Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms. - Wikidata - awgldk - TriplyDB

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

http://www.wikidata.org/entity/Q34540483

about

Molecular reclassification of Crohn's disease: a cautionary note on population stratification Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort Differential effect of genetic burden on disease phenotypes in Crohn's disease and ulcerative colitis: analysis of a North American cohort.Associations between PTPN2 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis.Associations between STAT3 rs744166 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis Association between NCF4 rs4821544T/C polymorphism and inflammatory bowel disease risk in Caucasian: a meta-analysis.Association of Interleukin-23 receptor gene polymorphisms with susceptibility to Crohn's disease: A meta-analysis Association between NOD2/CARD15 gene polymorphisms and Crohn's disease in Chinese Zhuang patients.Towards personalized care in IBD.The use of prognostic factors in inflammatory bowel diseases.Overcoming difficulty in diagnosis and differential diagnosis of Crohn's disease: the potential role of serological and genetic tests.A Personalized Approach to Managing Inflammatory Bowel Disease.Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.JAK2 rs10758669 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis.NOD2 and bacterial recognition as therapeutic targets for Crohn's disease.Genetic polymorphism in ATG16L1 gene is associated with adalimumab use in inflammatory bowel disease.Beyond disease susceptibility-Leveraging genome-wide association studies for new insights into complex disease biology.Association between ATG16L1 gene polymorphism and the risk of Crohn's disease.Genome-wide association studies in Crohn's disease: Past, present and future.New Trends in Inflammatory Bowel Disease.

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P2860

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

http://www.wikidata.org/entity/Q34540483

description

2012 nî lūn-bûn

@nan

2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

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2012年論文

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2012年论文

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name

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@ast

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@en

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@nl

type

label

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@ast

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@en

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@nl

prefLabel

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@ast

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@en

Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

@nl

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Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.

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Camille Jung

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Christian Libersa

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Frank M Ruemmele

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Françoise Merlin

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Gilles Thomas

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Gwenola Vernier-Massouille

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Habib Zouali

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Jacques Cosnes

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Jean-Marc Gornet

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Jean-Pierre Cezard

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P2860

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

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

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

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

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

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

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12

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Jean-Frédéric Colombel

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Laurent Beaugerie

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2012-12-27T00:00:00Z

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234090219

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23300620

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Crohn's disease

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3531408

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