Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci. - Wikidata - thesis-toulmin - TriplyDB

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci.

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci.

http://www.wikidata.org/entity/Q36101099

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Update on inflammatory bowel disease in patients with primary sclerosing cholangitis How Should Cancer Surveillance in Primary Sclerosing Cholangitis Be Performed?Biliary Mucosal Barrier and Microbiome The genetics of complex cholestatic disorders Expression of the Blood-Group-Related Gene B4galnt2 Alters Susceptibility to Salmonella Infection The Role of Genetic and Immune Factors for the Pathogenesis of Primary Sclerosing Cholangitis in Childhood Impact of Microbes on the Pathogenesis of Primary Biliary Cirrhosis (PBC) and Primary Sclerosing Cholangitis (PSC)Exploring Relationships between Host Genome and Microbiome: New Insights from Genome-Wide Association Studies The Immunogenetics of Autoimmune Cholestasis Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.Primary sclerosing cholangitis and the microbiota: current knowledge and perspectives on etiopathogenesis and emerging therapies Pathogenesis and clinical spectrum of primary sclerosing cholangitis.Gene-gene and gene-environment interactions in ulcerative colitis.Small duct primary sclerosing cholangitis without inflammatory bowel disease is genetically different from large duct disease.Immune and genetic gardening of the intestinal microbiome.Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.Genetically dictated change in host mucus carbohydrate landscape exerts a diet-dependent effect on the gut microbiota Advances and controversies in the pathogenesis and management of primary sclerosing cholangitis.Innate lymphoid cells regulate intestinal epithelial cell glycosylation Association of Ulcerative Colitis with FUT2 and FUT3 Polymorphisms in Patients from Southeast China A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.Association of cardiovascular and metabolic disease genes with psoriasis Lymphotoxin network pathways shape the tumor microenvironment The TNF Receptor Superfamily in Co-stimulating and Co-inhibitory Responses The inhibitory receptor BTLA controls γδ T cell homeostasis and inflammatory responses.Decoding norovirus infection in Crohn's disease.Genetics in PSC: what do the "risk genes" teach us?Extraintestinal manifestations and complications in inflammatory bowel disease: from shared genetics to shared biological pathways.Fucosyltransferase 2: a genetic risk factor for primary sclerosing cholangitis and Crohn's disease--a comprehensive review.Mechanisms of tissue injury in autoimmune liver diseases.Primary sclerosing cholangitis - the Norwegian experience.Primary sclerosing cholangitis: a clinical update.Genetics of Inflammatory Bowel Diseases.A common genetic variant of fucosyltransferase 2 correlates with serum carcinoembryonic antigen levels and affects cancer screening in patients with primary sclerosing cholangitis.Are Dominant Strictures in Primary Sclerosing Cholangitis a Risk Factor for Cholangiocarcinoma?Imaging of autoimmune biliary disease.Epithelial glycosylation in gut homeostasis and inflammation.Antineutrophil antibodies define clinical and genetic subgroups in primary sclerosing cholangitis.Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.

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P2860

Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci.

http://www.wikidata.org/entity/Q36101099

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Journal of Hepatology

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Alexey Shiryaev

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Andre Franke

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Andreas Teufel

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Annika Bergquist

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Brian D Juran

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Christian Rust

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Cyriel Y Ponsioen

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Daniel Nils Gotthardt

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David Ellinghaus

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Einar Björnsson

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P2860

Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype

Genome-wide association meta-analysis for total serum bilirubin levels

PLINK: a tool set for whole-genome association and population-based linkage analyses

Principal components analysis corrects for stratification in genome-wide association studies

Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling

B and T lymphocyte attenuator regulates T cell activation through interaction with herpesvirus entry mediator

Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

METAL: fast and efficient meta-analysis of genomewide association scans

LocusZoom: regional visualization of genome-wide association scan results

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10.1016/J.JHEP.2012.03.031

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2

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Christian Gieger

Philip Rosenstiel

Jon K. Laerdahl

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Johannes Roksund Hov

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2012-04-18T00:00:00Z

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224809869

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