| Item Type | Name |
|
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-Barré 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.
|