The architecture of gene regulatory variation across multiple human tissues: the MuTHER study. - Wikidata - awgldk - TriplyDB

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study.

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study.

http://www.wikidata.org/entity/Q33815387

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Exploiting gene expression variation to capture gene-environment interactions for disease Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis Cohort Profile: TwinsUK and healthy ageing twin study Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes Autoimmune diseases - connecting risk alleles with molecular traits of the immune system.Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation Progress in the genetics of polygenic brain disorders: significant new challenges for neurobiology Prediction of Causal Candidate Genes in Coronary Artery Disease Loci A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1 Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma Systematic genetic analysis identifies Cis-eQTL target genes associated with glioblastoma patient survival A statistical framework for joint eQTL analysis in multiple tissues Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation The genetic architecture of the genome-wide transcriptional response to ER stress in the mouse Context Sensitive Modeling of Cancer Drug Sensitivity Genetics of gene expression in immunity to infection A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS Functional genomic annotation of genetic risk loci highlights inflammation and epithelial biology networks in CKD Identification of inherited genetic variations influencing prognosis in early-onset breast cancer Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations Genome-wide association analysis identifies susceptibility loci for migraine without aura.Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene.Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways.RNA-Seq optimization with eQTL gold standards.

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P2860

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study.

http://www.wikidata.org/entity/Q33815387

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Gabriela Surdulescu

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P2860

Genome-wide associations of gene expression variation in humans

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

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

Variations in DNA elucidate molecular networks that cause disease

An atlas of combinatorial transcriptional regulation in mouse and man

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Statistical significance for genomewide studies

Mapping the genetic architecture of gene expression in human liver

Understanding mechanisms underlying human gene expression variation with RNA sequencing

Transcriptome genetics using second generation sequencing in a Caucasian population

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