheral nervous systems during human HSV-2 reactivation. The Journal of Experimental Medicine, 214, 2315-2329. PMCID: PMC5551564. doi: 10.1084/jem.20160581.

Vilboux, T., Doherty, D. A., Glass, I. A., Parisi, M. A., Phelps, I. G., Cullinane, A. R., … Gunay-Aygun, M. (2017). Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center. Genetics in Medicine, 19, 875-882. doi: 10.1038/gim.2016.204.

Yao, Z., Mich, J. K., Ku, S., Menon, V., Krostag, A. R., Martinez, R. A., … Glass, I. A., … Ramanathan, S. (2017). A single-cell roadmap of lineage bifurcation in human ESC models of embryonic brain development. Cell Stem Cell, 20, 120-134. PMCID: PMC5261831. doi: 10.1016/j.stem.2016.09.011.

Joan M. Goverman Goverman, J. M., Mathews, K., Goldstein, R., Holavanahalli, R., Kowalske, K., Esselman, P., … Schneider, J. C. (2017). Pediatric contractures in burn injury: A burn model system national database study. Journal of Burn Care & Research, 38, e469-e481. doi: 10.1097/BCR.0000000000000341.

Pierson, E. R., Goverman, J. M. (2017). GM-CSF is not essential for experimental autoimmune encephalomyelitis but promotes brain-targeted disease. JCI Insight, 2, e92362. PMCID: PMC5374070. doi: 10.1172/jci.insight.92362.

Thomas J. Grabowski, Jr. Boord, P., Madhyastha, T. M., Askren, M. K., Grabowski, T. J. (2017). Executive attention networks show altered relationship with default mode network in PD. NeuroImage: Clinical, 13, 1-8. PMCID: PMC5121155. doi: 10.1016/j.nicl.2016.11.004.

Lee, A. K. C., Sarkka, A., Madhyastha, T. M., Grabowski, T. J. (2017). Characterizing cross-subject spatial interaction patterns in functional magnetic resonance imaging studies: A two-stage point-process model. Biometrical Journal, 59, 1352-1381. doi: 10.1002/bimj.201600212.

Madhyastha, T. M., Koh, N., Day, T. K. M., Hernandez-Fernandez, M., Kelley, A., Peterson, D. J., … Grabowski, T. J. (2017). Running neuroimaging applications on Amazon web services: How, when, and at what cost? Frontiers in Neuroinformatics, 11, 63. PMCID: PMC5675877. doi: 10.3389/fninf.2017.00063.

Wang, S., Peterson, D. J., Gatenby, J. C., Li, W., Grabowski, T. J., Madhyastha, T. M. (2017). Evaluation of field map and nonlinear registration methods for correction of susceptibility artifacts in diffusion MRI. Frontiers in Neuroinformatics, 11, 17. PMCID: PMC5318394. doi: 10.3389/fninf.2017.00017.

Michael Guralnick Guralnick, M. J. (2017). Early intervention for children with intellectual disabilities: An update. Journal of Applied Research in Intellectual Disabilities, 30, 211-229. doi: 10.1111/jar.12233.

Robert Hevner Alcantara, D., Timms, A. E., Gripp, K., Baker, L., Park, K., Collins, S., … Hevner, R. F., Dobyns, W. B., … Mirzaa, G. M. (2017). Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly. Brain, 140, 2610-2622. PMCID: PMC6080423. doi: 10.1093/brain/awx203.

Ha, S., Tripathi, P. P., Mihalas, A. B., Hevner, R. F., Beier, D. R. (2017). C-terminal region truncation of RELN disrupts an interaction with VLDLR, causing abnormal development of the cerebral cortex and hippocampus. The Journal of Neuroscience, 37, 960-971. PMCID: PMC5296787. doi: 10.1523/JNEUROSCI.1826-16.2016.

Kaplan, E. S., Ramos-Laguna, K. A., Mihalas, A. B., Daza, R. A. M., Hevner, R. F. (2017). Neocortical Sox9+ radial glia generate glutamatergic neurons for all layers, but lack discernible evidence of early laminar fate restriction. Neural Development, 12, 14. PMCID: PMC5559824. doi: 10.1186/s13064-017-0091-4.

Mihalas, A. B., Hevner, R. F. (2017). Control of neuronal development by T-box genes in the brain. Current Topics in Developmental Biology, 122, 279-312. doi: 10.1016/bs.ctdb.2016.08.001.

Probst, S., Daza, R. A., Bader, N., Hummel, J. F., Weiss, M., Tanriver, Y., Hevner, R. F., Arnold, S. J. (2017). A dual-fluorescence reporter in the Eomes locus for live imaging and medium-term lineage tracing. Genesis, 55, PMCID: PMC5568967. doi: 10.1002/dvg.23043.

Anne Hing Wenger, T. L., Dahl, J., Bhoj, E. J., Rosen, A., McDonald-McGinn, D., Zackai, E., … Hing, A. V., … Cunningham, M. L., Perkins, J. (2017). Tracheal cartilaginous sleeves in children with syndromic craniosynostosis. Genetics in Medicine, 19, 62-68. PMCID: PMC5846326. doi: 10.1038/gim.2016.60.

David Horn Horn, D. L., Won, J. H., Rubinstein, J. T., Werner, L. A. (2017). Spectral ripple discrimination in normal-hearing infants. Ear and Hearing, 38, 212-222. PMCID: PMC5321869. doi: 10.1097/AUD.0000000000000373.

Horn, D. L., Dudley, D. J., Dedhia, K., Nie, K., Drennan, W. R., Won, J. H., Rubinstein, J. T., Werner, L. A. (2017). Effects of age and hearing mechanism on spectral resolution in normal hearing and cochlear-implanted listeners. Journal of the Acoustical Society of America, 141, 613. PMCID: PMC5848837. doi: 10.1121/1.4974203.

Purcell, P. L., Shinn, J. R., Coggeshall, S. S., Phillips, G., Paladin, A., Sie, K. C. Y., Horn, D. L. (2017). Progression of unilateral hearing loss in children with and without ipsilateral cochlear nerve canal stenosis: A hazard analysis. Otology & Neurotology, 38, e138-e144. PMCID: PMC5639713. doi: 10.1097/MAO.0000000000001452.

Philip Horner Zhao, T., Sellers, D. L., Cheng, Y., Horner, P. J., Pun, S. H. (2017). Tunable, injectable hydrogels based on peptide-cross-linked, cyclized polymer nanoparticles for neural progenitor cell delivery. Biomacromolecules, 18, 2723-2731. doi: 10.1021/acs.biomac.7b00510.

Marshall S. Horwitz Wlodarski, M. W., Collin, M., Horwitz, M. S. (2017). GATA2 deficiency and related myeloid neoplasms. Seminars in Hematology, 54, 81-86. PMCID: PMC5650112. doi: 10.1053/j.seminhematol.2017.05.002.

Roxanne Hudson

Hudson, R. F., Sanders, E. A., Greenway, R., Xie, S., Smith, M., Gasamis, C., … Hackett, J. (2017). Effects of emergent literacy interventions for preschoolers with autism spectrum disorder. Exceptional Children, 84, 55-75. PMCID: PMC5950721. doi: 10.1177/0014402917705855.

Nina Isoherranen Stevison, F., Hogarth, C., Tripathy, S., Kent, T., Isoherranen, N. (2017). Inhibition of the all-trans retinoic acid (atRA) hydroxylases CYP26A1 and CYP26B1 results in dynamic, tissue-specific changes in endogenous atRA signaling. Drug Metabolism and Disposition, 45, 846-854. PMCID: PMC5469401. doi: 10.1124/dmd.117.075341.

Suman Jayadev Amos, P. J., Fung, S., Case, A., Kifelew, J., Osnis, L., Smith, C. L., … Garden, G. A., Jayadev, S. (2017). Modulation of hematopoietic lineage specification impacts TREM2 expression in microglia-like cells derived from human stem cells. ASN Neuro, 9, 1759091417716610. PMCID: PMC5548325. doi: 10.1177/1759091417716610.

Latimer, C. S., Flanagan, M. E., Cimino, P. J., Jayadev, S., Davis, M., Hoffer, Z. S., … Keene, C. D. (2017). Neuropathological comparison of adult onset and juvenile Huntington's disease with cerebellar atrophy: A report of a father and son. Journal of Huntington’s Disease, 6, 337-348. PMCID: PMC5832043. doi: 10.3233/JHD-170261.

Pearl, J. R., Heath, L. M., Bergey, D. E., Kelly, J. P., Smith, C., Laurino, M. Y., … Jayadev, S. (2017). Enhanced retinal responses in Huntington's disease patients. Journal of Huntington’s Disease, 6, 237-247. doi: 10.3233/JHD-170255.

Tracy Jirikowic Berg, L. A., Jirikowic, T. L., Haerling, K., MacDonald, G. (2017). Navigating the hidden curriculum of higher education for postsecondary students with intellectual disabilities. American Journal of Occupational Therapy, 71, 7103100020p1-7103100020p9. doi: 10.5014/ajot.2017.024703.

Murphy, A. D., Griffith, V. M., Mroz, T. M., Jirikowic, T. L. (2017). Primary care for underserved populations: Navigating policy to incorporate occupational therapy into federally qualified health centers. American Journal of Occupational Therapy, 71, 7102090010p1-7102090010p5. doi: 10.5014/ajot.2017.712001.

Umeda, C. J., Fogelberg, D. J., Jirikowic, T. L., Pitonyak, J. S., Mroz, T. M., Ideishi, R. I. (2017). Expanding the implementation of the Americans with Disabilities Act for populations with intellectual and developmental disabilities: The role of organization-level occupational therapy consultation. American Journal of Occupational Therapy, 71, 7104090010p1-7104090010p6. doi: 10.5014/ajot.2017.714001.

Sandra Juul Frymoyer, A., Juul, S. E., Massaro, A. N., Bammler, T. K., Wu, Y. W. (2017). High-dose erythropoietin population pharmacokinetics in neonates with hypoxic-ischemic encephalopathy receiving hypothermia. Pediatric Research, 81, 865-872. PMCID: PMC5476365. doi: 10.1038/pr.2017.15.

German, K., Vu, P. T., Grelli, K. N., Denton, C., Lee, G., Juul, S. E. (2017). Zinc protoporphyrin-to-heme ratio and ferritin as measures of iron sufficiency in the neonatal intensive care unit. The Journal of Pediatrics, 06 Dec 2017. doi: 10.1016/j.jpeds.2017.10.041.

McAdams, R. M., Fleiss, B., Traudt, C., Schwendimann, L., Snyder, J. M., Haynes, R. L., … Juul, S. E. (2017). Long-term neuropathological changes associated with Cerebral Palsy in a nonhuman primate model of hypoxic-ischemic encephalopathy. Developmental Neuroscience, 39, 124-140. PMCID: PMC5519434. doi: 10.1159/000470903.

McAdams, R. M., McPherson, R. J., Kapur, R. P., Juul, S. E. (2017). Focal brain injury associated with a model of severe hypoxic-ischemic encephalopathy in nonhuman primates. Developmental Neuroscience, 39, 107-123. PMCID: PMC5519439. doi: 10.1159/000456658.

Mulkey, S. B., Ramakrishnaiah, R. H., McKinstry, R. C., Chang, T., Mathur, A. M., Mayock, D. E., … Juul, S. E., Wu, Y. W. (2017). Erythropoietin and brain magnetic resonance imaging findings in hypoxic-ischemic encephalopathy: Volume of acute brain injury and 1-year neurodevelopmental outcome. The Journal of Pediatrics, 186, 196-199. doi: 10.1016/j.jpeds.2017.03.053.

Parikh, P., Juul, S. E. (2018). Neuroprotective strategies in neonatal brain injury. The Journal of Pediatrics, 192, 22-32. doi: 10.1016/j.jpeds.2017.08.031.

Starr, M. C., Askenazi, D. J., Goldstein, S. L., MacDonald, J. W., Bammler, T. K., Afsharinejad, Z., … Juul, S. E., … Hingorani, S. R. (2017). Impact of processing methods on urinary biomarkers analysis in neonates. Pediatric Nephrology, 19 Aug 2017. PMCID: PMC5700848. doi: 10.1007/s00467-017-3779-0.

Raj P. Kapur McAdams, R. M., McPherson, R. J., Kapur, R. P., Juul, S. E. (2017). Focal brain injury associated with a model of severe hypoxic-ischemic encephalopathy in nonhuman primates. Developmental Neuroscience, 39, 107-123. PMCID: PMC5519439. doi: 10.1159/000456658.

Bryan King de Lacy, N., Doherty, D. A., King, B. H., Rachakonda, S., Calhoun, V. D. (2017). Disruption to control network function correlates with altered dynamic connectivity in the wider autism spectrum. NeuroImage: Clinical, 15, 513-524. PMCID: PMC5473646. doi: 10.1016/j.nicl.2017.05.024.

Natalia Kleinhans Velasquez, F., Qin, X. A., Reilly, M. A., Neuhaus, E., Estes, A. M., Aylward, E. H., Kleinhans, N. M. (2017). Neural correlates of emotional inhibitory control in autism spectrum disorders. Research in Developmental Disabilities, 64, 64-77. doi: 10.1016/j.ridd.2017.03.008.

Sara T. Kover Rausch, T. L., Kendall, D. L., Kover, S. T., Louw, E. M., Zsilavecz, U. L., Van der Merwe, A. (2017). The effect of methylphenidate-OROS® on the narrative ability of children with attention-deficit hyperactivity disorder. The South African Journal of Communication Disorders, 64, e1-e12. PMCID: PMC5843053. doi: 10.4102/sajcd.v64i1.180.

Thurman, A. J., Kover, S. T., Ted Brown, W., Harvey, D. J., Abbeduto, L. (2017). Noncomprehension signaling in males and females with fragile X syndrome. Journal of Speech, Language, and Hearing Research, 60, 1606-1621. PMCID: PMC5544413. doi: 10.1044/2016_JSLHR-L-15-0358.

Patricia Kuhl Ramirez-Esparza, N., Garcia-Sierra, A., Kuhl, P. K. (2017). Look who's talking NOW! Parentese speech, social context, and language development across time. Frontiers in Psychology, 8, 1008. PMCID: PMC5477750. doi: 10.3389/fpsyg.2017.01008.

Zhao, T. C., Lam, H. T. G., Sohi, H., Kuhl, P. K. (2017). Neural processing of musical meter in musicians and non-musicians. Neuropsychologia, 106, 289-297. doi: 10.1016/j.neuropsychologia.2017.10.007.

Charles Laird Choi, M., Genereux, D. P., Goodson, J., Al-Azzawi, H., Allain, S. Q., Simon, N., … Laird, C. D. (2017). Epigenetic memory via concordant DNA methylation is inversely correlated to developmental potential of mammalian cells. PLoS Genetics, 13, e1007060. PMCID: PMC5690686. doi: 10.1371/journal.pgen.1007060.

Adrian K.C. Lee Lee, A. K. C., Sarkka, A., Madhyastha, T. M., Grabowski, T. J. (2017). Characterizing cross-subject spatial interaction patterns in functional magnetic resonance imaging studies: A two-stage point-process model. Biometrical Journal, 59, 1352-1381. doi: 10.1002/bimj.201600212.

McCloy, D. R., Lau, B. K., Larson, E., Pratt, K. A. I., Lee, A. K. C. (2017). Pupillometry shows the effort of auditory attention switching. Journal of the Acoustical Society of America, 141, 2440. PMCID: PMC5848839. doi: 10.1121/1.4979340.

Kenneth Maravilla Wundes, A., Bowen, J. D., Kraft, G. H., Maravilla, K. R., McLaughlin, B., von Geldern, G., … Lu, J. Q. (2017). Brain pathology of a patient 7 years after autologous hematopoietic stem cell transplantation for multiple sclerosis. Journal of the Neurological Sciences, 373, 339-341. doi: 10.1016/j.jns.2017.01.016.

Ryan McAdams

Katie A. McLaughlin Busso, D. S., McLaughlin, K. A., Brueck, S., Peverill, M., Gold, A. L., Sheridan, M. A. (2017). Child abuse, neural structure, and adolescent psychopathology: A longitudinal study. Journal of the American Academy of Child and Adolescent Psychiatry, 56, 321-328 e1. PMCID: PMC5367472. doi: 10.1016/j.jaac.2017.01.013.

Busso, D. S., McLaughlin, K. A., Sheridan, M. A. (2017). Dimensions of adversity, physiological reactivity, and externalizing psychopathology in adolescence: Deprivation and threat. Psychosomatic Medicine, 79, 162-171. PMCID: PMC5237627. doi: 10.1097/PSY.0000000000000369.

Christensen, K. A., Aldao, A., Sheridan, M. A., McLaughlin, K. A. (2017). Habitual reappraisal in context: peer victimisation moderates its association with physiological reactivity to social stress. Cognition & Emotion, 31, 384-394. PMCID: PMC4907884. doi: 10.1080/02699931.2015.1103701.

Cooper-Vince, Christine E., DeSerisy, Mariah, Cornacchio, Danielle, Sanchez, Amanda, McLaughlin, K. A., Comer, Jonathan S. (2017). Parasympathetic reactivity and disruptive behavior problems in young children during interactions with their mothers and other adults: A preliminary investigation. Developmental Psychobiology, 59, 543-550. PMCID: PMC5417687. doi: 10.1002/dev.21511.

Dorsey, S., McLaughlin, K. A., Kerns, S. E. U., Harrison, J. P., Lambert, H. K., Briggs, E. C., … Amaya-Jackson, L. (2017). Evidence base update for psychosocial treatments for children and adolescents exposed to traumatic events. Journal of Clinical Child and Adolescent Psychology, 46, 303-330. PMCID: PMC5395332. doi: 10.1080/15374416.2016.1220309.

Dunn, E. C., Wang, Y., Tse, J., McLaughlin, K. A., Fitzmaurice, G., Gilman, S. E., Susser, E. S. (2017). Sensitive periods for the effect of childhood interpersonal violence on psychiatric disorder onset among adolescents. The British Journal of Psychiatry, 211, 365-372. PMCID: PMC5709674. doi: 10.1192/bjp.bp.117.208397.

Jenness, J. L., Rosen, M. L., Sambrook, K. A., Dennison, M. J., Lambert, H. K., Sheridan, M. A., McLaughlin, K. A. (2017). Violence exposure and neural systems underlying working memory for emotional stimuli in youth. Developmental Psychopathology, 1-12. doi: 10.1017/S0954579417001638.

Kerns, C. E., Pincus, D. B., McLaughlin, K. A., Comer, J. S. (2017). Maternal emotion regulation during child distress, child anxiety accommodation, and links between maternal and child anxiety. Journal of Anxiety Disorders, 50, 52-59. doi: 10.1016/j.janxdis.2017.05.002.

Lambert, H. K., Sheridan, M. A., Sambrook, K. A., Rosen, M. L., Askren, M. K., McLaughlin, K. A. (2017). Hippocampal contribution to context encoding across development is disrupted following early-life adversity. The Journal of Neuroscience, 37, 1925-1934. PMCID: PMC5320618. doi: 10.1523/JNEUROSCI.2618-16.2017.

Lambert, H. K., King, K. M., Monahan, K. C., McLaughlin, K. A. (2017). Differential associations of threat and deprivation with emotion regulation and cognitive control in adolescence. Developmental Psychopathology, 29, 929-940. PMCID: PMC5243929. doi: 10.1017/S0954579416000584.

LeWinn, K. Z., Sheridan, M. A., Keyes, K. M., Hamilton, A., McLaughlin, K. A. (2017). Sample composition alters associations between age and brain structure. Nature Communications, 8, 874. PMCID: PMC5638928. doi: 10.1038/s41467-017-00908-7.

Logue, M. W., van Rooij, S. J. H., Dennis, E. L., Davis, S. L., Hayes, J. P., Stevens, J. S., … McLaughlin, K. A., … Morey, R. A. (2017). Smaller hippocampal volume in posttraumatic stress disorder: A multisite ENIGMA-PGC study: Subcortical volumetry results from posttraumatic stress disorder consortia. Biological Psychiatry, 20 Sept 2017. doi: 10.1016/j.biopsych.2017.09.006.

Madhyastha, T., Peverill, M., Koh, N., McCabe, C., Flournoy, J., Mills, K., … McLaughlin, K. A. (2017). Current methods and limitations for longitudinal fMRI analysis across development. Developmental Cognitive Neuroscience, 33, 118-128. doi: 10.1016/j.dcn.2017.11.006.

McGrath, J. J., Saha, S., Lim, C. C. W., Aguilar-Gaxiola, S., Alonso, J., Andrade, L. H., … McLaughlin, K. A., … W H O World Mental Health Survey Collaborators, (2017). Trauma and psychotic experiences: Transnational data from the World Mental Health Survey. The British Journal of Psychiatry, 211, 373-380. PMCID: PMC5709675. doi: 10.1192/bjp.bp.117.205955.

McGrath, J. J., McLaughlin, K. A., Saha, S., Aguilar-Gaxiola, S., Al-Hamzawi, A., Alonso, J., … Kessler, R. C. (2017). The association between childhood adversities and subsequent first onset of psychotic experiences: A cross-national analysis of 23 998 respondents from 17 countries. Psychological Medicine, 47, 1230-1245. PMCID: PMC5590103. doi: 10.1017/S0033291716003263.

McLaughlin, K. A., Sheridan, M. A., Nelson, C. A. (2017). Neglect as a violation of species-expectant experience: Neurodevelopmental consequences. Biological Psychiatry, 82, 462-471. PMCID: PMC5572554. doi: 10.1016/j.biopsych.2017.02.1096.

McLaughlin, K. A., Lambert, H. K. (2017). Child trauma exposure and psychopathology: Mechanisms of risk and resilience. Current Opinion in Psychology, 14, 29-34. PMCID: PMC5111863. doi: 10.1016/j.copsyc.2016.10.004.

Platt, J. M., Colich, N. L., McLaughlin, K. A., Gary, D., Keyes, K. M. (2017). Transdiagnostic psychiatric disorder risk associated with early age of menarche: A latent modeling approach. Comprehensive Psychology, 79, 70-79. PMCID: PMC5643227. doi: 10.1016/j.comppsych.2017.06.010.

Rosen, M. L., Sheridan, M. A., Sambrook, K. A., Dennison, M. J., Jenness, J. L., Askren, M. K., Meltzoff, A. N., McLaughlin, K. A. (2017). Salience network response to changes in emotional expressions of others is heightened during early adolescence: Relevance for social functioning. Developmental Science, 30 May 2017.PMCID: PMC5709230. doi: 10.1111/desc.12571.

Sheridan, M. A., Peverill, M., Finn, A. S., McLaughlin, K. A. (2017). Dimensions of childhood adversity have distinct associations with neural systems underlying executive functioning. Developmental Psychopathology, 29, 1777-1794. PMCID: PMC5733141. doi: 10.1017/S0954579417001390.

Troller-Renfree, Sonya, McLaughlin, K. A., Sheridan, Margaret A., Nelson, Charles H., Fox, Nathan A. (2017). The beneficial effects of a positive attention bias amongst children with a history of psychosocial deprivation. Biological Psychology, 122, 110-120. PMCID: PMC5074922. doi: 10.1016/j.biopsycho.2016.04.008.

Walsh, K., McLaughlin, K. A., Hamilton, A., Keyes, K. M. (2017). Trauma exposure, incident psychiatric disorders, and disorder transitions in a longitudinal population representative sample. Journal of Psychiatric Research, 92, 212-218. PMCID: PMC5539922. doi: 10.1016/j.jpsychires.2017.05.001.

Heather Mefford Byers, H. M., Adam, M. P., LaCroix, A., Leary, S. E., Cole, B., Dobyns, W. B., Mefford, H. C. (2017). Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22. American Journal of Medical Genetics. Part A, 173, 245-249. PMCID: PMC5999866. doi: 10.1002/ajmg.a.37993.

Dejanovic, B., Djemie, T., Grunewald, N., Suls, A., Kress, V., Hetsch, F., … Mefford, H. C., … Schwarz, G. (2017). Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy. EMBO Molecular Medicine, 9, 1764. PMCID: PMC5709744. doi: 10.15252/emmm.201708525.

Graustein, A. D., Horne, D. J., Fong, J. J., Schwarz, F., Mefford, H. C., Peterson, G. J., … Hawn, T. R. (2017). The SIGLEC14 null allele is associated with Mycobacterium tuberculosis- and BCG-induced clinical and immunologic outcomes. Tuberculosis (Edinb), 104, 38-45. doi: 10.1016/j.tube.2017.02.005.

Hamdan, F. F., Myers, C. T., Cossette, P., Lemay, P., Spiegelman, D., Laporte, A. D., … Mefford, H. C., … Michaud, J. L. (2017). High rate of recurrent de novo mutations in developmental and epileptic encephalopathies. American Journal of Human Genetics, 101, 664-685. PMCID: PMC5673604. doi: 10.1016/j.ajhg.2017.09.008.

Kruszka, P., Tanpaiboon, P., Neas, K., Crosby, K., Berger, S. I., Martinez, A. F., … Mefford, H. C., … Muenke, M. (2017). Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects. Journal of Medical Genetics, 54, 825-829. doi: 10.1136/jmedgenet-2017-104611.

Moller, R. S., Wuttke, T. V., Helbig, I., Marini, C., Johannesen, K. M., Brilstra, E. H., … Mefford, H. C., … Maljevic, S. (2017). Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. Neurology, 88, 483-492. PMCID: PMC5278942. doi: 10.1212/WNL.0000000000003565.

Myers, C. T., Stong, N., Mountier, E. I., Helbig, K. L., Freytag, S., Sullivan, J. E., … Mefford, H. C., Heinzen, E. L. (2017). De novo mutations in PPP3CA cause severe neurodevelopmental disease with seizures. American Journal of Human Genetics, 101, 516-524. PMCID: PMC5630160. doi: 10.1016/j.ajhg.2017.08.013.

Sadleir, L. G., Mountier, E. I., Gill, D., Davis, S., Joshi, C., DeVile, C., … Mefford, H. C., Scheffer, I. E. (2017). Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype. Neurology, 89, 1035-1042. PMCID: PMC5589790. doi: 10.1212/WNL.0000000000004331.

Andrew Meltzoff Loucks, J., Mutschler, C., Meltzoff, A. N. (2017). Children's representation and imitation of events: How goal organization influences 3-year-old children's memory for action sequences. Cognitive Science, 41, 1904-1933. doi: 10.1111/cogs.12446.

Master, A., Cheryan, S., Meltzoff, A. N. (2017). Social group membership increases STEM engagement among preschoolers. Developmental Psychology, 53, 201-209. doi: 10.1037/dev0000195.

Rabinowitch, T. C., Meltzoff, A. N. (2017). Synchronized movement experience enhances peer cooperation in preschool children. Journal of Experimental Child Psychology, 160, 21-32. doi: 10.1016/j.jecp.2017.03.001.

Rogers, L. O., Meltzoff, A. N. (2017). Is gender more important and meaningful than race? An analysis of racial and gender identity among Black, White, and mixed-race children. Cultural Diversity and Ethnic Minority Psychology, 23, 323-334. doi: 10.1037/cdp0000125.

Waismeyer, A., Meltzoff, A. N. (2017). Learning to make things happen: Infants' obervational learning of social and physical causal events. Journal of Experimental Child Psychology, 162, 58-71. doi: 10.1016/j.jecp.2017.04.018.

Kathleen J. Millen Haldipur, P., Dang, D., Aldinger, K. A., Janson, O. K., Guimiot, F., Adle-Biasette, H., Dobyns, W. B., … Millen, K. J. (2017). Phenotypic outcomes in mouse and human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms. eLife, 6, PMCID: PMC5271606. doi: 10.7554/eLife.20898.

Ghayda Mirzaa Alcantara, D., Timms, A. E., Gripp, K., Baker, L., Park, K., Collins, S., … Hevner, R. F., Dobyns, W. B., … Mirzaa, G. M. (2017). Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly. Brain, 140, 2610-2622. PMCID: PMC6080423. doi: 10.1093/brain/awx203.

Michels, S., Foss, K., Park, K., Golden-Grant, K., Saneto, R., Lopez, J., Mirzaa, G. M. (2017). Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development. American Journal of Medical Genetics. Part A, 173, 3127-3131. PMCID: PMC5687290. doi: 10.1002/ajmg.a.38496.

Sheri Mizumori Baker, P. M., Raynor, S. A., Francis, N. T., Mizumori, S. J. (2017). Lateral habenula integration of proactive and retroactive information mediates behavioral flexibility. Neuroscience, 345, 89-98. doi: 10.1016/j.neuroscience.2016.02.010.

Cecilia B. Moens Miller, A. C., Whitebirch, A. C., Shah, A. N., Marsden, K. C., Granato, M., O'Brien, J., Moens, C. B. (2017). A genetic basis for molecular asymmetry at vertebrate electrical synapses. eLife, 6, PMCID: PMC5462537. doi: 10.7554/eLife.25364.

Pierre D. Mourad Khaing, Z. Z., Cates, L. N., Fischedick, A. E., McClintic, A. M., Mourad, P. D., Hofstetter, C. P. (2017). Temporal and spatial evolution of raised intraspinal pressure after traumatic spinal cord injury. Journal of Neurotrauma, 34, 645-651. doi: 10.1089/neu.2016.4490.

Jeffrey Munson Cidav, Z., Munson, J., Estes, A. M., Dawson, G., Rogers, S., Mandell, D. (2017). Cost offset associated with Early Start Denver Model for children with autism. Journal of the American Academy of Child and Adolescent Psychiatry, 56, 777-783. doi: 10.1016/j.jaac.2017.06.007.

Scott Murray Mikkelsen, M., Barker, P. B., Bhattacharyya, P. K., Brix, M. K., Buur, P. F., Cecil, K. M., … Murray, S. O., … Edden, R. A. E. (2017). Big GABA: Edited MR spectroscopy at 24 research sites. Neuroimage, 159, 32-45. PMCID: PMC5700835. doi: 10.1016/j.neuroimage.2017.07.021.

Michael Mustari Bakst, L., Fleuriet, J., Mustari, M. J. (2017). Temporal dynamics of retinal and extraretinal signals in the FEFsem during smooth pursuit eye movements. Journal of Neurophysiology, 117, 1987-2003. PMCID: PMC5411476. doi: 10.1152/jn.00786.2016.

Bakst, L., Fleuriet, J., Mustari, M. J. (2017). FEFsem neuronal response during combined volitional and reflexive pursuit. Journal of Vision, 17, 13. PMCID: PMC5445972. doi: 10.1167/17.5.13.

McMillan, A., Mustari, M. J., Horn, A. (2017). Identification of secondary vestibulo-ocular neurons in human based on their histochemical characteristics found in monkey. Journal of Neurology, 264, 583-585. PMCID: PMC5337153. doi: 10.1007/s00415-017-8397-z.

Mustari, M. J. (2017). Nonhuman primate studies to advance vision science and prevent blindness. ILAR Journal, 58, 216-225. PMCID: PMC5886335. doi: 10.1093/ilar/ilx009.

Pallus, A. C., Walton, M. M. G., Mustari, M. J. (2017). Response of supra oculomotor area neurons during combined saccade-vergence movements. Journal of Neurophysiology, 119, 585-596 doi: 10.1152/jn.00193.2017.

