Nancy Jean Cox to Models, Genetic
This is a "connection" page, showing publications Nancy Jean Cox has written about Models, Genetic.
Connection Strength
1.995
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Rational inferences about departures from Hardy-Weinberg equilibrium. Am J Hum Genet. 2005 Jun; 76(6):967-86.
Score: 0.178
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A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. Nat Genet. 2020 11; 52(11):1239-1246.
Score: 0.130
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Genetic inheritance of body mass index in African-American and African families. Genet Epidemiol. 2000 Apr; 18(4):360-76.
Score: 0.126
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Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nat Commun. 2018 05 08; 9(1):1825.
Score: 0.110
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Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet. 1997 Nov; 61(5):1179-88.
Score: 0.106
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Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet. 1997 Aug; 61(2):423-9.
Score: 0.104
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Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues. PLoS Genet. 2016 Nov; 12(11):e1006423.
Score: 0.099
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Structural architecture of SNP effects on complex traits. Am J Hum Genet. 2014 Nov 06; 95(5):477-89.
Score: 0.086
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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.
Score: 0.082
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Stuttering: a complex behavioral disorder for our times? Am J Med Genet. 1993 Dec 15; 48(4):177-8.
Score: 0.081
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A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk. Cell. 2013 Sep 26; 155(1):70-80.
Score: 0.080
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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.
Score: 0.076
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The 1200 patients project: creating a new medical model system for clinical implementation of pharmacogenomics. Clin Pharmacol Ther. 2012 Oct; 92(4):446-9.
Score: 0.074
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Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes. Genet Epidemiol. 2012 Dec; 36(8):820-8.
Score: 0.074
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Power and sample size calculations for SNP association studies with censored time-to-event outcomes. Genet Epidemiol. 2012 Sep; 36(6):538-48.
Score: 0.073
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Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. PLoS Genet. 2006 May; 2(5):e67.
Score: 0.048
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No bias in linkage analysis. Am J Hum Genet. 2004 Oct; 75(4):722-3; author reply 723-7.
Score: 0.043
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Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED. Genet Epidemiol. 1984; 1(2):167-70.
Score: 0.041
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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.
Score: 0.035
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Discovery and implications of polygenicity of common diseases. Science. 2021 Sep 24; 373(6562):1468-1473.
Score: 0.035
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Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families. Genet Epidemiol. 2001 Apr; 20(3):340-55.
Score: 0.034
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A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk. Cancer Res. 2020 10 15; 80(20):4346-4354.
Score: 0.032
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Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. PLoS One. 2017; 12(10):e0185730.
Score: 0.026
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A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis. Bioinformatics. 2015 May 01; 31(9):1452-9.
Score: 0.022
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Poly-omic prediction of complex traits: OmicKriging. Genet Epidemiol. 2014 Jul; 38(5):402-15.
Score: 0.021
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An exponential combination procedure for set-based association tests in sequencing studies. Am J Hum Genet. 2012 Dec 07; 91(6):977-86.
Score: 0.019
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Genetic architecture of microRNA expression: implications for the transcriptome and complex traits. Am J Hum Genet. 2012 Jun 08; 90(6):1046-63.
Score: 0.018
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Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases. Stat Appl Genet Mol Biol. 2010; 9:Article18.
Score: 0.016
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The insulin gene and susceptibility to IDDM. Genet Epidemiol. 1989; 6(1):65-9.
Score: 0.014
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Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees. J Psychiatr Res. 1989; 23(2):109-23.
Score: 0.014
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Some effects of selection strategies on linkage analysis. Genet Epidemiol. 1988; 5(4):289-97.
Score: 0.013
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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.
Score: 0.013
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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.
Score: 0.012
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Linkage analysis for psychiatric disorders. II. Methodological considerations. Psychiatr Dev. 1985; 3(4):369-82.
Score: 0.011
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Linkage analysis for psychiatric disorders. I. Basic concepts. Psychiatr Dev. 1985; 3(3):219-43.
Score: 0.011
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Segregation analyses of stuttering. Genet Epidemiol. 1984; 1(3):245-53.
Score: 0.010
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A statistical method for identification of polymorphisms that explain a linkage result. Am J Hum Genet. 2002 Feb; 70(2):399-411.
Score: 0.009
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Segregation analysis of speech and language disorders. Behav Genet. 1993 May; 23(3):291-7.
Score: 0.005
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Genetic studies of variation in Rayleigh and photometric matches in normal trichromats. Vision Res. 1990; 30(1):149-62.
Score: 0.004
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Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity. Genet Epidemiol. 1988; 5(1):1-15.
Score: 0.003
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Ascertainment considerations in the analysis of affected sib shared haplotype data. Genet Epidemiol Suppl. 1986; 1:319-22.
Score: 0.003
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The detection of major loci by segregation and linkage analysis: a simulation study. Genet Epidemiol. 1984; 1(3):285-96.
Score: 0.003