| Item Type | Name |
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Concept
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DiGeorge Syndrome
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Concept
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Bone Marrow Diseases
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Concept
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Bone Marrow Examination
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Concept
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Tourette Syndrome
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Concept
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Immunologic Deficiency Syndromes
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Concept
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Heart Failure
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Concept
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Dysplastic Nevus Syndrome
|
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Concept
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Reye Syndrome
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Concept
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Bone Marrow Transplantation
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Concept
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Syndrome
|
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Concept
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Kidney Failure, Chronic
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Concept
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Post-Concussion Syndrome
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Concept
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Exfoliation Syndrome
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Concept
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Severe Acute Respiratory Syndrome
|
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Concept
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Metabolic Syndrome
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Concept
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Porcine Reproductive and Respiratory Syndrome
|
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Concept
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Polycystic Ovary Syndrome
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|
Concept
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Respiratory Distress Syndrome, Newborn
|
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Concept
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Sleep Apnea Syndromes
|
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Concept
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Treatment Failure
|
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Concept
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Guillain-Barre Syndrome
|
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Concept
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Neurotoxicity Syndromes
|
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Concept
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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.
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Academic Article
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Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome.
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Academic Article
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Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome.
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Academic Article
|
Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome.
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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.
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Academic Article
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Antigenic and genetic variation in influenza A (H1N1) virus isolates recovered from a persistently infected immunodeficient child.
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Academic Article
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The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
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Academic Article
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Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
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Academic Article
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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.
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Academic Article
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Prolonged shedding of amantadine-resistant influenzae A viruses by immunodeficient patients: detection by polymerase chain reaction-restriction analysis.
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Academic Article
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Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome.
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Academic Article
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Heritability of insulin secretion and insulin action in women with polycystic ovary syndrome and their first degree relatives.
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Academic Article
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Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling.
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Academic Article
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Amantadine-resistant influenza A in nursing homes. Identification of a resistant virus prior to drug use.
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Academic Article
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The total influenza vaccine failure of 1947 revisited: major intrasubtypic antigenic change can explain failure of vaccine in a post-World War II epidemic.
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Academic Article
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Genome-wide association study of Tourette's syndrome.
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Academic Article
|
An influenza A (H1N1) virus, closely related to swine influenza virus, responsible for a fatal case of human influenza.
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Academic Article
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Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
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Academic Article
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Genetic association signal near NTN4 in Tourette syndrome.
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Academic Article
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Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
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Academic Article
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Influenza.
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Academic Article
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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
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Academic Article
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Chemotherapy-induced peripheral neurotoxicity and ototoxicity: new paradigms for translational genomics.
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Academic Article
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Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.
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Academic Article
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Anti-ganglioside antibody induction by swine (A/NJ/1976/H1N1) and other influenza vaccines: insights into vaccine-associated Guillain-Barré syndrome.
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Academic Article
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Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration.
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Academic Article
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Common emergence of amantadine- and rimantadine-resistant influenza A viruses in symptomatic immunocompromised adults.
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Academic Article
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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.
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Academic Article
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A novel coronavirus associated with severe acute respiratory syndrome.
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Academic Article
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
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Academic Article
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Classification of common human diseases derived from shared genetic and environmental determinants.
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Academic Article
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Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
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Academic Article
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Diagnostic Algorithms to Study Post-Concussion Syndrome Using Electronic Health Records: Validating a Method to Capture an Important Patient Population.
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Academic Article
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Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies.
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Academic Article
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Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.
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Academic Article
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Synaptic processes and immune-related pathways implicated in Tourette syndrome.
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Academic Article
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Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
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Academic Article
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TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results.
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Academic Article
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Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
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Academic Article
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Pharmacogenomics of cisplatin-induced neurotoxicities: Hearing loss, tinnitus, and peripheral sensory neuropathy.
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Academic Article
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Association of Genetically Predicted Fibroblast Growth Factor-23 with Heart Failure: A Mendelian Randomization Study.
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Academic Article
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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.
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Academic Article
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APOL1 and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus.
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