NATURE No. 1 Weekly Science Journal, with Highest Ever Impact Factor Impact Factor: 41.456
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Bibliometric Tools Applied to Analytical Articles: the Example of Gene
The current issue and full text archive of this journal is available at www.emeraldinsight.com/1065-075X.htm OCLC 25,3 Bibliometric tools applied to analytical articles: the example of gene transfer-related research 186 Donghui Wen College of Environmental Sciences and Engineering, Peking University, Beijing, Received December 2008 Reviewed January 2009 China, and Accepted January 2009 Te-Chen Yu and Yuh-Shan Ho Bibliometric Research Centre, I-Shou University, Kaohsiung, Taiwan Abstract Purpose – The objective of this study is to conduct a bibliometric indicator and to conduct an analysis of citations per publication of all horizontal gene transfer-related publications in the Science Citation Index (SCI). A systematic search was performed using the SCI for publications during the period 1991-2005. Design/methodology/approach – The data were based on the online version of the Science Citation Index (SCI), Web of Science. Analyzed parameters included authorship, patterns of international collaboration, journal, language, document type, number of times cited, author, and KeyWords Plus. Findings – The USA and Germany produced 57 percent of the total articles and 77 percent of the total times cited in three years after publication. In addition, a simulation model was applied to describe the relationship between the cumulative number of citations and the article life. Originality/value – This is one of the first studies that uses analysis of citations per publication, defined as the ratio of the number of citations per publication in a certain period, to assess the impact relative to the entire field. Keywords Serials, Genetics, Research results, Publishing Paper type Research paper Introduction Horizontal gene transfer (HGT), or lateral gene transfer (LGT), is the collective name for processes that permit the exchange of DNA among organisms of different species (Jain et al., 2003). -
Top Peer Reviewed Journals – Molecular Biology & Genetics
Top Peer Reviewed Journals – Molecular Biology & Genetics Presented to Iowa State University Presented by Thomson Reuters Molecular Biology & Genetics The subject discipline for Molecular Biology & Genetics is made of 5 narrow subject categories from the Web of Science. The 5 categories that make up Molecular Biology & Genetics are: 1. Biochemistry & Molecular Biology 4. Developmental Biology 2. Cell Biology 5. Genetics & Heredity 3. Cytology & Histology The chart below provides an ordered view of the top peer reviewed journals within the 1st quartile for Molecular Biology & Genetics based on Impact Factors (IF), three year averages and their quartile ranking. Journal 2009 IF 2010 IF 2011 IF Average IF NATURE REVIEWS MOLECULAR CELL 42.19 38.65 39.12 39.99 BIOLOGY NATURE GENETICS 34.28 36.37 35.53 35.39 NATURE REVIEWS GENETICS 27.82 32.74 38.07 32.88 CELL 31.15 32.4 32.4 31.98 NATURE CELL BIOLOGY 19.52 19.4 19.48 19.47 ANNUAL REVIEW OF GENETICS 13.23 21.77 22.23 19.08 ANNUAL REVIEW OF CELL AND 19.57 14.07 15.83 16.49 DEVELOPMENTAL BIOLOGY Cell Metabolism 17.35 18.2 13.66 16.40 ANNUAL REVIEW OF GENOMICS AND 11.56 17.18 14.82 14.52 HUMAN GENETICS MOLECULAR CELL 14.6 14.19 14.17 14.32 DEVELOPMENTAL CELL 13.36 13.94 14.03 13.78 CURRENT OPINION IN CELL BIOLOGY 14.15 13.54 12.89 13.53 GENOME RESEARCH 11.34 13.58 13.6 12.84 TRENDS IN CELL BIOLOGY 12.11 12.14 12.35 12.20 GENES & DEVELOPMENT 12.07 12.88 11.65 12.20 AMERICAN JOURNAL OF HUMAN 12.3 11.68 10.6 11.53 GENETICS Journal of Molecular Cell Biology 13.4 7.66 10.53 Molecular Systems Biology -
An Introduction of C. Yung Yu's Research at the Research Institute
An Introduction of C. Yung Yu’s Research at the Research Institute, Nationwide Children’s Hospital (12/13/2011) I received my major postgraduate trainings in Oxford and Cambridge, U.K., before moving across the Atlantic to Columbus, Ohio in June, 1990. During the past 21 years, I witnessed the tremendous growth and development of the Research Institute at Nationwide Children’s Hospital and the Ohio State University, by which I am currently a principal investigator or a tenured faculty member. The theme of my research projects is centered on the molecular biology and genetics of immune effector proteins in human autoimmune diseases. My research team did the original work that contributed to the establishment of copy number variations (CNVs) among healthy subjects, and determination of differential susceptibilities for immune effector gene CNVs in systemic lupus erythematosus (SLE), type 1 diabetes and rheumatoid arthritis. The discovery of common, continuous CNVs provides important conceptual and technical advance in the genetics of complex diseases. Since joining Nationwide/Columbus Children’s Hospital, 8 doctorate (PhD) students, 4 clinical research fellows, and 4 masters (MS) students successfully graduated from my laboratory. Many postdoctoral fellows, visiting professors, scholars, professional and undergraduate students performed research or collaborative experiments in our laboratory. Our research projects were sponsored by three primary NIH R01 grants and one program project P01 grant, which were focused on the immunogenetics of complement C4 in human SLE. In addition, we received awards and subcontracts from NIH and private foundations. I have published a total of 94 research articles. During my tenure at NCH/OSU, my research team has authored/co-authored a total of 75 papers, among them were 60 peer-reviewed original articles, 7 peer-reviewed review articles, and 8 editor-reviewed book chapters. -
Human Gene Function Publications That Describe Wrongly Identified Nucleotide Sequence
bioRxiv preprint doi: https://doi.org/10.1101/2021.07.29.453321; this version posted July 31, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 1 Human gene function publications that describe wrongly identified nucleotide sequence 2 reagents are unacceptably frequent within the genetics literature 3 Short title: Wrongly identified nucleotide sequences in gene function papers 4 Yasunori Park1, Rachael A West1,2, Pranujan Pathmendra1, Bertrand Favier3, Thomas 5 Stoeger4,5,6, Amanda Capes-Davis1,7, Guillaume Cabanac8, Cyril Labbé9, Jennifer A 6 Byrne1,10,* 7 1Faculty of Medicine and Health, The University of Sydney, NSW, Australia 8 2Children’s Cancer Research Unit, Kids Research, The Children’s Hospital at Westmead, 9 Westmead, NSW, Australia 10 3Univ. Grenoble Alpes, TIMC, Grenoble, France 11 4Successful Clinical Response in Pneumonia Therapy (SCRIPT) Systems Biology Center, 12 Northwestern University, Evanston, United States. 13 5Department of Chemical and Biological Engineering, Northwestern University, Evanston, 14 United States. 15 6Center for Genetic Medicine, Northwestern University School of Medicine, Chicago, United 16 States 17 7CellBank Australia, Children’s Medical Research Institute, Westmead, New South Wales, 18 Australia 19 8Computer Science Department, IRIT UMR 5505 CNRS, University of Toulouse, 118 route 20 de Narbonne, 31062 Toulouse Cedex 9, France 21 9Univ. Grenoble Alpes, CNRS, Grenoble INP, LIG, Grenoble, France 22 10NSW Health Statewide Biobank, NSW Health Pathology, Camperdown, NSW, Australia 23 *Corresponding author 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.07.29.453321; this version posted July 31, 2021.