Marylyn D. Ritchie

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"Marylyn Ritchie"

Parents

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Jason H. Moore grad student 2004 Vanderbilt
 (Genetic programming optimized neural networks for identifying gene -gene interactions.)

Children

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Anna 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
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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
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