Walton, M. M. G., Pallus, A., Fleuriet, J., Mustari, M. J., Tarczy-Hornoch, K. (2017). Neural mechanisms of oculomotor abnormalities in the infantile strabismus syndrome. Journal of Neurophysiology, 118, 280-299. PMCID: PMC5498729. doi: 10.1152/jn.00934.2016.

Walton, M. M. G., Mustari, M. J. (2017). Comparison of three models of saccade disconjugacy in strabismus. Journal of Neurophysiology, 118, 3175-3193. PMCID: PMC5814716. doi: 10.1152/jn.00983.2016.

Elizabeth A. Nance Curtis, C., Zhang, M., Liao, R., Wood, T., Nance, E. (2017). Systems-level thinking for nanoparticle-mediated therapeutic delivery to neurological diseases. Wiley Interdisciplinary Reviews: Nanomedicine and Nanobiotechnology, 9. doi: 10.1002/wnan.1422.

Nance, E., Kambhampati, S. P., Smith, E. S., Zhang, Z., Zhang, F., Singh, S., … Kannan, S. (2017). Dendrimer-mediated delivery of N-acetyl cysteine to microglia in a mouse model of Rett syndrome. Journal of Neuroinflammation, 14, 252. PMCID: PMC5735803. doi: 10.1186/s12974-017-1004-5.

Nance, E. (2017). Brain-penetrating nanoparticles for analysis of the brain microenvironment. Methods in Molecular Biology, 1570, 91-104. doi: 10.1007/978-1-4939-6840-4_6.

Smith, J., Sprenger, K. G., Liao, R., Joseph, A., Nance, E., Pfaendtner, J. (2017). Determining dominant driving forces affecting controlled protein release from polymeric nanoparticles. Biointerphases, 12, 02D412. PMCID: PMC5648550. doi: 10.1116/1.4983154.

Edward J. Novotny, Jr. Berg, A. T., Coryell, J., Saneto, R. P., Grinspan, Z. M., Alexander, J. J., Kekis, M., … Dobyns, W. B., … Novotny, E. J., Jr., Koh, S. (2017). Early-life epilepsies and the emerging role of genetic testing. JAMA Pediatrics, 171, 863-871. PMCID: PMC5710404. doi: 10.1001/jamapediatrics.2017.1743.

Novotny, E. J., Jr. (2017). Early genetic testing for neonatal epilepsy: When, why, and how? Neurology, 89, 880-881. doi: 10.1212/WNL.0000000000004287.

Jeffrey Ojemann Amlie-Lefond, C., Ojemann, J. G. (2017). Neonatal hemorrhagic stroke. JAMA Pediatrics, 171, 220 -221. doi: 10.1001/jamapediatrics.2016.4466.

Friedman, S. D., Poliakov, A. V., Budech, C., Shaw, D. W. W., Breiger, D., Jinguji, T., … Ojemann, J. G. (2017). GABA alterations in pediatric sport concussion. Neurology, 89, 2151-2156. PMCID: PMC5696637. doi: 10.1212/WNL.0000000000004666.

Herron, J. A., Thompson, M. C., Brown, T., Chizeck, H. J., Ojemann, J. G., Ko, A. L. (2017). Chronic electrocorticography for sensing movement intention and closed-loop deep brain stimulation with wearable sensors in an essential tremor patient. Journal of Neurosurgery, 127, 580-587. doi: 10.3171/2016.8.JNS16536.

Kim, Y. J., Tsai, J. J., Ojemann, J. G., Verghese, P. (2017). Attention to multiple objects facilitates their integration in prefrontal and parietal cortex. The Journal of Neuroscience, 37, 4942-4953. PMCID: PMC5426182. doi: 10.1523/JNEUROSCI.2370-16.2017.

Laoprasert, P., Ojemann, J. G., Handler, M. H. (2017). Insular epilepsy surgery. Epilepsia, 58, 35-45. doi: 10.1111/epi.13682.

Miller, K. J., Hermes, D., Pestilli, F., Wig, G. S., Ojemann, J. G. (2017). Face percept formation in human ventral temporal cortex. Journal of Neurophysiology, 118, 2614-2627. PMCID: PMC5668462. doi: 10.1152/jn.00113.2017.

Prince, E., Hakimian, S., Ko, A. L., Ojemann, J. G., Kim, M. S., Miller, J. W. (2017). Laser interstitial thermal therapy for epilepsy. Current Neurology and Neuroscience Reports, 17, 63. doi: 10.1007/s11910-017-0772-8.

Szaflarski, J. P., Gloss, D., Binder, J. R., Gaillard, W. D., Golby, A. J., Holland, S. K., Ojemann, J. G., … Theodore, W. H. (2017). Practice guideline summary: Use of fMRI in the presurgical evaluation of patients with epilepsy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology, 88, 395-402. PMCID: PMC5272968. doi: 10.1212/WNL.0000000000003532.

Jay Parrish Boiko, N., Medrano, G., Montano, E., Jiang, N., Williams, C. R., Madungwe, N. B., … Parrish, J. Z., … Eaton, B. A. (2017). TrpA1 activation in peripheral sensory neurons underlies the ionic basis of pain hypersensitivity in response to vinca alkaloids. PLoS One, 12, e0186888. PMCID: PMC5662086. doi: 10.1371/journal.pone.0186888.

Williams, C. R., Baccarella, A., Parrish, J. Z., Kim, C. C. (2017). Empirical assessment of analysis workflows for differential expression analysis of human samples using RNA-Seq. BMC Bioinformatics, 18, 38. PMCID: PMC5240434. doi: 10.1186/s12859-016-1457-z.

David J. Perkel Budzillo, A., Duffy, A., Miller, K. E., Fairhall, A. L., Perkel, D. J. (2017). Dopaminergic modulation of basal ganglia output through coupled excitation-inhibition. Proceedings of the National Academy of Sciences of the United States of America, 114, 5713-5718. PMCID: PMC5465888. doi: 10.1073/pnas.1611146114.

James Phillips Kelly, J. P., Phillips, J. O., Weiss, A. H. (2017). The relationship of nystagmus waveform on the VEP response in infantile nystagmus syndrome: A small case series. Documenta Ophthalmologica, 134, 37-44. doi: 10.1007/s10633-016-9568-4.

Nicholas Poolos Poolos, N. P., Castagna, C. E., Williams, S., Miller, A. B., Story, T. J. (2017). Association between antiepileptic drug dose and long-term response in patients with refractory epilepsy. Epilepsy & Behavior, 69, 59-68. doi: 10.1016/j.yebeh.2016.10.010.

Suzie Pun Zhao, T., Sellers, D. L., Cheng, Y., Horner, P. J., Pun, S. H. (2017). Tunable, injectable hydrogels based on peptide-cross-linked, cyclized polymer nanoparticles for neural progenitor cell delivery. Biomacromolecules, 18, 2723-2731. doi: 10.1021/acs.biomac.7b00510.

Jan-Marino (Nino) Ramirez Pollak, J., Rai, K. G., Funk, C. C., Arora, S., Lee, E., Zhu, J., … Ramirez, J. M., Rostomily, R. C. (2017). Ion channel expression patterns in glioblastoma stem cells with functional and therapeutic implications for malignancy. PLoS One, 12, e0172884. PMCID: PMC5338779. doi: 10.1371/journal.pone.0172884.

Wendy Raskind Chou, S. T., Kacena, M. A., Weiss, M. J., Raskind, W. H. (2017). GATA1-Related X-Linked Cytopenia. GeneReviews®, May 11, 2017. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1364/

Phowthongkum, P., Chen, D. H., Raskind, W. H., Bird, T. (2017). SAMD9L-Related Ataxia-Pancytopenia Syndrome. GeneReviews®, May 11, 2017. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1364/

Raskind, W. H., Friedman, J. R., Roze, E., Meneret, A., Chen, D. H., Bird, T. D. (2017). ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severity. Movement Disorders, 32, 305-306. PMCID: PMC5318268. doi: 10.1002/mds.26888.

Rujano, M. A., Cannata Serio, M., Panasyuk, G., Peanne, R., Reunert, J., Rymen, D., … Raskind, W. H., … Simons, M. (2017). Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects. The Journal of Experimental Medicine, 214, 3707-3729. PMCID: PMC5716037. doi: 10.1084/jem.20170453.

Thomas A. Reh Chao, J. R., Lamba, D. A., Klesert, T. R., Torre, A., Hoshino, A., Taylor, R. J., … Reh, T. A. (2017). Transplantation of human embryonic stem cell-derived retinal cells into the subretinal space of a non-human primate. Translational Vision Science & Technology, 6, 4. PMCID: PMC5433804. doi: 10.1167/tvst.6.3.4.

Jorstad, N. L., Wilken, M. S., Grimes, W. N., Wohl, S. G., VandenBosch, L. S., Yoshimatsu, T., … Reh, T. A. (2017). Stimulation of functional neuronal regeneration from Muller glia in adult mice. Nature, 548, 103-107. PMCID: PMC5991837. doi: 10.1038/nature23283.

Nakamura, P. A., Shimchuk, A. A., Tang, S., Wang, Z., DeGolier, K., Ding, S., Reh, T. A. (2017). Small molecule Photoregulin3 prevents retinal degeneration in the Rho(P23H) mouse model of retinitis pigmentosa. eLife, 6, PMCID: PMC5693111. doi: 10.7554/eLife.30577.

Wohl, S. G., Jorstad, N. L., Levine, E. M., Reh, T. A. (2017). Muller glial microRNAs are required for the maintenance of glial homeostasis and retinal architecture. Nature Communications, 8, 1603. PMCID: PMC5693933. doi: 10.1038/s41467-017-01624-y.

Todd Richards Berninger, V. W., Richards, T. L., Abbott, R. D. (2017). Brain and behavioral assessment of executive functions for self-regulating levels of language in reading brain. Journal of Nature and Science, 3, e464. PMCID: PMC5662027.

Elkins, R. L., Richards, T. L., Nielsen, R., Repass, R., Stahlbrandt, H., Hoffman, H. G. (2017). The neurobiological mechanism of chemical aversion (emetic) therapy for alcohol use disorder: An fMRI study. Frontiers in Behavioral Neuroscience, 11, 182. PMCID: PMC5625029. doi: 10.3389/fnbeh.2017.00182.

Robert Rostomily Brito da Silva, H., Straus, D., Barber, J. K., Rostomily, R. C., Ferreira, M., Jr., Sekhar, L. N. (2017). Cranial chordoma: A new preoperative grading system. Neurosurgery, 3 Nov 2017. doi: 10.1093/neuros/nyx423.

Pollak, J., Rai, K. G., Funk, C. C., Arora, S., Lee, E., Zhu, J., … Ramirez, J. M., Rostomily, R. C. (2017). Ion channel expression patterns in glioblastoma stem cells with functional and therapeutic implications for malignancy. PLoS One, 12, e0172884. PMCID: PMC5338779. doi: 10.1371/journal.pone.0172884.

Edwin Rubel Chowdhury, S., Owens, K. N., Herr, R. J., Jiang, Q., Chen, X., Johnson, G., … Rubel, E. W., Simon, J. A. (2017). Phenotypic optimization of urea-thiophene carboxamides to yield potent, well tolerated, and orally active protective agents against aminoglycoside-induced hearing loss. Journal of Medicinal Chemistry, 61, 84-97. doi: 10.1021/acs.jmedchem.7b00932.

Weatherstone, J. H., Kopp-Scheinpflug, C., Pilati, N., Wang, Y., Forsythe, I. D., Rubel, E. W., Tempel, B. L. (2017). Maintenance of neuronal size gradient in MNTB requires sound-evoked activity. Journal of Neurophysiology, 117, 756-766. PMCID: PMC5304411. doi: 10.1152/jn.00528.2016.

Zorio, D. A., Jackson, C. M., Liu, Y., Rubel, E. W., Wang, Y. (2017). Cellular distribution of the fragile X mental retardation protein in the mouse brain. The Journal of Comparative Neurology, 525, 818-849. PMCID: PMC5558202. doi: 10.1002/cne.24100.

Craig Rubens Bianchi-Jassir, F., Seale, A. C., Kohli-Lynch, M., Lawn, J. E., Baker, C. J., Bartlett, L., … Rubens, C. E. (2017). Preterm birth associated with group B streptococcus maternal colonization worldwide: Systematic review and meta-analyses. Clinical Infectious Diseases, 65, S133-S142. PMCID: PMC5850429. doi: 10.1093/cid/cix661.

Kohli-Lynch, M., Russell, N. J., Seale, A. C., Dangor, Z., Tann, C. J., Baker, C. J., … Rubens, C. E., … Lawn, J. E. (2017). Neurodevelopmental impairment in children after group B streptococcal disease worldwide: Systematic review and meta-analyses. Clinical Infectious Diseases, 65, S190-S199. PMCID: PMC5848372. doi: 10.1093/cid/cix663.

Madrid, L., Seale, A. C., Kohli-Lynch, M., Edmond, K. M., Lawn, J. E., Heath, P. T., … Rubens, C. E., … Infant G. B. S. Disease Investigator Group, (2017). Infant group B streptococcal disease incidence and serotypes worldwide: Systematic review and meta-analyses. Clinical Infectious Diseases, 65, S160-S172. PMCID: PMC5850457. doi: 10.1093/cid/cix656.

Jay Rubinstein Horn, D. L., Won, J. H., Rubinstein, J. T., Werner, L. A. (2017). Spectral ripple discrimination in normal-hearing infants. Ear and Hearing, 38, 212-222. PMCID: PMC5321869. doi: 10.1097/AUD.0000000000000373.

Meredith, M. A., Rubinstein, J. T., Sie, K. C. Y., Norton, S. J. (2017). Cochlear implantation in children with postlingual progressive steeply sloping high-frequency hearing loss. Journal of the American Academy of Audiology, 28, 913-919. doi: 10.3766/jaaa.16115.

Hannele Ruohola-Baker

Moody, J. D., Levy, S., Mathieu, J., Xing, Y., Kim, W., Dong, C., … Ruohola-Baker, H. (2017). First critical repressive H3K27me3 marks in embryonic stem cells identified using designed protein inhibitor. Proceedings of the National Academy of Sciences of the United States of America, 114, 10125-10130. PMCID: PMC5617284. doi: 10.1073/pnas.1706907114.

Ilene Schwartz Fleury, Veronica P., Schwartz, I. S. (2017). A modified dialogic reading intervention for preschool children with autism spectrum disorder. Topics in Early Childhood Special Education, 37, 16-28. doi: 10.1177/0271121416637597.

C. Ronald Scott Bodamer, O. A., Scott, C. R., Giugliani, R., Pompe Disease Newborn Screening Working, Group (2017). Newborn screening for Pompe disease. Pediatrics, 140, S4-S13. doi: 10.1542/peds.2016-0280C.

Liao, H. C., Spacil, Z., Ghomashchi, F., Escolar, M. L., Kurtzberg, J., Orsini, J. J., … Scott, C. R., Gelb, M. H. (2017). Lymphocyte galactocerebrosidase activity by LC-MS/MS for post-newborn screening evaluation of Krabbe disease. Clinical Chemistry, 63, 1363-1369. PMCID: PMC5533636. doi: 10.1373/clinchem.2016.264952.

Mistry, P. K., Batista, J. L., Andersson, H. C., Balwani, M., Burrow, T. A., Charrow, J., … Scott, C. R., Weinreb, N. (2017). Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry. American Journal of Hematology, 92, 929-939. PMCID: PMC5600096. doi: 10.1002/ajh.24801.

Sniderman King, L., Trahms, C., Scott, C. R. (2017). Tyrosinemia Type I. GeneReviews®, May 24, 2017. Available from: https://www.ncbi.nlm.nih.gov/pubmed/20301688

Dennis Shaw Friedman, S. D., Poliakov, A. V., Budech, C., Shaw, D. W. W., Breiger, D., Jinguji, T., … Ojemann, J. G. (2017). GABA alterations in pediatric sport concussion. Neurology, 89, 2151-2156. PMCID: PMC5696637. doi: 10.1212/WNL.0000000000004666.

Sweet, K. M., Shaw, D. W. W., Chapman, T. (2017). Cerebral palsy and seizures in a child with tubulinopathy pattern dysgenesis and focal cortical dysplasia. Radiology Case Reports, 12, 396-400. PMCID: PMC5417618. doi: 10.1016/j.radcr.2016.12.008.

Frederick Shic Ness, S. L., Manyakov, N. V., Bangerter, A., Lewin, D., Jagannatha, S., Boice, M., … Shic, F., … Pandina, G. (2017). JAKE® multimodal data capture system: Insights from an observational study of autism spectrum disorder. Frontiers in Neuroscience, 11, 517. PMCID: PMC5623040. doi: 10.3389/fnins.2017.00517.

Matthew Speltz Aldridge, K., Collett, B. R., Wallace, E. R., Birgfeld, C., Austin, J. R., Yeh, R., … Aylward, E. H., Cunningham, M. L., Speltz, M. L. (2017). Structural brain differences in school-age children with and without single-suture craniosynostosis. Journal of Neurosurgery. Pediatrics, 19, 479-489. PMCID: PMC5642047. doi: 10.3171/2016.9.PEDS16107.

Collett, B. R., Kapp-Simon, K. A., Wallace, E., Cradock, M. M., Buono, L., Speltz, M. L. (2017). Attention and executive function in children with and without single-suture craniosynostosis. Child Neuropsychology, 23, 83-98. PMCID: PMC5181850. doi: 10.1080/09297049.2015.1085005.

Susan Spieker Granqvist, P., Sroufe, L. A., Dozier, M., Hesse, E., Steele, M., van Ijzendoorn, M., … Spieker, S. J., … Duschinsky, R. (2017). Disorganized attachment in infancy: A review of the phenomenon and its implications for clinicians and policy-makers. Attachment & Human Development, 19, 534-558. PMCID: PMC5600694. doi: 10.1080/14616734.2017.1354040.

Mark Stein Kim, S. J., Shonka, S., French, W. P., Strickland, J., Miller, L., Stein, M. A. (2017). Dose-response effects of long-acting liquid methylphenidate in children with attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD): A pilot study. Journal of Autism and Developmental Disorders, 47, 2307-2313. doi: 10.1007/s10803-017-3125-1.

Schulz, K. P., Bedard, A. V., Fan, J., Hildebrandt, T. B., Stein, M. A., Ivanov, I., … Newcorn, J. H. (2017). Striatal activation predicts differential therapeutic responses to methylphenidate and atomoxetine. Journal of the American Academy of Child and Adolescent Psychiatry, 56, 602-609 e2. doi: 10.1016/j.jaac.2017.04.005.

Nephi Stella Deng, L., Ng, L., Ozawa, T., Stella, N. (2017). Quantitative analyses of synergistic responses between cannabidiol and DNA-damaging agents on the proliferation and viability of glioblastoma and neural progenitor cells in culture. Journal of Pharmacology and Experimental Therapeutics, 360, 215-224. PMCID: PMC5193074. doi: 10.1124/jpet.116.236968.

Fung, S., Xu, C., Hamel, E., Wager-Miller, J. B., Woodruff, G., Miller, A., … Stella, N. (2017). Novel indole-based compounds that differentiate alkylindole-sensitive receptors from cannabinoid receptors and microtubules: Characterization of their activity on glioma cell migration. Pharmacological Research, 115, 233-241. doi: 10.1016/j.phrs.2016.10.025.

Jennifer Stone Bucks, S. A., Cox, B. C., Vlosich, B. A., Manning, J. P., Nguyen, T. B., Stone, J. S. (2017). Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice. eLife, 6, PMCID: PMC5338920. doi: 10.7554/eLife.18128.

Burns, J. C., Stone, J. S. (2017). Development and regeneration of vestibular hair cells in mammals. Seminars in Cell and Developmental Biology, 65, 96-105. PMCID: PMC5423856. doi: 10.1016/j.semcdb.2016.11.001.

Stone, J. S., Daudet, N. (2017). Editorial. Seminars in Cell and Developmental Biology, 65, 38. doi: 10.1016/j.semcdb.2017.04.005.

Wendy Stone Edmunds, S. R., Rozga, A., Li, Y., Karp, E. A., Ibanez, L. V., Rehg, J. M., Stone, W. L. (2017). Brief report: Using a point-of-view camera to measure eye gaze in young children with autism spectrum disorder during naturalistic social interactions: A pilot study. Journal of Autism and Developmental Disorders, 47, 898-904. doi: 10.1007/s10803-016-3002-3.

Foss-Feig, J. H., Schauder, K. B., Key, A. P., Wallace, M. T., Stone, W. L. (2017). Audition-specific temporal processing deficits associated with language function in children with autism spectrum disorder. Autism Research, 10, 1845-1856. doi: 10.1002/aur.1820.

Karp, E. A., Ibanez, L. V., Warren, Z., Stone, W. L. (2017). Brief report: What drives parental concerns about their 18-month-olds at familial risk for autism spectrum disorder? Journal of Autism and Developmental Disorders, 47, 1535-1541. doi: 10.1007/s10803-017-3060-1.

Simon, D. M., Damiano, C. R., Woynaroski, T. G., Ibanez, L. V., Murias, M., Stone, W. L., … Cascio, C. J. (2017). Neural correlates of sensory hyporesponsiveness in toddlers at high risk for autism spectrum disorder. Journal of Autism and Developmental Disorders, 47, 2710-2722. doi: 10.1007/s10803-017-3191-4.

Colin Studholme Blazejewska, A. I., Seshamani, S., McKown, S. K., Caucutt, J. S., Dighe, M., Gatenby, C., Studholme, C. (2017). 3D in utero quantification of T2* relaxation times in human fetal brain tissues for age optimized structural and functional MRI. Magnetic Resonance in Medicine, 78, 909-916. PMCID: PMC5378686. doi: 10.1002/mrm.26471.

Pontabry, J., Rousseau, F., Studholme, C., Koob, M., Dietemann, J. L. (2017). A discriminative feature selection approach for shape analysis: Application to fetal brain cortical folding. Medical Image Analysis, 35, 313-326. PMCID: PMC5501094. doi: 10.1016/j.media.2016.07.005.

Rajagopalan, V., Scott, J. A., Liu, M., Poskitt, K., Chau, V., Miller, S., Studholme, C. (2017). Complementary cortical gray and white matter developmental patterns in healthy, preterm neonates. Human Brain Mapping, 38, 4322-4336. PMCID: PMC5546945. doi: 10.1002/hbm.23618.

Wang, X., Studholme, C., Grigsby, P. L., Frias, A. E., Cuzon Carlson, V. C., Kroenke, C. D. (2017). Folding, but not surface area expansion, is associated with cellular morphological maturation in the fetal cerebral cortex. The Journal of Neuroscience, 37, 1971-1983. PMCID: PMC5338750. doi: 10.1523/JNEUROSCI.3157-16.2017.

Wild, H. M., Heckemann, R. A., Studholme, C., Hammers, A. (2017). Gyri of the human parietal lobe: Volumes, spatial extents, automatic labelling, and probabilistic atlases. PLoS One, 12, e0180866. PMCID: PMC5573296. doi: 10.1371/journal.pone.0180866.

Stephen Tapscott

Mason, A. G., Slieker, R. C., Balog, J., Lemmers, Rjlf, Wong, C. J., Yao, Z., … Tapscott, S. J., van der Maarel, S. M. (2017). SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes. Skeletal Muscle, 7, 12. PMCID: PMC5461771. doi: 10.1186/s13395-017-0129-7.

Shadle, S. C., Zhong, J. W., Campbell, A. E., Conerly, M. L., Jagannathan, S., Wong, C. J., … Tapscott, S. J. (2017). DUX4-induced dsRNA and MYC mRNA stabilization activate apoptotic pathways in human cell models of facioscapulohumeral dystrophy. PLoS Genetics, 13, e1006658. PMCID: PMC5362247. doi: 10.1371/journal.pgen.1006658.

Watanabe, T., Marotta, M., Suzuki, R., Diede, S. J., Tapscott, S. J., Niida, A., … Tanaka, H. (2017). Impediment of replication forks by long non-coding RNA provokes chromosomal rearrangements by error-prone restart. Cell Reports, 21, 2223-2235. PMCID: PMC5710012. doi: 10.1016/j.celrep.2017.10.103.

Bruce Tempel Minich, R. R., Li, J., Tempel, B. L. (2017). Early growth response protein 1 regulates promoter activity of alpha-plasma membrane calcium ATPase 2, a major calcium pump in the brain and auditory system. BMC Molecular Biology, 18, 14. PMCID: PMC5441030. doi: 10.1186/s12867-017-0092-1.

Jeffrey Tsai Kim, Y. J., Tsai, J. J., Ojemann, J. G., Verghese, P. (2017). Attention to multiple objects facilitates their integration in prefrontal and parietal cortex. The Journal of Neuroscience, 37, 4942-4953. PMCID: PMC5426182. doi: 10.1523/JNEUROSCI.2370-16.2017.

Won, D., Kim, W., Chaovalitwongse, W. A., Tsai, J. J. (2017). Altered visual contrast gain control is sensitive for idiopathic generalized epilepsies. Clinical Neurophysiology, 128, 340-348. PMCID: PMC5823846. doi: 10.1016/j.clinph.2016.12.008.

Hannah Tully Dempsey, J. C., Phelps, I. G., Bachmann-Gagescu, R., Glass, I. A., Tully, H. M., Doherty, D. A. (2017). Mortality in Joubert syndrome. American Journal of Medical Genetics. Part A, 173, 1237-1242. doi: 10.1002/ajmg.a.38158.

Eric Turner Quina, L. A., Harris, J., Zeng, H., Turner, E. E. (2017). Specific connections of the interpeduncular subnuclei reveal distinct components of the habenulopeduncular pathway. The Journal of Comparative Neurology, 525, 2632-2656. PMCID: PMC5873981. doi: 10.1002/cne.24221.

Jashvant Unadkat Ishida, K., Ullah, M., Toth, B., Juhasz, V., Unadkat, J. D. (2017). Successful prediction of in vivo hepatobiliary clearances and hepatic concentrations of rosuvastatin using sandwich-cultured rat hepatocytes, transporter-expressing cell lines, and quantitative proteomics. Drug Metabolism and Disposition, 30 Oct 2017. doi: 10.1124/dmd.117.076539.

Kumar, V., Nguyen, T. B., Toth, B., Juhasz, V., Unadkat, J. D. (2017). Optimization and application of a biotinylation method for quantification of plasma membrane expression of transporters in cells. The AAPS Journal, 19, 1377-1386. doi: 10.1208/s12248-017-0121-5.

Zhang, Z., Unadkat, J. D. (2017). Development of a novel maternal-fetal physiologically based pharmacokinetic model II: Verification of the model for passive placental permeability drugs. Drug Metabolism and Disposition, 45, 939-946. PMCID: PMC5506455. doi: 10.1124/dmd.116.073957.

Zhang, Z., Imperial, M. Z., Patilea-Vrana, G. I., Wedagedera, J., Gaohua, L., Unadkat, J. D. (2017). Development of a novel maternal-fetal physiologically based pharmacokinetic model I: Insights into factors that determine fetal drug exposure through simulations and sensitivity analyses. Drug Metabolism and Disposition, 45, 920-938. PMCID: PMC5506457. doi: 10.1124/dmd.117.075192.

Sara Jane Webb Charman, T., Young, G. S., Brian, J., Carter, A., Carver, L. J., Chawarska, K., … Stone, W. L., … Webb, S. J., … Zwaigenbaum, L. (2017). Non-ASD outcomes at 36 months in siblings at familial risk for autism spectrum disorder (ASD): A baby siblings research consortium (BSRC) study. Autism Research, 10, 169-178. PMCID: PMC5993543. doi: 10.1002/aur.1669.

Jones, E. J., Venema, K., Earl, R. K., Lowy, R., Webb, S. J. (2017). Infant social attention: an endophenotype of ASD-related traits? Journal of Child Psychology and Psychiatry and Allied Disciplines, 58, 270-281. PMCID: PMC5993542. doi: 10.1111/jcpp.12650.

Navot, N., Jorgenson, A. G., Webb, S. J. (2017). Maternal experience raising girls with autism spectrum disorder: a qualitative study. Child Care, Health, and Development, 43, 536-545. doi: 10.1111/cch.12470.

Webb, S. J., Neuhaus, E., Faja, S. (2017). Face perception and learning in autism spectrum disorders. Quarterly Journal of Experimental Psychology, 70, 970-986. PMCID: PMC5026554. doi: 10.1080/17470218.2016.1151059.

Jonathan Weinstein

McDonough, A., Lee, R. V., Noor, S., Lee, C., Le, T., Iorga, M., … Weinstein, J. R. (2017). Ischemia/reperfusion induces interferon-stimulated gene expression in microglia. The Journal of Neuroscience, 37, 8292-8308. PMCID: PMC5566872. doi: 10.1523/JNEUROSCI.0725-17.2017.

McDonough, A., Lee, R. V., Weinstein, J. R. (2017). Microglial interferon signaling and white matter. Neurochemical Research, 42, 2625-2638. PMCID: PMC5777301. doi: 10.1007/s11064-017-2307-8.

Weinstein, J. R., Asteria-Penaloza, R., Diaz-Artiga, A., Davila, G., Hammond, S. K., Ryde, I. T., … Thompson, L. M. (2017). Exposure to polycyclic aromatic hydrocarbons and volatile organic compounds among recently pregnant rural Guatemalan women cooking and heating with solid fuels. International Journal of Hygiene and Environmental Health, 220, 726-735. PMCID: PMC5474125. doi: 10.1016/j.ijheh.2017.03.002.

H. Steve White Aldana, B. I., Waagepetersen, H. S., Schousboe, A., White, H. S., Bulaj, G., Walls, A. B. (2017). The novel anticonvulsant neuropeptide and galanin analogue, NAX-5055, does not alter energy and amino acid metabolism in cultured brain cells. Journal of Neuroscience Research, 95, 2286-2296. doi: 10.1002/jnr.24057.

Barker-Haliski, M. L., Loscher, W., White, H. S., Galanopoulou, A. S. (2017). Neuroinflammation in epileptogenesis: Insights and translational perspectives from new models of epilepsy. Epilepsia, 58, 39-47. PMCID: PMC5604891. doi: 10.1111/epi.13785.

Bialer, M., Johannessen, S. I., Levy, R. H., Perucca, E., Tomson, T., White, H. S., Koepp, M. J. (2017). Seizure detection and neuromodulation: A summary of data presented at the XIII conference on new antiepileptic drug and devices (EILAT XIII). Epilepsy Research, 130, 27-36. doi: 10.1016/j.eplepsyres.2017.01.004.

Bialer, M., Johannessen, S. I., Levy, R. H., Perucca, E., Tomson, T., White, H. S. (2017). Progress report on new antiepileptic drugs: A summary of the Thirteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XIII). Epilepsia, 58, 181-221. doi: 10.1111/epi.13634.

Metcalf, C. S., Klein, B. D., Smith, M. D., Pruess, T., Ceusters, M., Lavreysen, H., … White, H. S. (2017). Efficacy of mGlu2 -positive allosteric modulators alone and in combination with levetiracetam in the mouse 6 Hz model of psychomotor seizures. Epilepsia, 58, 484-493. doi: 10.1111/epi.13659.

