As a Social Construction in Genetics Andrew Smart, Richard Tutton, Paul Martin and George T.H
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International Symposium of Human Genetics
ichg2022.com THE INTERNATIONAL The 14th International Congress of Human FEDERATION OF HUMAN Genetics was postponed GENETICS SOCIETIES by almost a year due to the COVID-19 pandemic, PRESENTS: and the LOC has decided to host a Symposium in 2021 as a taster of what will be expected at the International Congress in 2022. We are bringing together Symposium on exceptional speakers for two sessions on topics that are highly relevant to Human Genetics human geneticists and these discussions will be picked up again at the 9 & 10 March 2021 main meeting in 2022. DAY 1: The shaping of modern Tue 9 March 2021 3pm - 5pm human genomes: migration, admixture & Wed 10 March 2021 9am - 11 am ancient genomic Times are listed in SAST introgression DAY 2: Infectious diseases and Virtual Conference Platform our genome Programme: T U E S D A Y , 9 M A R C H 2 0 2 1 1 5 : 0 0 - 1 7 : 0 0 S A S T ( G M T + 2 ) The shaping of modern human genomes: migration, admixture and ancient genomic introgression - Chaired by Charles Rotimi & Michele Ramsay Since the emergence of modern man in Africa between 400,000 and 600,000 years ago, evolutionary forces have been shaping the human genome. Studies on the genomes of people living today and some who died thousands of years ago provide clues to our past and we begin to unravel a story of migration, admixture and adaptation. In this session we start with African population genomics, then adaptive signatures and introgression form extinct hominids to the peopling of Asia. -
2010-11 Events
2010-11 Events FEBRUARY 9/10 2011: BIOETHICS SEMINAR SERIES: “Developing Flourishing Research Practices in Tissue Engineering: A Proposal for a New Kind of Ethics Initiative.” Dr. George Khushf, Department of Philosophy, University of South Carolina Wednesday, 9th February 5:15-6:15 PM Greene Hall, Room 308, WFU Reynolda Campus. CBHS/PHILOSOPHY DEPT FORUM: Death as a Bridgework Concept Thursday, 10th February 4:30 – 6:00 PM Philosophy Library, B316 Tribble Hall, WFU Reynolda Campus. TALK: “DIVERSITY IN HEALTH CARE SETTINGS: WHY SHOULD IT MATTER?” Friday, 11th February 12:00-1:00PM Wake Forest University Baptist Medical Center, Comprehensive Cancer Center, Conference Room 1 A-B. FEBRUARY 17: BIOETHICS TEA TIME: “’It is My Duty to Resist Your Needles': Moral Challenges of Global Disease Eradication” Maria Merritt, PhD, John Hopkins Bloomberg School of Public Health 3:00-4:00 PM Location: Bioethics Commons, Piedmont Plaza II, 2nd Floor, Rm 2101. 4 February 2011 Page 1 FEBRUARY 22: PANEL DISCUSSION: Advocacy on Health & Healthcare Policy at Wake Forest University School of Medicine. Translation of research results into medical and public health policy and practice often involves policy change. Faculty members at Wake Forest Baptist Medical Center will discuss advocacy around public and institutional policy change at the international, national, state, and local level. The panelists will speak about their experience in the areas of health care reform, FDA regulation of alcoholic energy drinks, national vaccination policy, and enactment of North Carolina’s smoke free bars and restaurants law. Members of the audience will also share their experiences, challenges, and lessons in advocacy for health. -
Print Conference Brochure Now!Pdf Icon[PDF 1
YOU ARE INVITED The Planning Committee is very pleased to invite you to attend the Third National Conference on Genetics and Public Health. We hope the conference will be a strong learning and quality networking experience for you, one that enhances your abilities long after the conference ends. The conference highlights critical issues of how genetic information and technology are impacting all facets of Public Health including research, education, and practice. Importantly, the impact of genetics on the diverse communities we serve is of critical concern. This conference will be highly interactive, with emphasis on dialogue and exchange of information and ideas. Presenters will engage you in discussion on key topics in order to share their