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Connection

Jonathan Pritchard to Genome, Human

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

3.960
  1. Stable population structure in Europe since the Iron Age, despite high mobility. Elife. 2024 Jan 30; 13.
    View in: PubMed
    Score: 0.653
  2. Comment on "Widespread RNA and DNA sequence differences in the human transcriptome". Science. 2012 Mar 16; 335(6074):1302; author reply 1302.
    View in: PubMed
    Score: 0.287
  3. Whole-genome sequencing data offer insights into human demography. Nat Genet. 2011 Sep 28; 43(10):923-5.
    View in: PubMed
    Score: 0.277
  4. 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: 0.229
  5. 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: 0.197
  6. A map of recent positive selection in the human genome. PLoS Biol. 2006 Mar; 4(3):e72.
    View in: PubMed
    Score: 0.189
  7. A high-resolution survey of deletion polymorphism in the human genome. Nat Genet. 2006 Jan; 38(1):75-81.
    View in: PubMed
    Score: 0.185
  8. Haplotype blocks and linkage disequilibrium in the human genome. Nat Rev Genet. 2003 Aug; 4(8):587-97.
    View in: PubMed
    Score: 0.158
  9. High-resolution mapping of cancer cell networks using co-functional interactions. Mol Syst Biol. 2018 12 20; 14(12):e8594.
    View in: PubMed
    Score: 0.114
  10. Tracing the peopling of the world through genomics. Nature. 2017 01 18; 541(7637):302-310.
    View in: PubMed
    Score: 0.100
  11. Detection of human adaptation during the past 2000 years. Science. 2016 11 11; 354(6313):760-764.
    View in: PubMed
    Score: 0.098
  12. Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet. 2016 Jan; 48(1):22-9.
    View in: PubMed
    Score: 0.093
  13. The genetic and mechanistic basis for variation in gene regulation. PLoS Genet. 2015 Jan; 11(1):e1004857.
    View in: PubMed
    Score: 0.087
  14. fastSTRUCTURE: variational inference of population structure in large SNP data sets. Genetics. 2014 Jun; 197(2):573-89.
    View in: PubMed
    Score: 0.083
  15. Identification of genetic variants that affect histone modifications in human cells. Science. 2013 Nov 08; 342(6159):747-9.
    View in: PubMed
    Score: 0.080
  16. Controls of nucleosome positioning in the human genome. PLoS Genet. 2012; 8(11):e1003036.
    View in: PubMed
    Score: 0.075
  17. Genomics: ENCODE explained. Nature. 2012 Sep 06; 489(7414):52-5.
    View in: PubMed
    Score: 0.074
  18. A systematic survey of loss-of-function variants in human protein-coding genes. Science. 2012 Feb 17; 335(6070):823-8.
    View in: PubMed
    Score: 0.071
  19. DNase?I sensitivity QTLs are a major determinant of human expression variation. Nature. 2012 Feb 05; 482(7385):390-4.
    View in: PubMed
    Score: 0.071
  20. Dissecting the regulatory architecture of gene expression QTLs. Genome Biol. 2012 Jan 31; 13(1):R7.
    View in: PubMed
    Score: 0.071
  21. False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions. Bioinformatics. 2011 Aug 01; 27(15):2144-6.
    View in: PubMed
    Score: 0.068
  22. Adaptations to climate-mediated selective pressures in humans. PLoS Genet. 2011 Apr; 7(4):e1001375.
    View in: PubMed
    Score: 0.067
  23. DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol. 2011; 12(1):R10.
    View in: PubMed
    Score: 0.066
  24. How we are evolving. Sci Am. 2010 Oct; 303(4):40-7.
    View in: PubMed
    Score: 0.065
  25. Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data. Bioinformatics. 2009 Dec 15; 25(24):3207-12.
    View in: PubMed
    Score: 0.060
  26. The role of geography in human adaptation. PLoS Genet. 2009 Jun; 5(6):e1000500.
    View in: PubMed
    Score: 0.059
  27. Signals of recent positive selection in a worldwide sample of human populations. Genome Res. 2009 May; 19(5):826-37.
    View in: PubMed
    Score: 0.058
  28. High-resolution mapping of expression-QTLs yields insight into human gene regulation. PLoS Genet. 2008 Oct; 4(10):e1000214.
    View in: PubMed
    Score: 0.056
  29. 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: 0.054
  30. Completing the map of human genetic variation. Nature. 2007 May 10; 447(7141):161-5.
    View in: PubMed
    Score: 0.051
  31. Evidence for extensive transmission distortion in the human genome. Am J Hum Genet. 2004 Jan; 74(1):62-72.
    View in: PubMed
    Score: 0.040
  32. Linkage disequilibrium in humans: models and data. Am J Hum Genet. 2001 Jul; 69(1):1-14.
    View in: PubMed
    Score: 0.034
  33. Ancient Rome: A genetic crossroads of Europe and the Mediterranean. Science. 2019 11 08; 366(6466):708-714.
    View in: PubMed
    Score: 0.030
  34. The functional consequences of variation in transcription factor binding. PLoS Genet. 2014 Mar; 10(3):e1004226.
    View in: PubMed
    Score: 0.021
  35. 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: 0.013
  36. Sequencing and analysis of Neanderthal genomic DNA. Science. 2006 Nov 17; 314(5802):1113-8.
    View in: PubMed
    Score: 0.012
  37. Clines, clusters, and the effect of study design on the inference of human population structure. PLoS Genet. 2005 Dec; 1(6):e70.
    View in: PubMed
    Score: 0.012
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.