Metcalf, C. S., Klein, B. D., McDougle, D. R., Zhang, L., Kaufmann, D., Bulaj, G., White, H. S. (2017). Preclinical evaluation of intravenous NAX 810-2, a novel GalR2-preferring analog, for anticonvulsant efficacy and pharmacokinetics. Epilepsia, 58, 239-246. PMCID: PMC5291807. doi: 10.1111/epi.13647.

Metcalf, C. S., West, P. J., Thomson, K. E., Edwards, S. F., Smith, M. D., White, H. S., Wilcox, K. S. (2017). Development and pharmacologic characterization of the rat 6 Hz model of partial seizures. Epilepsia, 58, 1073-1084. PMCID: PMC5469205. doi: 10.1111/epi.13764.

Zhengui Xia

Engstrom, A. K., Snyder, J. M., Maeda, N., Xia, Z. (2017). Correction to: Gene-environment interaction between lead and Apolipoprotein E4 causes cognitive behavior deficits in mice. Molecular Neurodegeneration, 12, 81. PMCID: PMC5670524. doi: 10.1186/s13024-017-0223-7.

Wang, H., Engstrom, A. K., Xia, Z. (2017). Cadmium impairs the survival and proliferation of cultured adult subventricular neural stem cells through activation of the JNK and p38 MAP kinases. Toxicology, 380, 30-37. PMCID: PMC5413202. doi: 10.1016/j.tox.2017.01.013.

Jason Yeatman Joo, S. J., Donnelly, P. M., Yeatman, J. D. (2017). The causal relationship between dyslexia and motion perception reconsidered. Scientific Reports, 7, 4185. PMCID: PMC5482857. doi: 10.1038/s41598-017-04471-5.

Kay, K. N., Yeatman, J. D. (2017). Bottom-up and top-down computations in word- and face-selective cortex. eLife, 6, PMCID: PMC5358981. doi: 10.7554/eLife.22341.

Maier-Hein, K. H., Neher, P. F., Houde, J. C., Cote, M. A., Garyfallidis, E., Zhong, J., … Yeatman, J. D., … Descoteaux, M. (2017). The challenge of mapping the human connectome based on diffusion tractography. Nature Communications, 8, 1349. PMCID: PMC5677006. doi: 10.1038/s41467-017-01285-x.

Weiner, K. S., Yeatman, J. D., Wandell, B. A. (2017). The posterior arcuate fasciculus and the vertical occipital fasciculus. Cortex, 97, 274-276. doi: 10.1016/j.cortex.2016.03.012.

Jing Zhang Chang, I., Juric-Sekhar, G., Marshall, D., Zhang, J. (2017). An incidental finding of choroidal ganglioneuronal hamartoma in a patient with neurofibromatosis type 1. Ophthalmic Plastic and Reconstructive Surgery, 33, S40-S42. doi: 10.1097/IOP.0000000000000513.

Gwinn, K., David, K. K., Swanson-Fischer, C., Albin, R., Hillaire-Clarke, C. S., Sieber, B. A., … Zhang, J., … Rosenthal, L. S. (2017). Parkinson's disease biomarkers: Perspective from the NINDS Parkinson's Disease Biomarkers Program. Biomarkers in Medicine, 11, 451-473. PMCID: PMC5619098. doi: 10.2217/bmm-2016-0370.

Matsumoto, J., Stewart, T., Sheng, L., Li, N., Bullock, K., Song, N., … Zhang, J. (2017). Transmission of alpha-synuclein-containing erythrocyte-derived extracellular vesicles across the blood-brain barrier via adsorptive mediated transcytosis: Another mechanism for initiation and progression of Parkinson's disease? Acta Neuropathologica Communications, 5, 71. PMCID: PMC5598000. doi: 10.1186/s40478-017-0470-4.

Matsumoto, J., Stewart, T., Banks, W. A., Zhang, J. (2017). The transport mechanism of extracellular vesicles at the blood-brain barrier. Current Pharmaceutical Design, 23, 6206-6214. doi: 10.2174/1381612823666170913164738.

Mollenhauer, B., Batrla, R., El-Agnaf, O., Galasko, D. R., Lashuel, H. A., Merchant, K. M., … Zhang, J., … Investigating Synuclein Consortium of the Michael J. Fox Foundation for Parkinson's Research, (2017). A user's guide for alpha-synuclein biomarker studies in biological fluids: Perianalytical considerations. Movement Disorders, 32, 1117-1130. PMCID: PMC5638072. doi: 10.1002/mds.27090.

Song, N., Wang, W., Jia, F., Du, X., Xie, A., He, Q., … Zhang, J., … Jiang, H. (2017). Assessments of plasma ghrelin levels in the early stages of Parkinson's disease. Movement Disorders, 32, 1487-1491. doi: 10.1002/mds.27095.

Wile, D. J., Agarwal, P. A., Schulzer, M., Mak, E., Dinelle, K., Shahinfard, E., … Zhang, J., … Stoessl, A. J. (2017). Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: Cross-sectional studies. The Lancet Neurology, 16, 351-359. PMCID: PMC5477770. doi: 10.1016/S1474-4422(17)30056-X.

Yang, L., Stewart, T., Shi, M., Pottiez, G., Dator, R., Wu, R., … Zhang, J. (2017). An alpha-synuclein MRM assay with diagnostic potential for Parkinson's disease and monitoring disease progression. Proteomics. Clinical Applications, 11, PMCID: PMC5540649. doi: 10.1002/prca.201700045.

2018

Kristina Adams Waldorf

Adams Waldorf, K. M., Nelson, B. R., Stencel-Baerenwald, J. E., Studholme, C., Kapur, R. P., Armistead, B., … Shaw, D. W. W., … Dobyns, W. B., Hevner, R. F., … Rajagopal, L. (2018). Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brain. Nature Medicine, 24, 368-374. PMCID: PMC5839998. doi: 10.1038/nm.4485.

Lannon, S. M. R., Adams Waldorf, K. M., Fiedler, T., Kapur, R. P., Agnew, K., Rajagopal, L., … Fredricks, D. N. (2018). Parallel detection of lactobacillus and bacterial vaginosis-associated bacterial DNA in the chorioamnion and vagina of pregnant women at term. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of, 1-9. PMCID: PMC6135717. doi: 10.1080/14767058.2018.1446208.

Vornhagen, J., Armistead, B., Santana-Ufret, V., Gendrin, C., Merillat, S., Coleman, M., … Adams Waldorf, K. M., Nance, E., Rajagopal, L. (2018). Group B streptococcus exploits vaginal epithelial exfoliation for ascending infection. The Journal of Clinical Investigation, 128, 1985-1999. PMCID: PMC5919824. doi: 10.1172/JCI97043.

Susan Astley Ali, S., Kerns, K. A., Mulligan, B. P., Carmichael Olson, H., Astley, S. J. (2018). An investigation of intra-individual variability in children with fetal alcohol spectrum disorder (FASD). Child Neuropsychology, 24, 617-637. doi: 10.1080/09297049.2017.1302579.

Elizabeth Aylward Long, J. D., Lee, J. M., Aylward, E. H., Gillis, T., Mysore, J. S., Abu Elneel, K., … Gusella, J. F. (2018). Genetic modification of Huntington disease acts early in the prediagnosis phase. American Journal of Human Genetics, 103, 349-357. PMCID: PMC6128248. doi: 10.1016/j.ajhg.2018.07.017.

Melissa Barker-Haliski Barker-Haliski, M. L., Harte-Hargrove, L. C., Ravizza, T., Smolders, I., Xiao, B., Brandt, C., Loscher, W. (2018). A companion to the preclinical common data elements for pharmacologic studies in animal models of seizures and epilepsy. A Report of the TASK3 Pharmacology Working Group of the ILAE/AES Joint Translational Task Force. Epilepsia Open, 3, 53-68. PMCID: PMC6210039. doi: 10.1002/epi4.12254.

Koneval, Zachery, Knox, Kevin M., White, H. S., Barker-Haliski, M. L. (2018). Lamotrigine-resistant corneal-kindled mice: A model of pharmacoresistant partial epilepsy for moderate-throughput drug discovery. Epilepsia, 59, 1245-1256. doi: 10.1111/epi.14190. Raphael Bernier Arnett, A. B., Trinh, S., Bernier, R. A. (2018). The state of research on the genetics of autism spectrum disorder: Methodological, clinical and conceptual progress. Current Opinion in Psychology, 27, 1-5. doi: 10.1016/j.copsyc.2018.07.004.

Arnett, A. B., Rhoads, C. L., Hoekzema, K., Turner, T. N., Gerdts, J., Wallace, A. S., … Eichler, E. E., Bernier, R. A. (2018). The autism spectrum phenotype in ADNP syndrome. Autism Research, 11, 1300-1310. doi: 10.1002/aur.1980.

Arnett, A. B., Hudac, C. M., DesChamps, T. D., Cairney, B. E., Gerdts, J., Wallace, A. S., Bernier, R. A., Webb, S. J. (2018). Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder. Brain and Language, 187, 1-8. doi: 10.1016/j.bandl.2018.09.007.

Arnett, A. B., Cairney, B. E., Wallace, A. S., Gerdts, J., Turner, T. N., Eichler, E. E., Bernier, R. A. (2018). Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk. Journal of Child Psychology and Psychiatry and Allied Disciplines, 59, 268-276. PMCID: PMC5812799. doi: 10.1111/jcpp.12815.

Chapman, N. H., Bernier, R. A., Webb, S. J., Munson, J., Blue, E. M., Chen, D. H., … Raskind, W. H., Wijsman, E. M. (2018). Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder. Human Genetics, 137, 807-815. doi: 10.1007/s00439-018-1939-3.

Cheng, H., Dharmadhikari, A. V., Varland, S., Ma, N., Domingo, D., Kleyner, R., … Bernier, R. A., … Eichler, E. E., … Lyon, G. J. (2018). Truncating variants in NAA15 are associated with variable levels of intellectual disability, autism spectrum disorder, and congenital anomalies. American Journal of Human Genetics, 102, 985-994. PMCID: PMC5986698. doi: 10.1016/j.ajhg.2018.03.004.

Gerdts, J., Mancini, J., Fox, E., Rhoads, C., Ward, T., Easley, E., Bernier, R. A. (2018). Interdisciplinary team evaluation: An effective method for the diagnostic assessment of autism spectrum disorder. Journal of Developmental and Behavioral Pediatrics, 39, 271-281. doi: 10.1097/DBP.0000000000000549.

Guo, H., Duyzend, M. H., Coe, B. P., Baker, C., Hoekzema, K., Gerdts, J., … Bernier, R. A., Eichler, E. E. (2018). Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes. Genetics in Medicine, doi: 10.1038/s41436-018-0380-2.

Guo, H., Wang, T., Wu, H., Long, M., Coe, B. P., Li, H., … Bernier, R. A., Eichler, E. E., Xia, K. (2018). Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model. Molecular Autism, 9, 64. PMCID: PMC6293633. doi: 10.1186/s13229-018-0247-z.

Hudac, C. M., DesChamps, T. D., Arnett, A. B., Cairney, B. E., Ma, R., Webb, S. J., Bernier, R. A. (2018). Early enhanced processing and delayed habituation to deviance sounds in autism spectrum disorder. Brain and Cognition, 123, 110-119. PMCID: PMC5893357. doi: 10.1016/j.bandc.2018.03.004.

Jansen, S., Hoischen, A., Coe, B. P., Carvill, G. L., Van Esch, H., Bosch, D. G. M., … Bernier, R. A., … Mefford, H. C., … Eichler, E. E., de Vries, B. B. A. (2018). A genotye-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics, 26, 54-63. doi: 10.1038/s41431-017-0039-5.

Millin, R., Kolodny, T., Flevaris, A. V., Kale, A. M., Schallmo, M. P., Gerdts, J., Bernier, R. A., Murray, S. O. (2018). Reduced auditory cortical adaptation in autism spectrum disorder. eLife, 7, PMCID: PMC6203433. doi: 10.7554/eLife.36493.

Murray, S. O., Schallmo, M. P., Kolodny, T., Millin, R., Kale, A., Thomas, P., … Bernier, R. A., Tadin, D. (2018). Sex differences in visual motion processing. Current Biology, 28, 2794-2799 e3. PMCID: PMC6133755. doi: 10.1016/j.cub.2018.06.014.

Neuhaus, E., Bernier, R. A., Tham, S. W., Webb, S. J. (2018). Gastrointestinal and psychiatric symptoms among children and adolescents with autism spectrum disorder. Frontiers in Psychiatry, 9, 515. PMCID: PMC6204460. doi: 10.3389/fpsyt.2018.00515.

Neuhaus, E., Beauchaine, T. P., Bernier, R. A., Webb, S. J. (2018). Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms. Autism Research, 11, 476-487. PMCID: PMC5867206. doi: 10.1002/aur.1907.

Rubinstein, M., Patowary, A., Stanaway, I. B., McCord, E., Nesbitt, R. R., Archer, M., … Raskind, W. H., Wijsman, E. M., Bernier, R. A., Catterall, W. A., Brkanac, Z. (2018). Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism. Molecular Psychiatry, 23, 231-239. PMCID: PMC5468514. doi: 10.1038/mp.2016.222.

Sanders, S. J., Campbell, A. J., Cottrell, J. R., Moller, R. S., Wagner, F. F., Auldridge, A. L., Bernier, R. A., Catterall, W. A., … Bender, K. J. (2018). Progress in understanding and treating SCN2A-mediated disorders. Trends in Neurosciences, 41, 442-456. PMCID: PMC6015533. doi: 10.1016/j.tins.2018.03.011.

Schallmo, M. P., Kale, A. M., Millin, R., Flevaris, A. V., Brkanac, Z., Edden, R. A., Bernier, R. A., Murray, S. O. (2018). Suppression and facilitation of human neural responses. eLife, 7, PMCID: PMC5812713. doi: 10.7554/eLife.30334.

Van Dijck, A., Vulto-van Silfhout, A. T., Cappuyns, E., van der Werf, I. M., Mancini, G. M., Tzschach, A., Bernier, R. A., … Eichler, E. E., … Kooy, R. F. (2018). Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP. Biological Psychiatry, 15 Mar 2018. doi: 10.1016/j.biopsych.2018.02.1173.

Wallace, A. S., Hudac, C. M., Steinman, K. J., Peterson, J. L., DesChamps, T. D., Duyzend, M. H., … Eichler, E. E., Bernier, R. A. (2018). Longitudinal report of child with de novo 16p11.2 triplication. Clinical Case Reports, 6, 147-154. PMCID: PMC5771938. doi: 10.1002/ccr3.1236.

Virginia Berninger Nielsen, K., Andria-Habermann, K., Richards, T. L., Abbott, R., Mickail, T., Berninger, V. W. (2018). Emotional and behavioral correlates of persisting specific learning disabilities in written language during middle childhood and early adolescence. Journal of Psychoeducational Assessment, 36, 651-669. PMCID: PMC6291223. doi: 10.1177/0734282917698056.

Richards, T. L., Berninger, V. W., Yagle, K., Abbott, R. D., Peterson, D. (2018). Brain's functional network clustering coefficient changes in response to instruction (RTI) in students with and without reading disabilities: Multi-leveled reading brain's RTI. Cogent Psychology, 5, PMCID: PMC5877472. doi: 10.1080/23311908.2018.1424680.

Kristie F. Bjornson Andrews, M., Bjornson, K. F. (2018). Commentary on "Gait Analysis Parameters and Walking Activity Pre- and Postoperatively in Children With Cerebral Palsy". Pediatric Physical Therapy, 30, 208. doi: 10.1097/PEP.0000000000000522.

Bjornson, K. F., Moreau, N., Bodkin, A. W. (2018). Short-burst interval treadmill training walking capacity and performance in cerebral palsy: A pilot study. Developmental Neurorehabilitation, 1-8. doi: 10.1080/17518423.2018.1462270.

Braun, S., Bjornson, K. F., Dillon-Naftolin, E., Sheiko, M., Song, K., Kang, M. (2018). Reliability of StepWatch Activity Monitor to measure locomotor activity in youth with lower limb salvage. Pediatric Physical Therapy, 30, 217-221. doi: 10.1097/PEP.0000000000000518.

Liljenquist, K., O'Neil, M. E., Bjornson, K. F. (2018). Utilization of physical therapy services during transition for young people with Cerebral Palsy: A call for improved care into adulthood. Physical Therapy, 8 May 2018. doi: 10.1093/ptj/pzy068.

Omura, J., Fuentes, M., Bjornson, K. F. (2018). Participation in daily life: Influence on quality of life in ambulatory children with Cerebral Palsy. PM&R, 10, 1185-1191. doi: 10.1016/j.pmrj.2018.05.010.

Pham, K. L. D., Bjornson, K. F., Osorio, M., Whitlock, K. B., Massagli, T. L. (2018). A novel protocol for contact isolation for multidrug-resistant organisms in children on inpatient rehabilitation and effects on functional outcomes: A noninferiority study. PM&R, 10, 594-600. doi: 10.1016/j.pmrj.2017.11.006.

Wittry, S., Tsao, E., Bjornson, K. F. (2018). Are clinic-based walking measures associated with community walking activity in children with cerebral palsy? Journal of Pediatric Rehabilitation Medicine, 11, 23-30. doi: 10.3233/PRM-160425.

Cathryn Booth-LaForce Barstead, M. G., Smith, K. A., Laursen, B., Booth-LaForce, C., King, S., Rubin, K. H. (2018). Shyness, preference for solitude, and adolescent internalizing: The roles of maternal, paternal, and best-friend support. Journal of Research on Adolescence, 28, 488-504. doi: 10.1111/jora.12350.

Shepherd-Banigan, M., Bell, J. F., Basu, A., Booth-LaForce, C., Harris, J. R. (2018). Mothers' employment attributes and use of preventive child health services. Medical Care Research and Review, 74, 208-226. doi: 10.1177/1077558716634555.

Gittelsohn, J., Belcourt, A., Magarati, M., Booth-LaForce, C., Duran, B., Mishra, S. I., … Jernigan, V. B. B. (2018). Building capacity for productive indigenous community-university partnerships. Prevention Science: The Official Journal of the Society for Prevention Research, 4 Oct 2018. doi: 10.1007/s11121-018-0949-7. Eliot Brenowitz Larson, T. A., Thatra, N. M., Hou, D., Hu, R. A., Brenowitz, E. A. (2018). Seasonal changes in neuronal turnover in a forebrain nucleus in adult songbirds. The Journal of Comparative Neurology, 5 Oct 2018. doi: 10.1002/cne.24552.

Zoran Brkanac Rubinstein, M., Patowary, A., Stanaway, I. B., McCord, E., Nesbitt, R. R., Archer, M., … Raskind, W. H., Wijsman, E. M., Bernier, R. A., Catterall, W. A., Brkanac, Z. (2018). Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism. Molecular Psychiatry, 23, 231-239. PMCID: PMC5468514. doi: 10.1038/mp.2016.222.

Thomas Burbacher Grant, K. S., Petroff, R., Isoherranen, N. Stella, N., Burbacher, T. M. (2018). Cannabis use during pregnancy: Pharmacokinetics and effects on child development. Pharmacology and Therapeutics, 182, 133-151. doi: 10.1016/j.pharmthera.2017.08.014.

Gulinello, M., Mitchell, H. A., Chang, Q., Timothy O'Brien, W., Zhou, Z., Abel, T., … Burbacher, T. M., Crawley, J. N. (2018). Rigor and reproducibility in rodent behavioral research. Neurobiology of Learning and Memory, 4 Jan 2018. doi: 10.1016/j.nlm.2018.01.001.

Jing, J., Petroff, R., Shum, S., Crouthamel, B., Topletz, A. R., Grant, K. S., Burbacher, T. M., Isoherranen, N. (2018). Toxicokinetics and physiologically based pharmacokinetic modeling of the shellfish toxin Domoic acid in nonhuman primates. Drug Metabolism and Disposition, 46, 155-165. PMCID: PMC5776359. doi: 10.1124/dmd.117.078485.

Shum, S., Kirkwood, J. S., Jing, J., Petroff, R., Crouthamel, B., Grant, K. S., Burbacher, T. M., … Isoherranen, N. (2018). Validated HPLC-MS/MS method to quantify low levels of Domoic acid in plasma and urine after subacute exposure. ACS Omega, 3, 12079-12088. PMCID: PMC6175497. doi: 10.1021/acsomega.8b02115.

Heather Carmichael Olson Ali, S., Kerns, K. A., Mulligan, B. P., Carmichael Olson, H., Astley, S. J. (2018). An investigation of intra-individual variability in children with fetal alcohol spectrum disorder (FASD). Child Neuropsychology, 24, 617-637. doi: 10.1080/09297049.2017.1302579.

Hanlon-Dearman, A., Chen, M. L., Carmichael Olson, H. (2018). Understanding and managing sleep disruption in children with fetal alcohol spectrum disorder. Biochemistry and Cell Biology, 96, 267-274. doi: 10.1139/bcb-2017-0064.

Wagner, B., Fitzpatrick, J. P., Mazzucchelli, T. G., Symons, M., Carmichael Olson, H., Jirikowic, T. L., Cross, D. J., … Latimer, J. (2018). Study protocol for a self-controlled cluster randomised trial of the Alert Program to improve self-regulation and executive function in Australian Aboriginal children with fetal alcohol spectrum disorder. BMJ Open, 8, e021462. PMCID: PMC5875644. doi: 10.1136/bmjopen-2017-021462.

William Catterall Catterall, W. A. (2018). Dravet syndrome: A sodium channel interneuronopathy. Current Opinion in Physiology, 2, 42-50. PMCID: PMC6091224. doi: 10.1016/j.cophys.2017.12.007.

Gamal El-Din, T. M., Lenaeus, M. J., Catterall, W. A. (2018). Structural and functional analysis of sodium channels viewed from an evolutionary perspective. Handbook of Experimental Pharmacology, 246, 53-72. doi: 10.1007/164_2017_61.

Gamal El-Din, T. M., Lenaeus, M. J., Zheng, N., Catterall, W. A. (2018). Fenestrations control resting-state block of a voltage-gated sodium channel. Proceedings of the National Academy of Sciences of the United States of America, 115, 13111-13116. PMCID: PMC6304959. doi: 10.1073/pnas.1814928115.

Jiang, D., Gamal El-Din, T. M., Ing, C., Lu, P., Pomes, R., Zheng, N., Catterall, W. A. (2018).Structural basis for gating pore current in periodic paralysis. Nature, 557, 590-594. doi: 10.1038/s41586-018-0120-4.

Nanou, E., Lee, A. K. C., Catterall, W. A. (2018). Control of excitation/inhibition balance in a hippocampal circuit by calcium sensor protein regulation of presynaptic calcium channels. The Journal of Neuroscience, 38, 4430-4440. PMCID: PMC5932646. doi: 10.1523/JNEUROSCI.0022-18.2018.

Nanou, E., Catterall, W. A. (2018). Calcium channels, synaptic plasticity, and neuropsychiatric disease. Neuron, 98, 466-481. doi: 10.1016/j.neuron.2018.03.017.

Yu, H., Yuan, C., Westenbroek, R. E., Catterall, W. A. (2018). The AKAP Cypher/Zasp contributes to beta-adrenergic/PKA stimulation of cardiac CaV1.2 calcium channels. The Journal of General Physiology, 150, 883-889. PMCID: PMC5987873. doi: 10.1085/jgp.201711818.

Jeffrey Chamberlain Adams, M. E., Odom, G. L., Kim, M. J., Chamberlain, J. S., Froehner, S. C. (2018). Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16-17. Human Molecular Genetics, 27, 2978-2985 doi: 10.1093/hmg/ddy197.

Halbert, C. L., Allen, J. M., Chamberlain, J. S. (2018). Aav6 vector production and purification for muscle gene therapy. Methods in Molecular Biology, 1687, 257-266. doi: 10.1007/978-1-4939-7374-3_18.

Ho, P. P., Lahey, L. J., Mourkioti, F., Kraft, P. E., Filareto, A., Brandt, M., … Chamberlain, J. S., … Steinman, L. (2018). Engineered DNA plasmid reduces immunity to dystrophin while improving muscle force in a model of gene therapy of Duchenne dystrophy. Proceedings of the National Academy of Sciences of the United States of America, 115, E9182-E9191. PMCID: PMC6166850. doi: 10.1073/pnas.1808648115.

Kennedy, T. L., Guiraud, S., Edwards, B., Squire, S., Moir, L., Babbs, A., … Chamberlain, J. S., Davies, K. E. (2018). Micro-utrophin improves cardiac and skeletal muscle function of severely affected D2/mdx mice. Molecular Therapy Methods & Clinical Development, 11, 92-105. PMCID: PMC6216100. doi: 10.1016/j.omtm.2018.10.005.

Nelson, D. M., Lindsay, A., Judge, L. M., Duan, D., Chamberlain, J. S., Lowe, D. A., Ervasti, J. M. (2018). Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins. Human Molecular Genetics, 27, 2090-2100. PMCID: PMC5985723. doi: 10.1093/hmg/ddy113.

Park, J. S., Vohra, R., Klussmann, T., Bengtsson, N. E., Chamberlain, J. S., Lee, D. (2018). Non-invasive tracking of disease progression in young dystrophic muscles using multi-parametric MRI at 14T. PLoS One, 13, e0206323. doi: 10.1371/journal.pone.0206323.

Dimitri Christakis Christakis, D. A. (2018). JAMA Pediatrics-the year in review, 2018. JAMA Pediatrics, 172, 412-413. doi: 10.1001/jamapediatrics.2017.583.

Christakis, D. A., Ramirez, J. S. B., Ferguson, S. M., Ravinder, S., Ramirez, J. M. (2018). How early media exposure may affect cognitive function: A review of results from observations in humans and experiments in mice. Proceedings of the National Academy of Sciences of the United States of America, 115, 9851-9858. PMCID: PMC6176595. doi: 10.1073/pnas.1711548115.

Christakis, D. A. (2018). Jama pediatrics 2018 and beyond. JAMA Pediatrics, 172, 116. doi: 10.1001/jamapediatrics.2017.4867.

Tandon, P. S., Saelens, B. E., Zhou, C., Christakis, D. A. (2018). A comparison of preschoolers' physical activity indoors versus outdoors at child care. International Journal of Environmental Research and Public Health, 15, doi: 10.3390/ijerph15112463.

Walters, K., Christakis, D. A., Wright, D. R. (2018). Are Mechanical Turk worker samples representative of health status and health behaviors in the U.S.? PLoS One, 13, e0198835. PMCID: PMC5991724. doi: 10.1371/journal.pone.0198835.

Wright, D. R., Christakis, D. A., Lozano, P., Saelens, B. E. (2018). Healthy, wealthy, and wise? Exploring parent comparative optimism about future child outcomes. MDM Policy & Practice, 3, 2381468318774776. PMCID: PMC6157425. doi: 10.1177/2381468318774776.

Lucio Costa Chang, Y. C., Cole, T. B., Costa, L. G. (2018). Prenatal and early-life diesel exhaust exposure causes autism-like behavioral changes in mice. Particle and Fibre Toxicology, 15, 18. PMCID: PMC5910592. doi: 10.1186/s12989-018-0254-4.

Coburn, J. L., Cole, T. B., Dao, K. T., Costa, L. G. (2018). Acute exposure to diesel exhaust impairs adult neurogenesis in mice: Prominence in males and protective effect of pioglitazone. Archives of Toxicology, 92, 1815-1829. doi: 10.1007/s00204-018-2180-5.

Costa, L. G. (2018). Organophosphorus compounds at 80: Some old and new issues. Toxicological Sciences, 162, 24-35. doi: 10.1093/toxsci/kfx266.

Pellacani, C., Costa, L. G. (2018). Role of autophagy in environmental neurotoxicity. Environmental Pollution, 235, 791-805. doi: 10.1016/j.envpol.2017.12.102.

Timothy Cox Cox, L. L., Cox, T. C., Moreno Uribe, L. M., Zhu, Y., Richter, C. T., Nidey, N., … Hing, A. V., … Glass, I. A., … Roscioli, T. (2018). Mutations in the epithelial Cadherin-p120-Catenin complex cause Mendelian non-syndromic cleft lip with or without cleft palate. American Journal of Human Genetics, 102, 1143-1157. PMCID: PMC5992119.doi: 10.1016/j.ajhg.2018.04.009.

Gallagher, E. R., Siebold, B., Collett, B. R., Cox, T. C., Aziz, V., Cunningham, M. L. (2018). Associations between laterality of orofacial clefts and medical and academic outcomes. American Journal of Medical Genetics. Part A, 176, 1037. doi: 10.1002/ajmg.a.38663.

Donna Cross Wagner, B., Fitzpatrick, J. P., Mazzucchelli, T. G., Symons, M., Carmichael Olson, H., Jirikowic, T. L., Cross, D. J., … Latimer, J. (2018). Study protocol for a self-controlled cluster randomised trial of the Alert Program to improve self-regulation and executive function in Australian Aboriginal children with fetal alcohol spectrum disorder. BMJ Open, 8, e021462. PMCID: PMC5875644. doi: 10.1136/bmjopen-2017-021462. Michael Cunningham Gallagher, E. R., Siebold, B., Collett, B. R., Cox, T. C., Aziz, V., Cunningham, M. L. (2018). Associations between laterality of orofacial clefts and medical and academic outcomes. American Journal of Medical Genetics. Part A, 176, 1037. doi: 10.1002/ajmg.a.38663.

Gilbert, J. R., Losee, J. E., Mooney, M. P., Cray, J. J., Gustafson, J., Cunningham, M. L., Cooper, G. M. (2018). Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit. PLoS One, 13, e0204086. PMCID: PMC6147457. doi: 10.1371/journal.pone.0204086.

Kievit, A., Tessadori, F., Douben, H., Jordens, I., Maurice, M., Hoogeboom, J., … Cunningham, M. L., Hing, A. V., … van Haaften, G. (2018). Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, 26, 210-219. PMCID: PMC5838974. doi: 10.1038/s41431-017-0010-5.

Wenger, T. L., Hopper, R. A., Rosen, A., Tully, H. M., Cunningham, M. L., Lee, A. K. C. (2018). A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortality. Genetics in Medicine, 18 Jun 2018. doi: 10.1038/s41436-018-0073-x.

Stephen Dager Estes, A. M., Munson, J., John, T. S., Dager, S. R., Rodda, A., Botteron, K., … Guralnick, M. J., IBIS Network. (2018). Parent support of preschool peer relationships in younger siblings of children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 48, 1122-1132. PMCID: PMC5738288. doi: 10.1007/s10803-017-3202-5.

Marrus, N., Eggebrecht, A. T., Todorov, A., Elison, J. T., Wolff, J. J., Cole, L., … Estes, A. M., … Dager, S. R., … Pruett, J. R., Jr. (2018). Walking, gross motor development, and brain functional connectivity in infants and toddlers. Cerebral Cortex, 28, 750-763. PMCID: PMC6057546. doi: 10.1093/cercor/bhx313.

Marrus, N., Hall, L. P., Paterson, S. J., Elison, J. T., Wolff, J. J., Swanson, M. R., … Dager, S. R., Estes, A. M., … IBIS Network. (2018). Language delay aggregates in toddler siblings of children with autism spectrum disorder. Journal of Neurodevelopmental Disorders, 10, 29. PMCID: PMC6198516. doi: 10.1186/s11689-018-9247-8.

