Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1.

The European respiratory journal - 1 Apr 2006

Brøgger J, Steen V M, Eiken H G, Gulsvik A, Bakke P

Abstract excerpt

There is evidence of a hereditary component in chronic obstructive pulmonary disease (COPD). A number of genetic association studies have been performed to find susceptibility genes of COPD. The current authors performed a case-control, genetic-association study and a meta-analysis of 16 studies, involving seven polymorphisms in three well-studied genes: microsomal epoxide hydroxylase (EPHX1); tumour necrosis...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Epoxide Hydrolases
Share to Genetic Testing
Share to Pulmonary Disease, Chronic Obstructive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Receptors, Adrenergic, beta-2

Share to Smoking

Share to Smoking Cessation

Share to Statistics as Topic

Share to Tumor Necrosis Factor-alpha

Source

Identifiers

PMID: 16585076
DOI: 10.1183/09031936.06.00057005

Genes

EPHX1
ADRB2
TNF

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1.PMID 16585076Read ↗

Analyses of association between PPAR gamma and EPHX1 polymorphisms and susceptibility to COPD in a Hungarian cohort, a case-control study.Semantic proximity Read ↗

EPHX1 Y113H polymorphism is associated with increased risk of chronic obstructive pulmonary disease in Kazakhstan population.Semantic proximity Read ↗

EPHX1 polymorphisms, COPD and asthma in 47,000 individuals and in meta-analysis.Semantic proximity Read ↗

Glutathione S-transferase and microsomal epoxide hydrolase gene polymorphisms and risk of chronic obstructive pulmonary disease in Slovak population.Semantic proximity Read ↗

Polymorphism of microsomal epoxide hydrolase is associated with chronic obstructive pulmonary disease and bronchodilator response.Semantic proximity Read ↗

Genetic association analysis of functional impairment in chronic obstructive pulmonary disease.Semantic proximity Read ↗

Microsomal epoxide hydrolase gene polymorphisms and susceptibility to chronic obstructive pulmonary disease in the Tunisian population.Semantic proximity Read ↗

Combined analysis of EPHX1, GSTP1, GSTM1 and GSTT1 gene polymorphisms in relation to chronic obstructive pulmonary disease risk and lung function impairment.Semantic proximity Read ↗

Genetic associations with hypoxemia and pulmonary arterial pressure in COPD.Semantic proximity Read ↗

Association of functionally important polymorphism of microsomal epoxide hydrolase gene (EPHX1) with lung cancer susceptibility.Semantic proximity Read ↗

Association of the CYP1A1 MspI and TNFα-308 polymorphisms with chronic obstructive pulmonary disease in Inner Mongolia.Semantic proximity Read ↗

Association between polymorphisms of microsomal epoxide hydrolase and COPD: results from meta-analyses.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.