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| Genetic analyses of diverse populations improves discovery for complex traits GL Wojcik, M Graff, KK Nishimura, R Tao, J Haessler, CR Gignoux, ... Nature 570 (7762), 514-518, 2019 | 767 | 2019 |
| Detectable clonal mosaicism from birth to old age and its relationship to cancer CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ... Nature genetics 44 (6), 642-650, 2012 | 639 | 2012 |
| Discovery of common and rare genetic risk variants for colorectal cancer JR Huyghe, SA Bien, TA Harrison, HM Kang, S Chen, SL Schmit, ... Nature genetics, 1, 2018 | 428 | 2018 |
| Branched-chain amino acid levels are associated with improvement in insulin resistance with weight loss SH Shah, DR Crosslin, CS Haynes, S Nelson, CB Turer, RD Stevens, ... Diabetologia 55, 321-330, 2012 | 387 | 2012 |
| The trans-ancestral genomic architecture of glycemic traits J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ... Nature genetics 53 (6), 840-860, 2021 | 373 | 2021 |
| Genetic diversity and association studies in US Hispanic/Latino populations: applications in the Hispanic Community Health Study/Study of Latinos MP Conomos, CA Laurie, AM Stilp, SM Gogarten, CP McHugh, ... The American Journal of Human Genetics 98 (1), 165-184, 2016 | 303 | 2016 |
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| A genome-wide association meta-analysis of circulating sex hormone–binding globulin reveals multiple Loci implicated in sex steroid hormone regulation AD Coviello, R Haring, M Wellons, D Vaidya, T Lehtimäki, S Keildson, ... PLoS genetics 8 (7), e1002805, 2012 | 179 | 2012 |
| Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease L Wang, ER Hauser, SH Shah, MA Pericak-Vance, C Haynes, D Crosslin, ... The American Journal of Human Genetics 80 (4), 650-663, 2007 | 140 | 2007 |
| Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci T Aung, M Ozaki, MC Lee, U Schlötzer-Schrehardt, G Thorleifsson, ... Nature genetics 49 (7), 993-1004, 2017 | 136 | 2017 |
| Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network DR Crosslin, A McDavid, N Weston, SC Nelson, X Zheng, E Hart, ... Human genetics 131, 639-652, 2012 | 134 | 2012 |
| Characterization of large structural genetic mosaicism in human autosomes MJ Machiela, W Zhou, JN Sampson, MC Dean, KB Jacobs, A Black, ... The American Journal of Human Genetics 96 (3), 487-497, 2015 | 130 | 2015 |
| Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis SH Shah, NJ Freedman, L Zhang, DR Crosslin, DH Stone, C Haynes, ... PLoS genetics 5 (1), e1000318, 2009 | 127 | 2009 |
| Genome-wide association scan of dental caries in the permanent dentition X Wang, JR Shaffer, Z Zeng, F Begum, AR Vieira, J Noel, I Anjomshoaa, ... BMC oral health 12, 1-11, 2012 | 126 | 2012 |
| Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease PJ Martin, DM Levine, BE Storer, EH Warren, X Zheng, SC Nelson, ... Blood, The Journal of the American Society of Hematology 129 (6), 791-798, 2017 | 109 | 2017 |
| GATA2 is associated with familial early-onset coronary artery disease JJ Connelly, T Wang, JE Cox, C Haynes, L Wang, SH Shah, DR Crosslin, ... PLoS genetics 2 (8), e139, 2006 | 106 | 2006 |
| Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case–control and family datasets BS Sutton, DR Crosslin, SH Shah, SC Nelson, A Bassil, AB Hale, ... Human molecular genetics 17 (9), 1318-1328, 2008 | 98 | 2008 |
| Mice Heterozygous for Atp10c, a Putative Amphipath, Represent a Novel Model of Obesity and Type 2 Diabetes MS Dhar, CS Sommardahl, T Kirkland, S Nelson, R Donnell, DK Johnson, ... The Journal of nutrition 134 (4), 799-805, 2004 | 97 | 2004 |