Swanson, M. R., Shen, M. D., Wolff, J. J., Boyd, B., Clements, M., Rehg, J., … Dager, S. R., … Estes, A. M., … IBIS Network. (2018). Naturalistic language recordings reveal "hypervocal" infants at high familial risk for autism. Child Development, 89, e60-e73. PMCID: PMC5592123. doi: 10.1111/cdev.12777.

Wolff, J. J., Dimian, A. F., Botteron, K. N., Dager, S. R., Elison, J. T., Estes, A. M., … IBIS Network. (2018). A longitudinal study of parent-reported sensory responsiveness in toddlers at-risk for autism. Journal of Child Psychology and Psychiatry and Allied Disciplines, 23 Oct 2018. doi: 10.1111/jcpp.12978.

Woo, J., Kim, J. E., Im, J. J., Lee, J., Jeong, H. S., Park, S., … Dager, S. R., … Lee, C. J. (2018). Astrocytic water channel aquaporin-4 modulates brain plasticity in both mice and humans: A potential gliogenetic mechanism underlying language-associated learning. Molecular Psychiatry, 23, 1021-1030. doi: 10.1038/mp.2017.113.

Nina de Lacy de Lacy, N., Kodish, I., Rachakonda, S., Calhoun, V. D. (2018). Novel in silico multivariate mapping of intrinsic and anticorrelated connectivity to neurocognitive functional maps supports the maturational hypothesis of ADHD. Human Brain Mapping, 39, 3449-3467. doi: 10.1002/hbm.24187.

Fu, Z., Tu, Y., Di, X., Du, Y., Sui, J., Biswal, B. B., … de Lacy, N., Calhoun, V. D. (2018).Transient increased thalamic-sensory connectivity and decreased whole-brain dynamism in autism. Neuroimage, 06 Jun 2018. doi: 10.1016/j.neuroimage.2018.06.003.

Herzig, L., de Lacy, N., Capone, G., Radesky, J. (2018). Intellectual disability and psychotropic medications. Journal of Developmental and Behavioral Pediatrics, 39, 591-593. doi: 10.1097/DBP.0000000000000613.

Sureyya Dikmen

Alali, A. S., Temkin, N., Barber, J., Pridgeon, J., Chaddock, K., Dikmen, S. S., … Chesnut, R. M. (2018). A clinical decision rule to predict intracranial hypertension in severe traumatic brain injury. Journal of Neurosurgery, 1-8. doi: 10.3171/2018.4.JNS173166.

Christine Disteche Bonora, G., Deng, X., Fang, H., Ramani, V., Qiu, R., Berletch, J. B., … Disteche, C. M. (2018). Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome. Nature Communications, 9, 1445. PMCID: PMC5899087. doi: 10.1038/s41467-018-03694-y.

Ma, W., Ay, F., Lee, C., Gulsoy, G., Deng, X., Cook, S., … Disteche, C. M., … Duan, Z. (2018). Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution. Methods, 142, 59-73. PMCID: PMC5993575. doi: 10.1016/j.ymeth.2018.01.014.

William B. Dobyns Adams Waldorf, K. M., Nelson, B. R., Stencel-Baerenwald, J. E., Studholme, C., Kapur, R. P., Armistead, B., … Shaw, D. W. W., … Dobyns, W. B., Hevner, R. F., … Rajagopal, L. (2018). Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brain. Nature Medicine, 24, 368-374. PMCID: PMC5839998. doi: 10.1038/nm.4485.

Aldinger, K. A., Dempsey, J. C., Tully, H. M., Grout, M. E., Mehaffey, M. G., Dobyns, W. B., Doherty, D. A. (2018). Rhombencephalosynapsis: Fused cerebellum, confused geneticists. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 178, 432-439. doi: 10.1002/ajmg.c.31666.

Berg, A. T., Chakravorty, S., Koh, S., Grinspan, Z. M., Shellhaas, R. A., Saneto, R. P., … Dobyns, W. B., Hegde, M. (2018). Why West? Comparisons of clinical, genetic and molecular features of infants with and without spasms. PLoS One, 13, e0193599. PMCID: PMC5843222. doi: 10.1371/journal.pone.0193599.

Brock, S., Stouffs, K., Scalais, E., D'Hooghe, M., Keymolen, K., Guerrini, R., Dobyns, W. B., … Jansen, A. C. (2018). Tubulinopathies continued: Refining the phenotypic spectrum associated with variants in TUBG1. European Journal of Human Genetics, 26,1132-1142. doi: 10.1038/s41431-018-0146-y.

Di Donato, N., Timms, A. E., Aldinger, K. A., Mirzaa, G. M., Bennett, J. T., Collins, S., … Dobyns, W. B. (2018). Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. Genetics in Medicine, 19 Apr 2018. doi: 10.1038/gim.2018.8.

Dobyns, W. B., Aldinger, K. A., Ishak, G. E., Mirzaa, G. M., Timms, A. E., Grout, M. E., … Doherty, D. A., Mancini, G. M. S. (2018). MACF1 mutations encoding highly conserved zinc-binding residues of the GAR domain cause defects in neuronal migration and axon guidance. American Journal of Human Genetics, 103, 1009-1021. PMCID: PMC6288423. doi: 10.1016/j.ajhg.2018.10.019.

Fry, A. E., Fawcett, K. A., Zelnik, N., Yuan, H., Thompson, B. A. N., Shemer-Meiri, L., … Zhang, J., … Mirzaa, G. M., … Mefford, H. C., Dobyns, W. B., … Pilz, D. T. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain, 22 Jun 2018. PMCID: PMC5837214. doi: 10.1093/brain/awx358.

Heinzen, E. L., O'Neill, A. C., Zhu, X., Allen, A. S., Bahlo, M., Chelly, J., … Dobyns, W. B., … Epilepsy Phenome/Genome Project. (2018). De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. PLoS Genetics, 14, e1007281. PMCID: PMC5965900. doi: 10.1371/journal.pgen.1007281.

Leibovitz, Z., Mandel, H., Falik-Zaccai, T. C., Ben Harouch, S., Savitzki, D., Krajden-Haratz, K., … Dobyns, W. B., Lerman-Sagie, T. (2018). Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation. European Journal of Paediatric Neurology, 22, 525-531. doi: 10.1016/j.ejpn.2017.12.012.

Liu, W. A., Chen, S., Li, Z., Lee, C. H., Mirzaa, G. M., Dobyns, W. B., … Zhang, J., Shi, S. H. (2018). PARD3 dysfunction in conjunction with dynamic HIPPO signaling drives cortical enlargement with massive heterotopia. Genes & Development, 32, 763-780. doi: 10.1101/gad.313171.118.

Moog, U., Dobyns, W. B. (2018). An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 178, 414-422. doi: 10.1002/ajmg.c.31667.

Ramos, E. M., Carecchio, M., Lemos, R., Ferreira, J., Legati, A., Sears, R. L., … Dobyns, W. B., … Nicolas, G. (2018). Primary brain calcification: An international study reporting novel variants and associated phenotypes. European Journal of Human Genetics, 26, 1462-1477. doi: 10.1038/s41431-018-0185-4.

Schanze, I., Bunt, J., Lim, J. W. C., Schanze, D., Dean, R. J., Alders, M., … Dobyns, W. B., … Mirzaa, G. M., … Richards, L. J. (2018). NFIB haploinsufficiency is associated with intellectual disability and macrocephaly. American Journal of Human Genetics, 103, 752-768. PMCID: PMC6218805. doi: 10.1016/j.ajhg.2018.10.006.

Steiner, J. E., McCoy, G. N., Hess, C. P., Dobyns, W. B., Metry, D. W., Drolet, B. A., … Siegel, H. (2018). Structural malformations of the brain, eye, and pituitary gland in PHACE syndrome. American Journal of Medical Genetics. Part A, 176, 48-55. PMCID: PMC5844264. doi: 10.1002/ajmg.a.38523.

Stutterd, C. A., Dobyns, W. B., Jansen, A., Mirzaa, G. M., Leventer, R. J. (2018). Polymicrogyria overview. In M. P. Adam, H. H. Ardinger, R. A. Pagon, et. al. (Eds.). GeneReviews®, Aug 16, 2018. Available from: https://www.ncbi.nlm.nih.gov/pubmed/20301504.

Tripathy, R., Leca, I., van Dijk, T., Weiss, J., van Bon, B. W., Sergaki, M. C., … Dobyns, W. B., Mirzaa, G. M., … Keays, D. A. (2018). Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations. Neuron, 100, 1354-1368 e5. doi: 10.1016/j.neuron.2018.10.044. Daniel Doherty Aldinger, K. A., Dempsey, J. C., Tully, H. M., Grout, M. E., Mehaffey, M. G., Dobyns, W. B., Doherty, D. A. (2018). Rhombencephalosynapsis: Fused cerebellum, confused geneticists. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 178, 432-439. doi: 10.1002/ajmg.c.31666.

Brooks, B. P., Zein, W. M., Thompson, A. H., Mokhtarzadeh, M., Doherty, D. A., Parisi, M., Glass, I. A., … Gunay-Aygun, M. (2018). Joubert syndrome: Ophthalmological findings in correlation with genotype and hepatorenal disease in 99 patients prospectively evaluated at a single center. Ophthalmology, 125, 1937-1952. doi: 10.1016/j.ophtha.2018.05.026.

Strongin, A., Heller, T., Doherty, D. A., Glass, I. A., Parisi, M. A., Bryant, J., … NISC Comparative Sequencing Program (2018). Characteristics of liver disease in 100 individuals with Joubert syndrome prospectively evaluated at a single center. Journal of Pediatric Gastroenterology and Nutrition, 66, 428-435. PMCID: PMC5825259. doi: 10.1097/MPG.0000000000001816.

Valente, E. M., Nuovo, S., Doherty, D. A. (2018). Genetics of cerebellar disorders. Handbook of Clinical Neurology, 154, 267-286. doi: 10.1016/B978-0-444-63956-1.00016-3.

Evan Eichler

Aneichyk, T., Hendriks, W. T., Yadav, R., Shin, D., Gao, D., Vaine, C. A., … Eichler, E. E., … Talkowski, M. E. (2018). Dissecting the causal mechanism of X-linked Dystonia-Parkinsonism by integrating genome and transcriptome assembly. Cell, 172, 897-909 e21. PMCID: PMC5831509. doi: 10.1016/j.cell.2018.02.011.

Arnett, A. B., Rhoads, C. L., Hoekzema, K., Turner, T. N., Gerdts, J., Wallace, A. S., … Eichler, E., Bernier, R. A. (2018). The autism spectrum phenotype in ADNP syndrome. Autism Research, 11, 1300-1310. doi: 10.1002/aur.1980.

Cantsilieris, S., Nelson, B. J., Huddleston, J., Baker, C., Harshman, L., Penewit, K., … Eichler, E. E. (2018). Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family.Proceedings of the National Academy of Sciences of the United States of America, 115, E4433-E4442. PMCID: PMC5948961. doi: 10.1073/pnas.1717600115.

Catacchio, C. R., Maggiolini, F. A. M., D'Addabbo, P., Bitonto, M., Capozzi, O., Lepore Signorile, M., … Eichler, E. E., … Antonacci, F. (2018). Inversion variants in human and primate genomes. Genome Research, 28, 910-920. PMCID: PMC5991517. doi: 10.1101/gr.234831.118.

Dougherty, M. L., Underwood, J. G., Nelson, B. J., Tseng, E., Munson, K. M., Penn, O., … Eichler, E. E. (2018). Transcriptional fates of human-specific segmental duplications in brain.Genome Research, 28, 1566-1576. PMCID: PMC6169893. doi: 10.1101/gr.237610.118.

Fiddes, I. T., Lodewijk, G. A., Mooring, M., Bosworth, C. M., Ewing, A. D., Mantalas, G. L., … Eichler, E. E., … Haussler, D. (2018). Human-specific NOTCH2NL genes affect NOTCH signaling and cortical neurogenesis. Cell, 173, 1356-1369 e22. PMCID: PMC5986104. doi: 10.1016/j.cell.2018.03.051.

Ghareghani, M., Porubsk, D., Sanders, A. D., Meiers, S., Eichler, E. E., Korbel, J. O., Marschall, T. (2018). Strand-seq enables reliable separation of long reads by chromosome via expectation maximization. Bioinformatics, 34, i115-i123. doi: 10.1093/bioinformatics/bty290.

Huddleston, J., Chaisson, M. J. P., Steinberg, K. M., Warren, W., Hoekzema, K., Gordon, D., … Eichler, E. E. (2018). Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data. Genome Research, 28, 144. PMCID: PMC5749179. doi: 10.1101/gr.233007.117.

Jansen, S., Hoischen, A., Coe, B. P., Carvill, G. L., Van Esch, H., Bosch, D. G. M., … Bernier, R. A., … Mefford, H. C., … Eichler, E. E., de Vries, B. B. A. (2018). A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency. European Journal of Human Genetics, 26, 54-63. doi: 10.1038/s41431-017-0039-5.

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Annette Mercer Estes Estes, A. M., Munson, J., John, T. S., Dager, S. R., Rodda, A., Botteron, K., … Guralnick, M. J., IBIS Network. (2018). Parent support of preschool peer relationships in younger siblings of children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 48, 1122-1132. PMCID: PMC5738288. doi: 10.1007/s10803-017-3202-5.

Rogers, S. J., Estes, A. M., Vismara, L., Munson, J., Zierhut, C., Greenson, J., … Talbott, M. (2018). Enhancing low-intensity coaching in parent implemented Early Start Denver Model intervention for early autism: A randomized comparison treatment trial. Journal of Autism and Developmental Disorders, 10 Sep 2018. doi: 10.1007/s10803-018-3740-5.

Welsh, J. P., Estes, A. M. (2018). Exploring the social brain. eLife, 7, PMCID: PMC5832409. doi: 10.7554/eLife.35392.

Elaine Faustman Griffith, W. C., Vigoren, E. M., Smith, M. N., Workman, T., Thompson, B., Coronado, G. D., Faustman, E. M. (2018). Application of improved approach to evaluate a community intervention to reduce exposure of young children living in farmworker households to organophosphate pesticides. Journal of Exposure Science and Environmental Epidemiology, 17 Apr 2018. doi: 10.1038/s41370-018-0028-y.

Park, J. J., Weldon, B. A., Hong, S., Workman, T., Griffith, W. C., Park, J. H., Faustman, E. M. (2018). Characterization of 3D embryonic C57BL/6 and A/J mouse midbrain micromass in vitro culture systems for developmental neurotoxicity testing. Toxicology in Vitro, 48, 33-44. doi: 10.1016/j.tiv.2017.12.009.

Plascak, J. J., Griffith, W. C., Workman, T., Smith, M. N., Vigoren, E., Faustman, E. M., Thompson, B. (2018). Evaluation of the relationship between residential orchard density and dimethyl organophosphate pesticide residues in house dust. Journal of Exposure Science and Environmental Epidemiology, doi: 10.1038/s41370-018-0074-5.

Tamaro, C. M., Smith, M. N., Workman, T., Griffith, W. C., Thompson, B., Faustman, E. M. (2018). Characterization of organophosphate pesticides in urine and home environment dust in an agricultural community. Biomarkers, 23, 174-187. doi: 10.1080/1354750X.2017.1395080.

Wallace, J. C., Youngblood, J. E., Port, J. A., Cullen, A. C., Smith, M. N., Workman, T., Faustman, E. M. (2018). Variability in metagenomic samples from the Puget Sound: Relationship to temporal and anthropogenic impacts. PLoS One, 13, e0192412. PMCID: PMC5811002. doi: 10.1371/journal.pone.0192412.

Martin Frasch Escalona-Vargas, D., Wu, H. T., Frasch, M. G., Eswaran, H. (2018). A comparison of five algorithms for fetal magnetocardiography signal extraction. Cardiovascular Engineering and Technology, 9, 483-487. doi: 10.1007/s13239-018-0351-4.

Frasch, M. G., Baier, C. J., Antonelli, M. C., Metz, G. A. S. (2018). Perinatal psychoneuroimmunology: Protocols for the study of prenatal stress and its effects on fetal and postnatal brain development. Methods in Molecular Biology, 1781, 353-376. doi: 10.1007.978-1-4939-7828-1_19.

Frasch, M. G. (2018). Saving the brain one heartbeat at a time. The Journal of Physiology, 596, 5503-5504. doi: 10.1113/JP275776.

Frasch, M. G., Burns, P., Benito, J., Cortes, M., Cao, M., Fecteau, G., Desrochers, A. (2018). Sculpting the sculptors: Methods for studying the fetal cholinergic signaling on systems and cellular scales. Methods in Molecular Biology, 1781, 341-352. doi: 10.1007/978-1-4939-7828-1_18.

Frasch, M. G., Lobmaier, S. M., Stampalija, T., Desplats, P., Pallares, M. E., Pastor, V., … Antonelli, M. C. (2018). Non-invasive biomarkers of fetal brain development reflecting prenatal stress: An integrative multi-scale multi-species perspective on data collection and analysis. Neuroscience & Biobehavioral Reviews, 30 May 2018. doi: 10.1016/j.neubiorev.2018.05.026.

Morrison, J. L., Berry, M. J., Botting, K. J., Darby, J. R. T., Frasch, M. G., Gatford, K. L., … Tellam, R. L. (2018). Improving pregnancy outcomes in humans through studies in sheep. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 16 Oct 2018. doi: 10.1152/ajpregu.00391.2017.

Shen, C., Frasch, M. G., Wu, H. T., Herry, C. L., Cao, M., Desrochers, A., … Burns, P. (2018). Non-invasive acquisition of fetal ECG from the maternal xyphoid process: A feasibility study in pregnant sheep and a call for open data sets. Physiological Measurement, 39, 035005 doi: 10.1088/1361-6579/aaaaa4.

Wallingford, M. C., Benson, C., Chavkin, N. W., Chin, M. T., Frasch, M. G. (2018). Placental vascular calcification and cardiovascular health: It is time to determine how much of maternal and offspring health is written in stone. Frontiers in Physiology, 9, 1044. PMCID: PMC6090024. doi: 10.3389/fphys.2018.01044.

Clement Furlong Bagi, A., Soelberg, S. D., Furlong, C. E., Baussant, T. (2018). Implementing morpholino-based nucleic acid sensing on a portable surface plasmon resonance instrument for future application in environmental monitoring. Sensors, 18. PMCID: PMC6210944. doi: 10.3390/s18103259.

Meyer, W. K., Jamison, J., Richter, R., Woods, S. E., Partha, R., Kowalczyk, A., … Furlong, C. E., Clark, N. L. (2018). Ancient convergent losses of Paraoxonase 1 yield potential risks for modern marine mammals. Science, 361, 591-594. doi: 10.1126/science.aap7714.

Gwenn Garden Wang, D. B., Kinoshita, C., Kinoshita, Y., Sopher, B. L., Uo, T., Lee, R. J., … Murphy, S. P., … Garden, G. A., Morrison, R. S. (2018). Neuronal susceptibility to beta-amyloid toxicity and ischemic injury involves histone deacetylase-2 regulation of endophilin-B1. Brain Pathology (Zurich, Switzerland), 20 July 2018. doi: 10.1111/bpa.12647.

Adam Geballe Bayer, A., Brennan, G., Geballe, A. P. (2018). Adaptation by copy number variation in monopartite viruses. Current Opinion in Virology, 33, 7-12. doi: 10.1016/j.coviro.2018.07.001.

Child, S. J., Hickson, S. E., Bayer, A., Malouli, D., Fruh, K., Geballe, A. P. (2018). Antagonism of the protein Kinase R pathway in human cells by Rhesus cytomegalovirus. Journal of Virology, 92. PMCID: PMC5827409. doi: 10.1128/JVI.01793-17.

Hickson, S. E., Margineantu, D., Hockenbery, D. M., Simon, J. A., Geballe, A. P. (2018). Inhibition of vaccinia virus replication by nitazoxanide. Virology, 518, 398-405. PMCID: PMC5929478. doi: 10.1016/j.virol.2018.03.023.

Ian Glass Brooks, B. P., Zein, W. M., Thompson, A. H., Mokhtarzadeh, M., Doherty, D. A., Parisi, M., Glass, I. A., … Gunay-Aygun, M. (2018). Joubert syndrome: Ophthalmological findings in correlation with genotype and hepatorenal disease in 99 patients prospectively evaluated at a single center. Ophthalmology, 125, 1937-1952. doi: 10.1016/j.ophtha.2018.05.026.

Byers, H. M., Jensen, D. M., Glass, I. A., Bennett, J. T. (2018). Minimal mosaicism, maximal phenotype: Discordance between clinical and molecular findings in two patients with tuberous sclerosis. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 178, 374 -378. doi: 10.1002/ajmg.c.31656.

Byers, H. M., Chen, M., Gelfand, A. S., Ong, B., Jendras, M., Glass, I. A. (2018). Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions. American Journal of Medical Genetics. Part A, 176, 1398-1404. PMCID: PMC5992090. doi: 10.1002/ajmg.a.38726.

Chang, I. J., Adam, M. P., Jayadev, S., Bird, T. D., Natarajan, N., Glass, I. A. (2018). Novel pregnancy-triggered episodes of CAPOS syndrome. American Journal of Medical Genetics. Part A, 176, 235-240. PMCID: PMC5726903. doi: 10.1002/ajmg.a.38502.

Cox, L. L., Cox, T. C., Moreno Uribe, L. M., Zhu, Y., Richter, C. T., Nidey, N., … Hing, A. V., … Glass, I. A., … Roscioli, T. (2018). Mutations in the epithelial Cadherin-p120-Catenin complex cause Mendelian non-syndromic cleft lip with or without cleft palate. American Journal of Human Genetics, 102, 1143-1157. PMCID: PMC5992119. doi: 10.1016/j.ajhg.2018.04.009.

Gauthier, J., Meijer, I. A., Lessel, D., Mencacci, N. E., Krainc, D., Hempel, M., … Glass, I. A., … Campeau, P. M. (2018). Recessive mutations in >VPS13D cause childhood onset movement disorders. Annals of Neurology, 83, 1089-1095. doi: 10.1002/ana.25204.

Neradugomma, N. K., Drafton, K., O'Day, D. R., Liao, M. Z., Han, L. W., Glass, I. A., Mao, Q. (2018). Marijuana use differentially affects cannabinoid receptor expression in early gestational human endometrium and placenta. Placenta, 66, 36-39. PMCID: PMC5995327. doi: 10.1016/j.placenta.2018.05.002.

Strongin, A., Heller, T., Doherty, D. A., Glass, I. A., Parisi, M. A., Bryant, J., … NISC Comparative Sequencing Program. (2018). Characteristics of liver disease in 100 individuals with Joubert syndrome prospectively evaluated at a single center. Journal of Pediatric Gastroenterology and Nutrition, 66, 428-435. PMCID: PMC5825259. doi: 10.1097/MPG.0000000000001816.

Whitley, B., Lam, C., Cui, H., Haude, K., Bai, R., Escobar, L., … Glass, I. A., Hoppins, S. (2018). Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes. Human Molecular Genetics, 27, 3710-3719. doi: 10.1093/hmg/ddy287. Joan M. Goverman

Pierson, E. R., Wagner, C. A., Goverman, J. M. (2018). The contribution of neutrophils to CNS autoimmunity. Clinical Immunology, 189, 23-28. PMCID: PMC5203971.doi: 10.1016/j.clim.2016.06.017.

Thomas J. Grabowski, Jr.

Edlow, B. L., Keene, C. D., Perl, D. P., Iacono, D., Folkerth, R. D., Stewart, W., … Grabowski, T. J., … Dams-O'Connor, K. (2018). Multimodal characterization of the late effects of traumatic brain injury: A methodological overview of the late effects of traumatic brain injury project. Journal of Neurotrauma, 35, 1604-1619. PMCID: PMC6016096. doi: 10.1089/neu.2017.5457.

Weaver, K. E., Poliakov, A., Novotny, E. J., Jr., Olson, J. D., Grabowski, T. J., Ojemann, J. G. (2018). Electrocorticography and the early maturation of high-frequency suppression within the default mode network. Journal of Neurosurgery. Pediatrics, 21, 133-140. doi: 10.3171/2017.7.PEDS17269.

Michael J. Guralnick

Estes, A. M., Munson, J., John, T. S., Dager, S. R., Rodda, A., Botteron, K., … Guralnick, M. J., IBIS Network. (2018). Parent support of preschool peer relationships in younger siblings of children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 48, 1122-1132. PMCID: PMC5738288. doi: 10.1007/s10803-017-3202-5.

Robert Hevner Adams Waldorf, K. M., Nelson, B. R., Stencel-Baerenwald, J. E., Studholme, C., Kapur, R. P., Armistead, B., … Shaw, D. W. W., … Dobyns, W. B., Hevner, R. F., … Rajagopal, L. (2018). Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brain. Nature Medicine, 24, 368-374. PMCID: PMC5839998. doi: 10.1038/nm.4485.

Anne Hing Cox, L. L., Cox, T. C., Moreno Uribe, L. M., Zhu, Y., Richter, C. T., Nidey, N., … Hing, A. V., … Glass, I. A., … Roscioli, T. (2018). Mutations in the epithelial Cadherin-p120-Catenin complex cause Mendelian non-syndromic cleft lip with or without cleft palate. American Journal of Human Genetics, 102, 1143-1157. PMCID: PMC5992119. doi: 10.1016/j.ajhg.2018.04.009.

David Horn Coppess, S., Padia, R., Horn, D. L., Parikh, S. R., Inglis, A., Bly, R., … Johnson, K. (2018). Standardizing laryngeal cleft evaluations: Reliability of the interarytenoid assessment protocol. Otolaryngology--Head and Neck Surgery, 194599818806283. doi: 10.1177/0194599818806283.

Marshall S. Horwitz Farr Zuend, C., Nomellini, J. F., Smit, J., Horwitz, M. S. (2018). Generation of a dual-target, safe, inexpensive microbicide that protects against HIV-1 and HSV-2 disease. Scientific Reports, 8, 2786. PMCID: PMC5809452. doi: 10.1038/s41598-018-21134-1.

Hart, M. R., Anderson, D. J., Porter, C. C., Neff, T., Levin, M., Horwitz, M. S. (2018). Activating PAX gene family paralogs to complement PAX5 leukemia driver mutations. PLoS Genetics, 14, e1007642. doi: 10.1371/journal.pgen.1007642.

Volejnikova, J., Zapletalova, J., Jarosova, M., Urbankova, H., Petr, V., Klaskova, E., Horwitz, M. S., … Mihal, V. (2018). Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A case report. Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 162, 65-70. doi: 10.5507/bp.2018.002.

Nina Isoherranen Grant, K. S., Petroff, R., Isoherranen, N., Stella, N., Burbacher, T. M. (2018). Cannabis use during pregnancy: Pharmacokinetics and effects on child development. Pharmacology and Therapeutics, 182, 133-151. doi: 10.1016/j.pharmthera.2017.08.014.

Lefebvre, K. A., Hendrix, A., Halaska, B., Duignan, P., Shum, S., Isoherranen, N., Marcinek, D. J., Gulland, F. M. D. (2018). Domoic acid in California sea lion fetal fluids indicates continuous exposure to a neuroteratogen poses risks to mammals. Harmful Algae, 79, 53-57. doi: 10.1016/j.hal.2018.06.003.

Suman Jayadev Chang, I. J., Adam, M. P., Jayadev, S., Bird, T. D., Natarajan, N., Glass, I. A. (2018). Novel pregnancy-triggered episodes of CAPOS syndrome. American Journal of Medical Genetics. Part A, 176, 235-240. PMCID: PMC5726903. doi: 10.1002/ajmg.a.38502.

Ferreccio, A., Mathieu, J., Detraux, D., Somasundaram, L., Cavanaugh, C., Sopher, B., … Jayadev, S., … Ruohola-Baker, H. (2018). Inducible CRISPR genome editing platform in naive human embryonic stem cells reveals JARID2 function in self-renewal. Cell Cycle, 17, 535-549. PMCID: PMC5969550. doi: 10.1080/15384101.2018.1442621.

Tsuang, D. W., Greenwood, T. A., Jayadev, S., Davis, M., Shutes-David, A., Bird, T. D. (2018). A genetic study of psychosis in Huntington's disease: Evidence for the involvement of glutamate signaling pathways. Journal of Huntington’s Disease, 7, 51-59. doi: 10.3233/JHD-170277.

Turk, K. W., Flanagan, M. E., Josephson, S., Keene, C. D., Jayadev, S., Bird, T. D. (2018). Psychosis in spinocerebellar ataxias: A case series and study of Tyrosine Hydroxylase in substantia Nigra. Cerebellum (London, England), 17. 143-151. PMCID: PMC5843512. doi: 10.1007/s12311-017-0882-5.

Tracy Jirikowic Wagner, B., Fitzpatrick, J. P., Mazzucchelli, T. G., Symons, M., Carmichael Olson, H., Jirikowic, T. L., Cross, D. J., … Latimer, J. (2018). Study protocol for a self-controlled cluster randomised trial of the Alert Program to improve self-regulation and executive function in Australian Aboriginal children with fetal alcohol spectrum disorder. BMJ Open, 8, e021462. PMCID: PMC5875644. doi: 10.1136/bmjopen-2017-021462.

Sandra Juul

Brandler, W. M., Antaki, D., Gujral, M., Kleiber, M. L., Whitney, J., Maile, M. S., … Juul, S. E., … Sebat, J. (2018). Paternally inherited cis-regulatory structural variants are associated with autism. Science, 360, 327-331. doi: 10.1126/science.aan2261.

Dhillon, S. K., Lear, C. A., Galinsky, R., Wassink, G., Davidson, J. O., Juul, S. E., … Bennet, L. (2018). The fetus at the tipping point: Modifying the outcome of fetal asphyxia. The Journal of Physiology, 596, 5571-5592. doi: 10.1113/JP274949.

German, K., Vu, P. T., Grelli, K. N., Denton, C., Lee, G., Juul, S. E. (2018). Zinc protoporphyrin-to-heme ratio and ferritin as measures of iron sufficiency in the neonatal intensive care unit. The Journal of Pediatrics,194, 47-53. doi: 10.1016/j.jpeds.2017.10.041.

Juul, S. E., Comstock, B. A., Heagerty, P. J., Mayock, D. E., Goodman, A. M., Hauge, S., … Wu, Y. W. (2018). High-dose erythropoietin for asphyxia and encephalopathy (HEAL): A randomized controlled trial - background, aims, and study protocol. Neonatology, 113, 331-338. PMCID: PMC5980685. doi: 10.1159/000486820.

Massaro, A. N., Wu, Y. W., Bammler, T. K., Comstock, B., Mathur, A., McKinstry, R. C., … Juul, S. E. (2018). Plasma biomarkers of brain injury in neonatal hypoxic-ischemic encephalopathy.The Journal of Pediatrics, 194, 67-75 e1. doi: 10.1016/j.jpeds.2017.10.060.

Snyder, J. M., Wood, T. R., Corry, K., Moralejo, D. H., Parikh, P., Juul, S. E. (2018). Ontogeny of white matter, toll-like receptor expression, and motor skills in the neonatal ferret. International Journal of Developmental Neuroscience, 70, 25-33. doi: 10.1016/j.ijdevneu.2018.05.006.

