(Q34362719)

1 August 2017

title

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects (English)

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1 August 2017

Faith Pangilinan

1

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1 August 2017

Anne M Molloy

2

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1 August 2017

James L Mills

3

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1 August 2017

James F Troendle

4

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1 August 2017

Anne Parle-McDermott

5

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1 August 2017

Caroline Signore

6

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1 August 2017

Valerie B O'Leary

7

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1 August 2017

Peter Chines

8

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1 August 2017

Jessica M Seay

9

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1 August 2017

Kerry Geiler-Samerotte

10

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1 August 2017

Adam Mitchell

11

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1 August 2017

Julia E VanderMeer

12

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1 August 2017

Kristine M Krebs

13

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1 August 2017

Angelica Sanchez

14

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1 August 2017

Joshua Cornman-Homonoff

15

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1 August 2017

Nicole Stone

16

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1 August 2017

Mary Conley

17

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1 August 2017

Peadar N Kirke

18

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1 August 2017

Barry Shane

19

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1 August 2017

John M Scott

20

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1 August 2017

Lawrence C Brody

21

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1 August 2017

publication date

2 August 2012

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1 August 2017

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1 August 2017

volume

13

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1 August 2017

page(s)

62

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Correction for multiplicity in genetic association studies of triads: the permutational TDT

1 August 2017

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6 July 2018

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6 July 2018

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Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects

6 July 2018

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A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency

6 July 2018

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Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway

6 July 2018

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

6 July 2018

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

6 July 2018

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Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification

6 July 2018

1 reference

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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)

6 July 2018

1 reference

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Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts

6 July 2018

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Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Neural tube defects in the sample of genetic counselling

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Maternal vitamin B12 and the risk of fetal neural tube defects in Egyptian patients.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999-2001.

6 July 2018

1 reference

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Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Preventing neural tube defects in Europe: population based study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Haploview: analysis and visualization of LD and haplotype maps

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

The International HapMap Project

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

Prevention of neural-tube defects with folic acid in China. China-U.S. Collaborative Project for Neural Tube Defect Prevention

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

Maternal serum vitamin B12, folate and homocysteine and the risk of neural tube defects in the offspring in a high-risk area of China

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

Maternal serum B12 levels and risk for neural tube defects in a Texas-Mexico border population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

The human T locus and spina bifida risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

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/10.1186%2F1471-2350-13-62

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

Methylenetetrahydrofolate reductase mutation and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-62

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/10.1186%2F1471-2350-13-62

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3458983

[Relationship between folate, vitamin B12, total plasma homocysteine and mutation of reductase]

27 October 2018

1 reference

12 December 2020

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

1 reference

12 December 2020

A case-control study of maternal nutrition and neural tube defects in Northern Ireland

1 reference

12 December 2020

Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida

1 reference

12 December 2020

Activity of adenosine deaminase in mothers who have conceived a fetus with central nervous system malformations

1 reference

12 December 2020

Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: a multicenter case-control study

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-13-62

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

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