Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease - Wikidata - awgldk - TriplyDB

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

http://www.wikidata.org/entity/Q30426720

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Accurate and robust genomic prediction of celiac disease using statistical learning Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis A global reference for human genetic variation Improving outcomes of refractory celiac disease - current and emerging treatment strategies Autoimmune diseases - connecting risk alleles with molecular traits of the immune system.Making sense of GWAS: using epigenomics and genome engineering to understand the functional relevance of SNPs in non-coding regions of the human genome Intestinal Microbiota and Celiac Disease: Cause, Consequence or Co-Evolution?Immunogenetics of juvenile idiopathic arthritis: A comprehensive review Risk factors for celiac disease Therapeutic approaches for celiac disease A review of post-GWAS prioritization approaches Diet and psoriasis, part II: celiac disease and role of a gluten-free diet Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.Elderly Onset Celiac Disease: A Narrative Review Coeliac disease: a unique model for investigating broken tolerance in autoimmunity The immunogenetics of Behçet's disease: A comprehensive review Coeliac disease and autoimmune disease-genetic overlap and screening Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci Evaluation of European coeliac disease risk variants in a north Indian population CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation Genetic and epigenetic fine mapping of causal autoimmune disease variants Generation of primary human intestinal T cell transcriptomes reveals differential expression at genetic risk loci for immune-mediated disease High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis Bayesian test for colocalisation between pairs of genetic association studies using summary statistics The Genome of the Netherlands: design, and project goals Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese The genetics of East African populations: a Nilo-Saharan component in the African genetic landscape Identification of Non-HLA Genes Associated with Celiac Disease and Country-Specific Differences in a Large, International Pediatric Cohort Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity.Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping HLA-DPB1*04:01 Protects Genetically Susceptible Children from Celiac Disease Autoimmunity in the TEDDY Study.An ImmunoChip study of multiple sclerosis risk in African Americans.Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.Regulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cells Negligible impact of rare autoimmune-locus coding-region variants on missing heritability Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

http://www.wikidata.org/entity/Q30426720

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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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Agata Szperl

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Ajit Sood

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Anna Rybak

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Barbara Mora

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Carmen Ribes-Koninckx

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Cleo C van Diemen

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Concepción Núñez

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Cordelia Langford

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Donatella Barisani

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Emilio G de la Concha

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P2860

Searching for genetic determinants in the new millennium

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

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

Multiple common variants for celiac disease influencing immune gene expression

A map of human genome variation from population-scale sequencing

Shared and distinct genetic variants in type 1 diabetes and celiac disease

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

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1193-1201

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scholarly article

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10.1038/NG.998

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12

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43

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Vincent Plagnol

Alexandra Zhernakova

Isis Ricaño-Ponce

Jeffrey C Barrett

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2011-11-06T00:00:00Z

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51773696

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22057235

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3242065

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