Xiaoquan Wen - Publications

2011 Statistics University of Chicago, Chicago, IL 

27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Barbeira AN, Bonazzola R, Gamazon ER, Liang Y, Park Y, Kim-Hellmuth S, Wang G, Jiang Z, Zhou D, Hormozdiari F, Liu B, Rao A, Hamel AR, Pividori MD, Aguet F, ... ... Wen X, et al. Exploiting the GTEx resources to decipher the mechanisms at GWAS loci. Genome Biology. 22: 49. PMID 33499903 DOI: 10.1186/s13059-020-02252-4  0.96
2020 Barbeira AN, Melia OJ, Liang Y, Bonazzola R, Wang G, Wheeler HE, Aguet F, Ardlie KG, Wen X, Im HK. Fine-mapping and QTL tissue-sharing information improves the reliability of causal gene identification. Genetic Epidemiology. PMID 32964524 DOI: 10.1002/gepi.22346  0.96
2020 Kim-Hellmuth S, Aguet F, Oliva M, Muñoz-Aguirre M, Kasela S, Wucher V, Castel SE, Hamel AR, Viñuela A, Roberts AL, Mangul S, Wen X, Wang G, Barbeira AN, Garrido-Martín D, et al. Cell type-specific genetic regulation of gene expression across human tissues. Science (New York, N.Y.). 369. PMID 32913075 DOI: 10.1126/Science.Aaz8528  0.96
2016 Scott LJ, Erdos MR, Huyghe JR, Welch RP, Beck AT, Wolford BN, Chines PS, Didion JP, Narisu N, Stringham HM, Taylor DL, Jackson AU, Vadlamudi S, Bonnycastle LL, Kinnunen L, ... ... Wen X, et al. The genetic regulatory signature of type 2 diabetes in human skeletal muscle. Nature Communications. 7: 11764. PMID 27353450 DOI: 10.1038/Ncomms11764  0.96
2016 Wen X, Lee Y, Luca F, Pique-Regi R. Efficient Integrative Multi-SNP Association Analysis via Deterministic Approximation of Posteriors. American Journal of Human Genetics. PMID 27236919 DOI: 10.1016/J.Ajhg.2016.03.029  0.96
2016 Wen X. Molecular QTL discovery incorporating genomic annotations using Bayesian false discovery rate control Annals of Applied Statistics. 10: 1619-1638. DOI: 10.1214/16-Aoas952  0.96
2016 Wen X. Robust Bayesian FDR Control Using Bayes Factors, with Applications to Multi-tissue eQTL Discovery Statistics in Biosciences. 1-22. DOI: 10.1007/S12561-016-9153-0  0.96
2015 Wen X, Luca F, Pique-Regi R. Cross-population joint analysis of eQTLs: fine mapping and functional annotation. Plos Genetics. 11: e1005176. PMID 25906321 DOI: 10.1371/Journal.Pgen.1005176  0.96
2015 Wen X. Bayesian model comparison in genetic association analysis: linear mixed modeling and SNP set testing. Biostatistics (Oxford, England). 16: 701-12. PMID 25796429 DOI: 10.1093/Biostatistics/Kxv009  0.96
2015 Harvey CT, Moyerbrailean GA, Davis GO, Wen X, Luca F, Pique-Regi R. QuASAR: quantitative allele-specific analysis of reads. Bioinformatics (Oxford, England). 31: 1235-42. PMID 25480375 DOI: 10.1093/Bioinformatics/Btu802  0.96
2015 Ardlie KG, DeLuca DS, Segrè AV, Sullivan TJ, Young TR, Gelfand ET, Trowbridge CA, Maller JB, Tukiainen T, Lek M, Ward LD, Kheradpour P, Iriarte B, Meng Y, Palmer CD, ... ... Wen X, et al. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans Science. 348: 648-660. DOI: 10.1126/science.1262110  0.96
2014 Li S, Mukherjee B, Taylor JM, Rice KM, Wen X, Rice JD, Stringham HM, Boehnke M. The role of environmental heterogeneity in meta-analysis of gene-environment interactions with quantitative traits. Genetic Epidemiology. 38: 416-29. PMID 24801060 DOI: 10.1002/Gepi.21810  0.96
