Xiuwen Zheng, Ph.D.
Affiliations: | 2013 | Biostatistics - Public Health | University of Washington, Seattle, Seattle, WA |
Google:
"Xiuwen Zheng"Parents
Sign in to add mentor| Bruce S. Weir | grad student | 2013 | University of Washington | |
| (Statistical Prediction of HLA Alleles and Relatedness Analysis in Genome-Wide Association Studies.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Zheng X, Lee J. (2024) Imputation-Based HLA Typing with GWAS SNPs. Methods in Molecular Biology (Clifton, N.J.). 2809: 127-143 |
| Karczewski KJ, Solomonson M, Chao KR, et al. (2022) Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics. 2: 100168 |
| Zhou H, Arapoglou T, Li X, et al. (2022) FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Research |
| Sofer T, Zheng X, Laurie CA, et al. (2021) Variant-specific inflation factors for assessing population stratification at the phenotypic variance level. Nature Communications. 12: 3506 |
| Hu Y, Stilp AM, McHugh CP, et al. (2021) Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. 108: 1165 |
| Hu Y, Stilp AM, McHugh CP, et al. (2021) Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics |
| Zheng X, Davis JW. (2020) SAIGEgds - an efficient statistical tool for large-scale PheWAS with mixed models. Bioinformatics (Oxford, England) |
| Huang YH, Khor SS, Zheng X, et al. (2020) A high-resolution HLA imputation system for the Taiwanese population: a study of the Taiwan Biobank. The Pharmacogenomics Journal |
| Sarnowski C, Leong A, Raffield LM, et al. (2019) Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American Journal of Human Genetics |
| Sofer T, Zheng X, Gogarten SM, et al. (2019) A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Genetic Epidemiology |