Parents
Sign in to add mentorJason H. Moore | grad student | 2004 | Vanderbilt | |
(Genetic programming optimized neural networks for identifying gene -gene interactions.) |
Children
Sign in to add traineeAnna Okula Basile | grad student | Penn State | |
William S. Bush | grad student | Vanderbilt | |
Molly Hall | grad student | Penn State | |
Emily Holzinger | grad student | ||
Carrie Buchanan Moore | grad student | ||
Shefali Setia Verma | grad student | ||
Anurag Verma | grad student | ||
Xinyuan (Blair) Zhang | grad student | Penn State | |
Alison Motsinger-Reif | grad student | 2007 | Vanderbilt |
Todd Edwards | grad student | 2008 | Vanderbilt |
Stephen D. Turner | grad student | 2006-2010 | Vanderbilt |
Logan C. Dumitrescu | grad student | 2011 | Vanderbilt |
Ruowang Li | grad student | 2011-2016 | Penn State |
Binglan Li | grad student | 2015-2020 | Geisinger Health System |
Marta Byrska-Bishop | post-doc | ||
Jason E. Miller | post-doc | Geisinger Health System | |
Rebecca L. Zuvich | post-doc | Vanderbilt (Neurotree) | |
Sarah A. Pendergrass | post-doc | 2015 | |
Dokyoon Kim | post-doc | 2014-2016 | Penn State |
BETA: Related publications
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Publications
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Li R, Benz L, Duan R, et al. (2024) mixWAS: An efficient distributed algorithm for mixed-outcomes genome-wide association studies. Medrxiv : the Preprint Server For Health Sciences |
Verma SS, Gudiseva HV, Chavali VRM, et al. (2024) A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma. Cell. 187: 464-480.e10 |
Kember RL, Verma SS, Verma A, et al. (2023) Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 29: 611-626 |
Yang G, González P, Moneró M, et al. (2023) Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics. Medrxiv : the Preprint Server For Health Sciences |
Roychowdhury T, Klarin D, Levin MG, et al. (2023) Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. Nature Genetics |
Li B, Sangkuhl K, Whaley R, et al. (2023) Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank. American Journal of Human Genetics. 110: 1628-1647 |
Pividori M, Lu S, Li B, et al. (2023) Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. Nature Communications. 14: 5562 |
Safonov A, Nomakuchi TT, Chao E, et al. (2023) A genotype-first approach identifies high incidence of pathogenic variants with distinct disease associations. Medrxiv : the Preprint Server For Health Sciences |
Lee DSM, DePaolo JS, Aragam KG, et al. (2023) Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum. Medrxiv : the Preprint Server For Health Sciences |
Singhal P, Guare L, Morse C, et al. (2023) DETECT: Feature extraction method for disease trajectory modeling in electronic health records. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2023: 487-496 |