(Q37373025)

English

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

20 August 2017

0 references

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls (English)

1 reference

Europe PubMed Central

20 August 2017

congenital disorder

0 references

congenital heart disease

1 reference

based on heuristic

inferred from title

12

object named as

Diana Zelenika

1 reference

Europe PubMed Central

20 August 2017

37

object named as

G Mark Lathrop

1 reference

Europe PubMed Central

20 August 2017

Chrysovalanto Mamasoula

1

object named as

Chrysovalanto Mamasoula

1 reference

Europe PubMed Central

20 August 2017

9

object named as

Darroch Hall

1 reference

Europe PubMed Central

20 August 2017

27

object named as

David Winlaw

1 reference

Europe PubMed Central

20 August 2017

object named as

Huay L Tan

23

0 references

Shoumo Bhattacharya

object named as

Shoumo Bhattacharya

15

0 references

object named as

Alex V Postma

28

0 references

object named as

Marc Gewillig

34

0 references

object named as

James L Mills

5

0 references

33

object named as

Anita Rauch

1 reference

Europe PubMed Central

20 August 2017

A. Graham Stuart

25

object named as

A Graham Stuart

1 reference

Europe PubMed Central

20 August 2017

Heather Cordell

object named as

Heather J Cordell

40

1 reference

ORCID Public Data File 2021

Bernard Keavney

1 reference

ORCID Public Data File 2021

Judith A Goodship

39

object named as

Judith A Goodship

1 reference

Europe PubMed Central

20 August 2017

Javier T Granados-Riveron

16

object named as

Javier Granados Riveron

1 reference

Europe PubMed Central

20 August 2017

13

object named as

Jamie Bentham

1 reference

Europe PubMed Central

20 August 2017

Catherine Cosgrove

14

object named as

Catherine Cosgrove

1 reference

Europe PubMed Central

20 August 2017

Jeroen Breckpot

35

object named as

Jeroen Breckpot

1 reference

Europe PubMed Central

20 August 2017

Kerry Setchfield

17

object named as

Kerry Setchfield

1 reference

Europe PubMed Central

20 August 2017

Chris Thornborough

20

object named as

Chris Thornborough

1 reference

Europe PubMed Central

20 August 2017

21

object named as

Thahira J Rahman

1 reference

Europe PubMed Central

20 August 2017

26

object named as

Gillian Blue

1 reference

Europe PubMed Central

20 August 2017

10

object named as

Ana Töpf

1 reference

Europe PubMed Central

20 August 2017

Aelko H. Zwinderman

30

object named as

Aelko H Zwinderman

1 reference

Europe PubMed Central

20 August 2017

Antoon F. M. Moorman

32

object named as

Antoon F M Moorman

1 reference

Europe PubMed Central

20 August 2017

38

object named as

Martin Farrall

1 reference

Europe PubMed Central

20 August 2017

Julian Palomino Doza

22

object named as

Julian Palomino Doza

1 reference

Europe PubMed Central

20 August 2017

Klaartje van Engelen

31

object named as

Klaartje van Engelen

1 reference

Europe PubMed Central

20 August 2017

36

object named as

Koen Devriendt

1 reference

Europe PubMed Central

20 August 2017

author name string

R Reid Prentice

2

1 reference

Europe PubMed Central

20 August 2017

Tomasz Pierscionek

3

1 reference

Europe PubMed Central

20 August 2017

Faith Pangilinan

4

1 reference

Europe PubMed Central

20 August 2017

Charlotte Druschel

6

1 reference

Europe PubMed Central

20 August 2017

Kenneth Pass

7

1 reference

Europe PubMed Central

20 August 2017

Mark W Russell

8

1 reference

Europe PubMed Central

20 August 2017

Danielle L Brown

11

1 reference

Europe PubMed Central

20 August 2017

J David Brook

18

1 reference

Europe PubMed Central

20 August 2017

Frances A Bu'Lock

19

1 reference

Europe PubMed Central

20 August 2017

John O'Sullivan

24

1 reference

Europe PubMed Central

20 August 2017

Barbara J M Mulder

29

1 reference

Europe PubMed Central

20 August 2017

Lawrence C Brody

41

1 reference

Europe PubMed Central

20 August 2017

Bernard D Keavney

42

1 reference

Europe PubMed Central

20 August 2017

publication date

22 July 2013

1 reference

Europe PubMed Central

20 August 2017

Circulation: Cardiovascular Genetics

1 reference

Europe PubMed Central

20 August 2017

6

1 reference

Europe PubMed Central

20 August 2017

4

1 reference

Europe PubMed Central

20 August 2017

347-353

1 reference

Europe PubMed Central

20 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Meta analysis of the association between MTHFR C677T polymorphism and the risk of congenital heart defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Meta-analysis, funnel plots and sensitivity analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Quantifying heterogeneity in a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

The incidence of congenital heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 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=3855044

6 September 2017

Periconceptional folic acid containing multivitamin supplementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

6 September 2017

Random-effects meta-analyses are not always conservative.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

26 June 2018

Periconceptional multivitamin use and the occurrence of conotruncal heart defects: results from a population-based, case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

26 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3855044

2 September 2018

Non-Latin European descent could be a requirement for association of NTDs and MTHFR variant 677C > T: a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23876493

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Occurrence of congenital heart defects in relation to maternal mulitivitamin use

1 reference

https://pubmed.ncbi.nlm.nih.gov/23876493

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23876493

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multivitamin Supplementation and Risk of Brith Defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/23876493

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase C677T polymorphism and congenital heart disease: a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23876493

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1161/CIRCGENETICS.113.000191

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37373025&oldid=1858780317"