| 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 | 2631 | 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 | 2162 | 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 | 1803 | 2015 |
| The “All of Us” Research Program All of Us Research Program Investigators New England Journal of Medicine 381 (7), 668-676, 2019 | 1403 | 2019 |
| 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 | 1247 | 2010 |
| 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 | 1232 | 2018 |
| 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 | 1067 | 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 | 841 | 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 | 697 | 2018 |
| 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 | 651 | 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 | 628 | 2013 |
| 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 | 582 | 2017 |
| 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 | 522 | 2016 |
| 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 | 481 | 2014 |
| 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 | 455 | 2011 |
| 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 | 440 | 2013 |
| 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 | 428 | 2012 |
| R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment RJ Carroll, L Bastarache, JC Denny Bioinformatics 30 (16), 2375-2376, 2014 | 425 | 2014 |
| 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 | 422 | 2016 |
| Mapping ICD-10 and ICD-10-CM codes to phecodes: workflow development and initial evaluation P Wu, A Gifford, X Meng, X Li, H Campbell, T Varley, J Zhao, R Carroll, ... JMIR medical informatics 7 (4), e14325, 2019 | 418 | 2019 |
Dan RodenProfessor of Medicine, Pharmacology, and Biomedical Informatics, Vanderbilt University Medical Ctrvanderbilt.edu의 이메일 확인됨