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Connection

Matthew Stephens to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications Matthew Stephens has written about Polymorphism, Single Nucleotide.
  1. A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes. PLoS Genet. 2023 07; 19(7):e1010539.
    View in: PubMed
    Score: 0.488
  2. Fine-mapping from summary data with the "Sum of Single Effects" model. PLoS Genet. 2022 07; 18(7):e1010299.
    View in: PubMed
    Score: 0.456
  3. A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians. PLoS One. 2015; 10(4):e0120758.
    View in: PubMed
    Score: 0.276
  4. Efficient multivariate linear mixed model algorithms for genome-wide association studies. Nat Methods. 2014 Apr; 11(4):407-9.
    View in: PubMed
    Score: 0.254
  5. Genome-wide efficient mixed-model analysis for association studies. Nat Genet. 2012 Jun 17; 44(7):821-4.
    View in: PubMed
    Score: 0.227
  6. Bayesian statistical methods for genetic association studies. Nat Rev Genet. 2009 Oct; 10(10):681-90.
    View in: PubMed
    Score: 0.188
  7. Linkage disequilibrium-based quality control for large-scale genetic studies. PLoS Genet. 2008 Aug 01; 4(8):e1000147.
    View in: PubMed
    Score: 0.173
  8. Imputation-based analysis of association studies: candidate regions and quantitative traits. PLoS Genet. 2007 Jul; 3(7):e114.
    View in: PubMed
    Score: 0.160
  9. Automating sequence-based detection and genotyping of SNPs from diploid samples. Nat Genet. 2006 Mar; 38(3):375-81.
    View in: PubMed
    Score: 0.146
  10. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. Genetics. 2003 Dec; 165(4):2213-33.
    View in: PubMed
    Score: 0.125
  11. Bayesian multivariate reanalysis of large genetic studies identifies many new associations. PLoS Genet. 2019 10; 15(10):e1008431.
    View in: PubMed
    Score: 0.094
  12. Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions. Nat Genet. 2019 01; 51(1):187-195.
    View in: PubMed
    Score: 0.089
  13. Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes. Nat Commun. 2018 10 19; 9(1):4361.
    View in: PubMed
    Score: 0.088
  14. fastSTRUCTURE: variational inference of population structure in large SNP data sets. Genetics. 2014 Jun; 197(2):573-89.
    View in: PubMed
    Score: 0.064
  15. 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. PLoS Genet. 2013; 9(10):e1003770.
    View in: PubMed
    Score: 0.062
  16. Practical issues in imputation-based association mapping. PLoS Genet. 2008 Dec; 4(12):e1000279.
    View in: PubMed
    Score: 0.044
  17. A second generation human haplotype map of over 3.1 million SNPs. Nature. 2007 Oct 18; 449(7164):851-61.
    View in: PubMed
    Score: 0.041
  18. A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet. 2006 Mar; 78(3):437-50.
    View in: PubMed
    Score: 0.036
  19. The effects of genotype-dependent recombination, and transmission asymmetry, on linkage disequilibrium. Genetics. 2006 Mar; 172(3):2001-5.
    View in: PubMed
    Score: 0.036
  20. Evidence for substantial fine-scale variation in recombination rates across the human genome. Nat Genet. 2004 Jul; 36(7):700-6.
    View in: PubMed
    Score: 0.032
  21. Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits. Nat Genet. 2024 Feb; 56(2):336-347.
    View in: PubMed
    Score: 0.032
  22. Fine-mapping studies distinguish genetic risks for childhood- and adult-onset asthma in the HLA region. Genome Med. 2022 05 24; 14(1):55.
    View in: PubMed
    Score: 0.028
  23. Genotyping Polyploids from Messy Sequencing Data. Genetics. 2018 11; 210(3):789-807.
    View in: PubMed
    Score: 0.022
  24. The genetic architecture of gene expression levels in wild baboons. Elife. 2015 Feb 25; 4.
    View in: PubMed
    Score: 0.017
  25. A statin-dependent QTL for GATM expression is associated with statin-induced myopathy. Nature. 2013 Oct 17; 502(7471):377-80.
    View in: PubMed
    Score: 0.015
  26. Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13). PLoS One. 2012; 7(8):e42646.
    View in: PubMed
    Score: 0.014
  27. DNase?I sensitivity QTLs are a major determinant of human expression variation. Nature. 2012 Feb 05; 482(7385):390-4.
    View in: PubMed
    Score: 0.014
  28. Dissecting the regulatory architecture of gene expression QTLs. Genome Biol. 2012 Jan 31; 13(1):R7.
    View in: PubMed
    Score: 0.014
  29. Genome-wide association of lipid-lowering response to statins in combined study populations. PLoS One. 2010 Mar 22; 5(3):e9763.
    View in: PubMed
    Score: 0.012
  30. Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature. 2010 Apr 01; 464(7289):768-72.
    View in: PubMed
    Score: 0.012
  31. High-resolution mapping of expression-QTLs yields insight into human gene regulation. PLoS Genet. 2008 Oct; 4(10):e1000214.
    View in: PubMed
    Score: 0.011
  32. Genes mirror geography within Europe. Nature. 2008 Nov 06; 456(7218):98-101.
    View in: PubMed
    Score: 0.011
  33. Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. Am J Hum Genet. 2008 May; 82(5):1193-201.
    View in: PubMed
    Score: 0.011
  34. Genome-wide detection and characterization of positive selection in human populations. Nature. 2007 Oct 18; 449(7164):913-8.
    View in: PubMed
    Score: 0.010
  35. Automating resequencing-based detection of insertion-deletion polymorphisms. Nat Genet. 2006 Dec; 38(12):1457-62.
    View in: PubMed
    Score: 0.010
  36. Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion. Nat Genet. 2006 Dec; 38(12):1419-23.
    View in: PubMed
    Score: 0.010
  37. Absence of the TAP2 human recombination hotspot in chimpanzees. PLoS Biol. 2004 Jun; 2(6):e155.
    View in: PubMed
    Score: 0.008
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.