Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease - Wikidata - awgldk - TriplyDB

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

http://www.wikidata.org/entity/Q28300680

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An integrated map of genetic variation from 1,092 human genomes Recent Insights Into the Genetics of Inflammatory Bowel Disease Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease Five years of GWAS discovery Role of genetics in pediatric inflammatory bowel disease The immunogenetics of Behçet's disease: A comprehensive review The long and winding road from correlation to causation TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q Genetics and pathogenesis of inflammatory bowel disease Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.Negligible impact of rare autoimmune-locus coding-region variants on missing heritability Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease Microbiota activation and regulation of innate and adaptive immunity.SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data.Genetic predisposition to colorectal cancer: where we stand and future perspectives Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X.A genome-wide small interfering RNA (siRNA) screen reveals nuclear factor-κB (NF-κB)-independent regulators of NOD2-induced interleukin-8 (IL-8) secretion Targeted exon sequencing fails to identify rare coding variants with large effect in rheumatoid arthritis Improving indel detection specificity of the Ion Torrent PGM benchtop sequencer Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder.Role of the human endogenous retrovirus HERV-K18 in autoimmune disease susceptibility: study in the Spanish population and meta-analysis.The quest for genetic risk factors for Crohn's disease in the post-GWAS era Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes The dichotomous pattern of IL-12r and IL-23R expression elucidates the role of IL-12 and IL-23 in inflammation.At the end of the beginning. Foreword.A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.Rare and common variants: twenty arguments.Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.Network Modeling of Crohn's Disease Incidence.Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2

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Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

http://www.wikidata.org/entity/Q28300680

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Resequencing of positional can ...... nst inflammatory bowel disease

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Nature Genetics

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Resequencing of positional can ...... nst inflammatory bowel disease

@en

P2093

Catherine Reenaers

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Colm O'Morain

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Curt Tysk

http://www.w3.org/2001/XMLSchema#string

Denis Franchimont

http://www.w3.org/2001/XMLSchema#string

Edouard Louis

http://www.w3.org/2001/XMLSchema#string

Isabelle Cleynen

http://www.w3.org/2001/XMLSchema#string

Jurgen Del-Favero

http://www.w3.org/2001/XMLSchema#string

Kayo Nakamura

http://www.w3.org/2001/XMLSchema#string

Leila Amininejad

http://www.w3.org/2001/XMLSchema#string

Marc Lémann

http://www.w3.org/2001/XMLSchema#string

P2860

Finding the missing heritability of complex diseases

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

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Are rare variants responsible for susceptibility to complex diseases?

Genome sequencing in microfabricated high-density picolitre reactors

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

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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43-7

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scholarly article

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314969

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10.1038/NG.733

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P433

1

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43

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Jean-Frédéric Colombel

Cécile Libioulle

Jean-Pierre Hugot

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2011-01-01T00:00:00Z

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49676839

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21151126

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inflammatory bowel diseases