(Q73489115)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the Vikings (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

N Milman

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

P Pedersen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

publication date

1 July 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

64

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

36-47

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

C282Y and H63D mutation frequencies in a population from central Spain

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is Celtic origin a risk factor?

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Celtic origin of the C282Y mutation of hemochromatosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelated

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Comparative study of the two more frequent HFE mutations (C282Y and H63D): significant different allelic frequencies between the North and South of Portugal.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Haemochromatosis mutations and ferritin in myocardial infarction: a case-control study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Heterozygotes for HFE mutations have no increased risk of advanced alcoholic liver disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Heterozygosity for the hemochromatosis gene in liver diseases--prevalence and effects on liver histology

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

C282Y and H63D mutations in the HFE gene are not associated with porphyria cutanea tarda in Bulgaria

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

HFE mutations, iron deficiency and overload in 10,500 blood donors

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Allele frequencies of hereditary hemochromatosis gene mutations in a local population of west Brittany

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Frequency of the C282Y mutation of hemochromatosis in five French populations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Geography of HFE C282Y and H63D mutations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Global prevalence of putative haemochromatosis mutations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Haemochromatosis mutations in North-East Scotland

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population--implications for haemochromatosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

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/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Heterogeneity of hemochromatosis in Italy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Mutations of the HFE gene and the risk of hepatocellular carcinoma

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Hemochromatosis in Ireland and HFE

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Determination of gene frequencies for two common haemochromatosis mutations in the Danish population by a novel polymerase chain reaction with sequence-specific primers.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

The frequency of the haemochromatosis C282Y mutation in the ethnic Hungarian and Romany populations of eastern Hungary

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

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/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00083.X

7 January 2021

10.1034/J.1399-0004.2003.00083.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12791037%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference