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One or more keywords matched the following items that are connected to Stephens, Matthew
Item TypeName
Concept Polymorphism, Single Nucleotide
Academic Article The effects of genotype-dependent recombination, and transmission asymmetry, on linkage disequilibrium.
Academic Article Genome-wide detection and characterization of positive selection in human populations.
Academic Article Practical issues in imputation-based association mapping.
Academic Article Genome-wide association of lipid-lowering response to statins in combined study populations.
Academic Article Understanding mechanisms underlying human gene expression variation with RNA sequencing.
Academic Article Genome-wide efficient mixed-model analysis for association studies.
Academic Article Dissecting the regulatory architecture of gene expression QTLs.
Academic Article Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.
Academic Article Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13).
Academic Article A second generation human haplotype map of over 3.1 million SNPs.
Academic Article DNase?I sensitivity QTLs are a major determinant of human expression variation.
Academic Article Absence of the TAP2 human recombination hotspot in chimpanzees.
Academic Article High-resolution mapping of expression-QTLs yields insight into human gene regulation.
Academic Article Genes mirror geography within Europe.
Academic Article Automating resequencing-based detection of insertion-deletion polymorphisms.
Academic Article Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.
Academic Article A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.
Academic Article The genetic architecture of gene expression levels in wild baboons.
Academic Article Integrated enrichment analysis of variants and pathways in genome-wide association studies indicates central role for IL-2 signaling genes in type 1 diabetes, and cytokine signaling genes in Crohn's disease.
Academic Article A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians.
Academic Article Bayesian statistical methods for genetic association studies.
Academic Article fastSTRUCTURE: variational inference of population structure in large SNP data sets.
Academic Article A comparison of phasing algorithms for trios and unrelated individuals.
Academic Article Automating sequence-based detection and genotyping of SNPs from diploid samples.
Academic Article Linkage disequilibrium-based quality control for large-scale genetic studies.
Academic Article Evidence for substantial fine-scale variation in recombination rates across the human genome.
Academic Article Efficient multivariate linear mixed model algorithms for genome-wide association studies.
Academic Article Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data.
Academic Article Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes.
Academic Article Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions.
Academic Article Genotyping Polyploids from Messy Sequencing Data.
Academic Article Bayesian multivariate reanalysis of large genetic studies identifies many new associations.
Academic Article Fine-mapping studies distinguish genetic risks for childhood- and adult-onset asthma in the HLA region.
Academic Article Fine-mapping from summary data with the "Sum of Single Effects" model.
Grant Multipoint and significance methods for genome-wide association studies
Academic Article A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes.
Academic Article Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits.
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  • Polymorphism Single Nucleotide