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Connection

Jonathan Pritchard to Humans

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

1.205
  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: 0.032
  2. Bayesian estimation of gene constraint from an evolutionary model with gene features. Nat Genet. 2024 Aug; 56(8):1632-1643.
    View in: PubMed
    Score: 0.031
  3. Stable population structure in Europe since the Iron Age, despite high mobility. Elife. 2024 Jan 30; 13.
    View in: PubMed
    Score: 0.030
  4. 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: 0.027
  5. GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Elife. 2021 02 15; 10.
    View in: PubMed
    Score: 0.025
  6. Trans Effects on Gene Expression Can Drive Omnigenic Inheritance. Cell. 2019 05 02; 177(4):1022-1034.e6.
    View in: PubMed
    Score: 0.022
  7. Evidence for Weak Selective Constraint on Human Gene Expression. Genetics. 2019 02; 211(2):757-772.
    View in: PubMed
    Score: 0.021
  8. Post-translational buffering leads to convergent protein expression levels between primates. Genome Biol. 2018 06 27; 19(1):83.
    View in: PubMed
    Score: 0.021
  9. Frequent nonallelic gene conversion on the human lineage and its effect on the divergence of gene duplicates. Proc Natl Acad Sci U S A. 2017 11 28; 114(48):12779-12784.
    View in: PubMed
    Score: 0.020
  10. 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: 0.020
  11. An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell. 2017 Jun 15; 169(7):1177-1186.
    View in: PubMed
    Score: 0.019
  12. Rapid evolution of the human mutation spectrum. Elife. 2017 04 25; 6.
    View in: PubMed
    Score: 0.019
  13. Mutation Rate Variation is a Primary Determinant of the Distribution of Allele Frequencies in Humans. PLoS Genet. 2016 Dec; 12(12):e1006489.
    View in: PubMed
    Score: 0.019
  14. Detection of human adaptation during the past 2000 years. Science. 2016 11 11; 354(6313):760-764.
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    Score: 0.018
  15. Genetic variation in MHC proteins is associated with T cell receptor expression biases. Nat Genet. 2016 09; 48(9):995-1002.
    View in: PubMed
    Score: 0.018
  16. Thousands of novel translated open reading frames in humans inferred by ribosome footprint profiling. Elife. 2016 05 27; 5.
    View in: PubMed
    Score: 0.018
  17. Coregulation of tandem duplicate genes slows evolution of subfunctionalization in mammals. Science. 2016 May 20; 352(6288):1009-13.
    View in: PubMed
    Score: 0.018
  18. RNA splicing is a primary link between genetic variation and disease. Science. 2016 Apr 29; 352(6285):600-4.
    View in: PubMed
    Score: 0.018
  19. WASP: allele-specific software for robust molecular quantitative trait locus discovery. Nat Methods. 2015 Nov; 12(11):1061-3.
    View in: PubMed
    Score: 0.017
  20. The effect of freeze-thaw cycles on gene expression levels in lymphoblastoid cell lines. PLoS One. 2014; 9(9):e107166.
    View in: PubMed
    Score: 0.016
  21. fastSTRUCTURE: variational inference of population structure in large SNP data sets. Genetics. 2014 Jun; 197(2):573-89.
    View in: PubMed
    Score: 0.015
  22. Archaic humans: Four makes a party. Nature. 2014 Jan 02; 505(7481):32-4.
    View in: PubMed
    Score: 0.015
  23. Identification of genetic variants that affect histone modifications in human cells. Science. 2013 Nov 08; 342(6159):747-9.
    View in: PubMed
    Score: 0.015
  24. Inference of population splits and mixtures from genome-wide allele frequency data. PLoS Genet. 2012; 8(11):e1002967.
    View in: PubMed
    Score: 0.014
  25. Controls of nucleosome positioning in the human genome. PLoS Genet. 2012; 8(11):e1003036.
    View in: PubMed
    Score: 0.014
  26. 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: 0.013
  27. Exon-specific QTLs skew the inferred distribution of expression QTLs detected using gene expression array data. PLoS One. 2012; 7(2):e30629.