perspectives and expertise as well as to gain yours. In addition, there will be opportunities for you to meet informally with other conference attendees to discuss current issues and events of importance to you. So plan on joining us to share, learn and enjoy yourself! See you in Ann Arbor Genetics Program Planning Committee Co-Chairs: Carol Garlinghouse, MSN, RN Kathryn Peppe, RN, MS David Johnson, MD, MPH Manager, Clinical Services Unit Chief, Division of Family and Community Chief Medical Executive and Deputy Director Cancer Prevention and Control Section Health Services for Public Heatlh Michigan Dept. of Community Health Ohio Department of Health, and President, Michigan Department. of Community Health Association of Maternal and Child Health Grace Gorenflo Programs Associate Executive Director Noreen M. Clark, PhD National Association of County and City David Perlman, MPH Dean and Marshall H. Becker Professor Health Officials Director, Office of Academic Outreach School of Public Health School of Public Health University of Michigan James W. -
Global Health, Epidemiology and Genomics Call for Papers
Global Health, Epidemiology and Genomics Call for Papers - H3Africa and Genomics in Africa Guest Editors: Charles Rotimi, Center for Research on Genomics and Global Health, USA Michèle Ramsay, University of the Witwatersrand, South Africa Christian Happi, Redeemer’s University, Nigeria Jantina de Vries, University of Cape Town, South Africa Despite the global upsurge in genomic studies, populations from Africa remain understudied and poorly represented in health research. Recent large genomic studies have highlighted the considerable genetic diversity across the continent and the need for studying region specific ethnolinguistic groups to gain a better understanding of genomic and environmental influences in susceptibility to disease. The Human Heredity and Health in Africa Consortium (H3Africa) supports research on infectious and non-communicable diseases to enhance our knowledge and understanding of health on the continent and provide valuable region-specific base-line data to build upon. If Africans are to benefit from precision medicine it is imperative that research is done and interpreted in an appropriate local context. This special collection of articles in Global Health, Epidemiology and Genomics (GHEG) on H3Africa and Genomics in Africa is a unique opportunity to bring together a collection of original research, perspectives, commentaries, brief reports, protocols, research resources and blog articles to highlight the importance of genomic research in African populations as well as ethical considerations, good governance and -
Genomic Epidemiology in Africa
Genomic epidemiology in Africa Manjinder Sandhu [email protected] Genetic Epidemiology Group International Health Research Group Wellcome Trust Sanger Institute Department of Public Health and Primary Care What is the African Genome Variation Project? • Study of 16 ethno-linguistic groups across SSA from populations relevant to medical genomics • 100 individuals with dense (2.5M) genotype data in each • One of the largest diversity panel from Africa so far • Aim: to study genetic variation in Africa to inform large scale studies in African genomics Population structure in SSA 1 Population structure in SSA 3 Evidence for Eurasian and KhoeSan admixture YRI CEU Population structure in SSA 2 Confirming Eurasian and KhoeSan admixture pop A pop B pop C f3,C;A,B Z score pop Apop B pop C f3,C;A,B Z score CEU YRI Zulu 0.00543 33.528 YRI Juhoansi Zulu -0.00705 -44.604 CEU YRI Fula -0.01115 -59.361 YRI Juhoansi Sotho -0.00984 -64.773 CEU YRI Jola 0.005366 31.897 YRI Juhoansi Fula 0.005064 38.379 CEU YRI Mandinka -4.5E-05 -0.338 YRI Juhoansi Jola 0.007087 51.022 CEU YRI Wolof -0.00079 -5.376 YRI Juhoansi Mandinka 0.003206 29.069 CEU YRI Baganda -0.00316 -23.709 YRI Juhoansi Wolof 0.005002 40.037 CEU YRI Banyarwanda -0.01206 -74.707 YRI Juhoansi Baganda -0.00067 -6.157 CEU YRI Barundi -0.00904 -64.071 YRI Juhoansi Barundi -0.00207 -19.407 CEU YRI LWK -0.00322 -21.533 YRI Juhoansi Banyarwanda -0.00044 -3.81 CEU YRI Kalenjin -0.01042 -50.547 YRI Juhoansi LWK -0.00017 -1.394 CEU YRI Kikuyu -0.01618 -89.291 YRI Juhoansi Kikuyu 0.003081 20.333 CEU YRI SOMALI -
