Dr. Xiuwen Zheng
Dr. Xiuwen Zheng
AbbVie (Genomics Research Center)
Adresse e-mail validée de
Citée par
Citée par
A high-performance computing toolset for relatedness and principal component analysis of SNP data
X Zheng, D Levine, J Shen, SM Gogarten, C Laurie, BS Weir
Bioinformatics 28 (24), 3326-3328, 2012
Detectable clonal mosaicism from birth to old age and its relationship to cancer
CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ...
Nature genetics 44 (6), 642-650, 2012
Quality control and quality assurance in genotypic data for genome‐wide association studies
CC Laurie, KF Doheny, DB Mirel, EW Pugh, LJ Bierut, T Bhangale, ...
Genetic epidemiology 34 (6), 591-602, 2010
HIBAG—HLA genotype imputation with attribute bagging
X Zheng, J Shen, C Cox, JC Wakefield, MG Ehm, MR Nelson, BS Weir
The pharmacogenomics journal 14 (2), 192-200, 2014
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies
SM Gogarten, T Bhangale, MP Conomos, CA Laurie, CP McHugh, ...
Bioinformatics 28 (24), 3329-3331, 2012
HLA-DPB1 and HLA class I confer risk of and protection from narcolepsy
HM Ollila, JM Ravel, F Han, J Faraco, L Lin, X Zheng, G Plazzi, ...
The American Journal of Human Genetics 96 (1), 136-146, 2015
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network
DR Crosslin, A McDavid, N Weston, SC Nelson, X Zheng, E Hart, ...
Human genetics 131, 639-652, 2012
SeqArray—a storage-efficient high-performance data format for WGS variant calls
X Zheng, SM Gogarten, M Lawrence, A Stilp, MP Conomos, BS Weir, ...
Bioinformatics 33 (15), 2251-2257, 2017
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
KJ Karczewski, M Solomonson, KR Chao, JK Goodrich, G Tiao, W Lu, ...
Cell Genomics 2 (9), 2022
Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease
PJ Martin, DM Levine, BE Storer, EH Warren, X Zheng, SC Nelson, ...
Blood, The Journal of the American Society of Hematology 129 (6), 791-798, 2017
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals
JA Kosmicki, JE Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, ...
The American Journal of Human Genetics 108 (7), 1350-1355, 2021
Genetic variation associated with circulating monocyte count in the eMERGE Network
DR Crosslin, A McDavid, N Weston, X Zheng, E Hart, M de Andrade, ...
Human molecular genetics 22 (10), 2119-2127, 2013
A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies
T Sofer, X Zheng, SM Gogarten, CA Laurie, K Grinde, JR Shaffer, ...
Genetic epidemiology 43 (3), 263-275, 2019
High-accuracy imputation for HLA class I and II genes based on high-resolution SNP data of population-specific references
SS Khor, W Yang, M Kawashima, S Kamitsuji, X Zheng, N Nishida, ...
The pharmacogenomics journal 15 (6), 530-537, 2015
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ...
The American Journal of Human Genetics 108 (5), 874-893, 2021
Eigenanalysis of SNP data with an identity by descent interpretation
X Zheng, BS Weir
Theoretical population biology 107, 65-76, 2016
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome
H Zhou, T Arapoglou, X Li, Z Li, X Zheng, J Moore, A Asok, S Kumar, ...
Nucleic Acids Research 51 (D1), D1300-D1311, 2023
Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: the trans-omics for precision medicine program
C Sarnowski, A Leong, LM Raffield, P Wu, PS de Vries, D DiCorpo, X Guo, ...
The American Journal of Human Genetics 105 (4), 706-718, 2019
Phenome-wide association study maps new diseases to the human major histocompatibility complex region
J Liu, Z Ye, JG Mayer, BA Hoch, C Green, L Rolak, C Cold, SS Khor, ...
Journal of medical genetics 53 (10), 681-689, 2016
Significant variation between SNP-based HLA imputations in diverse populations: the last mile is the hardest
DJ Pappas, A Lizee, V Paunic, KR Beutner, A Motyer, D Vukcevic, ...
The pharmacogenomics journal 18 (3), 367-376, 2018
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20