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Sign in to add mentor| Marylyn D. Ritchie | grad student | 2008 | Vanderbilt | |
| (Extensions to and an application of the multifactor dimensionality reduction pedigree disequilibrium test.) | ||||
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Publications
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| Armstrong ND, Srinivasasainagendra V, Ammous F, et al. (2023) Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program. Frontiers in Genetics. 14: 1278215 |
| Wang A, Shen J, Rodriguez AA, et al. (2023) Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Nature Genetics |
| 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 |
| Chen F, Madduri RK, Rodriguez AA, et al. (2023) Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. European Urology |
| Jasper EA, Hellwege JN, Breeyear JH, et al. (2023) Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia. Medrxiv : the Preprint Server For Health Sciences |
| Pike MM, Schildcrout J, Baldwin S, et al. (2023) Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Journal of the American Heart Association. 12: e027993 |
| Vujkovic M, Ramdas S, Lorenz KM, et al. (2022) A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Nature Genetics |
| Piekos JA, Hellwege JN, Zhang Y, et al. (2022) Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid. Human Genetics |
| Park J, Lucas AM, Zhang X, et al. (2021) Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. Nature Medicine |
| Surendran P, Feofanova EV, Lahrouchi N, et al. (2020) Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nature Genetics |