Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A. (Q43864515)

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scientific article published in January 2002

Language	Label	Description	Also known as
English	Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.	scientific article published in January 2002

Statements

scholarly article

1 reference

Europe PubMed Central

27 November 2017

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A. (English)

1 reference

Europe PubMed Central

27 November 2017

author name string

Peter L Rady

1

1 reference

Europe PubMed Central

27 November 2017

Sylvia Szucs

2

1 reference

Europe PubMed Central

27 November 2017

James Grady

3

1 reference

Europe PubMed Central

27 November 2017

S David Hudnall

4

1 reference

Europe PubMed Central

27 November 2017

Leonard H Kellner

5

1 reference

Europe PubMed Central

27 November 2017

Harold Nitowsky

6

1 reference

Europe PubMed Central

27 November 2017

Stephen K Tyring

7

1 reference

Europe PubMed Central

27 November 2017

Reuben K Matalon

8

1 reference

Europe PubMed Central

27 November 2017

publication date

1 January 2002

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Europe PubMed Central

27 November 2017

American Journal of Medical Genetics Part A

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Europe PubMed Central

27 November 2017

107

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27 November 2017

162-168

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Europe PubMed Central

27 November 2017

2

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Europe PubMed Central

27 November 2017

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Neural-tube defects

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Hispanic origin and neural tube defects in Houston/Harris County, Texas. I. Descriptive epidemiology

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

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Spontaneous abortion-high risk factor for neural tube defects in subsequent pregnancy

1 reference

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Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

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Neural tube defect prevalence in California (1990-1994): eliciting patterns by type of defect and maternal race/ethnicity.

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https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Molecular genetics of methylenetetrahydrofolate reductase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring.

1 reference

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21 January 2018

Biological and clinical implications of the MTHFR C677T polymorphism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Neural tube defects and a disturbed folate dependent homocysteine metabolism.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Periconceptional vitamin use, dietary folate, and the occurrence of neural tube defects

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Molecular genetics of homocysteine metabolism.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Hispanic origin and neural tube defects in Houston/Harris County, Texas. II. Risk factors

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10122

21 January 2018

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10.1002/AJMG.10122

1 reference

Europe PubMed Central

27 November 2017

1 reference

Europe PubMed Central

27 November 2017

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