(Q50967534)

26 March 2018

title

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease. (English)

1 reference

26 March 2018

1 reference

Benjing Wang

1

1 reference

26 March 2018

Minjuan Liu

2

1 reference

26 March 2018

Wenhua Yan

3

1 reference

26 March 2018

Jun Mao

4

1 reference

26 March 2018

Dong Jiang

5

1 reference

26 March 2018

Hong Li

6

1 reference

26 March 2018

Ying Chen

7

1 reference

26 March 2018

publication date

10 June 2013

1 reference

26 March 2018

Journal of Maternal-Fetal and Neonatal Medicine

published in

1 reference

26 March 2018

volume

26

1 reference

26 March 2018

issue

18

1 reference

26 March 2018

page(s)

1768-1777

1 reference

26 March 2018

The changing epidemiology of congenital heart disease

cites work

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Prevalence of severe congenital heart disease after folic acid fortification of grain products: time trend analysis in Quebec, Canada

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

The MTHFR 677C->T polymorphism and the risk of congenital heart defects: a literature review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Role of polymorphisms in MTHFR and MTHFD1 genes in the outcome of childhood acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Human methionine synthase. cDNA cloning, gene localization, and expression

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Genetic basis of neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Polymorphism of the methionine synthase gene : association with homocysteine metabolism and late-onset vascular diseases in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

Abnormal folate metabolism in foetuses affected by neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Variants of folate metabolism genes and the risk of conotruncal cardiac defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Biochemistry and molecular genetics of cystathionine beta-synthase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Reduced folate carrier polymorphisms and neural tube defect risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Intron 1 and the 5'-flanking region of the human thymidylate synthase gene as a regulatory determinant of growth-dependent expression

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Transcobalamin C776G genotype modifies the association between vitamin B12 and homocysteine in older Hispanics

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Characterization of the human Omega class glutathione transferase genes and associated polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism and the age-at-onset of Alzheimer's and Parkinson's diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

NFE2L2 gene mutation in male Japanese squamous cell carcinoma of the lung

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Cancer chemoprevention mechanisms mediated through the Keap1-Nrf2 pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

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/10.3109%2F14767058.2013.799648

10.3109/14767058.2013.799648

21 January 2018

Identifiers

DOI

1 reference

26 March 2018

PubMed ID

23701284

1 reference

26 March 2018