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Systematic identification of trans eQTLs as putative drivers of known disease associations

Systematic identification of trans eQTLs as putative drivers of known disease associations

http://www.wikidata.org/entity/Q28659854

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Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits Genetic studies of body mass index yield new insights for obesity biology Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma 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 Diametrical diseases reflect evolutionary-genetic tradeoffs: Evidence from psychiatry, neurology, rheumatology, oncology and immunology Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation Applications of Next-generation Sequencing in Systemic Autoimmune Diseases Genetic studies of rheumatoid arthritis Genetics, Epigenetics, and Genomics of Systemic Sclerosis Genetics of human metabolism: an update Genome-wide association study of selenium concentrations Linking the genetic architecture of cytosine modifications with human complex traits MT-HESS: an efficient Bayesian approach for simultaneous association detection in OMICS datasets, with application to eQTL mapping in multiple tissues 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.High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry The Future is The Past: Methylation QTLs in Schizophrenia Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23 Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease Changes in DNA methylation over the growing season differ between North Carolina farmworkers and non-farmworkers Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types Genome-wide association study of blood lead shows multiple associations near ALAD The genetic and mechanistic basis for variation in gene regulation A meta-analysis of gene expression signatures of blood pressure and hypertension Use of genome-wide association studies for cancer research and drug repositioning Erythropoietin in the general population: reference ranges and clinical, biochemical and genetic correlates Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters Genetic regulation of expression of leukotriene A4 hydrolase RNA Sequencing and Analysis Genetics of gene expression in immunity to infection Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci Genetics of rheumatoid arthritis contributes to biology and drug discovery Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk Individualized medicine from prewomb to tomb Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.

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P2860

Systematic identification of trans eQTLs as putative drivers of known disease associations

http://www.wikidata.org/entity/Q28659854

description

2013 nî lūn-bûn

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2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի հոտեմբերին 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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Nature Genetics

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Astrid Suchy-Dicey

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David Melzer

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Dena G Hernandez

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Dörte Radke

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Eva Reinmaa

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Jennifer Brody

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Joyce B J van Meurs

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Katharina Schramm

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Leonard H Van den Berg

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Mari Nelis

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P2860

A genome-wide association study of the metabolic syndrome in Indian Asian men

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

An integrated encyclopedia of DNA elements in the human genome

Multiple common variants for celiac disease influencing immune gene expression

A map of human genome variation from population-scale sequencing

Biological, clinical and population relevance of 95 loci for blood lipids

New loci associated with kidney function and chronic kidney disease

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

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

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1238-43

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6503

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10.1038/NG.2756

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10

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45

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Juha Karjalainen

Thomas Meitinger

Alexander Teumer

Fernando Rivadeneira

Holger Prokisch

Claudia Schurmann

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2013-10-01T00:00:00Z

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24013639

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3991562

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