Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia (Q73055232)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

familial hypercholesterolemia

31 October 2019

main subject

coronary artery disease

1 reference

based on heuristic

inferred from title

1 reference

M Kawashiri

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

K Kajinami

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

A Nohara

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

K Yagi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

A Inazu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

J Koizumi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

H Mabuchi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 October 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Cardiology

31 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

volume

86

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

840-845

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Molecular variant of 5,10-methylenetetrahydrofolate reductase is a risk factor of ischemic heart disease in the Japanese population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Discrimination of familial hypercholesterolemia and secondary hypercholesterolemia by Achilles' tendon thickness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Development of coronary heart disease in familial hypercholesterolemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Coronary Artery Disease in Heterozygous Familial Hypercholesterolemia Patients With the Same LDL Receptor Gene Mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Comparison of the effect of two low-density lipoprotein receptor class mutations on coronary heart disease among French-Canadian patients heterozygous for familial hypercholesterolaemia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Plasma high-density lipoproteins and ischemic heart disease: studies in a large kindred with familial hypercholesterolemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Coronary artery disease in heterozygous familial hypercholesterolemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Apolipoprotein E phenotype and lipoprotein(a) in familial hypercholesterolaemia: implication for lipoprotein(a) metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Characteristics of coronary artery disease and lipoprotein abnormalities in patients with heterozygous familial hypercholesterolemia associated with diabetes mellitus or impaired glucose tolerance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Hyperhomocysteinemia: an independent risk factor for vascular disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Prevalence of familial hyperhomocyst(e)inemia in men with premature coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Association between plasma total homocysteine and parental history of cardiovascular disease in children with familial hypercholesterolemia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

Familial hypercholesterolemia and apolipoprotein E4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2800%2901103-6

10.1016/S0002-9149(00)01103-6

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11024398%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference