(Q44429688)

2 December 2017

title

Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects (English)

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2 December 2017

2

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2 December 2017

Anne Parle-McDermott

1

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2 December 2017

Peadar N Kirke

3

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2 December 2017

Valerie B O'Leary

4

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2 December 2017

Deborah A Swanson

5

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2 December 2017

Faith Pangilinan

6

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2 December 2017

Mary Conley

7

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2 December 2017

Anne M Molloy

8

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2 December 2017

Christopher Cox

9

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2 December 2017

John M Scott

10

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2 December 2017

Lawrence C Brody

11

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2 December 2017

publication date

5 March 2003

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Journal of Human Genetics

2 December 2017

published in

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2 December 2017

volume

48

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2 December 2017

issue

4

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2 December 2017

page(s)

190-193

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https://scigraph.springernature.com/pub.10.1007/s10038-003-0008-4

2 December 2017

exact match

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cites work

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

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12 December 2020

Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects

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12 December 2020

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

1 reference

12 December 2020

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

12 December 2020

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)

1 reference

12 December 2020

Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population

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12 December 2020

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor

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12 December 2020

Loss of heterozygosity at the 5,10-methylenetetrahydrofolate reductase locus in human ovarian carcinomas

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12 December 2020

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

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12 December 2020

Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase

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12 December 2020

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

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12 December 2020

Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

1 reference

12 December 2020

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

1 reference

12 December 2020

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population

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12 December 2020

The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

10.1007/S10038-003-0008-4

Identifiers

DOI

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2 December 2017

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