2014 Wen X. Bayesian model selection in complex linear systems, as illustrated in genetic association studies. Biometrics. 70: 73-83. PMID 24350677 DOI: 10.1111/Biom.12112  0.96
2013 Lonsdale J, Thomas J, Salvatore M, Phillips R, Lo E, Shad S, Hasz R, Walters G, Garcia F, Young N, Foster B, Moser M, Karasik E, Gillard B, Ramsey K, ... ... Wen X, et al. The Genotype-Tissue Expression (GTEx) project Nature Genetics. 45: 580-585. PMID 23715323 DOI: 10.1038/Ng.2653  0.96
2013 Flutre T, Wen X, Pritchard J, Stephens M. A statistical framework for joint eQTL analysis in multiple tissues. Plos Genetics. 9: e1003486. PMID 23671422 DOI: 10.1371/Journal.Pgen.1003486  0.96
2011 Maranville JC, Luca F, Richards AL, Wen X, Witonsky DB, Baxter S, Stephens M, Di Rienzo A. Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. Plos Genetics. 7: e1002162. PMID 21750684 DOI: 10.1371/Journal.Pgen.1002162  0.96
2010 Wen X, Stephens M. USING LINEAR PREDICTORS TO IMPUTE ALLELE FREQUENCIES FROM SUMMARY OR POOLED GENOTYPE DATA. The Annals of Applied Statistics. 4: 1158-1182. PMID 21479081 DOI: 10.1214/10-Aoas338  0.96
2010 De la Cruz O, Wen X, Ke B, Song M, Nicolae DL. Gene, region and pathway level analyses in whole-genome studies. Genetic Epidemiology. 34: 222-31. PMID 20013942 DOI: 10.1002/Gepi.20452  0.96
2009 Fledel-Alon A, Wilson DJ, Broman K, Wen X, Ober C, Coop G, Przeworski M. Broad-scale recombination patterns underlying proper disjunction in humans. Plos Genetics. 5: e1000658. PMID 19763175 DOI: 10.1371/Journal.Pgen.1000658  0.96
2008 Coop G, Wen X, Ober C, Pritchard JK, Przeworski M. High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans. Science (New York, N.Y.). 319: 1395-8. PMID 18239090 DOI: 10.1126/Science.1151851  0.96
2008 Wen X, Nicolae DL. Association studies for untyped markers with TUNA. Bioinformatics (Oxford, England). 24: 435-7. PMID 18057020 DOI: 10.1093/Bioinformatics/Btm603  0.96
2006 Conrad DF, Jakobsson M, Coop G, Wen X, Wall JD, Rosenberg NA, Pritchard JK. A worldwide survey of haplotype variation and linkage disequilibrium in the human genome. Nature Genetics. 38: 1251-60. PMID 17057719 DOI: 10.1038/Ng1911  0.96
2006 Nicolae DL, Wen X, Voight BF, Cox NJ. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. Plos Genetics. 2: e67. PMID 16680197 DOI: 10.1371/Journal.Pgen.0020067  0.96
2006 Voight BF, Kudaravalli S, Wen X, Pritchard JK. A map of recent positive selection in the human genome. Plos Biology. 4: e72. PMID 16494531 DOI: 10.1371/Journal.Pbio.0040072  0.96
2005 Zöllner S, Wen X, Pritchard JK. Association mapping and fine mapping with TreeLD. Bioinformatics (Oxford, England). 21: 3168-70. PMID 15855250 DOI: 10.1093/Bioinformatics/Bti453  0.96
2004 Zöllner S, Wen X, Hanchard NA, Herbert MA, Ober C, Pritchard JK. Evidence for extensive transmission distortion in the human genome. American Journal of Human Genetics. 74: 62-72. PMID 14681832 DOI: 10.1086/381131  0.96
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