    View in: PubMed
    Score: 0.013
  28. DNase?I sensitivity QTLs are a major determinant of human expression variation. Nature. 2012 Feb 05; 482(7385):390-4.
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    Score: 0.013
  29. Dissecting the regulatory architecture of gene expression QTLs. Genome Biol. 2012 Jan 31; 13(1):R7.
    View in: PubMed
    Score: 0.013
  30. Whole-genome sequencing data offer insights into human demography. Nat Genet. 2011 Sep 28; 43(10):923-5.
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    Score: 0.013
  31. Efficient counting of k-mers in DNA sequences using a bloom filter. BMC Bioinformatics. 2011 Aug 10; 12:333.
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    Score: 0.013
  32. 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: 0.013
  33. DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol. 2011; 12(1):R10.
    View in: PubMed
    Score: 0.012
  34. Noisy splicing drives mRNA isoform diversity in human cells. PLoS Genet. 2010 Dec 09; 6(12):e1001236.
    View in: PubMed
    Score: 0.012
  35. Accurate inference of transcription factor binding from DNA sequence and chromatin accessibility data. Genome Res. 2011 Mar; 21(3):447-55.
    View in: PubMed
    Score: 0.012
  36. How we are evolving. Sci Am. 2010 Oct; 303(4):40-7.
    View in: PubMed
    Score: 0.012
  37. Adaptation - not by sweeps alone. Nat Rev Genet. 2010 Oct; 11(10):665-7.
    View in: PubMed
    Score: 0.012
  38. Using environmental correlations to identify loci underlying local adaptation. Genetics. 2010 Aug; 185(4):1411-23.
    View in: PubMed
    Score: 0.012
  39. Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature. 2010 Apr 01; 464(7289):768-72.
    View in: PubMed
    Score: 0.012
  40. The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation. Curr Biol. 2010 Feb 23; 20(4):R208-15.
    View in: PubMed
    Score: 0.012
  41. 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: 0.011
  42. The role of geography in human adaptation. PLoS Genet. 2009 Jun; 5(6):e1000500.
    View in: PubMed
    Score: 0.011
  43. Signals of recent positive selection in a worldwide sample of human populations. Genome Res. 2009 May; 19(5):826-37.
    View in: PubMed
    Score: 0.011
  44. 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: 0.011
  45. High-resolution mapping of expression-QTLs yields insight into human gene regulation. PLoS Genet. 2008 Oct; 4(10):e1000214.
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    Score: 0.011
  46. Revealing the architecture of gene regulation: the promise of eQTL studies. Trends Genet. 2008 Aug; 24(8):408-15.
    View in: PubMed
    Score: 0.010
  47. Adaptive evolution of conserved noncoding elements in mammals. PLoS Genet. 2007 Sep; 3(9):1572-86.
    View in: PubMed
    Score: 0.010
  48. Overcoming the winner's curse: estimating penetrance parameters from case-control data. Am J Hum Genet. 2007 Apr; 80(4):605-15.
    View in: PubMed
    Score: 0.009
  49. 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: 0.009
  50. A map of recent positive selection in the human genome. PLoS Biol. 2006 Mar; 4(3):e72.
    View in: PubMed
    Score: 0.009
  51. A high-resolution survey of deletion polymorphism in the human genome. Nat Genet. 2006 Jan; 38(1):75-81.
    View in: PubMed
    Score: 0.009
  52. Confounding from cryptic relatedness in case-control association studies. PLoS Genet. 2005 Sep; 1(3):e32.
    View in: PubMed
    Score: 0.008
  53. Coalescent-based association mapping and fine mapping of complex trait loci. Genetics. 2005 Feb; 169(2):1071-92.
    View in: PubMed
    Score: 0.008
  54. Statistical tests for admixture mapping with case-control and cases-only data. Am J Hum Genet. 2004 Nov; 75(5):771-89.
