High-resolution mapping of expression-QTLs yields insight into human gene regulation. - Wikidata - wikimedia - TriplyDB

High-resolution mapping of expression-QTLs yields insight into human gene regulation.

High-resolution mapping of expression-QTLs yields insight into human gene regulation.

http://www.wikidata.org/entity/Q33375030

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Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines Human genetics and genomics a decade after the release of the draft sequence of the human genome Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosate GSTCD and INTS12 regulation and expression in the human lung Association of the anxiogenic and alerting effects of caffeine with ADORA2A and ADORA1 polymorphisms and habitual level of caffeine consumption RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk Long noncoding RNAs in hepatocellular carcinoma: Novel insights into their mechanism Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes Long-range regulatory polymorphisms affecting a GABA receptor constitute a quantitative trait locus (QTL) for social behavior in Caenorhabditis elegans Constructing 3D interaction maps from 1D epigenomes.Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity Systematic genetic analysis identifies Cis-eQTL target genes associated with glioblastoma patient survival A statistical framework for joint eQTL analysis in multiple tissues 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 Genetic modifiers of chromatin acetylation antagonize the reprogramming of epi-polymorphisms Protein quantitative trait loci identify novel candidates modulating cellular response to chemotherapy Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations The genetic and mechanistic basis for variation in gene regulation Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study Integrated enrichment analysis of variants and pathways in genome-wide association studies indicates central role for IL-2 signaling genes in type 1 diabetes, and cytokine signaling genes in Crohn's disease Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study Exon-specific QTLs skew the inferred distribution of expression QTLs detected using gene expression array data Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation Genome-wide association study identifies three novel loci for type 2 diabetes.Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.Mapping and analysis of chromatin state dynamics in nine human cell types Understanding mechanisms underlying human gene expression variation with RNA sequencing Transcriptome genetics using second generation sequencing in a Caucasian population Annotation of functional variation in personal genomes using RegulomeDB Common regulatory variation impacts gene expression in a cell type-dependent manner

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High-resolution mapping of expression-QTLs yields insight into human gene regulation.

http://www.wikidata.org/entity/Q33375030

description

2008 nî lūn-bûn

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2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

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2008年論文

@zh-tw

2008年论文

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name

High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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type

label

High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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prefLabel

High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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High-resolution mapping of expression-QTLs yields insight into human gene regulation.

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JOURNAL.PGEN.1000214

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High-resolution mapping of expression-QTLs yields insight into human gene regulation.

@en

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Emmanouil T Dermitzakis

http://www.w3.org/2001/XMLSchema#string

Jean-Baptiste Veyrieras

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Jonathan K Pritchard

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Matthew Stephens

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Sridhar Kudaravalli

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Su Yeon Kim

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Yoav Gilad

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P2860

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Transcriptional Regulatory Elements in the Human Genome

A genome-wide analysis of CpG dinucleotides in the human genome distinguishes two distinct classes of promoters.

Common genetic variants account for differences in gene expression among ethnic groups

Analysis of the vertebrate insulator protein CTCF-binding sites in the human genome

A second generation human haplotype map of over 3.1 million SNPs

Revealing the architecture of gene regulation: the promise of eQTL studies

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

A haplotype map of the human genome

BLAT--the BLAST-like alignment tool

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e1000214

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10.1371/JOURNAL.PGEN.1000214

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10

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4

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Jean-Baptiste Veyrieras

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2008-10-10T00:00:00Z

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23310496

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18846210

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2556086

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