Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease.

scientific article published on 15 January 2018

Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease. is …
instance of (P31):
scholarly articleQ13442814

External links are
P6179Dimensions Publication ID1100404293
P356DOI10.1186/S40246-018-0132-Z
P2888exact matchhttps://scigraph.springernature.com/pub.10.1186/s40246-018-0132-z
P932PMC publication ID5769240
P698PubMed publication ID29335020

P50authorJohn QuackenbushQ6253638
Kimberly GlassQ66816190
John PlatigQ66816418
P2093author name stringXiaobo Zhou
George R Washko
Craig P Hersh
Dawn L DeMeo
Edwin K Silverman
Michael H Cho
Weiliang Qiu
Gerard J Criner
Raphael Bueno
Nathaniel Marchetti
Jarrett D Morrow
Bartholome Celli
P2860cites workA flexible and accurate genotype imputation method for the next generation of genome-wide association studiesQ21129496
Chapter 11: Genome-wide association studiesQ21145310
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWASQ21563317
Genome-wide association study identifies novel loci associated with diisocyanate-induced occupational asthmaQ23910396
Genotype imputation with thousands of genomesQ24633967
A global reference for human genetic variationQ25909434
Principal components analysis corrects for stratification in genome-wide association studiesQ27860975
ENCODE data in the UCSC Genome Browser: year 5 updateQ28280234
Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signaturesQ28834473
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosisQ28943334
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association studyQ28943525
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysisQ29416987
Genome-wide association study of smoking behaviours in patients with COPDQ29417072
Systematic localization of common disease-associated variation in regulatory DNAQ29614895
Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summaryQ29614970
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosisQ30274832
BioMart and Bioconductor: a powerful link between biological databases and microarray data analysisQ30998448
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.Q33419815
Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associationsQ33549716
Variants in FAM13A are associated with chronic obstructive pulmonary diseaseQ33687879
Epigenomics reveals a functional genome anatomy and a new approach to common diseaseQ34207844
A linear complexity phasing method for thousands of genomesQ34237936
Sherlock: detecting gene-disease associations by matching patterns of expression QTL and GWASQ34342875
The ConsensusPathDB interaction database: 2013 updateQ34473397
Second-generation PLINK: rising to the challenge of larger and richer datasetsQ35125670
Family history is a risk factor for COPDQ35410963
The ensembl regulatory buildQ35531112
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.Q35816887
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestryQ35860362
Genome-wide association study of lung function decline in adults with and without asthmaQ35923186
Matrix eQTL: ultra fast eQTL analysis via large matrix operationsQ35947630
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK BiobankQ36123192
Bipartite Community Structure of eQTLsQ36130077
CHRNA3/5, IREB2, and ADCY2 are associated with severe chronic obstructive pulmonary disease in PolandQ36176931
High mobility group box 1-induced epithelial mesenchymal transition in human airway epithelial cellsQ36438398
Genetic control of gene expression at novel and established chronic obstructive pulmonary disease lociQ36724956
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma.Q36888604
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary DiseaseQ37125510
Integration of genomic and genetic approaches implicates IREB2 as a COPD susceptibility geneQ37373901
Systems genetics approaches to understand complex traitsQ37602800
Functional interactors of three genome-wide association study genes are differentially expressed in severe chronic obstructive pulmonary disease lung tissueQ37695214
Cadherins and epithelial-to-mesenchymal transitionQ38088483
Epithelial-mesenchymal transition as a fundamental underlying pathogenic process in COPD airways: fibrosis, remodeling and cancerQ38238991
DNA methylation profiling in human lung tissue identifies genes associated with COPD.Q41665058
Sushi.R: flexible, quantitative and integrative genomic visualizations for publication-quality multi-panel figuresQ41841675
Clinical significance of epithelial mesenchymal transition (EMT) in chronic obstructive pulmonary disease (COPD): potential target for prevention of airway fibrosis and lung cancerQ43217503
Genetic effects on gene expression across human tissuesQ46285732
PTBP3-Mediated Regulation of ZEB1 mRNA Stability Promotes Epithelial-Mesenchymal Transition in Breast CancerQ47350707
Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis.Q52241091
HNRNPAB induces epithelial-mesenchymal transition and promotes metastasis of hepatocellular carcinoma by transcriptionally activating SNAIL.Q53240716
Gene expression networks in COPD: microRNA and mRNA regulation.Q54347289
Siblings of patients with severe chronic obstructive pulmonary disease have a significant risk of airflow obstructionQ77158107
An integrated epigenetic and genetic approach to common human diseaseQ80357018
P433issue1
P921main subjectchronic obstructive pulmonary diseaseQ199804
P304page(s)1
P577publication date2018-01-15
P1433published inHuman genomicsQ26842690
P1476titleEnsemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease.
P478volume12

Reverse relations

cites work (P2860)
Q90608251Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study
Q89882349Integrated transcriptomic correlation network analysis identifies COPD molecular determinants
Q58592122Integrative Genomics Analysis Identifies ACVR1B as a Candidate Causal Gene of Emphysema Distribution
Q64086915RNA-sequencing across three matched tissues reveals shared and tissue-specific gene expression and pathway signatures of COPD

Search more.