Year: 2020
Type: article
Source: Nature
Authors: Melina Claussnitzer, Judy H. Cho, Rory Collins, Nancy J. Cox, Emmanouil T. Dermitzakis, Matthew E. Hurles, Sekar Kathiresan, Eimear E. Kenny, Cecilia M. Lindgren, Daniel G. MacArthur, Kathryn N. North, Sharon E. Plon, Heidi L. Rehm, Neil Risch, Charles N. Rotimi, Jay Shendure, Nicole Soranzo, Mark I. McCarthy
Institutions: Broad Institute, University of Hohenheim, Beth Israel Deaconess Medical Center, Harvard University, Icahn School of Medicine at Mount Sinai, University of Oxford, UK Biobank, Vanderbilt University, Vanderbilt University Medical Center, University of Geneva, Wellcome Sanger Institute, Massachusetts General Hospital, Verve Therapeutics (United States), Centre for Human Genetics, The University of Melbourne, Murdoch Children's Research Institute, Baylor College of Medicine, Texas Children's Hospital, University of California, San Francisco, National Institutes of Health, National Human Genome Research Institute, Howard Hughes Medical Institute, University of Washington, Brotman Baty Institute, University of Cambridge, Genentech, John Radcliffe Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
Funders: National Science Foundation, Howard Hughes Medical Institute, Leona M. and Harry B. Helmsley Charitable Trust, Li Ka Shing Foundation, Wellcome Trust, Broad Institute, National Institute for Health and Care Research, British Heart Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, National Institutes of Health, National Health and Medical Research Council, NIHR Oxford Biomedical Research Centre, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Human Genome Research Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute on Minority Health and Health Disparities, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: Large-scale data integration to advance mechanistic inference and precision medicine in type 2 diabetes, G1314613728, G1476847741, G154717235, G1632194876, G1706615277, G2043572114, Characterising causal alleles for common disease., Harvard Reproductive Endocrine Sciences Center, G2628120876, G2946763061, Preparing Australia for Genomic Medicine: A proposal by the Australian Genomics Health Alliance, PAGE III: Population Architecture using Genomics and Epidemiology, G4765065348, Integrating genome-scale data to reveal causal mechanisms in type 2 diabetes, G561653141, G574117291, Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics., G7118838674, Human Genetics and Disease Biology: Core Renewal for the Wellcome Trust Centre for Human Genetics, The Impact of Human Gene Knockouts in Type 2 Diabetes and Related Traits, Incorporating genomics into the clinical care of diverse NYC children, Discovering Biology for Neuropsychiatric Diseases Through Omics Studies on Comorbidities, A systematic approach to understanding the biology underpinning GWAS hits., A systematic approach to understanding the biology underpinning GWAS hits., NIHR Senior Investigator Award, G9000011408, G9000018693, G9000075328, G9000094210, G9000127894, G9000210335, G9000235966, Precision IBD via genetics and genomics: integrating International and multi-omic datasets, expanding studies in diverse populations, and defining mechanisms of unmet clinical needs in IBD, Mount Sinai NYC Genetics Research Center: Multi-omic integration across data-types, cell niches and populations, G905179811
OpenAlex ID: W2999574254