Starr, M. C., Askenazi, D. J., Goldstein, S. L., MacDonald, J. W., Bammler, T. K., Afsharinejad, Z., … Juul, S. E., … Hingorani, S. R. (2018). Impact of processing methods on urinary biomarkers analysis in neonates. Pediatric Nephrology, 33, 181-186. PMCID: PMC5700848. doi: 10.1007/s00467-017-3779-0.

Wassink, G., Davidson, J. O., Lear, C. A., Juul, S. E., Northington, F., Bennet, L., Gunn, A. J. (2018). A working model for hypothermic neuroprotection. The Journal of Physiology, 596, 5641-5654. doi: 10.1113/JP274928.

Franck Kalume

Carspecken, C. W., Chanprasert, S., Kalume, F., Sedensky, M. M., Morgan, P. G. (2018). Anesthetics have different effects on the electrocorticographic spectra of wild-type and mitochondrial mutant mice. Anesthesiology, 129, 744-755. PMCID: PMC6148376. doi: 10.1097/ALN.0000000000002368.

Raj P. Kapur Aceto, N., Bardia, A., Wittner, B. S., Donaldson, M. C., O'Keefe, R., Engstrom, A., … Kapur, R. P., … Maheswaran, S. (2018). AR expression in breast cancer CTCs associates with bone metastases. Molecular Cancer Research, 16, 720-727. PMCID: PMC5882540. doi: 10.1158/1541-7786.MCR-17-0480.

Appelbaum, J., Wells, D., Hiatt, J. B., Steinbach, G., Stewart, F. M., Thomas, H., … Kapur, R. P., … Bhatia, S. (2018). Fatal enteric plexus neuropathy after one dose of ipilimumab plus nivolumab: A case report. Journal for Immunotherapy of Cancer, 6, 82. PMCID: PMC6117974. doi: 10.1186/s40425-018-0396-9.

El Demellawy, D., Lee, J. Y., McDonell, L., Dyment, D. A., Knisely, A. S., McGowan-Jordan, J., … Kapur, R. P., Nasr, A. (2018). Atypical hepatic mesenchymal hamartoma: Histologic appearance, immunophenotype, and molecular findings. Pediatric and Developmental Pathology, 1093526618806750. doi: 10.1177/1093526618806750.

Hwang, S., Rudd, M. K., Finch, L., Peterson, S. E., Kapur, R. P. (2018). VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5. American Journal of Medical Genetics. Part A, 176, 502-504. doi: 10.1002/ajmg.a.38579.

Jenkins, Z. A., Macharg, A., Chang, C. Y., van Kogelenberg, M., Morgan, T., Frentz, S., … Kapur, R. P., Robertson, S. P. (2018). Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies. Human Mutation, 39, 103-113. doi: 10.1002/humu.23355.

Kapur, R. P., Reyes-Mugica, M. (2018). Intestinal neuronal dysplasia type B: An updated review of a problematic diagnosis. Archives of Pathology & Laboratory Medicine, 8 Aug 2018. doi: 10.5858/arpa.2017-0524-RA.

Lannon, S. M. R., Adams Waldorf, K. M., Fiedler, T., Kapur, R. P., Agnew, K., Rajagopal, L., … Fredricks, D. N. (2018). Parallel detection of lactobacillus and bacterial vaginosis-associated bacterial DNA in the chorioamnion and vagina of pregnant women at term. The Journal of Maternal-Fetal & Neonatal Medicine: The Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 1-9. 12 Mar 2018. PMCID: PMC6135717. doi: 10.1080/14767058.2018.1446208.

Thaker, A. I., Kapur, R. P. (2018). Colonic adventitial fibromuscular dysplasia: A nonspecific arteriopathy associated with hirschsprung disease and other obstructive disorders. Pediatric and Developmental Pathology: The Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society, 21, 363-370. doi: 10.1177/1093526617739772.

Sara T. Kover

Abdelaziz, A., Kover, S. T., Wagner, M., Naigles, L. R. (2018). The shape bias in children with autism spectrum disorder: Potential sources of individual differences. Journal of Speech, Language, and Hearing Research, 61, 2685-2702. doi: 10.1044/2018_JSLHR-L-RSAUT-18-0027.

Kover, S. T. (2018). Distributional cues to language learning in children with intellectual disabilities. Language, Speech, and Hearing Services in Schools, 49, 653-667. doi: 10.1044/2018_LSHSS-STLT1-17-0128.

Venker, C. E., Bean, A., Kover, S. T. (2018). Auditory-visual misalignment: A theoretical perspective on vocabulary delays in children with ASD. Autism Research, 11, 1621-1628. doi: 10.1002/aur.2038.

Patricia Kuhl Ferjan Ramirez, N., Lytle, S. R., Fish, M., Kuhl, P. K. (2018). Parent coaching at 6 and 10 months improves language outcomes at 14 months: A randomized controlled trial. Developmental Science, e12762. doi: 10.1111/desc.12762.

Lin, J. L., Imada, T., Kuhl, P. K., Lin, F. H. (2018). Incongruent pitch cues are associated with increased activation and functional connectivity in the frontal areas. Scientific Reports, 8, 5206. PMCID: PMC5980092. doi: 10.1038/s41598-018-23287-5.

Lytle, S. R., Garcia-Sierra, A., Kuhl, P. K. (2018). Two are better than one: Infant language learning from video improves in the presence of peers. Proceedings of the National Academy of Sciences of the United States of America, 115, 9859-9866. PMCID: PMC6176610. doi: 10.1073/pnas.1611621115.

Mamiya, P. C., Richards, T. L., Kuhl, P. K. (2018). Right forceps minor and anterior thalamic radiation predict executive function skills in young bilingual adults. Frontiers in Psychology, 9, 118. PMCID: PMC5811666. doi: 10.3389/fpsyg.2018.00118.

Zhao, T. C., Kuhl, P. K. (2018). Linguistic effect on speech perception observed at the brainstem. Proceedings of the National Academy of Sciences of the United States of America, 115, 8716-8721. PMCID: PMC6126758. doi: 10.1073/pnas.1800186115.

Adrian K.C. Lee Atilgan, H., Town, S. M., Wood, K. C., Jones, G. P., Maddox, R. K., Lee, A. K. C., Bizley, J. K. (2018). Integration of visual information in auditory cortex promotes auditory scene analysis through multisensory binding. Neuron, 97, 640-655 e4. PMCID: PMC5814679. doi: 10.1016/j.neuron.2017.12.034.

Clarke, C. M., Fok, V. T., Gustafson, J. A., Smyth, M. D., Timms, A. E., Frazar, C. D., … Lee, A. K. C., … Cunningham, M. L. (2018). Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. American Journal of Medical Genetics. Part A, 176, 290-300. PMCID: PMC5768450. doi: 10.1002/ajmg.a.38540.

McCloy, D. R., Larson, E., Lee, A. K. C. (2018). Auditory attention switching with listening difficulty: Behavioral and pupillometric measures. Journal of the Acoustical Society of America, 144, 2764. PMCID: PMC6232045. doi: 10.1121/1.5078618.

Maddox, R. K., Lee, A. K. C. (2018). Auditory brainstem responses to continuous natural speech in human listeners. eNeuro, 5, PMCID: PMC5806592. doi: 10.1523/ENEURO.0441-17.2018.

Wang, A. C., Ibrahim, G. M., Poliakov, A. V., Wang, P. I., Fallah, A., Mathern, G. W., … Shaw, D. W. W., … Novotny, E. J., Jr., Lee, A. K. C., … Ojemann, J. G. (2018). Corticospinal tract atrophy and motor fMRI predict motor preservation after functional cerebral hemispherectomy. Journal of Neurosurgery. Pediatrics, 21, 81-89. doi: 10.3171/2017.7.PEDS17137.

Donghoon Lee

Ali Murat Maga Oesch, G., Maga, A. M., Friedman, S. D., Poliachik, S. L., Budech, C. B., Wright, J. N., … Gospe, S. M., Jr. (2018). Geometric morphometrics reveal altered corpus callosum shape in pyridoxine-dependent epilepsy. Neurology, 91, e78-e86. doi: 10.1212/WNL.0000000000005748.

Roosenboom, J., Lee, M. K., Hecht, J. T., Heike, C. L., Wehby, G. L., Christensen, K., … Maga, A. M., … Weinberg, S. M. (2018). Mapping genetic variants for cranial vault shape in humans. PLoS One, 13, e0196148. PMCID: PMC5919379. doi: 10.1371/journal.pone.0196148.

Kenneth Maravilla McDonald, R. J., Levine, D., Weinreb, J., Kanal, E., Davenport, M. S., Ellis, J. H., … Maravilla, K. R., … Kressel, H. Y. (2018). Gadolinium retention: A research roadmap from the 2018 NIH/ACR/RSNA Workshop on gadolinium chelates. Radiology, 289, 517-534. doi: 10.1148/radiol.2018181151.

David Marcinek Kramer, P. A., Duan, J., Gaffrey, M. J., Shukla, A. K., Wang, L., Bammler, T. K., … Marcinek, D. J. (2018). Fatiguing contractions increase protein S-glutathionylation occupancy in mouse skeletal muscle. Redox Biology, 17, 367-376. PMCID: PMC6007084. doi: 10.1016/j.redox.2018.05.011.

Moyer, C. E., Hiolski, E. M., Marcinek, D. J., Lefebvre, K. A., Smith, D. R., Zuo, Y. (2018). Repeated low level Domoic acid exposure increases CA1 VGluT1 levels, but not bouton density, VGluT2 or VGAT levels in the hippocampus of adult mice. Harmful Algae, 79, 74-86. doi: 10.1016/j.hal.2018.08.008.

Katie A. McLaughlin Galbraith, T., Carliner, H., Keyes, K. M., McLaughlin, K. A., McCloskey, M. S., Heimberg, R. G. (2018). The co-occurrence and correlates of anxiety disorders among adolescents with intermittent explosive disorder. Aggressive Behavior, 44, 581-590. doi: 10.1002/ab.21783.

Heleniak, C., King, K. M., Monahan, K. C., McLaughlin, K. A. (2018). Disruptions in emotion regulation as a mechanism linking community violence exposure to adolescent internalizing problems. Journal of Research on Adolescence, 28, 229-244. doi: 10.1111/jora.12328.

Jenness, J. L., Rosen, M. L., Sambrook, K. A., Dennison, M. J., Lambert, H. K., Sheridan, M. A., McLaughlin, K. A. (2018). Violence exposure and neural systems underlying working memory for emotional stimuli in youth. Developmental Psychopathology, 30, 1517-1528. doi: 10.1017/S0954579417001638.

Logue, M. W., van Rooij, S. J. H., Dennis, E. L., Davis, S. L., Hayes, J. P., Stevens, J. S., … McLaughlin, K. A., … Morey, R. A. (2018). Smaller hippocampal volume in posttraumatic stress disorder: A multisite ENIGMA-PGC study: Subcortical volumetry results from posttraumatic stress disorder consortia. Biological Psychiatry, 83, 244-253. doi: 10.1016/j.biopsych.2017.09.006.

Platt, J. M., Keyes, K. M., McLaughlin, K. A., Kaufman, A. S. (2018). Intellectual disability and mental disorders in a US population representative sample of adolescents. Psychological Medicine, 1-10. doi: 10.1017/S0033291718001605.

Rosen, M. L., Sheridan, M. A., Sambrook, K. A., Peverill, M. R., Meltzoff, A. N., McLaughlin, K. A. (2018). The role of visual association cortex in associative memory formation across development. Journal of Cognitive Neuroscience, 30, 365-380. PMCID: PMC5792361. doi: 10.1162/jocn_a_01202.

Heather Mefford Bozarth, X., Dines, J. N., Cong, Q., Mirzaa, G. M., Foss, K., Lawrence Merritt, J., 2nd, … Mefford, H. C., Novotny, E. J., Jr. (2018). Expanding clinical phenotype in CACNA1C related disorders: From neonatal onset severe epileptic encephalopathy to late-onset epilepsy. American Journal of Medical Genetics. Part A, 176, 2733-2739. PMCID: PMC6312477. doi: 10.1002/ajmg.a.40657.

Bozarth, X., Foss, K., Mefford, H. C. (2018). A de novo in-frame deletion of CASK gene causes early onset infantile spasms and supratentorial cerebral malformation in a female patient. American Journal of Medical Genetics. Part A, 176, 2425-2429. doi: 10.1002/ajmg.a.40429.

Carvill, G. L., Engel, K. L., Ramamurthy, A., Cochran, J. N., Roovers, J., Stamberger, H., … Mefford, H. C. (2018). Aberrant inclusion of a poison exon causes Dravet syndrome and related SCN1A-associated genetic epilepsies. American Journal of Human Genetics, 103, 1022-1029. PMCID: PMC6288405. doi: 10.1016/j.ajhg.2018.10.023.

Carvill, G. L., Liu, A., Mandelstam, S., Schneider, A., Lacroix, A., Zemel, M., … Zhang, J., … Mefford, H. C., Scheffer, I. E. (2018). Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45. Epilepsia, 59, e5-e13. PMCID: PMC5760358. doi: 10.1111/epi.13957.

Chatron, N., Moller, R. S., Champaigne, N. L., Schneider, A. L., Kuechler, A., Labalme, A., … Mefford, H. C., … Lesca, G. (2018). The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. Annals of Neurology, 83, 926-934. PMCID: PMC6021218. doi: 10.1002/ana.25222.

Dines, J. N., Golden-Grant, K., LaCroix, A., Muir, A. M., Cintron, D. L., McWalter, K., … Mefford, H. C. (2018). TANGO2: Expanding the clinical phenotype and spectrum of pathogenic variants. Genetics in Medicine, 24 Sept 2018. doi: 10.1038/s41436-018-0137-y.

Esterhuizen, A. I., Mefford, H. C., Ramesar, R. S., Wang, S., Carvill, G. L., Wilmshurst, J. M. (2018). Dravet syndrome in South African infants: Tools for an early diagnosis. Seizure, 62, 99-105. doi: 10.1016/j.seizure.2018.09.010.

Fry, A. E., Fawcett, K. A., Zelnik, N., Yuan, H., Thompson, B. A. N., Shemer-Meiri, L., … Zhang, J., … Mirzaa, G. M., … Mefford, H. C., Dobyns, W. B., … Pilz, D. T. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain, 22 Jan 2018. PMCID: PMC5837214. doi: 10.1093/brain/awx358.

Gregor, A., Sadleir, L. G., Asadollahi, R., Azzarello-Burri, S., Battaglia, A., Ousager, L. B., … Mefford, H. C., … Zweier, C. (2018). De novo variants in the F-BOX protein FBX011 in 20 individuals with a variable neurodevelopmental disorder. American Journal of Human Genetics, 103, 305-316. PMCID: PMC6080769. doi: 10.1016/j.ajhg.2018.07.003.

Helbig, I., Heinzen, E. L., Mefford, H. C., International League Against Epilepsy Genetics Commission. (2018). Genetic literacy series: Primer part 2-Paradigm shifts in epilepsy genetics. Epilepsia, 59, 1138-1147. doi: 10.1111/epi.14193.

Helbig, I., Riggs, E. R., Barry, C. A., Klein, K. M., Dyment, D., Thaxton, C., … Mirzaa, G. M., … Mefford, H. C. (2018). The ClinGen Epilepsy Gene Curation Expert Panel-Bridging the divide between clinical domain knowledge and formal gene curation criteria. Human Mutation, 39, 1476-1484. doi: 10.1002/humu.23632.

Helbig, K. L., Lauerer, R. J., Bahr, J. C., Souza, I. A., Myers, C. T., Uysal, B., … Mefford, H. C. (2018). De novo pathogenic variants in cacna1e cause developmental and epileptic encephalopathy with contractures, macrocephaly, and dyskinesias. American Journal of Human Genetics, 103, 666-678. PMCID: PMC6216110. doi: 10.1016/j.ajhg.2018.09.006.

Howell, K. B., Eggers, S., Dalziel, K., Riseley, J., Mandelstam, S., Myers, C. T., … Mefford, H. C., … Harvey, A. S. (2018). A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancy. Epilepsia, 59, 1177-1187. PMCID: PMC5990455. doi: 10.1111/epi.14087.

Johannesen, K. M., Gardella, E., Linnankivi, T., Courage, C., de Saint Martin, A., Lehesjoki, A. E., … Mefford, H. C., Moller, R. S. (2018). Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia, 59, 389-402. PMCID: PMC5912688. doi: 10.1111/epi.13986.

Kumar, R., Gardner, A., Homan, C. C., Douglas, E., Mefford, H. C., Wieczorek, D., … Gecz, J. (2018). Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery. Human Mutation, 39, 1126-1138. doi: 10.1002/humu.23557.

Mefford, H. C. (2018). Expanding role of GABAA receptors in generalised epilepsies. The Lancet Neurology, 17, 657-658. doi: 10.1016/S1474-4422(18)30252-7.

Mulhern, M. S., Stumpel, C., Stong, N., Brunner, H. G., Bier, L., Lippa, N., … Mefford, H. C., … Sands, T. T. (2018). NBEA: Developmental disease gene with early generalized epilepsy phenotypes. Annals of Neurology, 84, 788-795. doi: 10.1002/ana.25350.

Myers, C. T., Hollingsworth, G., Muir, A. M., Schneider, A. L., Thuesmunn, Z., Knupp, A., … Mefford, H. C. (2018). Parental mosaicism in "de novo" epileptic encephalopathies. The New England Journal of Medicine, 378, 1646-1648. PMCID: PMC5966016. doi: 10.1056/NEJMc1714579.

Ottman, R., Freyer, C., Mefford, H. C., Poduri, A., Lowenstein, D. H., Epilepsy Return of Results Workshop Participants (2018). Return of individual results in epilepsy genomic research: A view from the field. Epilepsia, 59, 1635-1642. PMCID: PMC6119474. doi: 10.1111/epi.14530.

Andrew Meltzoff Meltzoff, A. N., Ramirez, R. R., Saby, J. N., Larson, E., Taulu, S., Marshall, P. J. (2018). Infant brain responses to felt and observed touch of hands and feet: An MEG study. Developmental Science, 21, e12651. PMCID: PMC6045975. doi: 10.1111/desc.12651.

Meltzoff, A. N., Murray, L., Simpson, E., Heimann, M., Nagy, E., Nadel, J., … Ferrari, P. F. (2018). Eliciting imitation in early infancy. Developmental Science, e12738. doi: 10.1111/desc.12738.

Meltzoff, A. N., Saby, J. N., Marshall, P. J. (2018). Neural representations of the body in 60-day-old human infants. Developmental Science, e12698. doi: 10.1111/desc.12698.

Shen, G., Smyk, N. J., Meltzoff, A. N., Marshall, P. J. (2018). Using somatosensory mismatch responses as a window into somatotopic processing of tactile stimulation. Psychophysiology, 55, e13030. doi: 10.1111/psyp.13030.

Shen, G., Meltzoff, A. N., Marshall, P. J. (2017). Touching lips and hearing fingers: Effector-specific congruency between tactile and auditory stimulation modulates N1 amplitude and alpha desynchronization. Experimental Brain Research, 236, 13-29. doi: 10.1007/s00221-017-5104-3.

Shen, G., Weiss, S. M., Meltzoff, A. N., Marshall, P. J. (2018). The somatosensory mismatch negativity as a window into body representations in infancy. International Journal of Psychophysiology, 134, 144-150. doi: 10.1016/j.ijpsycho.2018.10.013.

Weiss, S. M., Meltzoff, A. N., Marshall, P. J. (2018). Neural measures of anticipatory bodily attention in children: Relations with executive function. Developmental Cognitive Neuroscience, 34, 148-158. doi: 10.1016/j.dcn.2018.08.002.

Kathleen J. Millen Aruga, J., Millen, K. J. (2018). ZIC1 function in normal cerebellar development and human developmental pathology. Advances in Experimental Medicine and Biology, 1046, 249-268. doi: 10.1007/978-981-10-7311-3_13.

Haldipur, P., Dang, D., Millen, K. J. (2018). Embryology. Handbook of Clinical Neurology, 154, 29-44. doi: 10.1016/B978-0-444-63956-1.00002-3.

Kridsada, K., Niu, J., Haldipur, P., Wang, Z., Ding, L., Li, J. J., … Millen, K. J., Luo, W. (2018). Roof plate-derived radial glial-like cells support developmental growth of rapidly adapting mechanoreceptor ascending axons. Cell Reports, 23, 2928-2941. doi: 10.1016/j.celrep.2018.05.025.

Ghayda Mirzaa

Bozarth, X., Dines, J. N., Cong, Q., Mirzaa, G. M., Foss, K., Lawrence Merritt, J., 2nd, … Mefford, H. C., Novotny, E. J., Jr. (2018). Expanding clinical phenotype in CACNA1C related disorders: From neonatal onset severe epileptic encephalopathy to late-onset epilepsy. American Journal of Medical Genetics. Part A, 176, 2733-2739. PMCID: PMC6312477. doi: 10.1002/ajmg.a.40657.

Fry, A. E., Fawcett, K. A., Zelnik, N., Yuan, H., Thompson, B. A. N., Shemer-Meiri, L., … Zhang, J., … Mirzaa, G. M., … Mefford, H. C., Dobyns, W. B., … Pilz, D. T. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain, 22 Jan 2018. PMCID: PMC5837214. doi: 10.1093/brain/awx358.

Marcogliese, P. C., Shashi, V., Spillmann, R. C., Stong, N., Rosenfeld, J. A., Koenig, M. K., … Mirzaa, G. M., … Pena, L. D. M. (2018). IRF2BPL is associated with neurological phenotypes. American Journal of Human Genetics, 103, 456. PMCID: PMC6128320. doi: 10.1016/j.ajhg.2018.08.010.

Martinelli, S., Krumbach, O. H. F., Pantaleoni, F., Coppola, S., Amin, E., Pannone, L., … Mirzaa, G. M. (2018). Functional dysregulation of CDC42 causes diverse developmental phenotypes. American Journal of Human Genetics, 102, 309-320. PMCID: PMC5985417. doi: 10.1016/j.ajhg.2017.12.015.

Piacitelli, A. M., Jensen, D. M., Brandling-Bennett, H., Gray, M. M., Batra, M., Gust, J., … Mirzaa, G. M., Bennett, J. T. (2018). Characterization of a severe case of PIK3CA-related overgrowth at autopsy by droplet digital polymerase chain reaction and report of PIK3CA sequencing in 22 patients. American Journal of Medical Genetics. Part A, 176, 2301-2308. doi: 10.1002/ajmg.a.40487.

Priolo, M., Schanze, D., Tatton-Brown, K., Mulder, P. A., Tenorio, J., Kooblall, K., … Mirzaa, G. M., … Hennekam, R. C. (2018). Further delineation of Malan syndrome. Human Mutation, 39, 1226-1237. doi: 10.1002/humu.23563.

Ruggeri, G., Timms, A. E., Cheng, C., Weiss, A., Kollros, P., Chapman, T., Tully, H. M., Mirzaa, G. M. (2018). Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. American Journal of Medical Genetics. Part A, 176, 676-681. PMCID: PMC5871351. doi: 10.1002/ajmg.a.38592.

Shukla, A., Saneto, R. P., Hebbar, M., Mirzaa, G. M., Girisha, K. M. (2018). A neurodegenerative mitochondrial disease phenotype due to biallelic loss-of-function variants in PNPLA8 encoding calcium-independent phospholipase A2gamma. American Journal of Medical Genetics. Part A, 176, 1232-1237. PMCID: PMC5918416. doi: 10.1002/ajmg.a.38687.

Stutterd, C., McGillivray, G., Stark, Z., Messazos, B., Cameron, F., White, S., … Mirzaa, G. M., Leventer, R. (2018). Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway. European Journal of Medical Genetics, 61, 738-740. doi: 10.1016/j.ejmg.2018.06.002.

Cecilia B. Moens Kidwell, C. U., Su, C. Y., Hibi, M., Moens, C. B. (2018). Multiple zebrafish Atoh1 genes specify a diversity of neuronal types in the zebrafish cerebellum. Developmental Biology, 438, 44-56. PMCID: PMC5915903. doi: 10.1016/j.ydbio.2018.03.004.

Poudel, K. R., Roh-Johnson, M., Su, A., Ho, T., Mathsyaraja, H., Anderson, S., … Moens, C. B., … Bai, J. (2018). Competition between TIAM1 and membranes balances endophilin A3 activity in cancer metastasis. Developmental Cell, 45, 738-752 e6. PMCID: PMC6095642.doi: 10.1016/j.devcel.2018.05.021.

David Morris Pareek, G., Thomas, R. E., Vincow, E. S., Morris, D. R., Pallanck, L. J. (2018). Lon protease inactivation in Drosophila causes unfolded protein stress and inhibition of mitochondrial translation. Cell Death Discovery, 5, 51. PMCID: PMC6197249.doi: 10.1038/s41420-018-0110-1.

Richard Morrison Gilmore-Hall, S., Kuo, J., Ward, J. M., Zahra, R., Morrison, R. S., Perkins, G., La Spada, A. R. (2018). CCP1 promotes mitochondrial fusion and motility to prevent Purkinje cell neuron loss in pcd mice. Journal of Cell Biology, 18 Oct 2018. doi: 10.1083/jcb.201709028.

Morrison, R. S., Aldridge, M. D., Block, J., Chiu, L., Maroney, C., Morrison, C. A., Meier, D. E. (2018). The national palliative care research center: 10 years of promoting and developing research in palliative care. Journal of Palliative Medicine, 21, 1548-1557. doi: 10.1089/jpm.2018.0204.

Wang, D. B., Kinoshita, C., Kinoshita, Y., Sopher, B. L., Uo, T., Lee, R. J., … Murphy, S. P., … Garden, G. A., Morrison, R. S. (2018). Neuronal susceptibility to beta-amyloid toxicity and ischemic injury involves histone deacetylase-2 regulation of endophilin-B1. Brain Pathology (Zurich, Switzerland).20 Jul 2018. doi: 10.1111/bpa.12647.

Pierre D. Mourad Mourad, P. D., Friedly, J. L., McClintic, A. M., Olmstead, T. A., Loeser, J. D. (2018). Intense focused ultrasound preferentially stimulates transected nerves within residual limbs: Pilot study. Pain Medicine, 19, 541-549. doi: 10.1093/pm/pnx188.

Olmstead, T. A., Chiarelli, P. A., Griggs, D. J., McClintic, A. M., Myroniv, A. N., Mourad, P. D. (2018). Transcranial and pulsed focused ultrasound that activates brain can accelerate remyelination in a mouse model of multiple sclerosis. Journal of Therapeutic Ultrasound, 6, 11. PMCID: PMC6287362. doi: 10.1186/s40349-018-0119-1.

Webb, S. J., Mourad, P. D. (2018). Prenatal ultrasonography and the incidence of autism spectrum disorder. JAMA Pediatrics, 172, 319-320. doi: 10.1001/jamapediatrics.2017.5685.

Jeffrey Munson Chapman, N. H., Bernier, R. A., Webb, S. J., Munson, J., Blue, E. M., Chen, D. H., … Raskind, W. H., Wijsman, E. M. (2018). Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder. Human Genetics, 137, 807-815. doi: 10.1007/s00439-018-1939-3.

Rogers, S. J., Estes, A. M., Vismara, L., Munson, J., Zierhut, C., Greenson, J., … Talbott, M. (2018).Enhancing low-intensity coaching in parent implemented Early Start Denver Model intervention for early autism: A randomized comparison treatment trial. Journal of Autism and Developmental Disorders. 10 Sep 2018. doi: 10.1007/s10803-018-3740-5.

Scott Murray Millin, R., Kolodny, T., Flevaris, A. V., Kale, A. M., Schallmo, M. P., Gerdts, J., Bernier, R. A., Murray, S. O. (2018). Reduced auditory cortical adaptation in autism spectrum disorder. eLife, 7, PMCID: PMC6203433. doi: 10.7554/eLife.36493.

Michael Mustari Lienbacher, K., Ono, S., Fleuriet, J., Mustari, M. J., Horn, A. K. E. (2018). A subset of palisade endings only in the medial and inferior rectus muscle in monkey contain calretinin. Investigative Ophthalmology & Visual Science, 59, 2944-2954. PMCID: PMC5989861. doi: 10.1167/iovs.18-24322.

Pallus, A. C., Walton, M. M. G., Mustari, M. J. (2018). Activity of near response cells during disconjugate saccades in strabismic monkeys. Journal of Neurophysiology,15 Aug 2018 doi: 10.1152/jn.00219.2018.

Pallus, A. C., Walton, M. M. G., Mustari, M. J. (2018). Response of supraoculomotor area neurons during combined saccade-vergence movements. Journal of Neurophysiology, 119, 585-596. PMCID: PMC5867375. doi: 10.1152/jn.00193.2017.

Elizabeth A. Nance Alnasser, Y., Kambhampati, S. P., Nance, E., Rajbhandari, L., Shrestha, S., Venkatesan, A., … Kannan, S. (2018). Preferential and increased uptake of hydroxyl-terminated PAMAM dendrimers by activated microglia in rabbit brain mixed glial culture. Molecules, 23, doi: 10.3390/molecules23051025.

Nance, E., Kambhampati, S. P., Smith, E. S., Zhang, Z., Zhang, F., Singh, S., … Kannan, S. (2018). Correction to: Dendrimer-mediated delivery of N-acetyl cysteine to microglia in a mouse model of Rett syndrome. Journal of Neuroinflammation, 15, 14. PMCID: PMC5766996. doi: 10.1186/s12974-018-1056-1.

Edward J. Novotny, Jr.

Coryell, J., Gaillard, W. D., Shellhaas, R. A., Grinspan, Z. M., Wirrell, E. C., Knupp, K. G., … Novotny, E. J., Jr., … Berg, A. T. (2018). Neuroimaging of early life epilepsy. Pediatrics, 142, doi: 10.1542/peds.2018-0672.

Grassia, F., Poliakov, A. V., Poliachik, S. L., Casimo, K., Friedman, S. D., Shurtleff, H., … Novotny, E. J., Jr., Ojemann, J. G., Hauptman, J. S. (2018). Changes in resting-state connectivity in pediatric temporal lobe epilepsy. Journal of Neurosurgery. Pediatrics, 22, 270-275. doi: 10.3171/2018.3.PEDS17701.

Grinspan, Z. M., Shellhaas, R. A., Coryell, J., Sullivan, J. E., Wirrell, E. C., Mytinger, J. R., … Novotny, E. J., Jr., … Berg, A. T. (2018). Comparative effectiveness of levetiracetam vs phenobarbital for infantile epilepsy. JAMA Pediatrics, 172, 352-360. PMCID: PMC5875334. doi: 10.1001/jamapediatrics.2017.5211.

Kuo, C. H., Feroze, A. H., Poliachik, S. L., Hauptman, J. S., Novotny, E. J., Jr., Ojemann, J. G. (2018). Laser ablation therapy for pediatric patients with intracranial lesions in eloquent areas. World Neurosurgery. 25 Sep 2018. doi: 10.1016/j.wneu.2018.09.074.

