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Genetics|January 6, 2004
Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism dataNa Li, Matthew StephensCell and Tissue Research|February 10, 2018
Neutrophil-lymphatic interactions during acute and chronic diseaseMatthew Stephens, Shan LiaoAmerican Journal of Human Genetics|February 9, 2005
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputationMatthew Stephens, Paul ScheetBiostatistics (Oxford, England)|July 10, 2018
Empirical Bayes shrinkage and false discovery rate estimation, allowing for unwanted variationDavid Gerard, Matthew StephensThe Annals of Applied Statistics|February 6, 2018
BAYESIAN LARGE-SCALE MULTIPLE REGRESSION WITH SUMMARY STATISTICS FROM GENOME-WIDE ASSOCIATION STUDIESXiang Zhu, Matthew StephensThe Annals of Applied Statistics|February 6, 2018
WAVELET-BASED GENETIC ASSOCIATION ANALYSIS OF FUNCTIONAL PHENOTYPES ARISING FROM HIGH-THROUGHPUT SEQUENCING ASSAYSHeejung Shim, Matthew StephensNature Genetics|May 25, 2021
Separating measurement and expression models clarifies confusion in single-cell RNA sequencing analysisAbhishek Sarkar, Matthew StephensAmerican Journal of Human Genetics|October 24, 2003
A comparison of bayesian methods for haplotype reconstruction from population genotype dataMatthew Stephens, Peter DonnellyAmerican Journal of Human Genetics|March 15, 2006
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phasePaul Scheet, Matthew StephensNature Genetics|April 22, 2008
Interpreting principal component analyses of spatial population genetic variationJohn Novembre, Matthew StephensPageof 24