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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 Genotype
Academic Article Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children.
Academic Article Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.
Academic Article Genetic inheritance of body mass index in African-American and African families.
Academic Article Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
Academic Article A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance.
Academic Article Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families.
Academic Article Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
Academic Article Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
Academic Article Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
Academic Article Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
Academic Article A statistical method for identification of polymorphisms that explain a linkage result.
Academic Article Methods for analysis and visualization of SNP genotype data for complex diseases.
Academic Article Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
Academic Article Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.
Academic Article Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
Academic Article MERLIN...and the geneticist's stone?
Academic Article Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
Academic Article Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
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 Population-specific GSTM1 copy number variation.
Academic Article Rational inferences about departures from Hardy-Weinberg equilibrium.
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 Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.
Academic Article Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.
Academic Article Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
Academic Article Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2).
Academic Article Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.
Academic Article Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.
Academic Article The detection of major loci by segregation and linkage analysis: a simulation study.
Academic Article Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome.
Academic Article Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.
Academic Article Parent-of-origin effects of the serotonin transporter gene associated with autism.
Academic Article Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas.
Academic Article Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkage.
Academic Article Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
Academic Article Concordant gene expression in leukemia cells and normal leukocytes is associated with germline cis-SNPs.
Academic Article Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset.
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 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 GEL: a novel genotype calling algorithm using empirical likelihood.
Academic Article Genetic studies of stuttering in a founder population.
Academic Article Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
Academic Article Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
Academic Article Evolution of highly pathogenic H5N1 avian influenza viruses in Vietnam between 2001 and 2007.
Academic Article Genetic architecture of microRNA expression: implications for the transcriptome and complex traits.
Academic Article Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Academic Article Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease.
Academic Article Genome-wide association study of Tourette's syndrome.
Academic Article An exponential combination procedure for set-based association tests in sequencing studies.
Academic Article Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients.
Academic Article CYP2D6 genotype and tamoxifen activity: understanding interstudy variability in methodological quality.
Academic Article Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
Academic Article Integrative genomics: quantifying significance of phenotype-genotype relationships from multiple sources of high-throughput data.
Academic Article Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.
Academic Article Genome-wide association studies in pharmacogenomics: successes and lessons.
Academic Article Identification of molecular markers associated with alteration of receptor-binding specificity in a novel genotype of highly pathogenic avian influenza A(H5N1) viruses detected in Cambodia in 2013.
Academic Article Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
Academic Article Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.
Academic Article Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.
Academic Article Loss of heterozygosity at the CYP2D6 locus in breast cancer: implications for germline pharmacogenetic studies.
Academic Article Quantitative allelic test--a fast test for very large association studies.
Academic Article Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes.
Academic Article Establishment of CYP2D6 reference samples by multiple validated genotyping platforms.
Academic Article Re: Concordance between CYP2D6 genotypes obtained from tumor-derived and germline DNA.
Academic Article Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group.
Academic Article Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Academic Article Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx.
Academic Article Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits.
Academic Article Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.
Academic Article Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues.
Academic Article Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
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 Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer.
Academic Article Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Academic Article Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.
Academic Article Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Academic Article Sex-specific genetic predictors of Alzheimer's disease biomarkers.
Academic Article GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
Academic Article Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Academic Article APOE e4-specific associations of VEGF gene family expression with cognitive aging and Alzheimer's disease.
Academic Article A brief history of human disease genetics.
Academic Article Clinical evaluation of germline polymorphisms associated with capecitabine toxicity in breast cancer: TBCRC-015.
Academic Article Genetic variants and functional pathways associated with resilience to Alzheimer's disease.
Academic Article Host genetic effects in pneumonia.
Academic Article Synaptic processes and immune-related pathways implicated in Tourette syndrome.
Academic Article Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
Academic Article Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Academic Article Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
Academic Article Race, Genotype, and Azathioprine Discontinuation : A Cohort Study.
Academic Article FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Academic Article APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus.
Academic Article Association between APOL1 risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.
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