| Year |
Citation |
Score |
| 2022 |
Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-Gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, et al. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics. 2: 100168. PMID 36778668 DOI: 10.1016/j.xgen.2022.100168 |
0.344 |
|
| 2022 |
Zhou H, Arapoglou T, Li X, Li Z, Zheng X, Moore J, Asok A, Kumar S, Blue EE, Buyske S, Cox N, Felsenfeld A, Gerstein M, Kenny E, Li B, et al. FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Research. PMID 36350676 DOI: 10.1093/nar/gkac966 |
0.327 |
|
| 2021 |
Sofer T, Zheng X, Laurie CA, Gogarten SM, Brody JA, Conomos MP, Bis JC, Thornton TA, Szpiro A, O'Connell JR, Lange EM, Gao Y, Cupples LA, Psaty BM, et al. Variant-specific inflation factors for assessing population stratification at the phenotypic variance level. Nature Communications. 12: 3506. PMID 34108454 DOI: 10.1038/s41467-021-23655-2 |
0.672 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jain D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. 108: 1165. PMID 34087167 DOI: 10.1016/j.ajhg.2021.04.015 |
0.639 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.672 |
|
| 2020 |
Zheng X, Davis JW. SAIGEgds - an efficient statistical tool for large-scale PheWAS with mixed models. Bioinformatics (Oxford, England). PMID 32898220 DOI: 10.1093/bioinformatics/btaa731 |
0.325 |
|
| 2020 |
Huang YH, Khor SS, Zheng X, Chen HY, Chang YH, Chu HW, Wu PE, Lin YJ, Liao SF, Shen CY, Tokunaga K, Lee MH. A high-resolution HLA imputation system for the Taiwanese population: a study of the Taiwan Biobank. The Pharmacogenomics Journal. PMID 32042094 DOI: 10.1038/S41397-020-0156-3 |
0.362 |
|
| 2019 |
Sarnowski C, Leong A, Raffield LM, Wu P, de Vries PS, DiCorpo D, Guo X, Xu H, Liu Y, Zheng X, Hu Y, Brody JA, Goodarzi MO, Hidalgo BA, Highland HM, et al. 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. PMID 31564435 DOI: 10.1016/J.Ajhg.2019.08.010 |
0.373 |
|
| 2019 |
Sofer T, Zheng X, Gogarten SM, Laurie CA, Grinde K, Shaffer JR, Shungin D, O'Connell JR, Durazo-Arvizo RA, Raffield L, Lange L, Musani S, Vasan RS, Cupples LA, Reiner AP, et al. A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Genetic Epidemiology. PMID 30653739 DOI: 10.1002/Gepi.22188 |
0.395 |
|
| 2018 |
Zheng X. Imputation-Based HLA Typing with SNPs in GWAS Studies. Methods in Molecular Biology (Clifton, N.J.). 1802: 163-176. PMID 29858808 DOI: 10.1007/978-1-4939-8546-3_11 |
0.419 |
|
| 2017 |
Pappas DJ, Lizee A, Paunic V, Beutner KR, Motyer A, Vukcevic D, Leslie S, Biesiada J, Meller J, Taylor KD, Zheng X, Zhao LP, Gourraud PA, Hollenbach JA, Mack SJ, et al. Significant variation between SNP-based HLA imputations in diverse populations: the last mile is the hardest. The Pharmacogenomics Journal. PMID 28440342 DOI: 10.1038/Tpj.2017.7 |
0.392 |
|
| 2017 |
Zheng X, Gogarten SM, Lawrence M, Stilp A, Conomos MP, Weir BS, Laurie C, Levine D. SeqArray - A storage-efficient high-performance data format for WGS variant calls. Bioinformatics (Oxford, England). PMID 28334390 DOI: 10.1093/Bioinformatics/Btx145 |
0.697 |
|
| 2016 |
Martin PJ, Levine DM, Storer BE, Warren EH, Zheng X, Nelson SC, Smith AG, Mortensen BK, Hansen JA. Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease. Blood. PMID 27872059 DOI: 10.1182/Blood-2016-09-737700 |
0.335 |
|
| 2016 |
Liu J, Ye Z, Mayer JG, Hoch BA, Green C, Rolak L, Cold C, Khor SS, Zheng X, Miyagawa T, Tokunaga K, Brilliant MH, Hebbring SJ. Phenome-wide association study maps new diseases to the human major histocompatibility complex region. Journal of Medical Genetics. PMID 27287392 DOI: 10.1136/Jmedgenet-2016-103867 |
0.355 |
|
| 2015 |
Weir BS, Zheng X. SNPs and SNVs in forensic science. Forensic Science International. Genetics Supplement Series. 5: e267-e268. PMID 28794809 DOI: 10.1016/J.Fsigss.2015.09.106 |
0.576 |
|
| 2015 |
Zhu Z, Liang Z, Liany H, Yang C, Wen L, Lin Z, Sheng Y, Lin Y, Ye L, Cheng Y, Chang Y, Liu L, Yang L, Shi Y, Shen C, ... ... Zheng X, et al. Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus. Arthritis Research & Therapy. 17: 349. PMID 26635088 DOI: 10.1186/S13075-015-0857-1 |
0.407 |
|
| 2015 |
Nunes K, Zheng X, Torres M, Moraes ME, Piovezan BZ, Pontes GN, Kimura L, Carnavalli JE, Mingroni Netto RC, Meyer D. HLA imputation in an admixed population: An assessment of the 1000 Genomes data as a training set. Human Immunology. PMID 26582005 DOI: 10.1016/J.Humimm.2015.11.004 |
0.387 |
|
| 2015 |
Zheng X, Weir BS. Eigenanalysis of SNP data with an identity by descent interpretation. Theoretical Population Biology. PMID 26482676 DOI: 10.1016/J.Tpb.2015.09.004 |
0.605 |
|
| 2015 |
Weir BS, Zheng X. SNPs and SNVs in forensic science Forensic Science International: Genetics Supplement Series. DOI: 10.1016/j.fsigss.2015.09.106 |
0.474 |
|
| 2014 |
Zheng X, Shen J, Cox C, Wakefield JC, Ehm MG, Nelson MR, Weir BS. HIBAG--HLA genotype imputation with attribute bagging. The Pharmacogenomics Journal. 14: 192-200. PMID 23712092 DOI: 10.1038/Tpj.2013.18 |
0.594 |
|
| 2013 |
Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, et al. Genetic variation associated with circulating monocyte count in the eMERGE Network. Human Molecular Genetics. 22: 2119-27. PMID 23314186 DOI: 10.1093/Hmg/Ddt010 |
0.377 |
|
| 2012 |
Zheng X, Levine D, Shen J, Gogarten SM, Laurie C, Weir BS. A high-performance computing toolset for relatedness and principal component analysis of SNP data. Bioinformatics (Oxford, England). 28: 3326-8. PMID 23060615 DOI: 10.1093/Bioinformatics/Bts606 |
0.599 |
|
| 2012 |
Gogarten SM, Bhangale T, Conomos MP, Laurie CA, McHugh CP, Painter I, Zheng X, Crosslin DR, Levine D, Lumley T, Nelson SC, Rice K, Shen J, Swarnkar R, Weir BS, et al. GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies. Bioinformatics (Oxford, England). 28: 3329-31. PMID 23052040 DOI: 10.1093/Bioinformatics/Bts610 |
0.702 |
|
| 2012 |
Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang LE, Lee JE, Barnes KC, Hansel NN, ... ... Zheng X, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics. 44: 642-50. PMID 22561516 DOI: 10.1038/Ng.2271 |
0.671 |
|
| 2012 |
Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Pretel S, Saip A, et al. Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Human Genetics. 131: 639-52. PMID 22037903 DOI: 10.1007/S00439-011-1103-9 |
0.426 |
|
| 2010 |
Laurie CC, Doheny KF, Mirel DB, Pugh EW, Bierut LJ, Bhangale T, Boehm F, Caporaso NE, Cornelis MC, Edenberg HJ, Gabriel SB, Harris EL, Hu FB, Jacobs KB, Kraft P, ... ... Zheng X, et al. Quality control and quality assurance in genotypic data for genome-wide association studies. Genetic Epidemiology. 34: 591-602. PMID 20718045 DOI: 10.1002/Gepi.20516 |
0.619 |
|
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