| Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ... Nature genetics 50 (8), 1112-1121, 2018 | 2066 | 2018 |
| 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 | 712 | 2021 |
| The phenotypic legacy of admixture between modern humans and Neandertals CN Simonti, B Vernot, L Bastarache, E Bottinger, DS Carrell, RL Chisholm, ... Science 351 (6274), 737-741, 2016 | 348 | 2016 |
| A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022 | 282 | 2022 |
| Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma JNC Bailey, SJ Loomis, JH Kang, RR Allingham, P Gharahkhani, CC Khor, ... Nature genetics 48 (2), 189-194, 2016 | 255 | 2016 |
| Whole-genome sequencing reveals host factors underlying critical COVID-19 A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ... Nature 607 (7917), 97-103, 2022 | 220 | 2022 |
| Meta-analysis of genome-wide association studies for abdominal aortic aneurysm identifies four new disease-specific risk loci GT Jones, G Tromp, H Kuivaniemi, S Gretarsdottir, AF Baas, B Giusti, ... Circulation research 120 (2), 341-353, 2017 | 178 | 2017 |
| Stroke genetics informs drug discovery and risk prediction across ancestries A Mishra, R Malik, T Hachiya, T Jürgenson, S Namba, DC Posner, ... Nature 611 (7934), 115-123, 2022 | 172 | 2022 |
| Imputation and quality control steps for combining multiple genome-wide datasets SS Verma, M de Andrade, G Tromp, H Kuivaniemi, E Pugh, ... Frontiers in genetics 5, 370, 2014 | 150 | 2014 |
| GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network B Namjou, T Lingren, Y Huang, S Parameswaran, BL Cobb, IB Stanaway, ... BMC medicine 17, 1-19, 2019 | 126 | 2019 |
| Large-scale genome-wide association study of coronary artery disease in genetically diverse populations C Tcheandjieu, X Zhu, AT Hilliard, SL Clarke, V Napolioni, S Ma, KM Lee, ... Nature medicine 28 (8), 1679-1692, 2022 | 120 | 2022 |
| Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis Interleukin 1 Genetics Consortium The Lancet Diabetes & Endocrinology 3 (4), 243-253, 2015 | 117 | 2015 |
| Association of the V122I hereditary transthyretin amyloidosis genetic variant with heart failure among individuals of African or Hispanic/Latino ancestry SM Damrauer, K Chaudhary, JH Cho, LW Liang, E Argulian, L Chan, ... Jama 322 (22), 2191-2202, 2019 | 101 | 2019 |
| Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to … B Namjou, K Marsolo, RJ Caroll, JC Denny, MD Ritchie, SS Verma, ... Frontiers in genetics 5, 401, 2014 | 89 | 2014 |
| Genetic architecture of abdominal aortic aneurysm in the million veteran program D Klarin, SS Verma, R Judy, O Dikilitas, BN Wolford, I Paranjpe, MG Levin, ... Circulation 142 (17), 1633-1646, 2020 | 81 | 2020 |
| A simulation study investigating power estimates in phenome-wide association studies A Verma, Y Bradford, S Dudek, AM Lucas, SS Verma, SA Pendergrass, ... BMC bioinformatics 19, 1-8, 2018 | 75 | 2018 |
| PheWAS and beyond: the landscape of associations with medical diagnoses and clinical measures across 38,662 individuals from Geisinger A Verma, A Lucas, SS Verma, Y Zhang, N Josyula, A Khan, DN Hartzel, ... The American Journal of Human Genetics 102 (4), 592-608, 2018 | 75 | 2018 |
| Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms FNG van’t Hof, YM Ruigrok, CH Lee, S Ripke, G Anderson, M De Andrade, ... Journal of the American Heart Association 5 (7), e002603, 2016 | 71 | 2016 |
| Genetic variation in the HLA region is associated with susceptibility to herpes zoster DR Crosslin, DS Carrell, A Burt, DS Kim, JG Underwood, DS Hanna, ... Genes & Immunity 16 (1), 1-7, 2015 | 69 | 2015 |
| A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough JD Mosley, CM Shaffer, SL Van Driest, PE Weeke, QS Wells, JH Karnes, ... The pharmacogenomics journal 16 (3), 231-237, 2016 | 64 | 2016 |
Marylyn D RitchieUniversity of PennsylvaniaVerified email at upenn.edu
