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Article

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

Human genomics - 15 Jan 2018

Morrow Jarrett D, Cho Michael H, Platig John, Zhou Xiaobo, DeMeo Dawn L, Qiu Weiliang, Celli Bartholome, Marchetti Nathaniel, Criner Gerard J, Bueno Raphael, Washko George R, Glass Kimberly, Quackenbush John, Silverman Edwin K, Hersh Craig P

Abstract excerpt

BACKGROUND: Genome-wide association studies (GWAS) have identified single nucleotide polymorphisms (SNPs) significantly associated with chronic obstructive pulmonary disease (COPD). However, many genetic variants show suggestive evidence for association but do not meet the strict threshold for genome-wide significance. Integrative analysis of multiple omics datasets has the potential to identify novel genes...

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Share to Activin Receptors, Type I
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heterogeneous-Nuclear Ribonucleoprotein Group A-B

Share to Pulmonary Disease, Chronic Obstructive

Share to Quantitative Trait Loci

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Source

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Identifiers

PMID: 29335020
DOI: 10.1186/s40246-018-0132-z
PMCID: PMC5769240

Genes

HNRNPAB
MAPT
PCBP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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