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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 | 430 | 2013 |
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ... Nature genetics 54 (5), 560-572, 2022 | 394 | 2022 |
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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 | 342 | 2012 |
Variants near FOXE1 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 | 304 | 2011 |
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Portability of an algorithm to identify rheumatoid arthritis in electronic health records RJ Carroll, WK Thompson, AE Eyler, AM Mandelin, T Cai, RM Zink, ... Journal of the American Medical Informatics Association 19 (e1), e162-e169, 2012 | 246 | 2012 |
Comparative effectiveness of aspirin dosing in cardiovascular disease WS Jones, H Mulder, LM Wruck, MJ Pencina, S Kripalani, D Muñoz, ... New England Journal of Medicine 384 (21), 1981-1990, 2021 | 224 | 2021 |
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Genome-and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk MD Ritchie, JC Denny, RL Zuvich, DC Crawford, JS Schildcrout, ... Circulation 127 (13), 1377-1385, 2013 | 197 | 2013 |
A genome-and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects K Shameer, JC Denny, K Ding, H Jouni, DR Crosslin, M De Andrade, ... Human genetics 133, 95-109, 2014 | 164 | 2014 |
The All of Us Research Program: data quality, utility, and diversity AH Ramirez, L Sulieman, DJ Schlueter, A Halvorson, J Qian, ... Patterns 3 (8), 2022 | 159 | 2022 |
Design and implementation of a privacy preserving electronic health record linkage tool in Chicago AN Kho, JP Cashy, KL Jackson, AR Pah, S Goel, J Boehnke, ... Journal of the American Medical Informatics Association 22 (5), 1072-1080, 2015 | 150 | 2015 |
Desiderata for computable representations of electronic health records-driven phenotype algorithms H Mo, WK Thompson, LV Rasmussen, JA Pacheco, G Jiang, R Kiefer, ... Journal of the American Medical Informatics Association 22 (6), 1220-1230, 2015 | 147 | 2015 |
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records PL Peissig, LV Rasmussen, RL Berg, JG Linneman, CA McCarty, ... Journal of the American Medical Informatics Association 19 (2), 225-234, 2012 | 139 | 2012 |
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network DR Crosslin, A McDavid, N Weston, SC Nelson, X Zheng, E Hart, ... Human genetics 131, 639-652, 2012 | 136 | 2012 |
PCORnet® 2020: current state, accomplishments, and future directions CB Forrest, KM McTigue, AF Hernandez, LW Cohen, H Cruz, K Haynes, ... Journal of Clinical Epidemiology 129, 60-67, 2021 | 126 | 2021 |
Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus WQ Wei, CL Leibson, JE Ransom, AN Kho, PJ Caraballo, HS Chai, ... Journal of the American Medical Informatics Association 19 (2), 219-224, 2012 | 126 | 2012 |