Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
about
Autoimmune diseases - connecting risk alleles with molecular traits of the immune system.Dissecting the genetics of complex traits using summary association statisticsA method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseasesJoint genetic analysis using variant sets reveals polygenic gene-context interactions.Genetic-epigenetic interactions in cis: a major focus in the post-GWAS eraImmunomediated Pan-cancer Regulation Networks are Dominant Fingerprints After Treatment of Cell Lines with Demethylation.Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes.Detection and interpretation of shared genetic influences on 42 human traits.Progress in understanding type 1 diabetes through its genetic overlap with other autoimmune diseases.Pharmacogenetic Biomarkers to Predict Treatment Response in Multiple Sclerosis: Current and Future Perspectives.Should There be Concern About Autoimmune Diabetes in Adults? Current Evidence and Controversies.A method for identifying genetic heterogeneity within phenotypically defined disease subgroups.The genetics revolution in rheumatology: large scale genomic arrays and genetic mapping.Immunogenomic approaches to understand the function of immune disease variants.Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease.Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.Modeling disease risk through analysis of physical interactions between genetic variants within chromatin regulatory circuitry.Constraints on eQTL Fine Mapping in the Presence of Multisite Local Regulation of Gene Expression.The Genetic Architecture of Type 1 Diabetes.Genetic predisposition for beta cell fragility underlies type 1 and type 2 diabetesFunctional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis.Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types.Isogenic Cellular Systems Model the Impact of Genetic Risk Variants in the Pathogenesis of Type 1 Diabetes.HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes.The chromosome 6q22.33 region is associated with age at diagnosis of type 1 diabetes and disease risk in those diagnosed under 5 years of age.Genetics of immune-mediated inflammatory diseases.Adverse effects of gluten ingestion and advantages of gluten withdrawal in nonceliac autoimmune disease.COBLL1 modulates cell morphology and facilitates androgen receptor genomic binding in advanced prostate cancer.Public attitudes in Japan toward participation in whole genome sequencing studies.Erratum: Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls
P2860
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P2860
Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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2015年论文
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Statistical colocalization of ...... he context of common controls.
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Statistical colocalization of ...... he context of common controls.
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Statistical colocalization of ...... he context of common controls.
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Statistical colocalization of ...... he context of common controls.
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Statistical colocalization of ...... he context of common controls.
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P2093
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10.1038/NG.3330
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2015-06-08T00:00:00Z