| Analysis of protein-coding genetic variation in 60,706 humans M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ... Nature 536 (7616), 285-291, 2016 | 10559 | 2016 |
| Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases M Verbanck, CY Chen, B Neale, R Do Nature genetics 50 (5), 693-698, 2018 | 5743 | 2018 |
| 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 | 3049* | 2013 |
| Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ... The Lancet 380 (9841), 572-580, 2012 | 2658 | 2012 |
| Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ... Nature genetics 43 (4), 333-338, 2011 | 2256 | 2011 |
| A high-coverage genome sequence from an archaic Denisovan individual M Meyer, M Kircher, MT Gansauge, H Li, F Racimo, S Mallick, ... Science 338 (6104), 222-226, 2012 | 2233 | 2012 |
| Evolution and functional impact of rare coding variation from deep sequencing of human exomes JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ... science 337 (6090), 64-69, 2012 | 1910 | 2012 |
| Large-scale association analysis identifies new risk loci for coronary artery disease CARDIoGRAMplusC4D Consortium, P Deloukas, S Kanoni, C Willenborg, ... Nature genetics 45 (1), 25-33, 2013 | 1780 | 2013 |
| Modeling linkage disequilibrium increases accuracy of polygenic risk scores BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ... The american journal of human genetics 97 (4), 576-592, 2015 | 1422 | 2015 |
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ... Nature genetics 41 (3), 334-341, 2009 | 1313 | 2009 |
| 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 | 1058 | 2013 |
| 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 | 882 | 2019 |
| Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease TG and HDL Working Group of the Exome Sequencing Project, National Heart ... New England Journal of Medicine 371 (1), 22-31, 2014 | 858 | 2014 |
| Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 805 | 2021 |
| Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia K Musunuru, JP Pirruccello, R Do, GM Peloso, C Guiducci, C Sougnez, ... New England Journal of Medicine 363 (23), 2220-2227, 2010 | 804 | 2010 |
| Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ... Nature 518 (7537), 102-106, 2015 | 777 | 2015 |
| Searching for missing heritability: designing rare variant association studies O Zuk, SF Schaffner, K Samocha, R Do, E Hechter, S Kathiresan, MJ Daly, ... Proceedings of the National Academy of Sciences 111 (4), E455-E464, 2014 | 738 | 2014 |
| 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 | 587 | 2016 |
| Exome sequencing and the genetic basis of complex traits A Kiezun, K Garimella, R Do, NO Stitziel, BM Neale, PJ McLaren, N Gupta, ... Nature genetics 44 (6), 623-630, 2012 | 510 | 2012 |
| Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease Myocardial Infarction Genetics Consortium Investigators New England Journal of Medicine 371 (22), 2072-2082, 2014 | 477 | 2014 |
