Maternal and infant gene-folate interactions and the risk of neural tube defects. (Q55154986)

23 June 2018

title

Maternal and infant gene-folate interactions and the risk of neural tube defects. (English)

1 reference

23 June 2018

author

Richard H. Finnell

2

1 reference

23 June 2018

Suzan L Carmichael

3

object named as

Suzan L Carmichael

1 reference

23 June 2018

7

Gary M Shaw

1 reference

23 June 2018

4

Edward J Lammer

1 reference

23 June 2018

Huiping Zhu

5

object named as

Huiping Zhu

1 reference

23 June 2018

Analee J Etheredge

1

object named as

Analee J Etheredge

1 reference

23 June 2018

author name string

Laura E Mitchell

6

1 reference

23 June 2018

language of work or name

English

0 references

publication date

17 August 2012

1 reference

23 June 2018

American Journal of Medical Genetics

published in

1 reference

23 June 2018

volume

158A

1 reference

23 June 2018

issue

10

1 reference

23 June 2018

page(s)

2439-2446

1 reference

23 June 2018

Periconceptional nutrient intakes and risks of neural tube defects in California

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24 June 2018

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Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida

24 June 2018

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118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

24 June 2018

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Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview

24 June 2018

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An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1)

24 June 2018

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Analysis of the MTHFD1 promoter and risk of neural tube defects.

24 June 2018

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Evidence for small ubiquitin-like modifier-dependent nuclear import of the thymidylate biosynthesis pathway

24 June 2018

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Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk

24 June 2018

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Human neural tube defects: developmental biology, epidemiology, and genetics

24 June 2018

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects

24 June 2018

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Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

24 June 2018

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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

24 June 2018

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24 June 2018

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24 June 2018

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Validation of a self-administered diet history questionnaire using multiple diet records

24 June 2018

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24 June 2018

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

24 June 2018

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Update on prevention of folic acid-preventable spina bifida and anencephaly

24 June 2018

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The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects

13 August 2018

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The methylenetetrahydrofolate dehydrogenase (MTHFD1) 1958G>A variant is not associated with spina bifida risk in the Dutch population.

13 August 2018

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Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections

13 August 2018

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Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3448841

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3448841

Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3448841

Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels

13 August 2018

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Thymidylate synthase promoter polymorphism, interaction with folate intake, and risk of colorectal adenomas.

13 August 2018

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Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

13 August 2018

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Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium.

13 August 2018

1 reference

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Distinguishing the Effects of Maternal and Offspring Genes through Studies of "Case-Parent Triads"

13 August 2018

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https://api.crossref.org/works/10.1002%2FAJMG.A.35552

Thymidylate synthase repeat polymorphisms and risk of neural tube defects in a population from the northern United Kingdom

21 January 2018

1 reference

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Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35552

Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.35552

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22903727

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Trends of selected malformations in relation to folic acid recommendations and fortification: an international assessment

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22903727

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22903727

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.A.35552

1 reference

23 June 2018

PMC publication ID

3448841

1 reference

23 June 2018

PubMed publication ID

22903727

1 reference

23 June 2018