Wang, A. C., Ibrahim, G. M., Poliakov, A. V., Wang, P. I., Fallah, A., Mathern, G. W., … Shaw, D. W. W., … Novotny, E. J., Jr., Lee, A. K. C., … Ojemann, J. G. (2018).Corticospinal tract atrophy and motor fMRI predict motor preservation after functional cerebral hemispherectomy. Journal of Neurosurgery. Pediatrics, 21, 81-89.doi: 10.3171/2017.7.PEDS17137.

Jeffrey Ojemann Grassia, F., Poliakov, A. V., Poliachik, S. L., Casimo, K., Friedman, S. D., Shurtleff, H., … Novotny, E. J., Jr., Ojemann, J. G., Hauptman, J. S. (2018). Changes in resting-state connectivity in pediatric temporal lobe epilepsy. Journal of Neurosurgery. Pediatrics, 22, 270-275. doi: 10.3171/2018.3.PEDS17701.

Kalmbach, B. E., Buchin, A., Long, B., Close, J., Nandi, A., Miller, J. A., … Ojemann, J. G., … Ting, J. T. (2018). H-channels contribute to divergent intrinsic membrane properties of supragranular pyramidal neurons in human versus mouse cerebral cortex. Neuron, 100, 1194-1208 e5. doi: 10.1016/j.neuron.2018.10.012.

Kuo, C. C., Tucker, D. M., Luu, P., Jenson, K., Tsai, J. J., Ojemann, J. G., Holmes, M. D. (2018). EEG source imaging of epileptic activity at seizure onset. Epilepsy Research, 146, 160-171. doi: 10.1016/j.eplepsyres.2018.07.006.

Monica Oxford Hastings, P. D., Kahle, S., Fleming, C., Lohr, M. J., Katz, L. F., Oxford, M. L. (2018). An intervention that increases parental sensitivity in families referred to Child Protective Services also changes toddlers' parasympathetic regulation. Developmental Science, e12725. doi: 10.1111/desc.12725.

Oxford, M. L., Spieker, S. J., Lohr, M. J., Fleming, C. B., Dillon, C., Rees, J. (2018). Ensuring implementation fidelity of a 10-week home visiting program in two randomized clinical trials. Maternal and Child Health Journal, 22, 376-383. PMCID: PMC5845475. doi: 10.1007/s10995-017-2387-8.

Ransone, S. H., Graff, J. C., Bush, A. J., Oxford, M. L., Wicks, M. N. (2018). Psychometric evaluation of the nursing child assessment teaching (NCAT) scale in a community-based sample. Research in Nursing & Health, 41, 301-311. doi: 10.1002/nur.21867.

Spieker, S. J., Oxford, M. L., Fleming, Charles B., Lohr, Mary Jane (2018). Parental childhood adversity, depressive symptoms, and parenting quality: Effects on toddler self-regulation in child welfare services involved families. Infant Mental Health Journal, 39, 5-16. PMCID: PMC5812360. doi: 10.1002/imhj.21685.

Leo Pallanck Pareek, G., Pallanck, L. J. (2018). Inactivation of Lon protease reveals a link between mitochondrial unfolded protein stress and mitochondrial translation inhibition. Cell Death & Disease, 9, 1168. PMCID: PMC6281655. doi: 10.1038/s41419-018-1213-6.

Pareek, G., Thomas, R. E., Pallanck, L. J. (2018). Loss of the Drosophila m-AAA mitochondrial protease paraplegin results in mitochondrial dysfunction, shortened lifespan, and neuronal and muscular degeneration. Cell Death & Disease, 9, 304. PMCID: PMC5833341. doi: 10.1038/s41419-018-0365-8.

Pareek, G., Thomas, R. E., Vincow, E. S., Morris, D. R., Pallanck, L. J. (2018). Lon protease inactivation in Drosophila causes unfolded protein stress and inhibition of mitochondrial translation. Cell Death Discovery, 5, 51. PMCID: PMC6197249. doi: 10.1038/s41420-018-0110-1.

Thomas, R. E., Vincow, E. S., Merrihew, G. E., MacCoss, M. J., Davis, M. Y., Pallanck, L. J. (2018).Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles. PLoS Genetics, 14, e1007694. PMCID: PMC6175534. doi: 10.1371/journal.pgen.1007694.

Jay Parrish Baccarella, A., Williams, C. R., Parrish, J. Z., Kim, C. C. (2018). Empirical assessment of the impact of sample number and read depth on RNA-Seq analysis workflow performance. BMC Bioinformatics, 19, 423. PMCID: PMC6234607. doi: 10.1186/s12859-018-2445-2.

Yan, C., Wang, F., Peng, Y., Williams, C. R., Jenkins, B., Wildonger, J., … Parrish, J. Z. (2018). Microtubule acetylation is required for mechanosensation in Drosophila. Cell Reports, 25, 1051-1065 e6. PMCID: PMC6248335. doi: 10.1016/j.celrep.2018.09.075.

David J. Perkel Vaaga, C. E., Miller, K. E., Bodor, A. L., Perkel, D. J. (2018). Expression of the potassium-chloride co-transporter, KCC2, within the avian song system. The Journal of Comparative Neurology, 526, 944–956. doi: 10.1002/cne.24372.

James Phillips Kelly, J. P., Baran, F., Phillips, J. O., Weiss, A. H. (2018). Optical coherence tomography in optic nerve hypoplasia: Correlation with optic disc diameter, nerve fiber layer thickness, and visual function. Journal of Neuro-Ophthalmology, 38, 312-319. doi: 10.1097/WNO.0000000000000596.

Phillips, J. O., Ling, L., Nowack, A. L., Phillips, C. M., Nie, K., Rubinstein, J. T. (2018). The dynamics of prosthetically elicited vestibulo-ocular reflex function across frequency and context in the rhesus monkey. Frontiers in Neuroscience, 12, 88. PMCID: PMC5962652. doi: 10.3389/fnins.2018.00088.

Phillips, J. O., Butt, L. E., Henderson, C. A., Devonshire, M., Healy, J., Conway, S. J., … Callaghan, A. J. (2018). High-density functional-RNA arrays as a versatile platform for studying RNA-based interactions. Nucleic Acids Research, 46, e86. PMCID: PMC6101487. doi: 10.1093/nar/gky410.

Suzie Pun Lee, D. C., Lamm, R. J., Prossnitz, A. N., Boydston, A. J., Pun, S. H. (2018). Dual polymerizations: Untapped potential for biomaterials. Advanced Healthcare Materials, e1800861. doi: 10.1002/adhm.201800861.

Jan-Marino (Nino) Ramirez Christakis, D. A., Ramirez, J. S. B., Ferguson, S. M., Ravinder, S., Ramirez, J. M. (2018). How early media exposure may affect cognitive function: A review of results from observations in humans and experiments in mice. Proceedings of the National Academy of Sciences of the United States of America, 115, 9851-9858. PMCID: PMC6176595. doi: 10.1073/pnas.1711548115. Wendy Raskind

Chen, D. H., Ma, M., Scavina, M., Blue, E., Wolff, J., Karna, P., … Raskind, W. H., Bird, T. D. (2018). An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation of the pathogenicity of a 3' untranslated region mutation in GJB1 and its clinical features. Muscle & Nerve, 57, 859-862. PMCID: PMC5910283. doi: 10.1002/mus.26037.

Todd Richards Mamiya, P. C., Richards, T. L., Kuhl, P. K. (2018). Right forceps minor and anterior thalamic radiation predict executive function skills in young bilingual adults. Frontiers in Psychology, 9, 118. PMCID: PMC5811666. doi: 10.3389/fpsyg.2018.00118.

Nielsen, K., Andria-Habermann, K., Richards, T. L., Abbott, R., Mickail, T., Berninger, V. W. (2018). Emotional and behavioral correlates of persisting specific learning disabilities in written language during middle childhood and early adolescence. Journal of Psychoeducational Assessment, 36, 651-669. PMCID: PMC6291223. doi: 10.1177/0734282917698056.

Robert Rostomily Brito da Silva, H., Straus, D., Barber, J. K., Rostomily, R. C., Ferreira, M., Jr., Sekhar, L. N. (2018). Cranial chordoma: A new preoperative grading system. Neurosurgery, 83, 403-415. PMCID: PMC6140779. doi: 10.1093/neuros/nyx423.

Mikheev, A. M., Mikheeva, S. A., Severs, L. J., Funk, C. C., Huang, L., McFaline-Figueroa, J. L., … Rostomily, R. C. (2018). Targeting TWIST1 through loss of function inhibits tumorigenicity of human glioblastoma. Molecular Oncology, 12, 1188-1202. PMCID: PMC6026950. doi: 10.1002/1878-0261.12320.

Parada, C. A., Osbun, J., Kaur, S., Yakkioui, Y., Shi, M., Pan, C., … Rostomily, R. C., Zhang, J., Ferreira, M., Jr. (2018). Kinome and phosphoproteome of high-grade meningiomas reveal AKAP12 as a central regulator of aggressiveness and its possible role in progression. Scientific Reports, 8, 2098. PMCID: PMC5794791. doi: 10.1038/s41598-018-19308-y.

Edwin Rubel Bhandiwad, A. A., Raible, D. W., Rubel, E. W., Sisneros, J. A. (2018). Noise-induced hypersensitization of the acoustic startle response in larval zebrafish. Journal of the Association for Research in Otolaryngology, 19, 741-752. PMCID: PMC6249159. doi: 10.1007/s10162-018-00685-0.

Zorio, D. A. R., Monsma, S., Sanes, D. H., Golding, N. L., Rubel, E. W., Wang, Y. (2018). De novo sequencing and initial annotation of the Mongolian gerbil (Meriones unguiculatus) genome. Genomics. 8 Mar 2018. PMCID: PMC6129228. doi: 10.1016/j.ygeno.2018.03.001.

Jay Rubinstein Phillips, J. O., Ling, L., Nowack, A. L., Phillips, C. M., Nie, K., Rubinstein, J. T. (2018). The dynamics of prosthetically elicited vestibulo-ocular reflex function across frequency and context in the rhesus monkey. Frontiers in Neuroscience, 12, 88. PMCID: PMC5962652. doi: 10.3389/fnins.2018.00088.

Resnick, J. M., O'Brien, G. E., Rubinstein, J. T. (2018). Simulated auditory nerve axon demyelination alters sensitivity and response timing to extracellular stimulation. Hearing Research, 361, 121-137. PMCID: PMC5846345. doi: 10.1016/j.heares.2018.01.014.

Hannele Ruohola-Baker

C. Ronald Scott Dana, K. N., Hertig, J. B., Scott, C. R., Briscoe-Dwyer, L. (2018). Instruction on compounded sterile preparations at schools of pharmacy. American Journal of Health-System Pharmacy, 75, 847-849. doi: 10.2146/ajhp170636.

Masi, S., Chennamaneni, N., Turecek, F., Scott, C. R., Gelb, M. H. (2018). Specific substrate for the assay of lysosomal acid lipase. Clinical Chemistry, 64, 690-696. doi: 10.1373/clinchem.2017.282251.

Yi, F., Hong, X., Kumar, A. B., Zong, C., Boons, G. J., Scott, C. R., … Gelb, M. H. (2018). Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometry. Molecular Genetics and Metabolism,125, 59-63. doi: 10.1016/j.ymgme.2018.05.005.

Dennis Shaw Adams Waldorf, K. M., Nelson, B. R., Stencel-Baerenwald, J. E., Studholme, C., Kapur, R. P., Armistead, B., … Shaw, D. W. W., … Dobyns, W. B., Hevner, R. F., … Rajagopal, L. (2018). Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brain. Nature Medicine, 24, 368-374. PMCID: PMC5839998. doi: 10.1038/nm.4485.

Maloney, E., Stanescu, A. L., Perez, F. A., Iyer, R. S., Otto, R. K., Leary, S., … Shaw, D. W. W. (2018). Surveillance magnetic resonance imaging for isolated optic pathway gliomas: Is gadolinium necessary? Pediatric Radiology, 48, 1472-1484. doi: 10.1007/s00247-018-4154-4.

Pierce, D. B., Shivaram, G., Koo, K. S. H., Shaw, D. W. W., Meyer, K. F., Monroe, E. J. (2018). Ultrasound-guided lumbar puncture in pediatric patients: Technical success and safety. Pediatric Radiology, 48, 875-881. doi: 10.1007/s00247-018-4091-2.

Weaver, J. J., Natarajan, N., Shaw, D. W. W., Apkon, S. D., Koo, K. S. H., Shivaram, G. M., Monroe, E. J. (2018). Transforaminal intrathecal delivery of nusinersen using cone-beam computed tomography for children with spinal muscular atrophy and extensive surgical instrumentation: Early results of technical success and safety. Pediatric Radiology,48, 392-397. doi: 10.1007/s00247-017-4031-6.

Frederick Shic Del Valle Rubido, M., McCracken, J. T., Hollander, E., Shic, F., Noeldeke, J., Boak, L., … Umbricht, D. (2018). In search of biomarkers for autism spectrum disorder. Autism Research, 11, 1567-1579. doi: 10.1002/aur.2026.

Mademtzi, M., Singh, P., Shic, F., Koenig, K. (2018). Challenges of females with autism: A parental perspective. Journal of Autism and Developmental Disorders, 48, 1301-1310. doi: 10.1007/s10803-017-3341-8.

Manfredonia, J., Bangerter, A., Manyakov, N. V., Ness, S., Lewin, D., Skalkin, A., … Shic, F., Pandina, G. (2018). Automatic recognition of posed facial expression of emotion in individuals with autism spectrum disorder. Journal of Autism and Developmental Disorders, 8 Oct 2018. doi: 10.1007/s10803-018-3757-9.

Manyakov, N. V., Bangerter, A., Chatterjee, M., Mason, L., Ness, S., Lewin, D., … Shic, F., Pandina, G. (2018). Visual exploration in autism spectrum disorder: Exploring age differences and dynamic features using recurrence quantification analysis. Autism Research, 11, 1554-1566. doi: 10.1002/aur.2021.

Nordahl-Hansen, A., Oien, R. A., Volkmar, F., Shic, F., Cicchetti, D. V. (2018). Enhancing the understanding of clinically meaningful results: A clinical research perspective. Psychiatry Research, 270, 801-806. doi: 10.1016/j.psychres.2018.10.069.

Oien, R. A., Schjolberg, S., Volkmar, F. R., Shic, F., Cicchetti, D. V., Nordahl-Hansen, A., … Chawarska, K. (2018). Clinical features of children with autism who passed 18-month screening. Pediatrics, 141, doi: 10.1542/peds.2017-3596.

Oien, R. A., Vambheim, S. M., Hart, L., Nordahl-Hansen, A., Erickson, C., Wink, L., … Shic, F., … Grodberg, D. (2018). Sex-differences in children referred for assessment: An exploratory analysis of the Autism Mental Status Exam (AMSE). Journal of Autism and Developmental Disorders, 48, 2286-2292. doi: 10.1007/s10803-018-3488-y.

Wang, Q., Campbell, D. J., Macari, S. L., Chawarska, K., Shic, F. (2018). Operationalizing atypical gaze in toddlers with autism spectrum disorders: A cohesion-based approach. Molecular Autism, 9, 25. PMCID: PMC5894192. doi: 10.1186/s13229-018-0211-y.

Stephen E. P. Smith Brown, E. A., Lautz, J. D., Davis, T. R., Gniffke, E. P., VanSchoiack, A. A. W., Neier, S. C., … Smith, S. E. P. (2018). Clustering the autisms using glutamate synapse protein interaction networks from cortical and hippocampal tissue of seven mouse models. Molecular Autism, 9, 48. PMCID: PMC6139139. doi: 10.1186/s13229-018-0229-1.

Lautz, J. D., Brown, E. A., VanSchoiack, A. A. W., Smith, S. E. P. (2018). Synaptic activity induces input-specific rearrangements in a targeted synaptic protein interaction network. Journal of Neurochemistry, 146, 540-559. doi: 10.1111/jnc.14466.

Matthew Speltz Collett, B. R., Wallace, E. R., Kartin, D., Speltz, M. L. (2018). Infant/toddler motor skills as predictors of cognition and language in children with and without positional skull deformation. Child's Nervous System, 30 Oct 2018. doi: 10.1007/s00381-018-3986-4.

Susan Spieker Crittenden, P. M., Spieker, S. J. (2018). Dynamic-maturational model of attachment and adaptation versus ABC+D assessments of attachment in child protection and treatment: Reply to van IJzendoorn, Bakermans, Steele, & Granqvist (2018). Infant Mental Health Journal,39, 647-651. doi: 10.1002/imhj.21750.

Spieker, S. J., Crittenden, P. M. (2018). Can attachment inform decision-making in child protection and forensic settings? Infant Mental Health Journal, 39, 625-641. doi: 10.1002/imhj.21746.

Mark Stein Faraone, S. V., Silverstein, M. J., Antshel, K., Biederman, J., Goodman, D. W., Mason, O., … Stein, M. A., Adler, L. A. (2018). The Adult ADHD Quality Measures Initiative. Journal of Attention Disorders, 1087054718804354. doi: 10.1177/1087054718804354.

Froehlich, T. E., Becker, S. P., Nick, T. G., Brinkman, W. B., Stein, M. A., Peugh, J., Epstein, J. N. (2018). Sluggish cognitive tempo as a possible predictor of methylphenidate response in children with ADHD: A randomized controlled trial. The Journal of Clinical Psychiatry, 79. doi: 10.4088/JCP.17m11553.

Nephi Stella Cao, J. K., Detloff, P. J., Gardner, R. G., Stella, N. (2018). Sex-dependent behavioral impairments in the HdhQ350/+ mouse line. Behavioural Brain Research, 337, 34-45. PMCID: PMC5659761. doi: 10.1016/j.bbr.2017.09.026.

Day, A. L., Greisen, P., Doyle, L., Schena, A., Stella, N., Johnsson, K., … Stoddard, B. (2018). Unintended specificity of an engineered ligand-binding protein facilitated by unpredicted plasticity of the protein fold. Protein Engineering, Design and Selection, doi: 10.1093/protein/gzy031.

Diaz, P., Horne, E., Xu, C., Hamel, E., Wagenbach, M., Petrov, R. R., … Stella, N. (2018). Modified carbazoles destabilize microtubules and kill glioblastoma multiform cells. European Journal of Medicinal Chemistry, 159, 74-89. doi: 10.1016/j.ejmech.2018.09.026.

Grant, K. S., Petroff, R., Isoherranen, N. Stella, N., Burbacher, T. M. (2018). Cannabis use during pregnancy: Pharmacokinetics and effects on child development. Pharmacology and Therapeutics, 182, 133-151. doi: 10.1016/j.pharmthera.2017.08.014.

Huizenga, M. N., Fureman, B. E., Soltesz, I., Stella, N. (2018). Proceedings of the Epilepsy Foundation's 2017 Cannabinoids in Epilepsy Therapy Workshop. Epilepsy & Behavior, 85, 237-242. doi: 10.1016/j.yebeh.2018.05.016.

Jennifer Stone Scheibinger, M., Ellwanger, D. C., Corrales, C. E., Stone, J. S., Heller, S. (2018). Aminoglycoside damage and hair cell regeneration in the chicken utricle. Journal of the Association for Research in Otolaryngology, 19, 17-29. PMCID: PMC5783928. doi: 10.1007/s10162-017-0646-4.

Stone, J. S., Wisner, S. R., Bucks, S. A., Mellado Lagarde, M. M., Cox, B. C. (2018). Characterization of adult vestibular organs in 11 CreER mouse lines. Journal of the Association for Research in Otolaryngology, 19, 381-399. PMCID: PMC6081895. doi: 10.1007/s10162-018-0676-6.

Williams, A. M., Huang, W., Muir, K. W., Stinnett, S. S., Stone, J. S., Rosdahl, J. A. (2018). Identifying risk factors for blindness from primary open-angle glaucoma by race: A case-control study. Clinical Ophthalmology, 12, 377-383. PMCID: PMC5824746. doi: 10.2147/OPTH.S143417.

Wendy Stone Broder Fingert, S., Carter, A., Pierce, K., Stone, W. L., Wetherby, A., Scheldrick, C., … Feinberg, E. (2018). Implementing systems-based innovations to improve access to early screening, diagnosis, and treatment services for children with autism spectrum disorder: An Autism Spectrum Disorder Pediatric, Early Detection, Engagement, and Services network study. Autism, 1362361318766238. doi: 10.1177/1362361318766238.

Damiano-Goodwin, C. R., Woynaroski, T. G., Simon, D. M., Ibanez, L. V., Murias, M., Kirby, A., … Stone, W. L., Cascio, C. J. (2018). Developmental sequelae and neurophysiologic substrates of sensory seeking in infant siblings of children with autism spectrum disorder. Developmental Cognitive Neuroscience, 29, 41-53. PMCID: PMC5812859. doi: 10.1016/j.dcn.2017.08.005.

Foss-Feig, J. H., Stavropoulos, K. K. M., McPartland, J. C., Wallace, M. T., Stone, W. L., Key, A. P. (2018). Electrophysiological response during auditory gap detection: Biomarker for sensory and communication alterations in autism spectrum disorder? Developmental Neuropsychology, 43, 109-122. PMCID: PMC5972824. doi: 10.1080/87565641.2017.1365869.

Ibanez, L. V., Kobak, K., Swanson, A., Wallace, L., Warren, Z., Stone, W. L. (2018). Enhancing interactions during daily routines: A randomized controlled trial of a web-based tutorial for parents of young children with ASD. Autism Research, 11, 667-678. PMCID: PMC5903955. doi: 10.1002/aur.1919.

Colin Studholme Adams Waldorf, K. M., Nelson, B. R., Stencel-Baerenwald, J. E., Studholme, C., Kapur, R. P., Armistead, B., … Shaw, D. W. W., … Dobyns, W. B., Hevner, R. F., … Rajagopal, L. (2018). Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brain. Nature Medicine, 24, 368-374. PMCID: PMC5839998. doi: 10.1038/nm.4485.

Kamino, D., Studholme, C., Liu, M., Chau, V., Miller, S. P., Synnes, A., … Tam, E. W. Y. (2018). Postnatal polyunsaturated fatty acids associated with larger preterm brain tissue volumes and better outcomes. Pediatric Research, 83, 93-101. doi: 10.1038/pr.2017.230.

Stephen Tapscott Balog, J., Goossens, R., Lemmers, Rjlf, Straasheijm, K. R., van der Vliet, P. J., Heuvel, A. V. D., … Tapscott, S. J., … van der Maarel, S. M. (2018). Monosomy 18p is a risk factor for facioscapulohumeral dystrophy. Journal of Medical Genetics, 55, 469-478. PMCID: PMC6019561. doi: 10.1136/jmedgenet-2017-105153.

Campbell, A. E., Belleville, A. E., Resnick, R., Shadle, S. C., Tapscott, S. J. (2018). Facioscapulohumeral dystrophy: Activating an early embryonic transcriptional program in human skeletal muscle. Human Molecular Genetics, 27, R153-R162. PMCID: PMC6061842. doi: 10.1093/hmg/ddy162.

Campbell, A. E., Shadle, S. C., Jagannathan, S., Lim, J. W., Resnick, R., Tawil, R., … Tapscott, S. J. (2018). NuRD and CAF-1-mediated silencing of the D4Z4 array is modulated by DUX4-induced MBD3L proteins. eLife, 7. PMCID: PMC5849414. doi: 10.7554/eLife.31023.

de Greef, J. C., Krom, Y. D., den Hamer, B., Snider, L., Hiramuki, Y., van den Akker, R. F. P., … Tapscott, S. J., van der Maarel, S. M. (2018). SMCHD1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. Human Molecular Genetics, 27, 716-731. PMCID: PMC5886298. doi: 10.1093/hmg/ddx437.

Heuvel, A. V. D., Mahfouz, A., Kloet, S. L., Balog, J., Engelen, Bgmv, Tawil, R., Tapscott, S. J., Maarel, S. M. V. (2018). Single-cell RNA-sequencing in facioscapulohumeral muscular dystrophy disease etiology and development. Human Molecular Genetics, doi: 10.1093/hmg/ddy400.

Hiramuki, Y., Tapscott, S. J. (2018). Identification of SMCHD1 domains for nuclear localization, homo-dimerization, and protein cleavage. Skeletal Muscle, 8, 24. PMCID: PMC6090946. doi: 10.1186/s13395-018-0172-z.

Lemmers, R. J., van der Vliet, P. J., Balog, J., Goeman, J. J., Arindrarto, W., Krom, Y. D., … Tapscott, S. J., … van der Maarel, S. M. (2018). Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2. European Journal of Human Genetics, 26, 94-106. doi: 10.1038/s41431-017-0015-0.

Lim, J. W., Wong, C. J., Yao, Z., Tawil, R., van der Maarel, S. M., Miller, D. G., Tapscott, S. J., Filippova, G. N. (2018). Small noncoding RNAs in FSHD2 muscle cells reveal both DUX4- and SMCHD1-specific signatures. Human Molecular Genetics. 8 May 2018. PMCID: PMC6048983. doi: 10.1093/hmg/ddy173.

Mul, K., Lemmers, Rjlf, Kriek, M., van der Vliet, P. J., van den Boogaard, M. L., Badrising, U. A., … Tapscott, S. J., … van der Maarel, S. M. (2018). FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutation. Neurology, 91, e562-e570. PMCID: PMC6105048. doi: 10.1212/WNL.0000000000005958.

Jeffrey Tsai Kuo, C. C., Tucker, D. M., Luu, P., Jenson, K., Tsai, J. J., Ojemann, J. G., Holmes, M. D. (2018). EEG source imaging of epileptic activity at seizure onset. Epilepsy Research, 146, 160-171. doi: 10.1016/j.eplepsyres.2018.07.006.

Hannah Tully Aldinger, K. A., Dempsey, J. C., Tully, H. M., Grout, M. E., Mehaffey, M. G., Dobyns, W. B., Doherty, D. A. (2018). Rhombencephalosynapsis: Fused cerebellum, confused geneticists. American Journal of Medical Genetics Part C Seminars in Medical Genetics, 178, 432-439. doi: 10.1002/ajmg.c.31666.

Eric Turner Morton, G., Nasirova, N., Sparks, D. W., Brodsky, M., Sivakumaran, S., Lambe, E. K., Turner, E. E. (2018). CHRNA5-expressing neurons in the interpeduncular nucleus mediate aversion primed by prior stimulation or nicotine exposure. The Journal of Neuroscience, 28 Jun 2018. PMCID: PMC6070661. doi: 10.1523/JNEUROSCI.0023-18.2018.

Jashvant Unadkat Xu, M., Saxena, N., Vrana, M., Zhang, H., Kumar, V., Billington, S., … Unadkat, J. D., Prasad, B. (2018). Targeted LC-MS/MS proteomics-based strategy to characterize in vitro models used in drug metabolism and transport studies. Analytical Chemistry, 90, 11873-11882. doi: 10.1021/acs.analchem.8b01913.

Sara Jane Webb Arnett, A. B., Hudac, C. M., DesChamps, T. D., Cairney, B. E., Gerdts, J., Wallace, A. S.,Bernier, R. A., Webb, S. J. (2018). Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder. Brain and Language, 187, 1-8. doi: 10.1016/j.bandl.2018.09.007.

Bazelmans, T., Jones, E. J. H., Ghods, S., Corrigan, S., Toth, K., Charman, T., Webb, S. J. (2018). Heart rate mean and variability as a biomarker for phenotypic variation in preschoolers with autism spectrum disorder. Autism Research. 16 Aug 2018. doi: 10.1002/aur.1982.

Jones, E. J. H., Dawson, G., Webb, S. J. (2018). Sensory hypersensitivity predicts enhanced attention capture by faces in the early development of ASD. Developmental Cognitive Neuroscience, 29, 11-20. PMCID: PMC5638681. doi: 10.1016/j.dcn.2017.04.001.

Naumann, S., Senftleben, U., Santhosh, M., McPartland, J., Webb, S. J. (2018). Neurophysiological correlates of holistic face processing in adolescents with and without autism spectrum disorder. Journal of Neurodevelopmental Disorders, 10, 27. PMCID: PMC6118009. doi: 10.1186/s11689-018-9244-y.

Webb, S. J., Mourad, P. D. (2018). Prenatal ultrasonography and the incidence of autism spectrum disorder. JAMA Pediatrics, 172, 319-320. doi: 10.1001/jamapediatrics.2017.5685.

Jonathan Weinstein McDonough, A., Weinstein, J. R. (2018). Correction to: Neuroimmune response in ischemic preconditioning. Neurotherapeutics, 15, 511-524. doi: 10.1007/s13311-017-0580-5.

John P. Welsh Welsh, J. P., Estes, A. M. (2018). Exploring the social brain. eLife, 7, PMCID: PMC5832409. doi: 10.7554/eLife.35392.

H. Steve White Bialer, M., Johannessen, S. I., Koepp, M. J., Levy, R. H., Perucca, E., Tomson, T., White, H. S. (2018). Progress report on new antiepileptic drugs: A summary of the Fourteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XIV). II. Drugs in more advanced clinical development. Epilepsia, 59, 1842-1866. doi: 10.1111/epi.14555.

Bialer, M., Johannessen, S. I., Koepp, M. J., Levy, R. H., Perucca, E., Tomson, T., White, H. S. (2018). Progress report on new antiepileptic drugs: A summary of the Fourteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XIV). I. Drugs in preclinical and early clinical development. Epilepsia, 59, 1811-1841. doi: 10.1111/epi.14557.

Rho, J. M., White, H. S. (2018). Brief history of anti-seizure drug development. Epilepsia Open, 3, 114-119. PMCID: PMC6293064. doi: 10.1002/epi4.12268.

West, P. J., Saunders, G. W., Billingsley, P., Smith, M. D., White, H. S., Metcalf, C. S., Wilcox, K. S. (2018). Recurrent epileptiform discharges in the medial entorhinal cortex of kainate-treated rats are differentially sensitive to antiseizure drugs. Epilepsia, 59, 2035-2048. PMCID: PMC6215509. doi: 10.1111/epi.14563.

Ellen M. Wijsman Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., … Wijsman, E. M., … Murray, R. (2018). Analysis of shared heritability in common disorders of the brain. Science, 360, PMCID: PMC6097237. doi: 10.1126/science.aap8757.

Kunji, K., Ullah, E., Nato, A. Q., Jr., Wijsman, E. M., Saad, M. (2018). GIGI-Quick: A fast approach to impute missing genotypes in genome-wide association family data. Bioinformatics, 34, 1591-1593. PMCID: PMC5925782. doi: 10.1093/bioinformatics/btx782.

Zhengui Xia Wang, H., Zhang, L., Abel, G. M., Storm, D. R., Xia, Z. (2018). Cadmium exposure impairs cognition and olfactory memory in male C57BL/6 mice. Toxicological Sciences, 161, 87-102. doi: 10.1093/toxsci/kfx202.

Libin Xu Fliesler, S. J., Peachey, N. S., Herron, J., Hines, K. M., Weinstock, N. I., Rao, S. R., Xu, L. (2018). Prevention of retinal degeneration in a rat model of Smith-Lemli-Opitz syndrome. Scientific Reports, 8, 1286. doi: 10.1038/s41598-018-19592-8.

