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

Prevalence, characteristics, and prognostic significance of HFE gene mutations in type 2 diabetes: the Fremantle Diabetes Study.

Diabetes care - 1 Sept 2008

Davis Timothy M E, Beilby John, Davis Wendy A, Olynyk John K, Jeffrey Gary P, Rossi Enrico, Boyder Conchita, Bruce David G

Abstract excerpt

OBJECTIVE: To examine the relationship between iron status, hereditary hemochromatosis (HFE) gene mutations, and clinical features and outcomes of type 2 diabetes in a well-characterized representative sample of community-based patients. RESEARCH DESIGN AND METHODS: HFE genotype data were availab...

Read the complete abstract on PubMed

Topics

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

Share to Body Mass Index
Share to Ethnicity
Share to Ferritins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemochromatosis Protein

Share to Histocompatibility Antigens Class I

Share to Iron Overload

Share to Lipids

Source

Open in PubMed Open full text

Identifiers

PMID: 18566337
DOI: 10.2337/dc08-0248
PMCID: PMC2518347

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18566337-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence, characteristics, and prognostic significance of HFE gene mutations in type 2 diabetes: the Fremantle Diabetes Study.PMID 18566337Read ↗

Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study.Semantic proximity Read ↗

Diabetes in HFE Hemochromatosis.Semantic proximity Read ↗

Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.Semantic proximity Read ↗

HFE genetic variability, body iron stores, and the risk of type 2 diabetes in U.S. women.Semantic proximity Read ↗

Total mortality by elevated transferrin saturation in patients with diabetes.Semantic proximity Read ↗

Higher ferritin levels, but not serum iron or transferrin saturation, are associated with Type 2 diabetes mellitus in adult men and women free of genetic haemochromatosis.Semantic proximity Read ↗

Diabetes and hemochromatosis.Semantic proximity Read ↗

Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study.Semantic proximity Read ↗

Hemochromatosis gene (HFE) polymorphisms and risk of type 2 diabetes mellitus: a meta-analysis.Semantic proximity Read ↗

Relations among serum ferritin, C282Y and H63D mutations in the HFE gene and type 2 diabetes mellitus in the Czech population.Semantic proximity Read ↗

A diabetes-associated genetic variant is associated with diastolic dysfunction and cardiovascular disease.Semantic proximity Read ↗

Correlation between HFE gene polymorphisms and increased risk of coronary artery disease among patients with type 2 diabetes in Iran.Semantic proximity Read ↗

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