118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects (Q33459545)

27 July 2017

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

1 reference

27 July 2017

1 reference

Richard H Finnell

9

0 references

Suzan L Carmichael

series ordinal

6

object named as

Suzan L Carmichael

1 reference

27 July 2017

1

Gary M Shaw

1 reference

27 July 2017

7

Lisa F Barcellos

1 reference

27 July 2017

8

Edward J Lammer

1 reference

27 July 2017

3

Huiping Zhu

1 reference

27 July 2017

Wei Lu

2

1 reference

27 July 2017

Wei Yang

series ordinal

4

1 reference

27 July 2017

Farren B S Briggs

series ordinal

5

1 reference

27 July 2017

3 June 2009

1 reference

27 July 2017

1 reference

27 July 2017

10

1 reference

27 July 2017

49

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-49

27 July 2017

0 references

cites work

Methionine synthase reductase deficiency results in adverse reproductive outcomes and congenital heart defects in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Multiple displacement amplification to create a long-lasting source of DNA for genetic studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Genetic variation in genes of folate metabolism and neural-tube defect risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Effects of DNA mass on multiple displacement whole genome amplification and genotyping performance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Exploring whole genome amplification as a DNA recovery tool for molecular genetic studies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Redox regulation and reaction mechanism of human cystathionine-beta-synthase: a PLP-dependent hemesensor protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Distribution of mutations in human thymidylate synthase yielding resistance to 5-fluorodeoxyuridine

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Thymidylate synthase as a translational regulator of cellular gene expression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Point: population stratification: a problem for case-control studies of candidate-gene associations?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Maternal multivitamin use and orofacial clefts in offspring

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Oral clefts and vitamin supplementation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Quality control of birth defect registry data: a case study.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Birth defects monitoring in California: a resource for epidemiological research

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Risks of orofacial clefts in children born to women using multivitamins containing folic acid periconceptionally

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Hungarian cohort-controlled trial of periconceptional multivitamin supplementation shows a reduction in certain congenital abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Association between 5,10-Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms and Conotruncal Heart Defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Reduced folate carrier polymorphism (80A-->G) and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

Multivitamin Supplementation and Risk of Brith Defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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%2F1471-2350-10-49

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Counterpoint: bias from population stratification is not a major threat to the validity of conclusions from epidemiological studies of common polymorphisms and cancer.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700092

Methylenetetrahydrofolate reductase mutation and neural tube defects

31 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-49

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%2F1471-2350-10-49

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%2F1471-2350-10-49

Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes

21 January 2018

1 reference

12 December 2020

Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism

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

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

12 December 2020

Is mutated MTHFR a risk factor for neural tube defects?

1 reference

12 December 2020

Reduction of urinary tract and cardiovascular defects by periconceptional multivitamin supplementation

1 reference

12 December 2020

Population-based case control study of folic acid supplementation during pregnancy

1 reference

12 December 2020

Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring

1 reference

12 December 2020

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

1 reference

12 December 2020

Occurrence of congenital heart defects in relation to maternal mulitivitamin use

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-10-49

1 reference

Dimensions Publication ID

27 July 2017

0 references

1 reference

27 July 2017

1 reference