Fliesler, S. J., Xu, L. (2018). Oxysterols and retinal degeneration in a rat model of Smith-Lemli-Opitz syndrome: Implications for an improved therapeutic intervention. Molecules, 23, E2720. PMCID: PMC6222618. doi: 10.3390/molecules23102720.

Herron, J., Hines, K. M., Xu, L. (2018). Assessment of altered cholesterol homeostasis by xenobiotics using ultra-high performance liquid chromatography-tandem mass spectrometry. Current Protocols in Toxicology, 78, e65. PMCID: PMC6205911. doi: 10.1002/cptx.65.

Jason Yeatman Huber, E., Donnelly, P. M., Rokem, A., Yeatman, J. D. (2018). Rapid and widespread white matter plasticity during an intensive reading intervention. Nature Communications, 9, 2260. PMCID: PMC5993742. doi: 10.1038/s41467-018-04627-5.

Joo, S. J., White, A. L., Strodtman, D. J., Yeatman, J. D. (2018). Optimizing text for an individual's visual system: The contribution of visual crowding to reading difficulties. Cortex, 103, 291-301. doi: 10.1016/j.cortex.2018.03.013.

Jing Zhang Fry, A. E., Fawcett, K. A., Zelnik, N., Yuan, H., Thompson, B. A. N., Shemer-Meiri, L., … Zhang, J., … Mirzaa, G. M., … Mefford, H. C., Dobyns, W. B., … Pilz, D. T. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain, 22 Jan 2018. PMCID: PMC5837214. doi: 10.1093/brain/awx358.

2019

Kristina Adams Waldorf

Al-Haddad, B. J. S., Oler, E., Armistead, B., Elsayed, N. A., Weinberger, D. R., Bernier, R. A., … Kapur, R. P., … Adams Waldorf, K. M. (2019). The fetal origins of mental illness. American Journal of Obstetrics and Gynecology, Jun 15 2019. doi: 10.1016/j.ajog.2019.06.013.

Al-Haddad, B. J. S., Jacobsson, B., Chabra, S., Modzelewska, D., Olson, E. M., Bernier, R. A., … Adams Waldorf, K. M., Sengpiel, V. (2019). Long-term risk of neuropsychiatric disease after exposure to infection in utero. JAMA Psychiatry, Mar 6 2019. doi: 10.1001/jamapsychiatry.2019.0029.

Armistead, B., Oler, E., Adams Waldorf, K. M., Rajagopal, L. (2019). The double life of group B streptococcus: Asymptomatic colonizer and potent pathogen. Journal of Molecular Biology, Jan 31 2019. doi: 10.1016/j.jmb.2019.01.035.

Kachikis, A., Walker, C. L., McAdams, R. M., Gyamfi-Bannerman, C., Adams Waldorf, K. M. (2019). Phenotypic overlap in neonatal respiratory morbidity following preterm premature rupture of membranes versus spontaneous preterm labor. The Journal of Maternal-Fetal & Neonatal Medicine, 1-8. doi: 10.1080/14767058.2019.1651280.

Robbiani, D. F., Olsen, P. C., Costa, F., Wang, Q., Oliveira, T. Y., Nery, N., Jr., … Adams Waldorf, K. M., … Nussenzweig, M. C. (2019). Risk of Zika microcephaly correlates with features of maternal antibodies. The Journal of Experimental Medicine, Aug 14 2019. doi: 10.1084/jem.20191061.

Susan Astley Jarmasz, J. S., Stirton, H., Basalah, D., Davie, J. R., Clarren, S. K., Astley, S. J., Del Bigio, M. R. (2019). Global DNA methylation and histone posttranslational modifications in human and nonhuman primate brain in association with prenatal alcohol exposure. Alcoholism: Clinical and Experimental Research, 43, 1145-1162. PMCID: PMC6593679. doi: 10.1111/acer.14052.

Raphael Bernier Al-Haddad, B. J. S., Oler, E., Armistead, B., Elsayed, N. A., Weinberger, D. R., Bernier, R. A., … Kapur, R. P., … Adams Waldorf, K. M. (2019). The fetal origins of mental illness. American Journal of Obstetrics and Gynecology, Jun 15 2019. doi: 10.1016/j.ajog.2019.06.013.

Cao, M., MacDonald, J. W., Liu, H. L., Weaver, M., Cortes, M., Durosier, L. D., … Bernier, R. A., … Frasch, M. G. (2019). Alpha7 nicotinic acetylcholine receptor signaling modulates ovine fetal brain astrocytes transcriptome in response to endotoxin. Frontiers in Immunology, 10, 1063. PMCID: PMC6520997. doi: 10.3389/fimmu.2019.01063.

Fenckova, M., Blok, L. E. R., Asztalos, L., Goodman, D. P., Cizek, P., Singgih, E. L., … Eichler, E. E., … Bernier, R. A., … Schenck, A. (2019). Habituation learning is a widely affected mechanism in Drosophila models of intellectual disability and autism spectrum disorders. Biological Psychiatry, 86, 294-305. doi: 10.1016/j.biopsych.2019.04.029.

Nellaker, C., Alkuraya, F. S., Baynam, G., Bernier, R. A., Bernier, F. P. J., Boulanger, V., … Eichler, E. E., … Minerva Consortium. (2019). Enabling global clinical collaborations on identifiable patient data: The Minerva Initiative. Frontiers in Genetics, 10, 611. PMCID: PMC6681681. doi: 10.3389/fgene.2019.00611.

Niarchou, M., Chawner, Sjra, Doherty, J. L., Maillard, A. M., Jacquemont, S., Chung, W. K., … Bernier, R. A., … van den Bree, M. B. (2019). Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry, 9, 8. PMCID: PMC6341088. doi: 10.1038/s41398-018-0339-8.

Patowary, A., Won, S. Y., Oh, S. J., Nesbitt, R. R., Archer, M., Nickerson, D., Raskind, W. H., Bernier, R. A., … Brkanac, Z. (2019). Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene. Translational Psychiatry, 9, 4. PMCID: PMC6341097. doi: 10.1038/s41398-018-0343-z.

Sabatos-DeVito, M., Murias, M., Dawson, G., Howell, T., Yuan, A., Marsan, S., Bernier, R. A., … Shic, F., … Webb, S. J., … Autism Biomarkers Consortium for Clinical Trials. (2019). Methodological considerations in the use of Noldus EthoVision XT video tracking of children with autism in multi-site studies. Biological Psychology, 146, 107712. doi: 10.1016/j.biopsycho.2019.05.012.

Kristie F. Bjornson Bjornson, K. F., Fiss, A., Avery, L., Wentz, E., Kerfeld, C., Cicirello, N., Hanna, S. E. (2019). Longitudinal trajectories of physical activity and walking performance by gross motor function classification system level for children with cerebral palsy. Disability and Rehabilitation, 1-9. doi: 10.1080/09638288.2018.1534995.

Cathryn Booth-LaForce

Bradley, R., Booth-LaForce, C., Hanes, D., Scott, C., Sherman, K. J., Lin, Y. S., Zwickey, H. (2019). Design of a multidisciplinary training program in complementary and integrative health clinical research: Building research across interdisciplinary gaps. Journal of Alternative and Complementary Medicine, Feb 13 2019. doi: 10.1089/acm.2018.0454.

Haltigan, J. D., Roisman, G. I., Groh, A. M., Holland, A. S., Booth-LaForce, C., Rogosch, F. A., Cicchetti, D. (2019). Antecedents of attachment states of mind in normative-risk and high-risk caregiving: cross-race and cross-sex generalizability in two longitudinal studies. Journal of Child Psychology and Psychiatry and Allied Disciplines, Jun 19 2019. doi: 10.1111/jcpp.13086.

Zoran Brkanac

Thomas Burbacher Burbacher, T. M., Grant, K. S., Petroff, R., Shum, S., Crouthamel, B., Stanley, C., … Isoherranen, N. (2019). Effects of oral domoic acid exposure on maternal reproduction and infant birth characteristics in a preclinical nonhuman primate model. Neurotoxicology and Teratology, 72, 10-21. PMCID: PMC6408264. doi: 10.1016/j.ntt.2019.01.001.

Grant, K. S., Crouthamel, B., Kenney, C., McKain, N., Petroff, R., Shum, S., … Isoherranen, N., Burbacher, T. M. (2019). Preclinical modeling of exposure to a global marine bio-contaminant: Effects of in utero Domoic acid exposure on neonatal behavior and infant memory. Neurotoxicology and Teratology, 73, 1-8. doi: 10.1016/j.ntt.2019.01.003.

Petroff, R., Richards, T. L., Crouthamel, B., McKain, N., Stanley, C., Grant, K. S., … Isoherranen, N., Burbacher, T. M. (2019). Chronic, low-level oral exposure to marine toxin, domoic acid, alters whole brain morphometry in nonhuman primates. Neurotoxicology, Feb 28 2019. doi: 10.1016/j.neuro.2019.02.016.

William Catterall Konoki, K., Baden, D. G., Scheuer, T., Catterall, W. A. (2019). Molecular determinants of brevetoxin binding to voltage-gated sodium channels. Toxins, 11, Sep 3 2019. doi: 10.3390/toxins11090513.

Sanchez, R. E. A., Bussi, I. L., Ben-Hamo, M., Caldart, C. S., Catterall, W. A., de la Iglesia, H. O. (2019). Circadian regulation of sleep in a pre-clinical model of Dravet syndrome: Dynamics of sleep stage and siesta re-entrainment. Sleep, Jul 26 2019. doi: 10.1093/sleep/zsz173.

Stein, R. E., Kaplan, J. S., Li, J., Catterall, W. A. (2019). Hippocampal deletion of NaV1.1 channels in mice causes thermal seizures and cognitive deficit characteristic of Dravet Syndrome. Proceedings of the National Academy of Sciences of the United States of America, 116, 16571-16576. PMCID: PMC6697805. doi: 10.1073/pnas.1906833116.

Tang, L., Gamal El-Din, T. M., Lenaeus, M. J., Zheng, N., Catterall, W. A. (2019). Structural basis for diltiazem block of a voltage-gated Ca(2+) channel. Molecular Pharmacology, 96, 485-492. doi: 10.1124/mol.119.117531.

Weyrer, C., Turecek, J., Niday, Z., Liu, P. W., Nanou, E., Catterall, W. A., … Regehr, W. G. (2019). The role of CaV2.1 channel facilitation in synaptic facilitation. Cell Reports, 26, 2289-2297 e3. doi: 10.1016/j.celrep.2019.01.114.

Williams, A. D., Kalume, F., Westenbroek, R. E., Catterall, W. A. (2019). A more efficient conditional mouse model of Dravet syndrome: Implications for epigenetic selection and sex-dependent behaviors. Journal of Neuroscience Methods, 325, 108315. PMCID: PMC6686874. doi: 10.1016/j.jneumeth.2019.108315.

Wisedchaisri, G., Tonggu, L., McCord, E., Gamal El-Din, T. M., Wang, L., Zheng, N., Catterall, W. A. (2019). Resting-state structure and gating mechanism of a voltage-gated sodium channel. Cell, 178, 993-1003 e12. PMCID: PMC6688928. doi: 10.1016/j.cell.2019.06.031.

Jeffrey Chamberlain Crudele, J. M., Chamberlain, J. S. (2019). AAV-based gene therapies for the muscular dystrophies. Human Molecular Genetics, Jun 25 2019. doi: 10.1093/hmg/ddz128.

Parvatiyar, M. S., Brownstein, A. J., Kanashiro-Takeuchi, R. M., Collado, J. R., Dieseldorff Jones, K. M., Gopal, J., … Chamberlain, J. S., … Crosbie, R. H. (2019). Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy. JCI Insight, 5, Apr 30 2019. PMCID: PMC6629091. doi: 10.1172/jci.insight.123855.

Ramos, J. N., Hollinger, K., Bengtsson, N. E., Allen, J. M., Hauschka, S. D., Chamberlain, J. S. (2019). Development of novel micro-dystrophins with enhanced functionality. Molecular Therapy, 27, 623-635. PMCID: PMC6403485. doi: 10.1016/j.ymthe.2019.01.002.

Dimitri Christakis Christakis, D. A., Lowry, S. J., Goldberg, G., Violette, H., Garrison, M. M. (2019). Assessment of a Parent-Child Interaction Intervention for Language Development in Children. JAMA Network Open, 2, e195738. PMCID: PMC6575141. doi: 10.1001/jamanetworkopen.2019.5738.

Christakis, D. A. (2019). Decision to Publish Study on Maternal Fluoride Exposure During Pregnancy. JAMA Pediatrics, Aug 19 2019. doi: 10.1001/jamapediatrics.2019.3120.

Tandon, P. S., Sasser, T., Gonzalez, E. S., Whitlock, K. B., Christakis, D. A., Stein, M. A. (2019). Physical activity, screen time, and sleep in children with ADHD. Journal of Physical Activity & Health, 16, 416-422. doi: 10.1123/jpah.2018-0215.

Lucio Costa Chang, Y. C., Daza, R., Hevner, R. F., Costa, L. G., Cole, T. B. (2019). Prenatal and early life diesel exhaust exposure disrupts cortical lamina organization: Evidence for a reelin-related pathogenic pathway induced by interleukin-6. Brain, Behavior, and Immunity, 78, 105-115. doi: 10.1016/j.bbi.2019.01.013.

Timothy Cox Cox, T. C., Lidral, A. C., McCoy, J. C., Liu, H., Cox, L. L., Zhu, Y., … Glass, I. A., … Roscioli, T. (2019). Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. Human Mutation, Jun 18 2019. doi: 10.1002/humu.23793.

Michael Cunningham

Collett, B. R., Wallace, E. R., Kartin, D., Cunningham, M. L., Speltz, M. L. (2019). Cognitive outcomes and positional plagiocephaly. Pediatrics, 143, Feb 2019. PMCID: PMC6361360. doi: 10.1542/peds.2018-2373.

Gustafson, J. A., Park, S. S., Cunningham, M. L. (2019). Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model. PLoS One, 14, e0221402. PMCID: PMC6707563. doi: 10.1371/journal.pone.0221402.

Stephen Dager Estes, A. M., St John, T., Dager, S. R. (2019). What to tell a parent who worries a young child has autism. JAMA Psychiatry, Aug 7 2019. doi: 10.1001/jamapsychiatry.2019.1234.

Swanson, M. R., Donovan, K., Paterson, S., Wolff, J. J., Parish-Morris, J., Meera, S. S., … Estes, A. M., … Dager, S. R., … IBIS Network. (2019). Early language exposure supports later language skills in infants with and without autism. Autism Research, Jun 28 2019. doi: 10.1002/aur.2163.

Nina de Lacy de Lacy, N., Calhoun, V. D. (2019). Dynamic connectivity and the effects of maturation in youth with attention deficit hyperactivity disorder. Network Neuroscience, 3, 195-216. PMCID: PMC6372020. doi: 10.1162/netn_a_00063.

Sureyya Dikmen Alali, A. S., Temkin, N., Vavilala, M. S., Lele, A. V., Barber, J., Dikmen, S. S., Chesnut, R. M. (2019). Matching early arterial oxygenation to long-term outcome in severe traumatic brain injury: Target values. Journal of Neurosurgery, 1-8. doi: 10.3171/2018.10.JNS18964.

William B. Dobyns

Aldinger, K. A., Timms, A. E., Thomson, Z., Mirzaa, G. M., Bennett, J. T., Rosenberg, A. B., … Glass, I. A., Millen, K. J., Doherty, D. A., Dobyns, W. B. (2019). Redefining the etiologic landscape of cerebellar malformations. American Journal of Human Genetics, 105, 606-615. doi: 10.1016/j.ajhg.2019.07.019.

Dobyns, W. B., Mirzaa, G. M. (2019). Megalencephaly syndromes associated with mutations of core components of the PI3K-AKT-MTOR pathway: PIK3CA, PIK3R2, AKT3, and MTOR. American Journal of Medical Genetics Part C Seminars in Medical Genetics, Aug 23 2019. doi: 10.1002/ajmg.c.31736.

Gripp, K. W., Morse, L. A., Axelrad, M., Chatfield, K. C., Chidekel, A., Dobyns, W. B., … Rauen, K. A. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics. Part A, 179, 1725-1744. doi: 10.1002/ajmg.a.61270.

Holt, R. J., Young, R. M., Crespo, B., Ceroni, F., Curry, C. J., Bellacchio, E., … Dobyns, W. B., … Ragge, N. K. (2019). De novo missense variants in FBXW11 cause diverse developmental phenotypes including brain, eye, and digit anomalies. American Journal of Human Genetics, 105, 640-657. doi: 10.1016/j.ajhg.2019.07.005.

Kanca, O., Andrews, J. C., Lee, P. T., Patel, C., Braddock, S. R., Slavotinek, A. M., … Dobyns, W. B., … Malicdan, M. C. V. (2019). De novo variants in WDR37 are associated with epilepsy, colobomas, dysmorphism, developmental delay, intellectual disability, and cerebellar hypoplasia. American Journal of Human Genetics, 105, 413-424. PMCID: PMC6699142. doi: 10.1016/j.ajhg.2019.06.014.

Monteiro, F. P., Curry, C. J., Hevner, R. F., Elliott, S., Fisher, J. H., Turocy, J., Dobyns, W. B., … Kok, F. (2019). Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European Journal of Medical Genetics, Jan 25 2019. doi: 10.1016/j.ejmg.2019.01.014.

Oegema, R., Barkovich, A. J., Mancini, G. M. S., Guerrini, R., Dobyns, W. B. (2019). Subcortical heterotopic gray matter brain malformations: Classification study of 107 individuals. Neurology, Sep 4 2019. doi: 10.1212/WNL.0000000000008200.

Vandervore, L. V., Schot, R., Kasteleijn, E., Oegema, R., Stouffs, K., Gheldof, A., … Dobyns, W. B., … Mancini, G. M. S. (2019). Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics. Brain, 142, 867-884. PMCID: PMC6439326. doi: 10.1093/brain/awz045.

Daniel Doherty Aldinger, K. A., Timms, A. E., Thomson, Z., Mirzaa, G. M., Bennett, J. T., Rosenberg, A. B., … Glass, I. A., Millen, K. J., Doherty, D. A., Dobyns, W. B. (2019). Redefining the etiologic landscape of cerebellar malformations. American Journal of Human Genetics, 105, 606-615. doi: 10.1016/j.ajhg.2019.07.019.

Ward Drennan Nie, K., Hannaford, S., Director, H. M., Nishigaki, M. A., Drennan, W. R., Rubinstein, J. T. (2019). Mandarin tone recognition in English speakers with normal hearing and with cochlear implants. International Journal of Audiology, 1-10. doi: 10.1080/14992027.2019.1632498.

Evan Eichler Ang, C. E., Ma, Q., Wapinski, O. L., Fan, S., Flynn, R. A., Lee, Q. Y., … Eichler, E. E., … Chang, H. Y. (2019). The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders. eLife, 8, Jan 10 2019. PMCID: PMC6380841. doi: 10.7554/eLife.41770.

Audano, P. A., Sulovari, A., Graves-Lindsay, T. A., Cantsilieris, S., Sorensen, M., Welch, A. E., … Eichler, E. E. (2019). Characterizing the major structural variant alleles of the human genome. Cell, 176, 663-675 e19. PMCID: PMC6438697. doi: 10.1016/j.cell.2018.12.019.

Cogne, B., Ehresmann, S., Beauregard-Lacroix, E., Rousseau, J., Besnard, T., Garcia, T., … Eichler, E. E., … Campeau, P. M. (2019). Missense variants in the histone acetyltransferase complex component gene TRRAP cause autism and syndromic intellectual disability. American Journal of Human Genetics, 104, 530-541. PMCID: PMC6407527. doi: 10.1016/j.ajhg.2019.01.010.

Eichler, E. E. (2019). Genetic variation, comparative genomics, and the diagnosis of disease. The New England Journal of Medicine, 381, 64-74. PMCID: PMC6681822. doi: 10.1056/NEJMra1809315.

Feliciano, P., Zhou, X., Astrovskaya, I., Turner, T. N., Wang, T., Brueggeman, L., … Eichler, E. E., … Chung, W. K. (2019). Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes. NPJ Genomic Medicine, 4, 19. PMCID: PMC6707204. doi: 10.1038/s41525-019-0093-8.

Gao, L. Z., Liu, Y. L., Zhang, D., Li, W., Gao, J., Liu, Y., … Eichler, E. E. (2019). Evolution of Oryza chloroplast genomes promoted adaptation to diverse ecological habitats. Communications Biology, 2, 278. PMCID: PMC6659635. doi: 10.1038/s42003-019-0531-2.

Maggiolini, F. A. M., Cantsilieris, S., D'Addabbo, P., Manganelli, M., Coe, B. P., Dumont, B. L., … Eichler, E. E., Antonacci, F. (2019). Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus. PLoS Genetics, 15, e1008075. PMCID: PMC6436712. doi: 10.1371/journal.pgen.1008075.

Nellaker, C., Alkuraya, F. S., Baynam, G., Bernier, R. A., Bernier, F. P. J., Boulanger, V., … Eichler, E. E., … Minerva Consortium (2019). Enabling global clinical collaborations on identifiable patient data: The Minerva Initiative. Frontiers in Genetics, 10, 611. PMCID: PMC6681681. doi: 10.3389/fgene.2019.00611.

Pollen, A. A., Bhaduri, A., Andrews, M. G., Nowakowski, T. J., Meyerson, O. S., Mostajo-Radji, M. A., … Eichler, E. E., Kriegstein, A. R. (2019). Establishing cerebral organoids as models of human-specific brain evolution. Cell, 176, 743-756 e17. doi: 10.1016/j.cell.2019.01.017.

Annette Mercer Estes Davlantis, K. S., Estes, A. M., Dawson, G., Rogers, S. J. (2019). A novel method for measuring learning opportunities provided by parents to young children with autism spectrum disorder. Autism, 1362361318817303. doi: 10.1177/1362361318817303.

Estes, A. M., St John, T., Dager, S. R. (2019). What to tell a parent who worries a young child has autism. JAMA Psychiatry, Aug 7 2019. doi: 10.1001/jamapsychiatry.2019.1234.

Iverson, J. M., Shic, F., Wall, C. A., Chawarska, K., Curtin, S., Estes, A. M., … Stone, W. L., … Young, G. S. (2019). Early motor abilities in infants at heightened versus low risk for ASD: A Baby Siblings Research Consortium (BSRC) study. Journal of Abnormal Psychology, 128, 69-80. PMCID: PMC6338079. doi: 10.1037/abn0000390.

Rogers, S. J., Estes, A. M., Lord, C., Munson, J., Rocha, M., Winter, J., … Talbott, M. (2019). A multisite randomized controlled two-phase trial of the Early Start Denver Model compared to treatment as usual. Journal of the American Academy of Child and Adolescent Psychiatry, Jan 24 2019. doi: 10.1016/j.jaac.2019.01.004.

Elaine Faustman Park, J. D., Kim, J. K., Jo, M. S., Kim, Y. H., Jeon, K. S., Lee, J. H., Faustman, E. M., … Yu, I. J. (2019). Lobar evenness of deposition/retention in rat lungs of inhaled silver nanoparticles: An approach for reducing animal use while maximizing endpoints. Particle and Fibre Toxicology, 16, 2. PMCID: PMC6322301. doi: 10.1186/s12989-018-0286-9.

Petroff, R., Hendrix, A., An, S., Anderson, M., Jo, Y., Lim, J., … Faustman, E. M. (2019). A call to include indirect effects of marine microplastics in human health risk assessments. Integrated Environmental Assessment and Management, 15, 819-820. doi: 10.1002/ieam.4195.

Martin Frasch Cao, M., MacDonald, J. W., Liu, H. L., Weaver, M., Cortes, M., Durosier, L. D., … Bernier, R. A., … Frasch, M. G. (2019). Alpha7 nicotinic acetylcholine receptor signaling modulates ovine fetal brain astrocytes transcriptome in response to endotoxin. Frontiers in Immunology, 10, 1063. PMCID: PMC6520997. doi: 10.3389/fimmu.2019.01063.

Georgieva, A., Abry, P., Chudacek, V., Djuric, P. M., Frasch, M. G., Kok, R., … Vullings, R. (2019). Computer-based intrapartum fetal monitoring and beyond: A review of the 2nd Workshop on Signal Processing and Monitoring in Labor (October 2017, Oxford, UK). Acta Obstetricia et Gynecologica Scandinavica, 98, 1207-1217. doi: 10.1111/aogs.13639.

Herry, C. L., Burns, P., Desrochers, A., Fecteau, G., Durosier, L. D., Cao, M., … Frasch, M. G. (2019). Vagal contributions to fetal heart rate variability: An omics approach. Physiological Measurement, 40, 065004. doi: 10.1088/1361-6579/ab21ae.

Rivolta, M. W., Stampalija, T., Frasch, M. G., Sassi, R. (2019). Theoretical value of deceleration capacity points to deceleration reserve of fetal heart rate. IEEE Transactions on Biomedical Engineering, Aug 2 2019. doi: 10.1109/TBME.2019.2932808.

Gwenn Garden McDonough, A., Noor, S., Lee, R. V., Dodge, R., 3rd, Strosnider, J. S., Shen, J., … Garden, G. A., Weinstein, J. R. (2019). Ischemic preconditioning induces cortical microglial proliferation and a transcriptomic program of robust cell cycle activation. Glia, Aug 17 2019. doi: 10.1002/glia.23701.

Adam Geballe Limaye, A. P., Green, M. L., Edmison, B. C., Stevens-Ayers, T., Chatterton-Kirchmeier, S., Geballe, A. P., … Boeckh, M. (2019). Prospective assessment of cytomegalovirus immunity in high-risk donor-seropositive/recipient-seronegative liver transplant recipients receiving either preemptive therapy or antiviral prophylaxis. The Journal of Infectious Diseases, 220, 752-760. doi: 10.1093/infdis/jiz181.

Ian Glass Aldinger, K. A., Timms, A. E., Thomson, Z., Mirzaa, G. M., Bennett, J. T., Rosenberg, A. B., … Glass, I. A., Millen, K. J., Doherty, D. A., Dobyns, W. B. (2019). Redefining the etiologic landscape of cerebellar malformations. American Journal of Human Genetics, 105, 606-615. doi: 10.1016/j.ajhg.2019.07.019.

Carter, L. B., Battaglia, A., Cherry, A., Manning, M. A., Ruzhnikov, M. R., Bird, L. M., … Glass, I. A., … Hudgins, L. (2019). Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy. American Journal of Medical Genetics. Part A, 179, 1543-1546. doi: 10.1002/ajmg.a.61266.

Cox, T. C., Lidral, A. C., McCoy, J. C., Liu, H., Cox, L. L., Zhu, Y., … Glass, I. A., … Roscioli, T. (2019). Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. Human Mutation, Jun 18 2019. doi: 10.1002/humu.23793.

Paine, I., Posey, J. E., Grochowski, C. M., Jhangiani, S. N., Rosenheck, S., Kleyner, R., … Glass, I. A., … Lupski, J. R. (2019). Paralog studies augment gene discovery: DDX and D genes. American Journal of Human Genetics, 105, 302-316. PMCID: PMC6698803. doi: 10.1016/j.ajhg.2019.06.001.

Joan M. Goverman Kirby, L., Jin, J., Cardona, J. G., Smith, M. D., Martin, K. A., Wang, J., … Goverman, J. M., … Calabresi, P. A. (2019). Oligodendrocyte precursor cells present antigen and are cytotoxic targets in inflammatory demyelination. Nature Communications, 10, 3887. PMCID: PMC6715717. doi: 10.1038/s41467-019-11638-3.

Robert Hevner Chang, Y. C., Daza, R., Hevner, R. F., Costa, L. G., Cole, T. B. (2019). Prenatal and early life diesel exhaust exposure disrupts cortical lamina organization: Evidence for a reelin-related pathogenic pathway induced by interleukin-6. Brain, Behavior, and Immunity, 78, 105-115. doi: 10.1016/j.bbi.2019.01.013.

David Horn Liu, C. C., Anne, S., Horn, D. L. (2019). Advances in management of pediatric sensorineural hearing loss. Otolaryngologic Clinics of North America, 52, 847-861. doi: 10.1016/j.otc.2019.05.004.

Mitchell, R. M., Christianson, E., Ramirez, R., Onchiri, F. M., Horn, D. L., Pontis, L., … Sie, K. C. Y. (2019). Auditory comprehension outcomes in children who receive a cochlear implant before 12 months of age. The Laryngoscope, May 14 2019. doi: 10.1002/lary.28061.

Walker, B. A., Gerhards, C. M., Werner, L. A., Horn, D. L. (2019). Amplitude modulation detection and temporal modulation cutoff frequency in normal hearing infants. Journal of the Acoustical Society of America, 145, 3667. doi: 10.1121/1.5111757.

Nina Isoherranen Burbacher, T. M., Grant, K. S., Petroff, R., Shum, S., Crouthamel, B., Stanley, C., … Isoherranen, N. (2019). Effects of oral domoic acid exposure on maternal reproduction and infant birth characteristics in a preclinical nonhuman primate model. Neurotoxicology and Teratology, 72, 10-21. PMCID: PMC6408264. doi: 10.1016/j.ntt.2019.01.001.

Isoherranen, N., Zhong, G. (2019). Biochemical and physiological importance of the CYP26 retinoic acid hydroxylases. Pharmacology and Therapeutics, 107400. doi: 10.1016/j.pharmthera.2019.107400.

Lefebvre, K. A., Yakes, B. J., Frame, E., Kendrick, P., Shum, S., Isoherranen, N., … Marcinek, D. J., Grattan, L. (2019). Discovery of a potential human serum biomarker for chronic seafood toxin exposure using an SPR biosensor. Toxins, 11, May 23 2019. PMCID: PMC6563296. doi: 10.3390/toxins11050293.

Stevison, F., Kosaka, M., Kenny, J. R., Wong, S., Hogarth, C., Amory, J. K., Isoherranen, N. (2019). Does in vitro cytochrome P450 downregulation translate to in vivo drug-drug interactions? preclinical and clinical studies with 13-cis-retinoic acid. Clinical and Translational Science, Jan 25 2019. doi: 10.1111/cts.12616.

Sandra Juul German, K., Vu, P. T., Irvine, J. D., Juul, S. E. (2019). Trends in reticulocyte hemoglobin equivalent values in critically ill neonates, stratified by gestational age. Journal of Perinatology, 39, 1268-1274. doi: 10.1038/s41372-019-0434-6.

Juul, S. E., Derman, R. J., Auerbach, M. (2019). Perinatal iron deficiency: Implications for mothers and infants. Neonatology, 115, 269-274. doi: 10.1159/000495978.

Massaro, A. N., Wu, Y. W., Bammler, T. K., MacDonald, J. W., Mathur, A., Chang, T., … Juul, S. E. (2019). Dried blood spot compared to plasma measurements of blood-based biomarkers of brain injury in neonatal encephalopathy. Pediatric Research, 85, 655-661. doi: 10.1038/s41390-019-0298-7.

Wu, Y. W., Goodman, A. M., Chang, T., Mulkey, S. B., Gonzalez, F. F., Mayock, D. E., Juul, S. E., … Redline, R. W. (2019). Placental pathology and neonatal brain MRI in a randomized trial of erythropoietin for hypoxic-ischemic encephalopathy. Pediatric Research, Jul 1 2019. doi: 10.1038/s41390-019-0493-6.

