Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24601772

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Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology Five years of GWAS discovery In search of low-frequency and rare variants affecting complex traits Genetic and epigenetic regulation of intestinal fibrosis The role for protein tyrosine phosphatase non-receptor type 22 in regulating intestinal homeostasis Genetics and Therapeutics in Pediatric Ulcerative Colitis: the Past, Present and Future Autoimmune diseases - connecting risk alleles with molecular traits of the immune system.New developments in the genetics, pathogenesis, and therapy of IgA nephropathy To Extinguish the Fire from Outside the Cell or to Shutdown the Gas Valve Inside? Novel Trends in Anti-Inflammatory Therapies From genetics of inflammatory bowel disease towards mechanistic insights Role of genetics in pediatric inflammatory bowel disease Rare-variant association analysis: study designs and statistical tests Association of STAT4 gene rs7574865G > T polymorphism with ulcerative colitis risk: evidence from 1532 cases and 3786 controls Advances in inflammatory bowel disease pathogenesis: linking host genetics and the microbiome A functional framework for interpretation of genetic associations in T1D Exome sequencing and complex disease: practical aspects of rare variant association studies Effect of barrier microbes on organ-based inflammation.The MKK7 p.Glu116Lys Rare Variant Serves as a Predictor for Lung Cancer Risk and Prognosis in Chinese.Mapping asthma-associated variants in admixed populations The immunogenetics of Behçet's disease: A comprehensive review Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway Genetics and epigenetics of rheumatoid arthritis TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits Progress in methods for rare variant association Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study The Genome of the Netherlands: design, and project goals The mystery of missing heritability: Genetic interactions create phantom heritability Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility The contribution of rare and common variants in 30 genes to risk nicotine dependence 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 Congenital disorder of fucosylation type 2c (LADII) presenting with short stature and developmental delay with minimal adhesion defect A unified method for detecting secondary trait associations with rare variants: application to sequence data.Genomes and phenomes of a population of outbred rats and its progenitors Comparing a few SNP calling algorithms using low-coverage sequencing data.An evaluation of allele frequency estimation accuracy using pooled sequencing data

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

http://www.wikidata.org/entity/Q24601772

description

2011 nî lūn-bûn

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2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի նոյեմբերին 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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Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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type

label

Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

@en

Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

@nl

prefLabel

Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

@ast

Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

@en

Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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Nature Genetics

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Deep resequencing of GWAS loci ...... ith inflammatory bowel disease

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Agnes Gardet

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Andre Franke

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Andrew Kirby

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Benjamin Neale

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Caroline Lagacé

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Christine Stevens

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Clarence K Zhang

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Dermot P B McGovern

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Finny Kuruvilla

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Gabrielle Boucher

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P2860

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

Membrane recruitment of NOD2 in intestinal epithelial cells is essential for nuclear factor-{kappa}B activation in muramyl dipeptide recognition

Network organization of the human autophagy system

A map of human genome variation from population-scale sequencing

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

Generation of pathogenic T(H)17 cells in the absence of TGF-β signalling

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Mapping short DNA sequencing reads and calling variants using mapping quality scores

P2888

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1066-73

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scholarly article

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314970

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10.1038/NG.952

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P433

11

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43

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Talin Haritunians

David Ellinghaus

Mark Joseph Daly

Jonas Halfvarson

David Altshuler

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2011-11-01T00:00:00Z

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51703360

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1043485621

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21983784

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genome-wide association study

inflammatory bowel diseases

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3378381

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