(Q21089859)

English

Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies

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scholarly article

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Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies (English)

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author name string

Lifeng Yan

1

author given names

Lifeng

author last names

Yan

1 reference

PubMed publication ID

8 August 2022

Lin Zhao

2

author given names

Lin

author last names

Zhao

1 reference

PubMed publication ID

8 August 2022

Yan Long

3

author given names

Yan

author last names

Long

1 reference

PubMed publication ID

8 August 2022

Peng Zou

4

author given names

Peng

author last names

Zou

1 reference

PubMed publication ID

8 August 2022

Guixiang Ji

5

author given names

Guixiang

author last names

Ji

1 reference

PubMed publication ID

8 August 2022

Aihua Gu

6

author given names

Aihua

author last names

Gu

1 reference

PubMed publication ID

8 August 2022

Peng Zhao

7

author given names

Peng

author last names

Zhao

1 reference

PubMed publication ID

8 August 2022

language of work or name

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publication date

2012

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7

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10

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e41689

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copyright license

Creative Commons Attribution 4.0 International

3 October 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

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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.

1 reference

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19 March 2017

Bias in meta-analysis detected by a simple, graphical test

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19 March 2017

Statistical aspects of the analysis of data from retrospective studies of disease

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19 March 2017

Meta-analysis in clinical trials

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19 March 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

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

1 reference

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19 March 2017

A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis

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19 March 2017

MTHFR polymorphisms and breast cancer risk.

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12 September 2017

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria

1 reference

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12 September 2017

Importance of methyl donors during reproduction

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12 September 2017

Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Polymorphisms in genes involved in folate metabolism and colorectal neoplasia: a HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Folate, homocysteine and neural tube defects: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Biological and clinical implications of the MTHFR C677T polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Neural tube defects and a disturbed folate dependent homocysteine metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Susceptibility to spina bifida; an association study of five candidate genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Folate status, homocysteine metabolism, and methylene tetrahydrofolate reductase genotype in rural South African blacks with a history of pregnancy complicated by neural tube defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

12 September 2017

Methylenetetrahydrofolate reductase gene polymorphisms and the risk of anencephaly in Mexico.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

27 September 2017

Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

27 September 2017

Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

27 September 2017

Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

30 May 2018

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

30 May 2018

Effect on risk of anencephaly of gene-nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Methionine synthase reductase A66G polymorphism contributes to tumor susceptibility: evidence from 35 case-control studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

A case-control study on the risk factors of neural tube defects in Shanxi province

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Screening for new MTHFR polymorphisms and NTD risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Exploring gene-gene interactions in the etiology of neural tube defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463537

29 November 2018

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism of the methionine synthase gene: association with plasma folate, vitamin B12, homocyst(e)ine, and colorectal cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 677 C-->T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of colorectal cancer associated with the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in the Kashmiri population

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR)

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The common C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with neural tube defects and preeclampsia]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23056169

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0041689

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2012PLoSO...741689Y

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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