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

Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene.

Clinical chemistry - 1 Oct 2001

Koziol J A, Ho N J, Felitti V J, Beutler E

Abstract excerpt

BACKGROUND: The gene that causes most cases of hereditary hemochromatosis is designated HFE. Individuals with mutations in the HFE gene may have increased serum iron, transferrin saturation, and ferritin concentrations relative to individuals with the wild-type genotype. METHODS: We generated reference centiles for percentage of transferrin saturation and serum ferritin concentrations in normal (wild-type),...

Read the complete abstract on PubMed

Topics

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

Share to Ferritins
Share to Hemochromatosis
Share to Hemochromatosis Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Histocompatibility Antigens Class I

Share to HLA Antigens

Share to Reference Values

Share to Sex Factors

Share to Transferrin

Source

Identifiers

PMID: 11568090

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

Reference centiles for serum ferritin and percentage of transferrin saturation, with application to mutations of the HFE gene.PMID 11568090Read ↗

HFE Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.Semantic proximity Read ↗

The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis.Semantic proximity Read ↗

Compound heterozygous hemochromatosis genotype predicts increased iron and erythrocyte indices in women.Semantic proximity Read ↗

Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.Semantic proximity Read ↗

HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity # †Semantic proximity Read ↗

Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry.Semantic proximity Read ↗

Hemochromatosis and iron-overload screening in a racially diverse population.Semantic proximity Read ↗

HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.Semantic proximity Read ↗

HFE genotype and transferrin saturation in the United States.Semantic proximity Read ↗

Predicting C282Y homozygote genotype for hemochromatosis using serum ferritin and transferrin saturation values from 44,809 participants of the HEIRS study.Semantic proximity Read ↗

Effect of hemochromatosis genotype and lifestyle factors on iron and red cell indices in a community population.Semantic proximity Read ↗

HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis.Semantic proximity Read ↗

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