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Connection

Nancy Jean Cox to Models, Genetic

This is a "connection" page, showing publications Nancy Jean Cox has written about Models, Genetic.
Connection Strength

1.764
  1. Rational inferences about departures from Hardy-Weinberg equilibrium. Am J Hum Genet. 2005 Jun; 76(6):967-86.
    View in: PubMed
    Score: 0.154
  2. A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. Nat Genet. 2020 11; 52(11):1239-1246.
    View in: PubMed
    Score: 0.113
  3. Genetic inheritance of body mass index in African-American and African families. Genet Epidemiol. 2000 Apr; 18(4):360-76.
    View in: PubMed
    Score: 0.109
  4. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nat Commun. 2018 05 08; 9(1):1825.
    View in: PubMed
    Score: 0.095
  5. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet. 1997 Nov; 61(5):1179-88.
    View in: PubMed
    Score: 0.092
  6. Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet. 1997 Aug; 61(2):423-9.
    View in: PubMed
    Score: 0.090
  7. Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues. PLoS Genet. 2016 Nov; 12(11):e1006423.
    View in: PubMed
    Score: 0.086
  8. Structural architecture of SNP effects on complex traits. Am J Hum Genet. 2014 Nov 06; 95(5):477-89.
    View in: PubMed
    Score: 0.074
  9. Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines. Genome Biol. 2014 Mar 03; 15(3):R47.
    View in: PubMed
    Score: 0.071
  10. Stuttering: a complex behavioral disorder for our times? Am J Med Genet. 1993 Dec 15; 48(4):177-8.
    View in: PubMed
    Score: 0.070
  11. A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk. Cell. 2013 Sep 26; 155(1):70-80.
    View in: PubMed
    Score: 0.069
  12. Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases. J Am Med Inform Assoc. 2013 Jul-Aug; 20(4):619-29.
    View in: PubMed
    Score: 0.066
  13. The 1200 patients project: creating a new medical model system for clinical implementation of pharmacogenomics. Clin Pharmacol Ther. 2012 Oct; 92(4):446-9.
    View in: PubMed
    Score: 0.064
  14. Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes. Genet Epidemiol. 2012 Dec; 36(8):820-8.
    View in: PubMed
    Score: 0.064
  15. Power and sample size calculations for SNP association studies with censored time-to-event outcomes. Genet Epidemiol. 2012 Sep; 36(6):538-48.
    View in: PubMed
    Score: 0.063
  16. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. PLoS Genet. 2006 May; 2(5):e67.
    View in: PubMed
    Score: 0.041
  17. EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints-A study in asthma. Am J Hum Genet. 2025 May 01; 112(5):1199-1214.
    View in: PubMed
    Score: 0.038
  18. No bias in linkage analysis. Am J Hum Genet. 2004 Oct; 75(4):722-3; author reply 723-7.
    View in: PubMed
    Score: 0.037
  19. Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED. Genet Epidemiol. 1984; 1(2):167-70.
    View in: PubMed
    Score: 0.035
  20. Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: examples from studies of the calpain-10 gene. Hum Mol Genet. 2001 Oct 01; 10(20):2301-5.
    View in: PubMed
    Score: 0.030
  21. Discovery and implications of polygenicity of common diseases. Science. 2021 Sep 24; 373(6562):1468-1473.
    View in: PubMed
    Score: 0.030
  22. Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families. Genet Epidemiol. 2001 Apr; 20(3):340-55.
    View in: PubMed
    Score: 0.029
  23. A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk. Cancer Res. 2020 10 15; 80(20):4346-4354.
    View in: PubMed
    Score: 0.028
  24. Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. PLoS One. 2017; 12(10):e0185730.
    View in: PubMed
    Score: 0.023
  25. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis. Bioinformatics. 2015 May 01; 31(9):1452-9.
    View in: PubMed
    Score: 0.019
  26. Poly-omic prediction of complex traits: OmicKriging. Genet Epidemiol. 2014 Jul; 38(5):402-15.
    View in: PubMed
    Score: 0.018
  27. An exponential combination procedure for set-based association tests in sequencing studies. Am J Hum Genet. 2012 Dec 07; 91(6):977-86.
    View in: PubMed
    Score: 0.016
  28. Genetic architecture of microRNA expression: implications for the transcriptome and complex traits. Am J Hum Genet. 2012 Jun 08; 90(6):1046-63.
    View in: PubMed
    Score: 0.016
  29. Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases. Stat Appl Genet Mol Biol. 2010; 9:Article18.
    View in: PubMed
    Score: 0.014
  30. The insulin gene and susceptibility to IDDM. Genet Epidemiol. 1989; 6(1):65-9.
    View in: PubMed
    Score: 0.012
  31. Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees. J Psychiatr Res. 1989; 23(2):109-23.
    View in: PubMed
    Score: 0.012
  32. Some effects of selection strategies on linkage analysis. Genet Epidemiol. 1988; 5(4):289-97.
    View in: PubMed
    Score: 0.012
  33. Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium. Hum Hered. 2008; 66(1):35-49.
    View in: PubMed
    Score: 0.011
  34. Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? Eur J Hum Genet. 2007 Mar; 15(3):260-3.
    View in: PubMed
    Score: 0.011
  35. Linkage analysis for psychiatric disorders. II. Methodological considerations. Psychiatr Dev. 1985; 3(4):369-82.
    View in: PubMed
    Score: 0.009
  36. Linkage analysis for psychiatric disorders. I. Basic concepts. Psychiatr Dev. 1985; 3(3):219-43.
    View in: PubMed
    Score: 0.009
  37. Segregation analyses of stuttering. Genet Epidemiol. 1984; 1(3):245-53.
    View in: PubMed
    Score: 0.009
  38. A statistical method for identification of polymorphisms that explain a linkage result. Am J Hum Genet. 2002 Feb; 70(2):399-411.
    View in: PubMed
    Score: 0.008
  39. Segregation analysis of speech and language disorders. Behav Genet. 1993 May; 23(3):291-7.
    View in: PubMed
    Score: 0.004
  40. Genetic studies of variation in Rayleigh and photometric matches in normal trichromats. Vision Res. 1990; 30(1):149-62.
    View in: PubMed
    Score: 0.003
  41. Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity. Genet Epidemiol. 1988; 5(1):1-15.
    View in: PubMed
    Score: 0.003
  42. Ascertainment considerations in the analysis of affected sib shared haplotype data. Genet Epidemiol Suppl. 1986; 1:319-22.
    View in: PubMed
    Score: 0.003
  43. The detection of major loci by segregation and linkage analysis: a simulation study. Genet Epidemiol. 1984; 1(3):285-96.
    View in: PubMed
    Score: 0.002
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.