    View in: PubMed
    Score: 0.008
  55. Invasive Treatment Strategy for Older Patients with Myocardial Infarction. N Engl J Med. 2024 Nov 07; 391(18):1673-1684.
    View in: PubMed
    Score: 0.008
  56. Diversity of ribosomes at the level of rRNA variation associated with human health and disease. Cell Genom. 2024 Sep 11; 4(9):100629.
    View in: PubMed
    Score: 0.008
  57. Base-editing mutagenesis maps alleles to tune human T cell functions. Nature. 2024 Jan; 625(7996):805-812.
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    Score: 0.008
  58. Informativeness of genetic markers for inference of ancestry. Am J Hum Genet. 2003 Dec; 73(6):1402-22.
    View in: PubMed
    Score: 0.008
  59. CRISPR screens decode cancer cell pathways that trigger ?d T cell detection. Nature. 2023 Sep; 621(7977):188-195.
    View in: PubMed
    Score: 0.007
  60. A genetic history of continuity and mobility in the Iron Age central Mediterranean. Nat Ecol Evol. 2023 09; 7(9):1515-1524.
    View in: PubMed
    Score: 0.007
  61. A genome-wide genetic screen uncovers determinants of human pigmentation. Science. 2023 08 11; 381(6658):eade6289.
    View in: PubMed
    Score: 0.007
  62. Haplotype blocks and linkage disequilibrium in the human genome. Nat Rev Genet. 2003 Aug; 4(8):587-97.
    View in: PubMed
    Score: 0.007
  63. On the number of genealogical ancestors tracing to the source groups of an admixed population. Genetics. 2023 07 06; 224(3).
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    Score: 0.007
  64. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. Nat Commun. 2023 05 15; 14(1):2709.
    View in: PubMed
    Score: 0.007
  65. Precise modulation of transcription factor levels identifies features underlying dosage sensitivity. Nat Genet. 2023 05; 55(5):841-851.
    View in: PubMed
    Score: 0.007
  66. The allelic architecture of human disease genes: common disease-common variant...or not? Hum Mol Genet. 2002 Oct 01; 11(20):2417-23.
    View in: PubMed
    Score: 0.007
  67. RNA editing underlies genetic risk of common inflammatory diseases. Nature. 2022 08; 608(7923):569-577.
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    Score: 0.007
  68. Systematic discovery and perturbation of regulatory genes in human T cells reveals the architecture of immune networks. Nat Genet. 2022 08; 54(8):1133-1144.
    View in: PubMed
    Score: 0.007
  69. A highly virulent variant of HIV-1 circulating in the Netherlands. Science. 2022 02 04; 375(6580):540-545.
    View in: PubMed
    Score: 0.007
  70. Case-control studies of association in structured or admixed populations. Theor Popul Biol. 2001 Nov; 60(3):227-37.
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    Score: 0.007
  71. 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: 0.006
  72. Linkage disequilibrium in humans: models and data. Am J Hum Genet. 2001 Jul; 69(1):1-14.
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    Score: 0.006
  73. Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet. 2001 Jul; 69(1):124-37.
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    Score: 0.006
  74. Shared heritability of human face and brain shape. Nat Genet. 2021 06; 53(6):830-839.
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    Score: 0.006
  75. 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: 0.006
  76. Genetics of 35 blood and urine biomarkers in the UK Biobank. Nat Genet. 2021 02; 53(2):185-194.
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    Score: 0.006
  77. Inference of population structure using multilocus genotype data. Genetics. 2000 Jun; 155(2):945-59.
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    Score: 0.006
  78. Association mapping in structured populations. Am J Hum Genet. 2000 Jul; 67(1):170-81.
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    Score: 0.006
  79. DNA analysis in a paternity case involving a triploid fetus. Transfusion. 2000 Feb; 40(2):240-4.
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    Score: 0.006
  80. Variable prediction accuracy of polygenic scores within an ancestry group. Elife. 2020 01 30; 9.
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    Score: 0.006
  81. Chromatin accessibility dynamics in a model of human forebrain development. Science. 2020 01 24; 367(6476).
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    Score: 0.006
  82. Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol Biol Evol. 1999 Dec; 16(12):1791-8.
