| 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 | 1151 | 2018 |
| Precision medicine, AI, and the future of personalized health care KB Johnson, WQ Wei, D Weeraratne, ME Frisse, K Misulis, K Rhee, ... Clinical and translational science 14 (1), 86-93, 2021 | 791 | 2021 |
| The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021 | 531 | 2021 |
| Trans-ethnic association study of blood pressure determinants in over 750,000 individuals A Giri, JN Hellwege, JM Keaton, J Park, C Qiu, HR Warren, ES Torstenson, ... Nature genetics 51 (1), 51-62, 2019 | 395 | 2019 |
| 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 | 384 | 2019 |
| 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 | 341 | 2012 |
| Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record WQ Wei, LA Bastarache, RJ Carroll, JE Marlo, TJ Osterman, ER Gamazon, ... PloS one 12 (7), e0175508, 2017 | 334 | 2017 |
| Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins I Postmus, S Trompet, HA Deshmukh, MR Barnes, X Li, HR Warren, ... Nature communications 5 (1), 5068, 2014 | 286 | 2014 |
| Extracting research-quality phenotypes from electronic health records to support precision medicine WQ Wei, JC Denny Genome Medicine 7 (41), 2015 | 269 | 2015 |
| IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes Y Momozawa, J Dmitrieva, E Théâtre, V Deffontaine, S Rahmouni, ... Nature communications 9 (1), 2427, 2018 | 233 | 2018 |
| Combining billing codes, clinical notes, and medications from electronic health records provides superior phenotyping performance JCD Wei-Qi Wei, Pedro L Teixeira, Huan Mo, Robert M Cronin, Jeremy L Warner Journal of the American Medical Informatics Association, 2015 | 219* | 2015 |
| Learning from longitudinal data in electronic health record and genetic data to improve cardiovascular event prediction J Zhao, QP Feng, P Wu, RA Lupu, RA Wilke, QS Wells, JC Denny, ... Scientific reports 9 (1), 717, 2019 | 213 | 2019 |
| Clinical and pharmacogenetic predictors of circulating atorvastatin and rosuvastatin concentrations in routine clinical care MK DeGorter, RG Tirona, UI Schwarz, YH Choi, GK Dresser, N Suskin, ... Circulation: Cardiovascular Genetics 6 (4), 400-408, 2013 | 213 | 2013 |
| Phenotype risk scores identify patients with unrecognized Mendelian disease patterns L Bastarache, JJ Hughey, S Hebbring, J Marlo, W Zhao, WT Ho, ... Science 359 (6381), 1233-1239, 2018 | 207 | 2018 |
| Genome-wide modeling of polygenic risk score in colorectal cancer risk M Thomas, LC Sakoda, M Hoffmeister, EA Rosenthal, JK Lee, ... The American journal of human genetics 107 (3), 432-444, 2020 | 156 | 2020 |
| A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease CA Emdin, ME Haas, AV Khera, K Aragam, M Chaffin, D Klarin, G Hindy, ... PLoS genetics 16 (4), e1008629, 2020 | 150 | 2020 |
| 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 | 135 | 2019 |
| Use of genetic variants related to antihypertensive drugs to inform on efficacy and side effects D Gill, MK Georgakis, F Koskeridis, L Jiang, Q Feng, WQ Wei, ... Circulation 140 (4), 270-279, 2019 | 135 | 2019 |
| Development and evaluation of an ensemble resource linking medications to their indications WQ Wei, RM Cronin, H Xu, TA Lasko, L Bastarache, JC Denny Journal of the American Medical Informatics Association 20 (5), 954-961, 2013 | 125 | 2013 |
| 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 | 123 | 2012 |
Joshua C. DennyCEO, All of Us Research ProgramVerified email at nih.gov
