| Genetics of rheumatoid arthritis contributes to biology and drug discovery Y Okada, D Wu, G Trynka, T Raj, C Terao, K Ikari, Y Kochi, K Ohmura, ... Nature 506 (7488), 376-381, 2014 | 2278 | 2014 |
| Defining the role of common variation in the genomic and biological architecture of adult human height AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ... Nature genetics 46 (11), 1173-1186, 2014 | 1995 | 2014 |
| A gene-based association method for mapping traits using reference transcriptome data ER Gamazon, HE Wheeler, KP Shah, SV Mozaffari, K Aquino-Michaels, ... Nature genetics 47 (9), 1091-1098, 2015 | 1434 | 2015 |
| PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations JC Denny, MD Ritchie, MA Basford, JM Pulley, L Bastarache, ... Bioinformatics 26 (9), 1205-1210, 2010 | 1070 | 2010 |
| Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data JC Denny, L Bastarache, MD Ritchie, RJ Carroll, R Zink, JD Mosley, ... Nature biotechnology 31 (12), 1102-1111, 2013 | 917 | 2013 |
| Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies W Zhou, JB Nielsen, LG Fritsche, R Dey, ME Gabrielsen, BN Wolford, ... Nature genetics 50 (9), 1335-1341, 2018 | 865 | 2018 |
| The “All of Us” Research Program All of Us Research Program Investigators New England Journal of Medicine 381 (7), 668-676, 2019 | 773 | 2019 |
| MedEx: a medication information extraction system for clinical narratives H Xu, SP Stenner, S Doan, KB Johnson, LR Waitman, JC Denny Journal of the American Medical Informatics Association 17 (1), 19, 2010 | 601 | 2010 |
| The electronic medical records and genomics (eMERGE) network: past, present, and future O Gottesman, H Kuivaniemi, G Tromp, WA Faucett, R Li, TA Manolio, ... Genetics in Medicine 15 (10), 761-771, 2013 | 560 | 2013 |
| Artificial intelligence, bias and clinical safety R Challen, J Denny, M Pitt, L Gompels, T Edwards, K Tsaneva-Atanasova BMJ Quality & Safety 28 (3), 231-237, 2019 | 553 | 2019 |
| Multi-ethnic genome-wide association study for atrial fibrillation C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ... Nature genetics 50 (9), 1225-1233, 2018 | 515 | 2018 |
| 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 | 509 | 2017 |
| 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 | 442 | 2014 |
| Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ... Nature communications 7 (1), 10023, 2016 | 438 | 2016 |
| Data from clinical notes: a perspective on the tension between structure and flexible documentation ST Rosenbloom, JC Denny, H Xu, N Lorenzi, WW Stead, KB Johnson Journal of the American Medical Informatics Association 18 (2), 181-186, 2011 | 395 | 2011 |
| Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project JM Pulley, JC Denny, JF Peterson, GR Bernard, CL Vnencak-Jones, ... Clinical Pharmacology & Therapeutics, 2012 | 393 | 2012 |
| Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network KM Newton, PL Peissig, AN Kho, SJ Bielinski, RL Berg, V Choudhary, ... Journal of the American Medical Informatics Association 20 (e1), e147-e154, 2013 | 390 | 2013 |
| Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators New England Journal of Medicine 374 (12), 1134-1144, 2016 | 374 | 2016 |
| Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record MD Ritchie, JC Denny, DC Crawford, AH Ramirez, JB Weiner, JM Pulley, ... The American Journal of Human Genetics 86 (4), 560-572, 2010 | 365 | 2010 |
| PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study AF Schmidt, DI Swerdlow, MV Holmes, RS Patel, Z Fairhurst-Hunter, ... The lancet Diabetes & endocrinology 5 (2), 97-105, 2017 | 364 | 2017 |
Dan RodenProfessor of Medicine and Pharmacology, Vanderbilt UniversityVerified email at vanderbilt.edu