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    Score: 0.006
  83. Ancient Rome: A genetic crossroads of Europe and the Mediterranean. Science. 2019 11 08; 366(6466):708-714.
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    Score: 0.006
  84. Landscape of stimulation-responsive chromatin across diverse human immune cells. Nat Genet. 2019 10; 51(10):1494-1505.
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    Score: 0.006
  85. Use of unlinked genetic markers to detect population stratification in association studies. Am J Hum Genet. 1999 Jul; 65(1):220-8.
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    Score: 0.006
  86. Public Discussion Affects Question Asking at Academic Conferences. Am J Hum Genet. 2019 07 03; 105(1):189-197.
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    Score: 0.006
  87. Reduced signal for polygenic adaptation of height in UK Biobank. Elife. 2019 03 21; 8.
    View in: PubMed
    Score: 0.005
  88. High-resolution mapping of cancer cell networks using co-functional interactions. Mol Syst Biol. 2018 12 20; 14(12):e8594.
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    Score: 0.005
  89. Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes. Elife. 2018 05 08; 7.
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    Score: 0.005
  90. Impact of regulatory variation across human iPSCs and differentiated cells. Genome Res. 2018 01; 28(1):122-131.
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    Score: 0.005
  91. Quantification of transplant-derived circulating cell-free DNA in absence of a donor genotype. PLoS Comput Biol. 2017 Aug; 13(8):e1005629.
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    Score: 0.005
  92. Tracing the peopling of the world through genomics. Nature. 2017 01 18; 541(7637):302-310.
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    Score: 0.005
  93. Batch effects and the effective design of single-cell gene expression studies. Sci Rep. 2017 01 03; 7:39921.
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    Score: 0.005
  94. Genetic data and the African origin of humans. Science. 1996 Nov 29; 274(5292):1548-9.
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    Score: 0.005
  95. Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution. Nat Genet. 2016 10; 48(10):1193-203.
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    Score: 0.005
  96. Genetic Variation, Not Cell Type of Origin, Underlies the Majority of Identifiable Regulatory Differences in iPSCs. PLoS Genet. 2016 Jan; 12(1):e1005793.
    View in: PubMed
    Score: 0.004
  97. Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet. 2016 Jan; 48(1):22-9.
    View in: PubMed
    Score: 0.004
  98. 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: 0.004
  99. Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions. Cell. 2015 Aug 27; 162(5):1051-65.
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    Score: 0.004
  100. Reprogramming LCLs to iPSCs Results in Recovery of Donor-Specific Gene Expression Signature. PLoS Genet. 2015 May; 11(5):e1005216.
    View in: PubMed
    Score: 0.004
  101. The genetic and mechanistic basis for variation in gene regulation. PLoS Genet. 2015 Jan; 11(1):e1004857.
    View in: PubMed
    Score: 0.004
  102. Genomic variation. Impact of regulatory variation from RNA to protein. Science. 2015 Feb 06; 347(6222):664-7.
    View in: PubMed
    Score: 0.004
  103. 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: 0.004
  104. The functional consequences of variation in transcription factor binding. PLoS Genet. 2014 Mar; 10(3):e1004226.
    View in: PubMed
    Score: 0.004
  105. The deleterious mutation load is insensitive to recent population history. Nat Genet. 2014 Mar; 46(3):220-4.
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    Score: 0.004
  106. Admixture facilitates genetic adaptations to high altitude in Tibet. Nat Commun. 2014; 5:3281.
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    Score: 0.004
  107. Epigenetic modifications are associated with inter-species gene expression variation in primates. Genome Biol. 2014; 15(12):547.
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    Score: 0.004
  108. Primate transcript and protein expression levels evolve under compensatory selection pressures. Science. 2013 Nov 29; 342(6162):1100-4.
