| 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 | 1415 | 2014 |
| 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 | 1408 | 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, 2015 | 687 | 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 | 664 | 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 | 535 | 2013 |
| 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 | 448 | 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 | 354 | 2013 |
| 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 | 333 | 2014 |
| 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 | 315 | 2012 |
| 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 | 302 | 2010 |
| Electronic medical records for genetic research: results of the eMERGE consortium AN Kho, JA Pacheco, PL Peissig, L Rasmussen, KM Newton, N Weston, ... Sci Transl Med 3, 79re1, 2011 | 301 | 2011 |
| 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 | 280 | 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 | 276 | 2013 |
| 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), 1-19, 2016 | 271 | 2016 |
| Computational phenotype discovery using unsupervised feature learning over noisy, sparse, and irregular clinical data TA Lasko, JC Denny, MA Levy PloS one 8 (6), e66341, 2013 | 258 | 2013 |
| Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study AN Kho, MG Hayes, L Rasmussen-Torvik, JA Pacheco, WK Thompson, ... Journal of the American Medical Informatics Association 19 (2), 212-218, 2012 | 240 | 2012 |
| Variants Near< i> FOXE1</i> Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome-and Phenome-wide Studies JC Denny, DC Crawford, MD Ritchie, SJ Bielinski, MA Basford, Y Bradford, ... The American Journal of Human Genetics 89 (4), 529-542, 2011 | 237 | 2011 |
| 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 | 215 | 2017 |
| 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 | 212 | 2017 |
| A study of machine-learning-based approaches to extract clinical entities and their assertions from discharge summaries M Jiang, Y Chen, M Liu, ST Rosenbloom, S Mani, JC Denny, H Xu Journal of the American Medical Informatics Association 18 (5), 601-606, 2011 | 212 | 2011 |
Dan RodenProfessor of Medicine and Pharmacology, Vanderbilt UniversityVerified email at vanderbilt.edu