Franck Kalume Bolea, I., Gella, A., Sanz, E., Prada-Dacasa, P., Menardy, F., Bard, A. M., … Kalume, F., Quintana, A. (2019). Defined neuronal populations drive fatal phenotype in a mouse model of Leigh syndrome. eLife, 8, Aug 12 2019. PMCID: PMC6731060. doi: 10.7554/eLife.47163.

Raj P. Kapur Al-Haddad, B. J. S., Oler, E., Armistead, B., Elsayed, N. A., Weinberger, D. R., Bernier, R. A., … Kapur, R. P., … Adams Waldorf, K. M. (2019). The fetal origins of mental illness. American Journal of Obstetrics and Gynecology, Jun 15 2019. doi: 10.1016/j.ajog.2019.06.013.

Crow, A. R., Kapur, R. P., Koernig, S., Campbell, I. K., Jen, C. C., Mott, P. J., … Lazarus, A. H. (2019). Treating murine inflammatory diseases with an anti-erythrocyte antibody. Science Translational Medicine, 11, Aug 21 2019. doi: 10.1126/scitranslmed.aau8217.

Patricia Kuhl Zhao, T. C., Masapollo, M., Polka, L., Menard, L., Kuhl, P. K. (2019). Effects of formant proximity and stimulus prototypicality on the neural discrimination of vowels: Evidence from the auditory frequency-following response. Brain and Language, 194, 77-83. PMCID: PMC6697130. doi: 10.1016/j.bandl.2019.05.002.

Adrian K.C. Lee McLaughlin, S. A., Larson, E., Lee, A. K. C. (2019). Neural switch asymmetry in feature-based auditory attention tasks. Journal of the Association for Research in Otolaryngology, 20, 205-215. PMCID: PMC6453991. doi: 10.1007/s10162-018-00713-z.

David Marcinek

Heather Mefford Carapito, R., Ivanova, E. L., Morlon, A., Meng, L., Molitor, A., Erdmann, E., … Mefford, H. C., … Bahram, S. (2019). ZMIZ1 variants cause a syndromic neurodevelopmental disorder. American Journal of Human Genetics, 104, 319-330. PMCID: PMC6369415. doi: 10.1016/j.ajhg.2018.12.007.

Coppola, A., Cellini, E., Stamberger, H., Saarentaus, E., Cetica, V., Lal, D., … Mefford, H. C., … EpiCNV Consortium (2019). Diagnostic implications of genetic copy number variation in epilepsy plus. Epilepsia, 60, 689-706. doi: 10.1111/epi.14683.

Cowley, M. J., Liu, Y. C., Oliver, K. L., Carvill, G., Myers, C. T., Gayevskiy, V., … Mefford, H. C., … Roscioli, T. (2019). Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection. Human Mutation, 40, 374-79. PMCID: PMC6492103. doi: 10.1002/humu.23699.

Mefford, H. C. (2019). The road to diagnosis: Shortening the diagnostic odyssey in epilepsy. Epilepsy Currents, 1535759719871593. doi: 10.1177/1535759719871593.

Muir, A. M., King, C., Schneider, A. L., Buttar, A. S., Scheffer, I. E., Sadleir, L. G., Mefford, H. C. (2019). Double somatic mosaicism in a child with Dravet syndrome. Neurology Genetics, 5, e333. PMCID: PMC6481227. doi: 10.1212/NXG.0000000000000333.

Nabais Sa, M. J., Jensik, P. J., McGee, S. R., Parker, M. J., Lahiri, N., McNeil, E. P., … Mefford, H. C., … Vulto-vanSilfhout, A. T. (2019). De novo and biallelic DEAF1 variants cause a phenotypic spectrum. Genetics in Medicine, Mar 29 2019. doi: 10.1038/s41436-019-0473-6.

Pippucci, T., Licchetta, L., Baldassari, S., Marconi, C., De Luise, M., Myers, C., … Mefford, H. C., … Collaborative Group of Italian League Against Epilepsy Genetic Commission (2019). Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies. Annals of Clinical and Translational Neurology, 6, 475-485. PMCID: PMC6414475. doi: 10.1002/acn3.722.

Sands, T. T., Miceli, F., Lesca, G., Beck, A. E., Sadleir, L. G., Arrington, D. K., … Mefford, H. C., … Cilio, M. R. (2019). Autism and developmental disability caused by KCNQ3 gain-of-function variants. Annals of Neurology, 86, 181-192. doi: 10.1002/ana.25522.

Ye, Z., McQuillan, L., Poduri, A., Green, T. E., Matsumoto, N., Mefford, H. C., … Hildebrand, M. S. (2019). Somatic mutation: The hidden genetics of brain malformations and focal epilepsies. Epilepsy Research, 155, 106161. doi: 10.1016/j.eplepsyres.2019.106161.

Andrew Meltzoff Brooks, R., Singleton, J. L., Meltzoff, A. N. (2019). Enhanced gaze following behavior in deaf infants of deaf parents. Developmental Science, e12900. doi: 10.1111/desc.12900.

Ruba, A. L., Meltzoff, A. N., Repacholi, B. M. (2019). How do you feel? Preverbal infants match negative emotions to events. Developmental Psychology, Mar 4 2019. doi: 10.1037/dev0000711.

Shen, G., Meltzoff, A. N., Marshall, P. J. (2019). Body representations as indexed by oscillatory EEG activities in the context of tactile novelty processing. Neuropsychologia, 132, 107144. doi: 10.1016/j.neuropsychologia.2019.107144.

Kathleen J. Millen Aldinger, K. A., Timms, A. E., Thomson, Z., Mirzaa, G. M., Bennett, J. T., Rosenberg, A. B., … Glass, I. A., Millen, K. J., Doherty, D. A., Dobyns, W. B. (2019). Redefining the etiologic landscape of cerebellar malformations. American Journal of Human Genetics, 105, 606-615. doi: 10.1016/j.ajhg.2019.07.019.

Ghayda Mirzaa Aldinger, K. A., Timms, A. E., Thomson, Z., Mirzaa, G. M., Bennett, J. T., Rosenberg, A. B., … Glass, I. A., Millen, K. J., Doherty, D. A., Dobyns, W. B. (2019). Redefining the etiologic landscape of cerebellar malformations. American Journal of Human Genetics, 105, 606-615. doi: 10.1016/j.ajhg.2019.07.019.

Blackburn, A. T. M., Bekheirnia, N., Uma, V. C., Corkins, M. E., Xu, Y., Rosenfeld, J. A., … Mirzaa, G. M., … Bekheirnia, M. R. (2019). DYRK1A-related intellectual disability: A syndrome associated with congenital anomalies of the kidney and urinary tract. Genetics in Medicine, Jul 2 2019. doi: 10.1038/s41436-019-0576-0.

Fischer-Zirnsak, B., Segebrecht, L., Schubach, M., Charles, P., Alderman, E., Brown, K., … Mirzaa, G. M., Ehmke, N. (2019). Haploinsufficiency of the Notch Ligand DLL1 causes variable neurodevelopmental disorders. American Journal of Human Genetics, 105, 631-639. doi: 10.1016/j.ajhg.2019.07.002.

Cecilia B. Moens Iulianella, A., Wingate, R. J., Moens, C. B., Capaldo, E. (2019). The generation of granule cells during the development and evolution of the cerebellum. Developmental Dynamics, 248, 506-513. doi: 10.1002/dvdy.64.

Navajas Acedo, J., Voas, M. G., Alexander, R., Woolley, T., Unruh, J. R., Li, H., Moens, C. B., Piotrowski, T. (2019). PCP and Wnt pathway components act in parallel during zebrafish mechanosensory hair cell orientation. Nature Communications, 10, 3993. doi: 10.1038/s41467-019-12005-y.

Richard Morrison Cherry, A. E., Vicente, J. J., Xu, C., Morrison, R. S., Ong, S. E., Wordeman, L., Stella, N. (2019). GPR124 regulates microtubule assembly, mitotic progression, and glioblastoma cell proliferation. Glia, 67, 1558-1570. PMCID: PMC6557680. doi: 10.1002/glia.23628.

Ward, J. M., Stoyas, C. A., Switonski, P. M., Ichou, F., Fan, W., Collins, B., … Morrison, R. S., … La Spada, A. R. (2019). Metabolic and organelle morphology defects in mice and human patients define spinocerebellar ataxia type 7 as a mitochondrial disease. Cell Reports, 26, 1189-1202 e6. PMCID: PMC6420346. doi: 10.1016/j.celrep.2019.01.028.

Pierre D. Mourad Bobola, M. S., Ezeokeke, C. K., Kuznetslova, K., Lahti, A. C., Loeser, J. D., Olmstead, T. A., … Mourad, P. D. (2019). A pre-clinical study of the response threshold of intact and transected nerves to stimulation by transcutaneous intense focused ultrasound. Ultrasound in Medicine and Biology, 45, 2094-2103. doi: 10.1016/j.ultrasmedbio.2019.04.014.

Jeffrey Munson Rogers, S. J., Estes, A. M., Lord, C., Munson, J., Rocha, M., Winter, J., … Talbott, M. (2019). A multisite randomized controlled two-phase trial of the Early Start Denver Model compared to treatment as usual. Journal of the American Academy of Child and Adolescent Psychiatry, Jan 24 2019. doi: 10.1016/j.jaac.2019.01.004.

Scott Murray Mikkelsen, M., Rimbault, D. L., Barker, P. B., Bhattacharyya, P. K., Brix, M. K., Buur, P. F., … Murray, S. O., … Edden, R. A. E. (2019). Big GABA II: Water-referenced edited MR spectroscopy at 25 research sites. Neuroimage, 191, 537-548. doi: 10.1016/j.neuroimage.2019.02.059.

Michael Mustari Mayadali, U. S., Lienbacher, K., Mustari, M. J., Strupp, M., Horn, A. K. E. (2019). Potassium channels in omnipause neurons. Progress in Brain Research, 249, 117-123. doi: 10.1016/bs.pbr.2019.04.017.

Elizabeth A. Nance

Yellepeddi, V., Joseph, A., Nance, E. (2019). Pharmacokinetics of nanotechnology-based formulations in pediatric populations. Advanced Drug Delivery Reviews, Sep 5 2019. doi: 10.1016/j.addr.2019.08.008.

Edward J. Novotny, Jr. Sanchez Fernandez, I., Gainza-Lein, M., Abend, N. S., Amengual-Gual, M., Anderson, A., Arya, R., … Novotny, E. J., Jr., … Pediatric Status Epilepticus Research Group. (2019). The onset of pediatric refractory status epilepticus is not distributed uniformly during the day. Seizure, 70, 90-96. doi: 10.1016/j.seizure.2019.06.017.

Jeffrey Ojemann Bledsoe, J. C., Breiger, D., Breiger, M., Shonka, S., Ermoian, R. P., Ojemann, J. G., … Geyer, J. R. (2019). Differential trajectories of neurocognitive functioning in females versus males following treatment for pediatric brain tumors. Neuro-Oncology, May 23 2019. doi: 10.1093/neuonc/noz092.

Caldwell, D. J., Cronin, J. A., Wu, J., Weaver, K. E., Ko, A. L., Rao, R. P. N., Ojemann, J. G. (2019). Direct stimulation of somatosensory cortex results in slower reaction times compared to peripheral touch in humans. Scientific Reports, 9, 3292. PMCID: PMC6397274. doi: 10.1038/s41598-019-38619-2.

Holdgraf, C., Appelhoff, S., Bickel, S., Bouchard, K., D'Ambrosio, S., David, O., … Ojemann, J. G., … Hermes, D. (2019). iEEG-BIDS, extending the Brain Imaging Data Structure specification to human intracranial electrophysiology. Scientific Data, 6, 102. PMCID: PMC6592874. doi: 10.1038/s41597-019-0105-7.

Kogan, M., Caldwell, D. J., Hakimian, S., Weaver, K. E., Ko, A. L., Ojemann, J. G. (2019). Differentiation of epileptic regions from voluntary high-gamma activation via interictal cross-frequency windowed power-power correlation. Journal of Neurosurgery, 1-11. doi: 10.3171/2019.2.JNS181991.

Wilson, N. R., Sarma, D., Wander, J. D., Weaver, K. E., Ojemann, J. G., Rao, R. P. N. (2019). Cortical topography of error-related high-frequency potentials during erroneous control in a continuous control brain-computer interface. Frontiers in Neuroscience, 13, 502. PMCID: PMC6541115. doi: 10.3389/fnins.2019.00502.

Wu, C., Jermakowicz, W. J., Chakravorti, S., Cajigas, I., Sharan, A. D., Jagid, J. R., … Ojemann, J. G., … D'Haese, P. F. (2019). Effects of surgical targeting in laser interstitial thermal therapy for mesial temporal lobe epilepsy: A multicenter study of 234 patients. Epilepsia, 60, 1171-1183. PMCID: PMC6551254. doi: 10.1111/epi.15565.

Jaime Olavarria Andelin, A. K., Olavarria, J. F., Fine, I., Taber, E. N., Schwartz, D., Kroenke, C. D., Stevens, A. A. (2019). The effect of onset age of visual deprivation on visual cortex surface area across-species. Cerebral Cortex, 29, 4321-4333. PMCID: PMC6735253 doi: 10.1093/cercor/bhy315.

Monica Oxford

Hash, J. B., Oxford, M. L., Fleming, C. B., Ward, T. M., Spieker, S. J. (2019). Sleep problems, daily napping behavior, and social-emotional functioning among young children from families referred to Child Protective Services. Behavioral Sleep Medicine, 1-13. doi: 10.1080/15402002.2019.1611579.

Hash, J. B., Oxford, M. L., Fleming, C. B., Ward, T. M., Spieker, S. J., Lohr, M. J. (2019). Impact of a home visiting program on sleep problems among young children experiencing adversity. Child Abuse & Neglect, 89, 143-154. doi: 10.1016/j.chiabu.2018.12.016.

Leo Pallanck Andreazza, S., Samstag, C. L., Sanchez-Martinez, A., Fernandez-Vizarra, E., Gomez-Duran, A., Lee, J. J., … Pallanck, L. J., … Whitworth, A. J. (2019). Mitochondrially-targeted APOBEC1 is a potent mtDNA mutator affecting mitochondrial function and organismal fitness in Drosophila. Nature Communications, 10, 3280. PMCID: PMC6650417. doi: 10.1038/s41467-019-10857-y.

Vincow, E. S., Thomas, R. E., Merrihew, G. E., Shulman, N. J., Bammler, T. K., MacDonald, J. W., … Pallanck, L. J. (2019). Autophagy accounts for approximately one-third of mitochondrial protein turnover and is protein selective. Autophagy, 1-14. doi: 10.1080/15548627.2019.1586258.

Jay Parrish Jiang, N., Rasmussen, J. P., Clanton, J. A., Rosenberg, M. F., Luedke, K. P., Cronan, M. R., … Parrish, J. Z. (2019). A conserved morphogenetic mechanism for epidermal ensheathment of nociceptive sensory neurites. eLife, 8, Mar 11 2019. PMCID: PMC6450671. doi: 10.7554/eLife.42455.

James Phillips Estrada, M., Kelly, J. P., Wright, J., Phillips, J. O., Weiss, A. (2019). Visual function, brain imaging, and physiological factors in children with asymmetric nystagmus due to chiasmal gliomas. Pediatric Neurology, 97, 30-37. doi: 10.1016/j.pediatrneurol.2019.03.021.

Suzie Pun Olden, B. R., Cheng, E., Cheng, Y., Pun, S. H. (2019). Identifying key barriers in cationic polymer gene delivery to human T cells. Biomaterials Science, 7, 789-797. PMCID: PMC6391219. doi: 10.1039/c8bm01262h.

Peng, J., Zuo, C., Xiao, Q., Deng, K., Meng, C., Liu, Y., … Pun, S. H., Wei, H. (2019). Synthesis of stimuli-responsive nanosized ring-like colloids and cyclic polymers via a dual-template approach. Chemical Science, 10, 3943-3948. PMCID: PMC6471857. doi: 10.1039/c9sc00450e.

Jan-Marino (Nino) Ramirez Nasirova, N., Quina, L. A., Agosto-Marlin, I. M., Ramirez, J. M., Lambe, E. K., Turner, E. E. (2019). Dual recombinase fate mapping reveals a transient cholinergic phenotype in multiple populations of developing glutamatergic neurons. The Journal of Comparative Neurology, Aug 9 2019. doi: 10.1002/cne.24753.

Wendy Raskind Doyle, T. B., Hayes, M. P., Chen, D. H., Raskind, W. H., Watts, V. J. (2019). Functional characterization of AC5 gain-of-function variants: Impact on the molecular basis of ADCY5-related dyskinesia. Biochemical Pharmacology, 163, 169-177. PMCID: PMC6470011. doi: 10.1016/j.bcp.2019.02.005.

Todd Richards Petroff, R., Richards, T. L., Crouthamel, B., McKain, N., Stanley, C., Grant, K. S., … Isoherranen, N., Burbacher, T. M. (2019). Chronic, low-level oral exposure to marine toxin, domoic acid, alters whole brain morphometry in nonhuman primates. Neurotoxicology, Feb 28 2019. doi: 10.1016/j.neuro.2019.02.016.

Jay Rubinstein Nie, K., Hannaford, S., Director, H. M., Nishigaki, M. A., Drennan, W. R., Rubinstein, J. T. (2019). Mandarin tone recognition in English speakers with normal hearing and with cochlear implants. International Journal of Audiology, 1-10. doi: 10.1080/14992027.2019.1632498.

Parkinson, A. J., Rubinstein, J. T., Drennan, W. R., Dodson, C., Nie, K. (2019). Hybrid music perception outcomes: Implications for melody and timbre recognition in cochlear implant recipients. Otology & Neurotology, 40, e283-e289. doi: 10.1097/MAO.0000000000002126.

Hannele Ruohola-Baker Battle, S. L., Doni Jayavelu, N., Azad, R. N., Hesson, J., Ahmed, F. N., Overbey, E. G., … Ruohola-Baker, H., … Hawkins, R. D. (2019). Enhancer chromatin and 3D genome architecture changes from naive to primed human embryonic stem cell states. Stem Cell Reports, 12, 1129-1144. PMCID: PMC6524944. doi: 10.1016/j.stemcr.2019.04.004.

C. Ronald Scott Jack, R. M., Scott, C. R. (2019). Validation of a therapeutic range for nitisinone in patients treated for tyrosinemia type 1 based on reduction of succinylacetone excretion. JMID Reports, 46, 75-78. PMCID: PMC6498826. doi: 10.1002/jmd2.12023.

Frederick Shic Bangerter, A., Ness, S., Lewin, D., Aman, M. G., Esbensen, A. J., Goodwin, M. S., … Shic, F., … Pandina, G. (2019). Clinical validation of the Autism Behavior Inventory: Caregiver-rated assessment of core and associated symptoms of autism spectrum disorder. Journal of Autism and Developmental Disorders, Mar 19 2019. doi: 10.1007/s10803-019-03965-7.

Bangerter, A., Manyakov, N. V., Lewin, D., Boice, M., Skalkin, A., Jagannatha, S., … Shic, F., … Pandina, G. (2019). Caregiver daily reporting of symptoms in Autism Spectrum Disorder: Observational study using web and mobile apps. JMIR Mental Health, 6, e11365. PMCID: PMC6454343. doi: 10.2196/11365.

Bradshaw, J., Shic, F., Holden, A. N., Horowitz, E. J., Barrett, A. C., German, T. C., Vernon, T. W. (2019). The use of eye tracking as a biomarker of treatment outcome in a pilot randomized clinical trial for young children with autism. Autism Research, Mar 20 2019. doi: 10.1002/aur.2093.

Ness, S. L., Bangerter, A., Manyakov, N. V., Lewin, D., Boice, M., Skalkin, A., … Shic, F., … Pandina, G. (2019). An observational study with the Janssen Autism Knowledge Engine (JAKE (R)) in individuals with autism spectrum disorder. Frontiers in Neuroscience, 13, 111. PMCID: PMC6402449. doi: 10.3389/fnins.2019.00111.

Sabatos-DeVito, M., Murias, M., Dawson, G., Howell, T., Yuan, A., Marsan, S., Bernier, R. A., … Shic, F., … Webb, S. J., … Autism Biomarkers Consortium for Clinical, Trials (2019). Methodological considerations in the use of Noldus EthoVision XT video tracking of children with autism in multi-site studies. Biological Psychology, 146, 107712. doi: 10.1016/j.biopsycho.2019.05.012.

Shic, F., Wang, Q., Macari, S. L., Chawarska, K. (2019). The role of limited salience of speech in selective attention to faces in toddlers with autism spectrum disorders. Journal of Child Psychology and Psychiatry and Allied Disciplines, Aug 30 2019. doi: 10.1111/jcpp.13118.

Wang, Q., Wall, C. A., Barney, E. C., Bradshaw, J. L., Macari, S. L., Chawarska, K., Shic, F. (2019). Promoting social attention in 3-year-olds with ASD through gaze-contingent eye tracking. Autism Research, Aug 30 2019. doi: 10.1002/aur.2199.

Stephen E. P. Smith

Lautz, J. D., Gniffke, E. P., Brown, E. A., Immendorf, K. B., Mendel, R. D., Smith, S. E. P. (2019). Activity-dependent changes in synaptic protein complex composition are consistent in different detergents despite differential solubility. Scientific Reports, 9, 10890. PMCID: PMC6659712. doi: 10.1038/s41598-019-46690-y.

Neier, S. C., Ferrer, A., Wilton, K. M., Smith, S. E. P., Kelcher, A. M. H., Pavelko, K. D., … Schrum, A. G. (2019). The early proximal alphabeta TCR signalosome specifies thymic selection outcome through a quantitative protein interaction network. Science Immunology, 4, Feb 15 2019. doi: 10.1126/sciimmunol.aal2201.

Matthew Speltz

Hammal, Z., Wallace, E. R., Speltz, M. L., Heike, C. L., Birgfeld, C. B., Cohn, J. F. (2019). Dynamics of face and head movement in infants with and without craniofacial microsomia: An automatic approach. Plastic and Reconstructive Surgery. Global Open, 7, e2081. PMCID: PMC6382247. doi: 10.1097/GOX.0000000000002081.

Luquetti, D. V., Speltz, M. L., Wallace, E. R., Siebold, B., Collett, B. R., Drake, A. F., … Heike, C. L. (2019). Methods and challenges in a cohort study of infants and toddlers with craniofacial microsomia: The clock study. The Cleft Palate-Craniofacial Journal, 1055665618821014. doi: 10.1177/1055665618821014.

Siebold, B., Heike, C. L., Leroux, B. G., Speltz, M. L., Drake, A. F., Johns, A. L., … Luquetti, D. V. (2019). Evaluation of prenatal diabetes mellitus and other risk factors for craniofacial microsomia. Birth Defects Research, Mar 30 2019. doi: 10.1002/bdr2.1502.

Susan Spieker Hash, J. B., Oxford, M. L., Fleming, C. B., Ward, T. M., Spieker, S. J., Lohr, M. J. (2019). Impact of a home visiting program on sleep problems among young children experiencing adversity. Child Abuse & Neglect, 89, 143-154. doi: 10.1016/j.chiabu.2018.12.016.

Mark Stein Russell, D., Weiss, M., Stein, M. A. (2019). A maximum dose for methylphenidate-How much is too much? JAMA Pediatrics, 173, 621-622. doi: 10.1001/jamapediatrics.2019.0911.

Steingard, R., Taskiran, S., Connor, D. F., Markowitz, J. S., Stein, M. A. (2019). New formulations of stimulants: An update for clinicians. Journal of Child and Adolescent Psychopharmacology, 29, 324-339. doi: 10.1089/cap.2019.0043.

Nephi Stella Cao, J. K., Viray, K., Zweifel, L., Stella, N. (2019). Sex-dependent impaired locomotion and motor coordination in the HdhQ200/200 mouse model of Huntington's Disease. Neurobiology of Disease, 104607. doi: 10.1016/j.nbd.2019.104607.

Cao, J. K., Kaplan, J., Stella, N. (2019). ABHD6: Its place in endocannabinoid signaling and beyond. Trends in Pharmacological Sciences, 40, 267-277. PMCID: PMC6445269. doi: 10.1016/j.tips.2019.02.002.

Cherry, A. E., Vicente, J. J., Xu, C., Morrison, R. S., Ong, S. E., Wordeman, L., Stella, N. (2019). GPR124 regulates microtubule assembly, mitotic progression, and glioblastoma cell proliferation. Glia, 67, 1558-1570. PMCID: PMC6557680. doi: 10.1002/glia.23628.

Jennifer Stone Warchol, M. E., Massoodnia, R., Pujol, R., Cox, B. C., Stone, J. S. (2019). Development of hair cell phenotype and calyx nerve terminals in the neonatal mouse utricle. The Journal of Comparative Neurology, Feb 6 2019. doi: 10.1002/cne.24658.

Wendy Stone Ibanez, L. V., Stoep, A. V., Myers, K., Zhou, C., Dorsey, S., Steinman, K. J., Stone, W. L. (2019). Promoting early autism detection and intervention in underserved communities: Study protocol for a pragmatic trial using a stepped-wedge design. BMC Psychiatry, 19, 169. PMCID: PMC6556010. doi: 10.1186/s12888-019-2150-3.

Colin Studholme Hunt, D., Dighe, M., Gatenby, C., Studholme, C. (2019). Automatic, age consistent reconstruction of the corpus callosum guided by coherency from in utero diffusion-weighted MRI. IEEE Transactions on Medical Imaging, Aug 2 2019. doi: 10.1109/TMI.2019.2932681.

Kamino, D., Chau, V., Studholme, C., Liu, M., Xu, D., Barkovich, A. J., … Tam, E. W. Y. (2019). Plasma cholesterol levels and brain development in preterm newborns. Pediatric Research, 85, 299-304. PMCID: PMC6433157. doi: 10.1038/s41390-018-0260-0.

Stephen Tapscott Jagannathan, S., Ogata, Y., Gafken, P. R., Tapscott, S. J., Bradley, R. K. (2019). Quantitative proteomics reveals key roles for post-transcriptional gene regulation in the molecular pathology of facioscapulohumeral muscular dystrophy. eLife, 8, Jan 15 2019. PMCID: PMC6349399. doi: 10.7554/eLife.41740.

Oliva, J., Galasinski, S., Richey, A., Campbell, A. E., Meyers, M. J., Modi, N., … Tapscott, S. J., Sverdrup, F. M. (2019). Clinically advanced p38 inhibitors suppress DUX4 expression in cellular and animal models of facioscapulohumeral muscular dystrophy. Journal of Pharmacology and Experimental Therapeutics, 370, 219-230. PMCID: PMC6652132. doi: 10.1124/jpet.119.259663.

Eric Turner Nasirova, N., Quina, L. A., Agosto-Marlin, I. M., Ramirez, J. M., Lambe, E. K., Turner, E. E. (2019). Dual recombinase fate mapping reveals a transient cholinergic phenotype in multiple populations of developing glutamatergic neurons. The Journal of Comparative Neurology, Aug 9 2019. doi: 10.1002/cne.24753.

Sara Jane Webb Sabatos-DeVito, M., Murias, M., Dawson, G., Howell, T., Yuan, A., Marsan, S., Bernier, R. A., … Shic, F., … Webb, S. J., … Autism Biomarkers Consortium for Clinical Trials. (2019). Methodological considerations in the use of Noldus EthoVision XT video tracking of children with autism in multi-site studies. Biological Psychology, 146, 107712. doi: 10.1016/j.biopsycho.2019.05.012.

Jonathan Weinstein McDonough, A., Weinstein, J. R. (2019). The role of microglia in ischemic preconditioning. Glia, Aug 6 2019. doi: 10.1002/glia.23695.

McDonough, A., Noor, S., Lee, R. V., Dodge, R., 3rd, Strosnider, J. S., Shen, J., … Garden, G. A., Weinstein, J. R. (2019). Ischemic preconditioning induces cortical microglial proliferation and a transcriptomic program of robust cell cycle activation. Glia, Aug 17 2019. doi: 10.1002/glia.23701.

H. Steve White Bialer, M., Johannessen, S. I., Koepp, M. J., Levy, R. H., Perucca, E., Tomson, T., White, H. S. (2019). A summary of data presented at the XIV conference on new antiepileptic drug and devices (EILAT XIV). Epilepsy Research, 153, 66-67. doi: 10.1016/j.eplepsyres.2019.03.002.

Hill, A. C., Rower, J. E., White, H. S. (2019). The pharmacokinetics of oral carbamazepine in rats dosed using an automated drug delivery system. Epilepsia, 60, 1829-1837. doi: 10.1111/epi.16293.

Hill, A. C., Thomson, K. E., Newell, T. G., White, H. S. (2019). Correction of medication nonadherence results in better seizure outcomes than dose escalation in a novel preclinical epilepsy model of adherence. Epilepsia, 60, 475-484. doi: 10.1111/epi.14655.

Libin Xu Fleurie, A., Zoued, A., Alvarez, L., Hines, K. M., Cava, F., Xu, L., … Waldor, M. K. (2019). A vibrio cholerae BolA-like protein is required for proper cell shape and cell envelope integrity. mBio, 10, Jul 9 2019. doi: 10.1128/mBio.00790-19.

Herron, J. M., Hines, K. M., Tomita, H., Seguin, R. P., Cui, J. Y., Xu, L. (2019). Multi-omics investigation reveals benzalkonium chloride disinfectants alter sterol and lipid homeostasis in the mouse neonatal brain. Toxicological Sciences, Jun 14 2019. doi: 10.1093/toxsci/kfz139.

Smita Yadav Yadav, S., Younger, S. H., Zhang, L., Thompson-Peer, K. L., Li, T., Jan, L. Y., Jan, Y. N. (2019). Glial ensheathment of the somatodendritic compartment regulates sensory neuron structure and activity. Proceedings of the National Academy of Sciences of the United States of America, 116, 5126-5134. PMCID: PMC6421456. doi: 10.1073/pnas.1814456116.

Jason Yeatman Bain, J. S., Yeatman, J. D., Schurr, R., Rokem, A., Mezer, A. A. (2019). Evaluating arcuate fasciculus laterality measurements across dataset and tractography pipelines. Human Brain Mapping, 40, 3695-3711. PMCID: PMC6679767. doi: 10.1002/hbm.24626.

Keshavan, A., Yeatman, J. D., Rokem, A. (2019). Combining citizen science and deep learning to amplify expertise in neuroimaging. Frontiers in Neuroinformatics, 13, 29. PMCID: PMC6517786. doi: 10.3389/fninf.2019.00029.

O'Brien, G. E., McCloy, D. R., Yeatman, J. D. (2019). Categorical phoneme labeling in children with dyslexia does not depend on stimulus duration. Journal of the Acoustical Society of America, 146, 245. PMCID: PMC6639114. doi: 10.1121/1.5116568.

White, A. L., Boynton, G. M., Yeatman, J. D. (2019). You can't recognize two words simultaneously. Trends in Cognitive Sciences, Jul 18 2019. doi: 10.1016/j.tics.2019.07.001.