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    Score: 0.004
  109. The genetic architecture of adaptations to high altitude in Ethiopia. PLoS Genet. 2012; 8(12):e1003110.
    View in: PubMed
    Score: 0.004
  110. 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: 0.003
  111. Genomics: ENCODE explained. Nature. 2012 Sep 06; 489(7414):52-5.
    View in: PubMed
    Score: 0.003
  112. 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: 0.003
  113. Comparative RNA sequencing reveals substantial genetic variation in endangered primates. Genome Res. 2012 Apr; 22(4):602-10.
    View in: PubMed
    Score: 0.003
  114. A genome sequence resource for the aye-aye (Daubentonia madagascariensis), a nocturnal lemur from Madagascar. Genome Biol Evol. 2012; 4(2):126-35.
    View in: PubMed
    Score: 0.003
  115. Haplotype variation and genotype imputation in African populations. Genet Epidemiol. 2011 Dec; 35(8):766-80.
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    Score: 0.003
  116. Adaptations to climate-mediated selective pressures in humans. PLoS Genet. 2011 Apr; 7(4):e1001375.
    View in: PubMed
    Score: 0.003
  117. 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: 0.003
  118. 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: 0.003
  119. Characterizing natural variation using next-generation sequencing technologies. Trends Genet. 2009 Oct; 25(10):463-71.
    View in: PubMed
    Score: 0.003
  120. 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: 0.003
  121. Adaptations to climate in candidate genes for common metabolic disorders. PLoS Genet. 2008 Feb; 4(2):e32.
    View in: PubMed
    Score: 0.003
  122. 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: 0.003
  123. Adaptive drool in the gene pool. Nat Genet. 2007 Oct; 39(10):1188-90.
    View in: PubMed
    Score: 0.002
  124. 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: 0.002
  125. Completing the map of human genetic variation. Nature. 2007 May 10; 447(7141):161-5.
    View in: PubMed
    Score: 0.002
  126. Convergent adaptation of human lactase persistence in Africa and Europe. Nat Genet. 2007 Jan; 39(1):31-40.
    View in: PubMed
    Score: 0.002
  127. Sequencing and analysis of Neanderthal genomic DNA. Science. 2006 Nov 17; 314(5802):1113-8.
    View in: PubMed
    Score: 0.002
  128. Long term morbidity and health related quality of life after multi-system Langerhans cell histiocytosis. Eur J Cancer. 2006 Oct; 42(15):2563-9.
    View in: PubMed
    Score: 0.002
  129. The effects of genotype-dependent recombination, and transmission asymmetry, on linkage disequilibrium. Genetics. 2006 Mar; 172(3):2001-5.
    View in: PubMed
    Score: 0.002
  130. 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: 0.002
  131. Evidence for extensive transmission distortion in the human genome. Am J Hum Genet. 2004 Jan; 74(1):62-72.
    View in: PubMed
    Score: 0.002
  132. 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: 0.002
  133. Traces of human migrations in Helicobacter pylori populations. Science. 2003 Mar 07; 299(5612):1582-5.
    View in: PubMed
    Score: 0.002
  134. Genetic structure of human populations. Science. 2002 Dec 20; 298(5602):2381-5.
    View in: PubMed
    Score: 0.002
  135. Distinctive genetic signatures in the Libyan Jews. Proc Natl Acad Sci U S A. 2001 Jan 30; 98(3):858-63.
    View in: PubMed
    Score: 0.002
  136. Recent common ancestry of human Y chromosomes: evidence from DNA sequence data. Proc Natl Acad Sci U S A. 2000 Jun 20; 97(13):7360-5.
    View in: PubMed
    Score: 0.001
  137. Defective alloantigen-presenting capacity of 'Langerhans cell histiocytosis cells'. Arch Dis Child. 1992 Nov; 67(11):1370-2.
    View in: PubMed
    Score: 0.001
  138. Documentation of Epstein-Barr virus infection in immunodeficient patients with life-threatening lymphoproliferative diseases by clinical, virological, and immunopathological studies. Cancer Res. 1981 Nov; 41(11 Pt 1):4226-36.
    View in: PubMed
    Score: 0.000
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.