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Cox, Nancy Jean

One or more keywords matched the following items that are connected to Cox, Nancy Jean

Item Type	Name
Concept	Haplotypes
Academic Article	The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
Academic Article	Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
Academic Article	Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Academic Article	Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
Academic Article	Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
Academic Article	Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
Academic Article	Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
Academic Article	Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
Academic Article	Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population.
Academic Article	Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
Academic Article	Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.
Academic Article	Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
Academic Article	Polymorphisms of GLUT2 and GLUT4 genes. Use in evaluation of genetic susceptibility to NIDDM in blacks.
Academic Article	Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene.
Academic Article	Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
Academic Article	Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses.
Academic Article	Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.
Academic Article	Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
Academic Article	Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans.
Academic Article	Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans.
Academic Article	The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
Academic Article	Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
Academic Article	Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
Academic Article	Genetic architecture of transcript-level variation in humans.
Academic Article	Ascertainment considerations in the analysis of affected sib shared haplotype data.
Academic Article	Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
Academic Article	Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred.
Academic Article	A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
Academic Article	Population differences in the rate of proliferation of international HapMap cell lines.
Academic Article	HLA and mate choice in humans.
Academic Article	Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease.
Academic Article	A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Academic Article	Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.
Academic Article	Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences.
Academic Article	Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood.

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Haplotypes