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Article

HFE alleles in an Irish cystic fibrosis population.

Genetic testing - 1 Jan 2003

Devaney J, Maher M, Smith T, Houghton J A, Glennon M

Abstract excerpt

The variable clinical manifestations of cystic fibrosis (CF) suggest the influence of modifier genes. Genetic and environmental factors that determine whether an individual will develop associated complications are still being determined. It has been proposed that the gene for hemochromatosis, HFE, may be a modifier locus for CF disease phenotype. Recent research has suggested a relationship between mutations to...

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Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Hemochromatosis Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Histocompatibility Antigens Class I

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Source

Identifiers

PMID: 12885340
DOI: 10.1089/109065703322146876

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HFE alleles in an Irish cystic fibrosis population.PMID 12885340Read ↗

Is the hemochromatosis gene a modifier locus for cystic fibrosis?Semantic proximity Read ↗

The Frequency and Potential Implications of HFE Genetic Variants in Children With Cystic Fibrosis.Semantic proximity Read ↗

Genetic hemochromatosis, a Celtic disease: is it now time for population screening?Semantic proximity Read ↗

Population-based study of cystic fibrosis disease severity and haemochromatosis gene mutations.Semantic proximity Read ↗

HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.Semantic proximity Read ↗

HFE mutations in patients with hereditary haemochromatosis in Sweden.Semantic proximity Read ↗

Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.Semantic proximity Read ↗

HFE haemochromatosis gene mutations in liver transplant patients.Semantic proximity Read ↗

Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.Semantic proximity Read ↗

S65C and other mutations in the haemochromatosis gene in the Czech population.Semantic proximity Read ↗

Prevalence of HFE mutations in California newborns.Semantic proximity Read ↗

A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.Semantic proximity Read ↗

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