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Connection

Jonathan Pritchard to Genome-Wide Association Study

This is a "connection" page, showing publications Jonathan Pritchard has written about Genome-Wide Association Study.
  1. Gene regulatory network inference from CRISPR perturbations in primary CD4+ T cells elucidates the genomic basis of immune disease. Cell Genom. 2024 Nov 13; 4(11):100671.
    View in: PubMed
    Score: 0.556
  2. Systematic differences in discovery of genetic effects on gene expression and complex traits. Nat Genet. 2023 Nov; 55(11):1866-1875.
    View in: PubMed
    Score: 0.519
  3. Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits. Am J Hum Genet. 2022 07 07; 109(7):1286-1297.
    View in: PubMed
    Score: 0.473
  4. GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Elife. 2021 02 15; 10.
    View in: PubMed
    Score: 0.431
  5. Inference of population splits and mixtures from genome-wide allele frequency data. PLoS Genet. 2012; 8(11):e1002967.
    View in: PubMed
    Score: 0.243
  6. Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Elife. 2022 09 08; 11.
    View in: PubMed
    Score: 0.120
  7. Variable prediction accuracy of polygenic scores within an ancestry group. Elife. 2020 01 30; 9.
    View in: PubMed
    Score: 0.100
  8. Trans Effects on Gene Expression Can Drive Omnigenic Inheritance. Cell. 2019 05 02; 177(4):1022-1034.e6.
    View in: PubMed
    Score: 0.095
  9. Inferring Relevant Cell Types for Complex Traits by Using Single-Cell Gene Expression. Am J Hum Genet. 2017 Nov 02; 101(5):686-699.
    View in: PubMed
    Score: 0.086
  10. An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell. 2017 Jun 15; 169(7):1177-1186.
    View in: PubMed
    Score: 0.084
  11. Detection of human adaptation during the past 2000 years. Science. 2016 11 11; 354(6313):760-764.
    View in: PubMed
    Score: 0.080
  12. Genome-wide association study of behavioral, physiological and gene expression traits in outbred CFW mice. Nat Genet. 2016 08; 48(8):919-26.
    View in: PubMed
    Score: 0.078
  13. RNA splicing is a primary link between genetic variation and disease. Science. 2016 Apr 29; 352(6285):600-4.
    View in: PubMed
    Score: 0.077
  14. The genetic architecture of adaptations to high altitude in Ethiopia. PLoS Genet. 2012; 8(12):e1003110.
    View in: PubMed
    Score: 0.061
  15. Adaptations to climate-mediated selective pressures in humans. PLoS Genet. 2011 Apr; 7(4):e1001375.
    View in: PubMed
    Score: 0.055
  16. DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol. 2011; 12(1):R10.
    View in: PubMed
    Score: 0.054
  17. Characterizing natural variation using next-generation sequencing technologies. Trends Genet. 2009 Oct; 25(10):463-71.
    View in: PubMed
    Score: 0.049
  18. The role of geography in human adaptation. PLoS Genet. 2009 Jun; 5(6):e1000500.
    View in: PubMed
    Score: 0.048
  19. Signals of recent positive selection in a worldwide sample of human populations. Genome Res. 2009 May; 19(5):826-37.
    View in: PubMed
    Score: 0.047
  20. A genome-wide genetic screen uncovers determinants of human pigmentation. Science. 2023 08 11; 381(6658):eade6289.
    View in: PubMed
    Score: 0.032
  21. RNA editing underlies genetic risk of common inflammatory diseases. Nature. 2022 08; 608(7923):569-577.
    View in: PubMed
    Score: 0.030
  22. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nat Genet. 2021 09; 53(9):1300-1310.
    View in: PubMed
    Score: 0.028
  23. Shared heritability of human face and brain shape. Nat Genet. 2021 06; 53(6):830-839.
    View in: PubMed
    Score: 0.027
  24. A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density. Cell Metab. 2021 03 02; 33(3):615-628.e13.
    View in: PubMed
    Score: 0.027
  25. Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes. Elife. 2018 05 08; 7.
    View in: PubMed
    Score: 0.022
  26. Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet. 2016 Jan; 48(1):22-9.
    View in: PubMed
    Score: 0.019
  27. Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions. Cell. 2015 Aug 27; 162(5):1051-65.
    View in: PubMed
    Score: 0.018
  28. The genetic and mechanistic basis for variation in gene regulation. PLoS Genet. 2015 Jan; 11(1):e1004857.
    View in: PubMed
    Score: 0.018
  29. Methylation QTLs are associated with coordinated changes in transcription factor binding, histone modifications, and gene expression levels. PLoS Genet. 2014 Sep; 10(9):e1004663.
    View in: PubMed
    Score: 0.017
  30. A statistical framework for joint eQTL analysis in multiple tissues. PLoS Genet. 2013 May; 9(5):e1003486.
    View in: PubMed
    Score: 0.016
  31. The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels. PLoS Genet. 2012; 8(10):e1003000.
    View in: PubMed
    Score: 0.015
  32. Haplotype variation and genotype imputation in African populations. Genet Epidemiol. 2011 Dec; 35(8):766-80.
    View in: PubMed
    Score: 0.014
  33. A genome-wide study of DNA methylation patterns and gene expression levels in multiple human and chimpanzee tissues. PLoS Genet. 2011 Feb; 7(2):e1001316.
    View in: PubMed
    Score: 0.014
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.