| Genetic studies of body mass index yield new insights for obesity biology AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ... Nature 518 (7538), 197-206, 2015 | 4781 | 2015 |
| Discovery and refinement of loci associated with lipid levels CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ... Nature genetics 45 (11), 1274, 2013 | 2996* | 2013 |
| New genetic loci link adipose and insulin biology to body fat distribution D Shungin, TW Winkler, DC Croteau-Chonka Nature 518 (7538), 187-196, 2015 | 1674 | 2015 |
| Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps A Mahajan, D Taliun, M Thurner, NR Robertson, JM Torres, NW Rayner, ... Nature genetics 50 (11), 1505-1513, 2018 | 1643 | 2018 |
| Common variants associated with plasma triglycerides and risk for coronary artery disease R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, ... Nature genetics 45 (11), 1345-1352, 2013 | 1041 | 2013 |
| Biobank-driven genomic discovery yields new insight into atrial fibrillation biology JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ... Nature genetics 50 (9), 1234-1239, 2018 | 655 | 2018 |
| Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease P Zanoni, SA Khetarpal, DB Larach, WF Hancock-Cerutti, JS Millar, ... Science 351 (6278), 1166-1171, 2016 | 570 | 2016 |
| Exome-wide association study of plasma lipids in> 300,000 individuals DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ... Nature genetics 49 (12), 1758-1766, 2017 | 553 | 2017 |
| The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021 | 489 | 2021 |
| The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals GB Ehret, T Ferreira, DI Chasman, AU Jackson, EM Schmidt, T Johnson, ... Nature genetics 48 (10), 1171-1184, 2016 | 444 | 2016 |
| Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics M Ghoussaini, E Mountjoy, M Carmona, G Peat, EM Schmidt, A Hercules, ... Nucleic acids research 49 (D1), D1311-D1320, 2021 | 369 | 2021 |
| Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ... Nature genetics 54 (5), 560-572, 2022 | 343 | 2022 |
| Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk OL Holmen, HE Zhang, Y Fan, DH Hovelson, EM Schmidt, W Zhou, Y Guo, ... Nature genetics 46 (4), 345-351, 2014 | 329 | 2014 |
| New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk Y Lu, FR Day, S Gustafsson, ML Buchkovich, J Na, V Bataille, ... Nature communications 7 (1), 10495, 2016 | 300 | 2016 |
| An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci E Mountjoy, EM Schmidt, M Carmona, J Schwartzentruber, G Peat, ... Nature genetics 53 (11), 1527-1533, 2021 | 286 | 2021 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 242 | 2014 |
| Association of polygenic risk scores for multiple cancers in a phenome-wide study: results from the Michigan Genomics Initiative LG Fritsche, SB Gruber, Z Wu, EM Schmidt, M Zawistowski, SE Moser, ... The American Journal of Human Genetics 102 (6), 1048-1061, 2018 | 170 | 2018 |
| Exploring and visualizing large-scale genetic associations by using PheWeb SA Gagliano Taliun, P VandeHaar, AP Boughton, RP Welch, D Taliun, ... Nature genetics 52 (6), 550-552, 2020 | 163 | 2020 |
| GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach EM Schmidt, J Zhang, W Zhou, J Chen, KL Mohlke, YE Chen, CJ Willer Bioinformatics 31 (16), 2601-2606, 2015 | 163 | 2015 |
| A fast and accurate algorithm to test for binary phenotypes and its application to PheWAS R Dey, EM Schmidt, GR Abecasis, S Lee The American Journal of Human Genetics 101 (1), 37-49, 2017 | 157 | 2017 |
