Xinyuan (Blair) Zhang
Affiliations: | Pennsylvania State University, State College, PA, United States |
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"Xinyuan Zhang"
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Publications
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Yengo L, Vedantam S, Marouli E, et al. (2022) A saturated map of common genetic variants associated with human height. Nature |
Zhang X, Lucas AM, Veturi Y, et al. (2022) Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature Communications. 13: 3428 |
Drivas TG, Lucas A, Zhang X, et al. (2021) Mendelian pathway analysis of laboratory traits reveals distinct roles for ciliary subcompartments in common disease pathogenesis. American Journal of 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 |
Li R, Duan R, Zhang X, et al. (2021) Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics. Nature Communications. 12: 168 |
Zhang X, Li R, Ritchie MD. (2020) Statistical Impact of Sample Size and Imbalance on Multivariate Analysis and A Case Study in the UK Biobank. Amia ... Annual Symposium Proceedings. Amia Symposium. 2020: 1383-1391 |
Huang J, Zhang X, Tong J, et al. (2019) Comparing drug safety of hepatitis C therapies using post-market data. Bmc Medical Informatics and Decision Making. 19: 147 |
Haggerty CM, Damrauer SM, Levin MG, et al. (2019) Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants. Circulation |
Zhang X, Veturi Y, Verma S, et al. (2019) Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 24: 272-283 |
Zhang X, Basile AO, Pendergrass SA, et al. (2019) Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico. Bmc Bioinformatics. 20: 46 |