A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study (Q43546781)

From Wikidata

Jump to navigation Jump to search

scientific article published in February 2001

Language	Label	Description	Also known as
English	A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study	scientific article published in February 2001

Statements

scholarly article

1 reference

Europe PubMed Central

24 November 2017

A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study (English)

1 reference

Europe PubMed Central

24 November 2017

atherosclerosis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Michael Y. Tsai

4

1 reference

Europe PubMed Central

24 November 2017

Aaron R. Folsom

2

object named as

A R Folsom

1 reference

Europe PubMed Central

24 November 2017

author name string

M L Rasmussen

1

1 reference

Europe PubMed Central

24 November 2017

D J Catellier

3

1 reference

Europe PubMed Central

24 November 2017

U Garg

5

1 reference

Europe PubMed Central

24 November 2017

J H Eckfeldt

6

1 reference

Europe PubMed Central

24 November 2017

publication date

1 February 2001

1 reference

Europe PubMed Central

24 November 2017

Atherosclerosis

1 reference

Europe PubMed Central

24 November 2017

154

1 reference

Europe PubMed Central

24 November 2017

3

1 reference

Europe PubMed Central

24 November 2017

739-746

1 reference

Europe PubMed Central

24 November 2017

Iron and the sex difference in heart disease risk

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

High stored iron levels are associated with excess risk of myocardial infarction in eastern Finnish men.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Body iron stores and the risk of coronary heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Low iron-binding capacity as a risk factor for myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Serum ferritin and ceruloplasmin as coronary risk factors

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Body iron stores and the risk of coronary heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Iron status and coronary heart disease: negative findings from the NHANES I epidemiologic follow-up study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Iron stores are not associated with acute myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Body iron stores, dietary iron intake and coronary heart disease mortality

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Body iron stores and mortality due to cancer and ischaemic heart disease: a 17-year follow-up study of elderly men and women

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Serum iron and risk of fatal acute myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

No association between serum ferritin and asymptomatic carotid atherosclerosis. The Atherosclerosis Risk in Communities (ARIC) Study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

The iron hypothesis--does iron cause atherosclerosis?

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Effects of positive iron status at a cellular level.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Iron status and risk of cardiovascular disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Is iron sufficiency a risk factor in ischemic heart disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Stimulation of lipid peroxidation and hydroxyl-radical generation by the contents of human atherosclerotic lesions

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

The role of lipid peroxidation and antioxidants in oxidative modification of LDL.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Reaction of NO with O2-. implications for the action of endothelium-derived relaxing factor (EDRF)

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Haemochromatosis and HLA-H

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hemochromatosis: a genetic defect in iron metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hemochromatosis: genetics helps to define a multifactorial disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hereditary hemochromatosis: gene discovery and its implications for population-based screening.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Heterozygosity for a hereditary hemochromatosis gene is associated with cardiovascular death in women

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Increased Risk of Acute Myocardial Infarction in Carriers of the Hemochromatosis Gene Cys282Tyr Mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

HFE gene mutations in coronary atherothrombotic disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Haemochromatosis gene mutations and risk of coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Community surveillance of coronary heart disease in the Atherosclerosis Risk in Communities (ARIC) Study: methods and initial two years' experience

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Robust variance estimation for the case-cohort design.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Heterozygous hemochromatosis as a risk factor for premature myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Coronary heart disease and iron status: meta-analyses of prospective studies

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hereditary hemochromatosis. Phenotypic expression of the disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Relation between iron stores and non-insulin dependent diabetes in men: case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hereditary haemochromatosis mutations (HFE) in patients with Type II diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Hemochromatosis and diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Mutation analysis in hereditary hemochromatosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

A population-based study of the clinical expression of the hemochromatosis gene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Global prevalence of putative haemochromatosis mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

Iron and heart disease: the epidemiologic data

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900623-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0021-9150(00)00623-7

1 reference

Europe PubMed Central

24 November 2017

1 reference

Europe PubMed Central

24 November 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q43546781&oldid=2102910288"