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Connection

Matthew Stephens to Models, Genetic

This is a "connection" page, showing publications Matthew Stephens has written about Models, Genetic.
Connection Strength

5.014
  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: 0.628
  2. Fine-mapping from summary data with the "Sum of Single Effects" model. PLoS Genet. 2022 07; 18(7):e1010299.
    View in: PubMed
    Score: 0.587
  3. Bayesian multivariate reanalysis of large genetic studies identifies many new associations. PLoS Genet. 2019 10; 15(10):e1008431.
    View in: PubMed
    Score: 0.484
  4. 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: 0.453
  5. Visualizing spatial population structure with estimated effective migration surfaces. Nat Genet. 2016 Jan; 48(1):94-100.
    View in: PubMed
    Score: 0.371
  6. msCentipede: Modeling Heterogeneity across Genomic Sites and Replicates Improves Accuracy in the Inference of Transcription Factor Binding. PLoS One. 2015; 10(9):e0138030.
    View in: PubMed
    Score: 0.366
  7. A unified framework for association analysis with multiple related phenotypes. PLoS One. 2013; 8(7):e65245.
    View in: PubMed
    Score: 0.314
  8. Fast and accurate estimation of the population-scaled mutation rate, theta, from microsatellite genotype data. Genetics. 2007 Jun; 176(2):1363-6.
    View in: PubMed
    Score: 0.206
  9. msHOT: modifying Hudson's ms simulator to incorporate crossover and gene conversion hotspots. Bioinformatics. 2007 Feb 15; 23(4):520-1.
    View in: PubMed
    Score: 0.199
  10. Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet. 2005 Mar; 76(3):449-62.
    View in: PubMed
    Score: 0.175
  11. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. Genetics. 2003 Dec; 165(4):2213-33.
    View in: PubMed
    Score: 0.161
  12. Separating measurement and expression models clarifies confusion in single-cell RNA sequencing analysis. Nat Genet. 2021 06; 53(6):770-777.
    View in: PubMed
    Score: 0.136
  13. Accurate genomic prediction of Coffea canephora in multiple environments using whole-genome statistical models. Heredity (Edinb). 2019 03; 122(3):261-275.
    View in: PubMed
    Score: 0.111
  14. Estimating Time to the Common Ancestor for a Beneficial Allele. Mol Biol Evol. 2018 04 01; 35(4):1003-1017.
    View in: PubMed
    Score: 0.109
  15. fastSTRUCTURE: variational inference of population structure in large SNP data sets. Genetics. 2014 Jun; 197(2):573-89.
    View in: PubMed
    Score: 0.083
  16. Polygenic modeling with bayesian sparse linear mixed models. PLoS Genet. 2013; 9(2):e1003264.
    View in: PubMed
    Score: 0.076
  17. Genome-wide efficient mixed-model analysis for association studies. Nat Genet. 2012 Jun 17; 44(7):821-4.
    View in: PubMed
    Score: 0.073
  18. Analysis of population structure: a unifying framework and novel methods based on sparse factor analysis. PLoS Genet. 2010 Sep 16; 6(9):e1001117.
    View in: PubMed
    Score: 0.065
  19. Practical issues in imputation-based association mapping. PLoS Genet. 2008 Dec; 4(12):e1000279.
    View in: PubMed
    Score: 0.057
  20. Linkage disequilibrium-based quality control for large-scale genetic studies. PLoS Genet. 2008 Aug 01; 4(8):e1000147.
    View in: PubMed
    Score: 0.056
  21. Using DNA to track the origin of the largest ivory seizure since the 1989 trade ban. Proc Natl Acad Sci U S A. 2007 Mar 06; 104(10):4228-33.
    View in: PubMed
    Score: 0.051
  22. A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet. 2003 Nov; 73(5):1162-9.
    View in: PubMed
    Score: 0.040
  23. Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. Genetics. 2003 Aug; 164(4):1567-87.
    View in: PubMed
    Score: 0.039
  24. Detailed modeling of positive selection improves detection of cancer driver genes. Nat Commun. 2019 07 30; 10(1):3399.
    View in: PubMed
    Score: 0.030
  25. Discovery and characterization of variance QTLs in human induced pluripotent stem cells. PLoS Genet. 2019 04; 15(4):e1008045.
    View in: PubMed
    Score: 0.029
  26. Genotyping Polyploids from Messy Sequencing Data. Genetics. 2018 11; 210(3):789-807.
    View in: PubMed
    Score: 0.028
  27. New evidence for hybrid zones of forest and savanna elephants in Central and West Africa. Mol Ecol. 2015 12; 24(24):6134-47.
    View in: PubMed
    Score: 0.023
  28. An estimate of the average number of recessive lethal mutations carried by humans. Genetics. 2015 Apr; 199(4):1243-54.
    View in: PubMed
    Score: 0.022
  29. 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: 0.018
  30. High-resolution mapping of expression-QTLs yields insight into human gene regulation. PLoS Genet. 2008 Oct; 4(10):e1000214.
    View in: PubMed
    Score: 0.014
  31. Absence of the TAP2 human recombination hotspot in chimpanzees. PLoS Biol. 2004 Jun; 2(6):e155.
    View in: PubMed
    Score: 0.010
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.