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One or more keywords matched the following items that are connected to Cox, Nancy Jean
Item TypeName
Concept DiGeorge Syndrome
Concept Tourette Syndrome
Concept Immunologic Deficiency Syndromes
Concept Dysplastic Nevus Syndrome
Concept Reye Syndrome
Concept Syndrome
Concept Post-Concussion Syndrome
Concept Exfoliation Syndrome
Concept Severe Acute Respiratory Syndrome
Concept Metabolic Syndrome
Concept Porcine Reproductive and Respiratory Syndrome
Concept Polycystic Ovary Syndrome
Concept Respiratory Distress Syndrome, Newborn
Concept Sleep Apnea Syndromes
Concept Guillain-Barre Syndrome
Concept Neurotoxicity Syndromes
Concept Irritable Bowel Syndrome
Academic Article Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.
Academic Article Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
Academic Article Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
Academic Article Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
Academic Article Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.
Academic Article Antigenic and genetic variation in influenza A (H1N1) virus isolates recovered from a persistently infected immunodeficient child.
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 Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
Academic Article A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
Academic Article Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome.
Academic Article Heritability of insulin secretion and insulin action in women with polycystic ovary syndrome and their first degree relatives.
Academic Article Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling.
Academic Article Genome-wide association study of Tourette's syndrome.
Academic Article An influenza A (H1N1) virus, closely related to swine influenza virus, responsible for a fatal case of human influenza.
Academic Article Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
Academic Article Genetic association signal near NTN4 in Tourette syndrome.
Academic Article Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
Academic Article Influenza.
Academic Article SCAN database: facilitating integrative analyses of cytosine modification and expression QTL.
Academic Article Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Academic Article Chemotherapy-induced peripheral neurotoxicity and ototoxicity: new paradigms for translational genomics.
Academic Article Anti-ganglioside antibody induction by swine (A/NJ/1976/H1N1) and other influenza vaccines: insights into vaccine-associated Guillain-Barr? syndrome.
Academic Article Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration.
Academic Article Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas.
Academic Article A novel coronavirus associated with severe acute respiratory syndrome.
Academic Article Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Academic Article Classification of common human diseases derived from shared genetic and environmental determinants.
Academic Article Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
Academic Article Diagnostic Algorithms to Study Post-Concussion Syndrome Using Electronic Health Records: Validating a Method to Capture an Important Patient Population.
Academic Article Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies.
Academic Article Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.
Academic Article Synaptic processes and immune-related pathways implicated in Tourette syndrome.
Academic Article Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
Academic Article Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy.
Academic Article Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.
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