Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions. - Wikidata - awgldk - TriplyDB

Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.

Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.

http://www.wikidata.org/entity/Q35911600

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Inflammation drives dysbiosis and bacterial invasion in murine models of ileal Crohn's disease Application of computational methods in genetic study of inflammatory bowel disease Role of genetics in the diagnosis and prognosis of Crohn's disease Endoplasmic reticulum stress in hepatic steatosis and inflammatory bowel diseases Interleukin-23R rs7517847 T/G Polymorphism Contributes to the Risk of Crohn's Disease in Caucasians: A Meta-Analysis Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians.Replication and meta-analysis of 13,000 cases defines the risk for interleukin-23 receptor and autophagy-related 16-like 1 variants in Crohn's disease.Inflammatory bowel disease in pediatric and adolescent patients: a biomolecular and histopathological review IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease Association of ATG16L1 and IRGM genes polymorphisms with inflammatory bowel disease: a meta-analysis approach.Role of genetics in the diagnosis and prognosis of Crohn's disease Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.Clinical predictors of inflammatory bowel disease in a genetically well-defined Caucasian population Association of Interleukin-23 receptor gene polymorphisms with susceptibility to Crohn's disease: A meta-analysis Trees Assembling Mann-Whitney approach for detecting genome-wide joint association among low-marginal-effect loci Bugs, genes, fatty acids, and serotonin: Unraveling inflammatory bowel disease?Role of Salmonella enterica exposure in Chilean Crohn's disease patients.Contribution of higher risk genes and European admixture to Crohn's disease in African Americans.Genome-wide association studies--a summary for the clinical gastroenterologist.Susceptibility to ulcerative colitis in Hungarian patients determined by gene-gene interactions.Links between autophagy, innate immunity, inflammation and Crohn's disease IL-23R mutation is associated with ulcerative colitis: A systemic review and meta-analysis.Autophagy and Crohn's disease: at the crossroads of infection, inflammation, immunity, and cancer.Meta-analysis of published studies identified eight additional common susceptibility loci for Crohn's disease and ulcerative colitis.Family history of inflammatory bowel disease among patients with ulcerative colitis: a systematic review and meta-analysis.ATG16L1 and IL23R variants and genetic susceptibility to crohn's disease: mode of inheritance based on meta-analysis of genetic association studies.Overcoming difficulty in diagnosis and differential diagnosis of Crohn's disease: the potential role of serological and genetic tests.From Genes to Mechanisms: The Expanding Spectrum of Monogenic Disorders Associated with Inflammatory Bowel Disease.T300A polymorphism of ATG16L1 and susceptibility to inflammatory bowel diseases: a meta-analysis.The Crohn's disease-associated polymorphism in ATG16L1 (rs2241880) reduces SHIP gene expression and activity in human subjects.Inflammasome activation has an important role in the development of spontaneous colitis.Crohn's disease as an immunodeficiency.Predicting complicated Crohn's disease and surgery: phenotypes, genetics, serology and psychological characteristics of a population-based cohort.Confirmation of three inflammatory bowel disease susceptibility loci in a Chinese cohort.Recent Advances in ADAM17 Research: A Promising Target for Cancer and Inflammation.Contribution of IL23R but not ATG16L1 to Crohn's disease susceptibility in Koreans.Association between ATG16L1 gene polymorphism and the risk of Crohn's disease.Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions.Interaction between CTLA4 gene and IBD5 locus in Hungarian Crohn's disease patients

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Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.

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Charles N Bernstein

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Lisa Wu Datta

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Michael Sargent

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Ming-Hsi Wang

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Systematic association mapping identifies NELL1 as a novel IBD disease gene

A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Functional variants of OCTN cation transporter genes are associated with Crohn disease

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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10.1002/IBD.20512

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18521914

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Crohn's disease

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3336049

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