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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	Genetic Variation
Academic Article	Genetic variation in neuraminidase genes of influenza A (H3N2) viruses.
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	Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
Academic Article	Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: examples from studies of the calpain-10 gene.
Academic Article	No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.
Academic Article	Variation within the type 2 diabetes susceptibility gene calpain-10 and 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	Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
Academic Article	Reappearance and global spread of variants of influenza B/Victoria/2/87 lineage viruses in the 2000-2001 and 2001-2002 seasons.
Academic Article	Antigenic and genetic variation in influenza A (H1N1) virus isolates recovered from a persistently infected immunodeficient child.
Academic Article	Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
Academic Article	Genetic studies of variation in Rayleigh and photometric matches in normal trichromats.
Academic Article	SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report.
Academic Article	Evaluation of genetic variation contributing to differences in gene expression between populations.
Academic Article	Human genetics: an expression of interest.
Academic Article	Identification of genetic variants and gene expression relationships associated with pharmacogenes in humans.
Academic Article	Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans.
Academic Article	A pharmacogene database enhanced by the 1000 Genomes Project.
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	Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
Academic Article	The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
Academic Article	Population differences in microRNA expression and biological implications.
Academic Article	Genome-wide meta-analysis for severe diabetic retinopathy.
Academic Article	The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy.
Academic Article	Genetic architecture of transcript-level variation in humans.
Academic Article	Antigenic drift in influenza virus H3 hemagglutinin from 1968 to 1980: multiple evolutionary pathways and sequential amino acid changes at key antigenic sites.
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	Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.
Academic Article	Nucleotide sequences of the neuraminidase genes of influenza A/Leningrad/134/57 (H2N2) virus and two of its live, attenuated, cold-adapted variants.
Academic Article	Nonimmunoselected intrastrain genetic variation detected in pairs of high-yielding influenza A (H3N2) vaccine and parental viruses.
Academic Article	Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants.
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	A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
Academic Article	Variation in the calpain-10 gene affects blood glucose levels in the British population.
Academic Article	Linkage of calpain 10 to type 2 diabetes: the biological rationale.
Academic Article	A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
Academic Article	Genetic architecture of microRNA expression: implications for the transcriptome and complex traits.
Academic Article	Avian-to-human transmission of H9N2 subtype influenza A viruses: relationship between H9N2 and H5N1 human isolates.
Academic Article	Genetic relatedness between influenza A (H1N1) viruses isolated from humans and pigs.
Academic Article	An exponential combination procedure for set-based association tests in sequencing studies.
Academic Article	Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans.
Academic Article	Genetic variation is the major determinant of individual differences in leukocyte endothelial adhesion.
Academic Article	Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity.
Academic Article	Genetic analysis of human H2N2 and early H3N2 influenza viruses, 1957-1972: evidence for genetic divergence and multiple reassortment events.
Academic Article	A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Academic Article	Structural architecture of SNP effects on complex traits.
Academic Article	Challenges in interpreting the evidence for genetic predictors of ototoxicity.
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	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	Influenza activity - United States, 2013-14 season and composition of the 2014-15 influenza vaccines.
Academic Article	Guidelines for investigating causality of sequence variants in human disease.
Academic Article	Establishment of CYP2D6 reference samples by multiple validated genotyping platforms.
Academic Article	Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver.
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	Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.
Academic Article	Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Academic Article	Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
Academic Article	Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.
Academic Article	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Academic Article	De novo pattern discovery enables robust assessment of functional consequences of non-coding variants.
Academic Article	Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Academic Article	Discovery and implications of polygenicity of common diseases.
Academic Article	Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults.
Academic Article	FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.

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Genetic Variation