| A second generation human haplotype map of over 3.1 million SNPs International HapMap Consortium Nature 449 (7164), 851, 2007 | 9334* | 2007 |
| A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8741 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8235 | 2012 |
| The international HapMap project RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ... Nature Publishing Group, 2003 | 6191 | 2003 |
| International network of cancer genome projects Data coordination centre Kasprzyk (Leader) Arek 1 Stein (Leader) Lincoln D ... Nature 464 (7291), 993-998, 2010 | 2247 | 2010 |
| Genome-wide detection and characterization of positive selection in human populations PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ... Nature 449 (7164), 913-918, 2007 | 2196 | 2007 |
| A haplotype map of the human genome D Altshuler Nature 437, 1299-1320, 2005 | 1187 | 2005 |
| Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ... Nature neuroscience 20 (4), 602-611, 2017 | 759 | 2017 |
| Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011 | 707 | 2011 |
| Whole-genome sequencing in health care CG Van El, MC Cornel, P Borry, RJ Hastings, F Fellmann, SV Hodgson, ... European Journal of Human Genetics 21 (6), 580-584, 2013 | 525 | 2013 |
| Managing incidental findings and research results in genomic research involving biobanks and archived data sets SM Wolf, BN Crock, B Van Ness, F Lawrenz, JP Kahn, LM Beskow, ... Genetics in Medicine 14 (4), 361-384, 2012 | 504 | 2012 |
| Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014 | 434 | 2014 |
| Human genetic research: emerging trends in ethics BM Knoppers, R Chadwick Nature Reviews Genetics 6 (1), 75-79, 2005 | 398 | 2005 |
| Trends in ethical and legal frameworks for the use of human biobanks A Cambon-Thomsen, E Rial-Sebbag, BM Knoppers European Respiratory Journal 30 (2), 373-382, 2007 | 381 | 2007 |
| International cooperation to enable the diagnosis of all rare genetic diseases KM Boycott, A Rath, JX Chong, T Hartley, FS Alkuraya, G Baynam, ... The American Journal of Human Genetics 100 (5), 695-705, 2017 | 380 | 2017 |
| Recommendations for returning genomic incidental findings? We need to talk! W Burke, AH Matheny Antommaria, R Bennett, J Botkin, EW Clayton, ... Genetics in Medicine 15 (11), 854-859, 2013 | 337 | 2013 |
| The emergence of an ethical duty to disclose genetic research results: international perspectives BM Knoppers, Y Joly, J Simard, F Durocher European Journal of Human Genetics 14 (11), 1170-1178, 2006 | 323 | 2006 |
| Research ethics recommendations for whole-genome research: consensus statement T Caulfield, AL McGuire, M Cho, JA Buchanan, MM Burgess, U Danilczyk, ... PLoS biology 6 (3), e73, 2008 | 301 | 2008 |
| FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ... The American Journal of Human Genetics 94 (6), 809-817, 2014 | 278 | 2014 |
| DataSHIELD: taking the analysis to the data, not the data to the analysis A Gaye, Y Marcon, J Isaeva, P LaFlamme, A Turner, EM Jones, J Minion, ... International journal of epidemiology 43 (6), 1929-1944, 2014 | 261 | 2014 |
