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Cox, Nancy Jean
One or more keywords matched the following items that are connected to Cox, Nancy Jean
Item TypeName
Concept Genetic Diseases, Inborn
Academic Article Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Academic Article Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
Academic Article A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
Academic Article Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
Academic Article MERLIN...and the geneticist's stone?
Academic Article Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
Academic Article Finding the missing heritability of complex diseases.
Academic Article Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
Academic Article Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
Academic Article Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees.
Academic Article Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium.
Academic Article Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
Academic Article Copy number polymorphisms and anticancer pharmacogenomics.
Academic Article Linkage of calpain 10 to type 2 diabetes: the biological rationale.
Academic Article Sequential imputation and multipoint linkage analysis.
Academic Article A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
Academic Article Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.
Academic Article Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder.
Academic Article Guidelines for investigating causality of sequence variants in human disease.
Academic Article A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
Academic Article The genetic architecture of type 2 diabetes.
Academic Article Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.
Academic Article Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Academic Article Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.
Academic Article Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping.
Academic Article Sex differences in the genetic predictors of Alzheimer's pathology.
Academic Article Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.
Academic Article Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Academic Article A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes.
Academic Article Discovery and implications of polygenicity of common diseases.
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  • Genetic Diseases Inborn