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 | 2163 | 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 | 641 | 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 | 554 | 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 | 419 | 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 | 209 | 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 | 145 | 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 | 135 | 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 | 115 | 2017 |
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 | 110 | 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 | 105 | 2022 |
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 | 82 | 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 | 68 | 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 | 62 | 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 | 53 | 2015 |
Eigenanalysis of SNP data with an identity by descent interpretation X Zheng, BS Weir Theoretical population biology 107, 65-76, 2016 | 46 | 2016 |
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 | 44 | 2021 |
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 | 44 | 2019 |
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 | 41 | 2023 |
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 | 41 | 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 | 38 | 2018 |