Genomics Research in Africa: Implications for Disease Diagnosis, Treatment
Genomics Research in Africa: Implications for Disease Diagnosis, Treatment and Drug Development Proceedings of the 5th Annual Meeting of the African Society of Human Genetics Short title: AfSHG proceedings 2007 Melanie J Newport 1, Sonia Abdelhak 2, Eman Abulezz 3, Adebowale Adeyemo 4, Gail Davey 5, Yehia Gad 3, Branwen J Hennig 6, Patricia A Marshall 7, Amal M. Mohamed 3, Charmaine D Royal 8, Himla Soodyall 9 and Charles N Rotimi 4 for the AfSHG. 1Department of Medicine, Brighton and Sussex Medical School, Falmer, Sussex, UK 2Institut Pasteur de Tunis, Tunis, Tunisia 3Division of Human Genetics and Genome Research, National Research Center, Elbehooth Street, Dokki, Giza, 12311 Egypt. 4NIH-Intramural Center for Genomics and Health Disparities, NHGRI/NIH, Bethesda, Maryland, USA 5School of Public Health, Addis Ababa University, Ethiopia 6Department of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK 7Department of Bioethics. School of Medicine, Case Western Reserve University. Cleveland, Ohio, USA 8Institute for Genome Sciences & Policy, Duke University, North Carolina, USA 9Human Genomic Diversity and Disease Research Unit, University of Witwatersand, Johannesburg, South Africa 1 Corresponding author: Melanie Newport, Department of Medicine, Brighton and Sussex Medical School, Falmer, Sussex, BN1 9PS, UK; tel: +44 (0) 1273 877882; fax +44(0)1273877884; email: [email protected] Key words: human genetics, African populations, African genome project, non- communicable diseases, infectious diseases, pharmacogenetics, 2 Abstract This paper presents the proceedings of the 5 th Annual Meeting of the African Society of Human Genetics, which took place in Cairo, Egypt, on 3 rd -5th November 2007. -
Genetic Structure in Four West African Population Groups Adebowale a Adeyemo*1,2, Guanjie Chen2, Yuanxiu Chen2 and Charles Rotimi2
BMC Genetics BioMed Central Research article Open Access Genetic structure in four West African population groups Adebowale A Adeyemo*1,2, Guanjie Chen2, Yuanxiu Chen2 and Charles Rotimi2 Address: 1College of Medicine, University of Ibadan, Ibadan. Nigeria and 2National Human Genome Center, Howard University, Washington DC, USA Email: Adebowale A Adeyemo* - [email protected]; Guanjie Chen - [email protected]; Yuanxiu Chen - [email protected]; Charles Rotimi - [email protected] * Corresponding author Published: 24 June 2005 Received: 01 December 2004 Accepted: 24 June 2005 BMC Genetics 2005, 6:38 doi:10.1186/1471-2156-6-38 This article is available from: http://www.biomedcentral.com/1471-2156/6/38 © 2005 Adeyemo et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Africa contains the most genetically divergent group of continental populations and several studies have reported that African populations show a high degree of population stratification. In this regard, it is important to investigate the potential for population genetic structure or stratification in genetic epidemiology studies involving multiple African populations. The presences of genetic sub-structure, if not properly accounted for, have been reported to lead to spurious association between a putative risk allele and a disease. Within the context of the Africa America Diabetes Mellitus (AADM) Study (a genetic epidemiologic study of type 2 diabetes mellitus in West Africa), we have investigated population structure or stratification in four ethnic groups in two countries (Akan and Gaa-Adangbe from Ghana, Yoruba and Igbo from Nigeria) using data from 372 autosomal microsatellite loci typed in 493 unrelated persons (986 chromosomes). -
The African Diaspora: History, Adaptation and Health
