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Search Results to Nancy Jean Cox

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

Item TypeName
Concept European Continental Ancestry Group
Academic Article Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Academic Article Genome-wide screen for atopy susceptibility alleles in the Hutterites.
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 Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
Academic Article Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.
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 in Europeans: results of pooled and meta-analyses.
Academic Article Population-specific GSTM1 copy number variation.
Academic Article Identification of genetic variants and gene expression relationships associated with pharmacogenes in humans.
Academic Article Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.
Academic Article Identification of common genetic variants that account for transcript isoform variation between human populations.
Academic Article Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
Academic Article Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
Academic Article Population differences in microRNA expression and biological implications.
Academic Article Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.
Academic Article The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy.
Academic Article Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
Academic Article HLA-DR typing "at the DNA level": RFLPs and subtypes detected with a DR beta cDNA probe.
Academic Article Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry.
Academic Article Genetic architecture of transcript-level variation in humans.
Academic Article Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from the International Association of Diabetes and Pregnancy Study Groups.
Academic Article A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
Academic Article Identification of novel germline polymorphisms governing capecitabine sensitivity.
Academic Article The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
Academic Article Variation in the calpain-10 gene affects blood glucose levels in the British population.
Academic Article Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
Academic Article A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
Academic Article Genome-wide association study of Tourette's syndrome.
Academic Article Genome-wide association study of obsessive-compulsive disorder.
Academic Article Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
Academic Article Genome-wide interrogation of longitudinal FEV1 in children with asthma.
Academic Article A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
Academic Article The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
Academic Article SCAN database: facilitating integrative analyses of cytosine modification and expression QTL.
Academic Article Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Academic Article Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Academic Article A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
Academic Article Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
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 A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
Academic Article Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Academic Article Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
Academic Article Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

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  • European Continental Ancestry Group