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

A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population.

Clinica chimica acta; international journal of clinical chemistry - 1 Jan 2023

Hubacek J A, Philipp T, Adamkova V, Majek O, Dusek L

Abstract excerpt

BACKGROUND: Coronavirus disease (COVID-19), which is caused by the SARS-CoV-2 virus, has become a global pandemic. While susceptibility to COVID-19 is subject to several external factors, including hypertension, BMI, and the presence of diabetes, it is also genetically determined to a significant extent. Infectious agents require iron (Fe) for proper functioning. Carriers of mutations resulting in increased iron...

Read the complete abstract on PubMed

Topics

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

Share to COVID-19
Share to Czech Republic

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hemochromatosis

Share to Hemochromatosis Protein

Share to Histocompatibility Antigens Class I

Share to Polymorphism, Single Nucleotide

Share to SARS-CoV-2

Source

Open in PubMed Open full text

Identifiers

PMID: 36572138
DOI: 10.1016/j.cca.2022.12.025
PMCID: PMC9788844

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population.PMID 36572138Read ↗

Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK BiobankSemantic proximity Read ↗

<i>HFE</i>genotypes, haemochromatosis diagnosis and clinical outcomes to age 80: a prospective cohort study in UK BiobankSemantic proximity Read ↗

Population-based analysis of the frequency of HFE gene polymorphisms: Correlation with the susceptibility to develop hereditary hemochromatosis.Semantic proximity Read ↗

HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank.Semantic proximity Read ↗

Penetrance, cancer incidence and survival in HFE haemochromatosis-A population-based cohort study.Semantic proximity Read ↗

An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.Semantic proximity Read ↗

Morbidity, risk of cancer and mortality in 3645 HFE mutations carriers.Semantic proximity Read ↗

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.Semantic proximity Read ↗

GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors.Semantic proximity Read ↗

The prevalence of haemochromatosis gene mutations in the West of Scotland and their relation to ischaemic heart disease.Semantic proximity Read ↗

GNPAT Variant associated with severe iron overload in HFE hemochromatosisSemantic proximity Read ↗

Haemochromatosis mutations in North-East Scotland.Semantic proximity Read ↗

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