Available online at www.sciencedirect.com ScienceDirect The African diaspora: history, adaptation and health Charles N Rotimi, Fasil Tekola-Ayele, Jennifer L Baker and Daniel Shriner The trans-Atlantic slave trade brought millions of Africans to the We illustrate opportunities offered by the African Dias- New World. Advances in genomics are providing novel insights pora to study interactions of old genes with modern into the history and health of Africans and the diasporan environments, thereby lending novel insights into disease populations. Recent examples reviewed here include the etiology, ancestry-based disease gene mapping, and unraveling of substantial hunter-gatherer and ‘Eurasian’ health disparities. admixtures across sub-Saharan Africa, expanding our understanding of ancestral African genetics; the global ubiquity The African diaspora — history and definition of mixed ancestry; the revealing of African ancestry in Latin The term ‘African Diaspora’ first appeared in the litera- Americans that likely derived from the slave trade; and ture in the 1950s and has been broadly defined to include understanding of the ancestral backgrounds of APOL1 and LPL all global communities descended from the historic found to influence kidney disease and lipid levels, respectively, th migrations of peoples from Africa since the 15 century providing specific insights into disease etiology and health [3,4]. This delineates it from the pre-historic Out-of- disparities. Africa migrations that led to the peopling of the world. Address The African Diaspora -
What Does Genomic Medicine Mean for Diverse Populations?
INVITED COMMENTARY What does genomic medicine mean for diverse populations? Adebowale Adeyemo & Charles Rotimi Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, 20892 doi: 10.1002/mgg3.63 The completion of the effort to sequence the human gen- ability of empirical evidence generated from research. It is ome opened up a new era in human genomics. The new gratifying that each new development in genomics has tools and technologies developed, as well as new models been followed by studies that apply the new tools and for collaboration, data sharing, and data release provided technologies to the study of disease and treatment a good foundation for the international projects that response. For example, the International HapMap Project attempted to characterize genomic variation in diverse was swiftly followed by GWAS, which have now been populations. The first of these global efforts, the Interna- applied to scores of diseases, resulting in over 1700 publi- tional HapMap Project (http://www.hapmap.org), gener- cations as of December 2013 (NHGRI GWAS catalog – ated a catalog of common genetic variation in eleven http://www.genome.gov/26525384), with implications for global populations reflecting different ancestries. The disease risk, pathogenesis, and treatment response. How- 1000 Genomes Project (http://www.1000genomes.org) ever, the vast majority of these applied studies have been greatly expanded the scope of known human variation by performed only in European ancestry populations (Hind- sequencing over 2500 individuals from 26 global popula- orff et al. 2009; Need and Goldstein 2009) and most of tions. -
Enabling the Genomic Revolution in Africa
INSIGHTS | PERSPECTIVES barrier that culminated in the RESEARCH CAPACITY speciation of these two crow taxa. Armed with this new very detailed genetic informa- Enabling tion, it is clear that none of the currently formulated species concepts fully apply to these the genomic two crow taxa (unless one is willing relax some stringency Sw in the various definitions). In- revolution deed, the genomes of German carrion crows are much more in Africa similar to those of hooded Po crows than to Spanish car- rion crows. Put simply, apart H3Africa is developing from the few carrion crow type capacity for health-related “speciation islands,” German Ge carrion crows could be con- genomics research in Africa sidered to represent hooded Sp crows with a black (carrion By The H3Africa Consortium * † crow) phenotype. There is a clear need for ad- ur understanding of genome biology, ditional population genomic genomics, and disease, and even hu- studies using a more dense man history, has advanced tremen- sampling, especially among dously with the completion of the 1.0 the fully black carrion crows, Human Genome Project. Technologi- on August 3, 2014 Ancestry 0.5 Sp Ge Po Sw before the complexity of repro- cal advances coupled with significant 0.0 ductive isolation and speciation Ocost reductions in genomic research have among these two taxa can be yielded novel insights into disease etiol- Speciation battleground. On either side of the narrow hybridization fully understood. The specia- ogy, diagnosis, and therapy for some of zone (dark brown), the carrion crow (Corvus corone) (dark area) tion genomics strategy already the world’s most intractable and devastat- and hooded crow (Corvus cornix) (pale area) ( 2) maintain their proved itself in unraveling the ing diseases—including ma- marked phenotypic differentiation, despite apparent lack of genetic complexities of mimicry among POLICY laria, HIV/AIDS, tuberculosis, differentiation. -
