Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci - sprookjes - yvandenbroek - TriplyDB

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

http://www.wikidata.org/entity/Q30417517

about

Microbiota and chronic inflammatory arthritis: an interwoven link Autoimmune diseases - connecting risk alleles with molecular traits of the immune system.Progress and promise in understanding the genetic basis of common diseases Decoding the non-coding genome: elucidating genetic risk outside the coding genome FOXP3(+) Treg Cells and Gender Bias in Autoimmune Diseases Immunogenetics of juvenile idiopathic arthritis: A comprehensive review HLA-B27 misfolding and ankylosing spondylitis Review: The interleukin-23/interleukin-17 axis in spondyloarthritis pathogenesis: Th17 and beyond Endoplasmic reticulum-associated amino-peptidase 1 and rheumatic disease: genetics The immunogenetics of Behçet's disease: A comprehensive review A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci Genetic and epigenetic fine mapping of causal autoimmune disease variants The eGenVar data management system--cataloguing and sharing sensitive data and metadata for the life sciences Genetics of rheumatoid arthritis contributes to biology and drug discovery Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis.Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data.VSEAMS: a pipeline for variant set enrichment analysis using summary GWAS data identifies IKZF3, BATF and ESRRA as key transcription factors in type 1 diabetes.Assessing the presence of shared genetic architecture between Alzheimer's disease and major depressive disorder using genome-wide association data.Investigation of a possible extended risk haplotype in the IL23R region associated with ankylosing spondylitis.A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine.Human IL-6RhiTIGIT- CD4+CD127lowCD25+ T cells display potent in vitro suppressive capacity and a distinct Th17 profile.The genetic basis of ankylosing spondylitis: new insights into disease pathogenesis Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes Bone morphogenetic protein 6 polymorphisms are associated with radiographic progression in ankylosing spondylitis.rs10865331 associated with susceptibility and disease severity of ankylosing spondylitis in a Taiwanese population.Autoimmune and autoinflammatory mechanisms in uveitis.Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2).Update on ankylosing spondylitis: current concepts in pathogenesis.Reverse interferon signature is characteristic of antigen-presenting cells in human and rat spondyloarthritis.A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk.Genetics, environment, and gene-environment interactions in the development of systemic rheumatic diseases Aberrant expression of shared master-key genes contributes to the immunopathogenesis in patients with juvenile spondyloarthritis.A role for naturally occurring alleles of endoplasmic reticulum aminopeptidases in tumor immunity and cancer pre-disposition.UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis.Identification of potential transcriptomic markers in developing ankylosing spondylitis: a meta-analysis of gene expression profiles.Does the microbiome play a causal role in spondyloarthritis?PharmGKB summary: very important pharmacogene information for human leukocyte antigen B.

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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

http://www.wikidata.org/entity/Q30417517

description

2013 nî lūn-bûn

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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2013 թվականի հունիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Identification of multiple ris ...... otyping of immune-related loci

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Adrian Cortes

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Australo-Anglo-American Spondyloarthritis Consortium (TASC)

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Benedicte A Lie

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Bryan Paul Wordsworth

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Carlos Lopez-Larrea

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Chung-Tei Chou

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Claire Farrah

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Consuelo Romero-Sánchez

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Dirk Elewaut

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Gilles Chiocchia

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P2860

Evidence for significant overlap between common risk variants for Crohn's disease and ankylosing spondylitis

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

An integrated encyclopedia of DNA elements in the human genome

TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis

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

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

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

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10.1038/NG.2667

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7

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Jaakko Tuomilehto

Matthew A. Brown

Dafna D. Gladman

Johannes C Nossent

Fernando Pimentel-Santos

Rubén Burgos-Vargas

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2013-06-09T00:00:00Z

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239525770

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23749187

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3757343

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