Genetic and lifestyle factors related to the periconception vitamin B12 status and congenital heart defects: a Dutch case-control study (Q40130140)

17 September 2017

Genetic and lifestyle factors related to the periconception vitamin B12 status and congenital heart defects: a Dutch case-control study (English)

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17 September 2017

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7

André G Uitterlinden

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Regine PM Steegers-Theunissen

17 September 2017

series ordinal

8

object named as

Régine P M Steegers-Theunissen

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17 September 2017

5

Eric A P Steegers

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17 September 2017

Anna C Verkleij-Hagoort

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1

object named as

Anna C Verkleij-Hagoort

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17 September 2017

2

Lydi M J W van Driel

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17 September 2017

4

Aaron Isaacs

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17 September 2017

Jan Lindemans

3

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17 September 2017

Willem A Helbing

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6

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17 September 2017

15 January 2008

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Molecular Genetics and Metabolism

17 September 2017

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17 September 2017

94

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17 September 2017

1

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17 September 2017

112-119

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Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.

17 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Congenital heart defects and abnormal maternal biomarkers of methionine and homocysteine metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Congenital heart defects and maternal derangement of homocysteine metabolism.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Dietary determinants of plasma homocysteine concentrations.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Cardiac outflow tract malformations in chick embryos exposed to homocysteine

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Vitamin supplements and the risk for congenital anomalies other than neural tube defects

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Low-dose folic acid supplementation decreases plasma homocysteine concentrations: a randomized trial

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

The effect of vitamin B12 inhibition in vivo: impaired folate polyglutamate biosynthesis indicating that 5-methyltetrahydropteroylglutamate is not its usual substrate

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Staging vitamin B-12 (cobalamin) status in vegetarians

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Kinetic and thermodynamic characterization of the common polymorphic variants of human methionine synthase reductase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Genetic polymorphisms predisposing to hyperhomocysteinemia in cardiac transplant patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Transcobalamin 776C->G polymorphism negatively affects vitamin B-12 metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Altered folate and vitamin B12 metabolism in families with spina bifida offspring

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Marginal maternal vitamin B12 status increases the risk of offspring with spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Vitamin and homocysteine status of mothers and infants and the risk of nonsyndromic orofacial clefts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Folic acid and homocysteine affect neural crest and neuroepithelial cell outgrowth and differentiation in vitro

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Dietary intake of B-vitamins in mothers born a child with a congenital heart defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Maternal nutritional status and the risk for orofacial cleft offspring in humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Proportioning whole-genome single-nucleotide-polymorphism diversity for the identification of geographic population structure and genetic ancestry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Validation of the assessment of folate and vitamin B12 intake in women of reproductive age: the method of triads

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Adjustment for total energy intake in epidemiologic studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

MTRR 66A>G polymorphism in relation to congenital heart defects.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Study of four genes belonging to the folate pathway: transcobalamin 2 is involved in the onset of non-syndromic cleft lip with or without cleft palate.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

776C>G polymorphism of the transcobalamin II gene as a risk factor for spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Environmental influence on the worldwide prevalence of a 776C->G variant in the transcobalamin gene (TCN2).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Hyperhomocysteinemia, pregnancy complications, and the timing of investigation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Holotranscobalamin as a predictor of vitamin B12 status

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

Measurement of total vitamin B12 and holotranscobalamin, singly and in combination, in screening for metabolic vitamin B12 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.12.002

10.1016/J.YMGME.2007.12.002

7 January 2021

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DOI

1 reference

17 September 2017

1 reference