Nigeria Is Poised to Become a Hub for Genetics Research, but a Few Stubborn Challenges Block the Way
Feature THE NEXT CHAPTER FOR AFRICAN GENOMICS Nigeria is poised to become a hub for genetics research, but a few stubborn challenges block the way. By Amy Maxmen 350 | Nature | Vol 578 | 20 February 2020 ©2020 Spri nger Nature Li mited. All ri ghts reserved. ©2020 Spri nger Nature Li mited. All ri ghts reserved. n the affluent, beach-side neighbour- meaning that dangerous pathogens could hoods of Lagos, finance and technology evade detection until an outbreak is too big entrepreneurs mingle with investors at to contain easily. art openings and chic restaurants. Now But Nigeria’s genetics revolution could just biotech is entering the scene. Thirty- as soon sputter as soar. Although the coun- four-year-old Abasi Ene-Obong has try is Africa’s largest economy, its research been traversing the globe for the past budget languishes at 0.2% of gross domestic six months, trying to draw investors and product (GDP). Biologists therefore need to Icollaborators into a venture called 54Gene. rely on private investment or on funding from Named to reflect the 54 countries in Africa, outside Africa. This threatens continuity: one the genetics company aims to build the con- of the largest US grants to Nigerian geneticists, tinent’s largest biobank, with backing from through a project known as H3Africa, is set to Silicon Valley venture firms such as Y Com- expire in two years. There are other challenges. binator and Fifty Years. The first step in that Human research in Africa requires copious effort is a study, launched earlier this month, communication and unique ethical consid- to sequence and analyse the genomes of eration given the vast economic disparities 100,000 Nigerians. -
Jessica W. Blanchard
Jessica W. Blanchard University of Oklahoma Center for Applied Social Research 5PP, 201 Stephenson Parkway, Ste 4100 Norman, OK 73072 Email: [email protected] Phone: (405) 740-3282 _______________________________ EDUCATION 2010 Ph.D. Cultural Anthropology, University of Oklahoma, Norman, Oklahoma. Dissertation: “They Came One At A Time”: Native-led Church Planting and Growing the Body of Christ from the Margins of Culture. Doctoral Committee: Morris W. Foster (chair), Daniel Swan, Sean O’Neill, Gus Palmer, Jr., Joe Watkins. 2004 M.A. Anthropology, University of Oklahoma, Norman, Oklahoma. Thesis: Perception and Management of Type II Diabetes: The Narrated Experience of Diabetes in an Absentee Shawnee Community. 2001 B.A. Anthropology Major, Art History Minor. Auburn University, Auburn, Alabama. PROFESSIONAL POSITIONS 2017- Research Scientist. Center for Applied Social Research; University of Oklahoma. Norman, Oklahoma. 2013-17 Lecturer and Undergraduate Faculty Advisor. Department of Anthropology; University of Oklahoma, Norman, Oklahoma. 2013-15 Adjunct Instructor. Department of Sociology and Substance Abuse Studies; University of Central Oklahoma, Edmond, Oklahoma. 2012-13 Research Scientist. Center for Applied Social Research; University of Oklahoma, Norman. Oklahoma. 2010-12 Post-doctoral Research Fellow. Center for Applied Social Research; University of Oklahoma, Norman, Oklahoma. 2007-10 Community Outreach Coordinator and Staff Researcher. Center for Applied Social Research; University of Oklahoma, Norman, Oklahoma. 2003-06 Project Coordinator. Center for Applied Social Research; University of Oklahoma, Norman, Oklahoma. HONORS AND AWARDS 2018 American Journal of Epidemiology Reviewer of the Year 2017 Student Mentoring Award, Spirit of Eagles Changing Patterns of Cancer in Native Communities. 2013-15 Hampton Faculty Fellow Awardee, Cohort II.