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Connection

Jonathan Pritchard to Haplotypes

This is a "connection" page, showing publications Jonathan Pritchard has written about Haplotypes.
Connection Strength

1.446
  1. A worldwide survey of haplotype variation and linkage disequilibrium in the human genome. Nat Genet. 2006 Nov; 38(11):1251-60.
    View in: PubMed
    Score: 0.238
  2. Assessing the performance of the haplotype block model of linkage disequilibrium. Am J Hum Genet. 2003 Sep; 73(3):502-15.
    View in: PubMed
    Score: 0.191
  3. Haplotype blocks and linkage disequilibrium in the human genome. Nat Rev Genet. 2003 Aug; 4(8):587-97.
    View in: PubMed
    Score: 0.190
  4. Detection of human adaptation during the past 2000 years. Science. 2016 11 11; 354(6313):760-764.
    View in: PubMed
    Score: 0.119
  5. WASP: allele-specific software for robust molecular quantitative trait locus discovery. Nat Methods. 2015 Nov; 12(11):1061-3.
    View in: PubMed
    Score: 0.110
  6. Haplotype variation and genotype imputation in African populations. Genet Epidemiol. 2011 Dec; 35(8):766-80.
    View in: PubMed
    Score: 0.085
  7. The role of geography in human adaptation. PLoS Genet. 2009 Jun; 5(6):e1000500.
    View in: PubMed
    Score: 0.071
  8. Haplotypic background of a private allele at high frequency in the Americas. Mol Biol Evol. 2009 May; 26(5):995-1016.
    View in: PubMed
    Score: 0.070
  9. Gene expression levels are a target of recent natural selection in the human genome. Mol Biol Evol. 2009 Mar; 26(3):649-58.
    View in: PubMed
    Score: 0.069
  10. The effects of genotype-dependent recombination, and transmission asymmetry, on linkage disequilibrium. Genetics. 2006 Mar; 172(3):2001-5.
    View in: PubMed
    Score: 0.056
  11. Coalescent-based association mapping and fine mapping of complex trait loci. Genetics. 2005 Feb; 169(2):1071-92.
    View in: PubMed
    Score: 0.052
  12. A novel quantitative trait locus implicates Msh3 in the propensity for genome-wide short tandem repeat expansions in mice. Genome Res. 2023 05; 33(5):689-702.
    View in: PubMed
    Score: 0.047
  13. A natural mutator allele shapes mutation spectrum variation in mice. Nature. 2022 05; 605(7910):497-502.
    View in: PubMed
    Score: 0.044
  14. 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: 0.040
  15. Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency. Proc Natl Acad Sci U S A. 2010 May 11; 107 Suppl 2:8924-30.
    View in: PubMed
    Score: 0.019
  16. High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans. Science. 2008 Mar 07; 319(5868):1395-8.
    View in: PubMed
    Score: 0.016
  17. Using population mixtures to optimize the utility of genomic databases: linkage disequilibrium and association study design in India. Ann Hum Genet. 2008 Jul; 72(Pt 4):535-46.
    View in: PubMed
    Score: 0.015
  18. Convergent adaptation of human lactase persistence in Africa and Europe. Nat Genet. 2007 Jan; 39(1):31-40.
    View in: PubMed
    Score: 0.015
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.