(Q35671289)

English

Evaluation of heterogeneity in the association between congenital heart defects and variants of folate metabolism genes: conotruncal and left-sided cardiac defects

scientific article published on 24 August 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 August 2017

Evaluation of heterogeneity in the association between congenital heart defects and variants of folate metabolism genes: conotruncal and left-sided cardiac defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

congenital disorder

0 references

1 reference

based on heuristic

inferred from title

Elizabeth Goldmuntz

3

object named as

Elizabeth Goldmuntz

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

Jin Long

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Philip J Lupo

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Laura E Mitchell

4

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

publication date

24 August 2011

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Birth Defects Research Part A: Clinical and Molecular Teratology

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

91

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

879-884

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

Variants of folate metabolism genes and risk of left-sided cardiac defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

Maternal effects as the cause of parent-of-origin effects that mimic genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

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=3257803

12 July 2018

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=3257803

12 July 2018

Testing for linkage disequilibrium, maternal effects, and imprinting with (In)complete case-parent triads, by use of the computer program LEM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

The use of case-parent triads to study joint effects of genotype and exposure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3257803

12 July 2018

Increased prevalence of cardiovascular defects among 56,709 California twin pairs.

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.22849

21 January 2018

Congenital heart defects, maternal homocysteine, smoking, and the 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene: evaluating gene-environment interactions

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.22849

21 January 2018

Distinguishing the Effects of Maternal and Offspring Genes through Studies of "Case-Parent Triads"

1 reference

https://api.crossref.org/works/10.1002%2FBDRA.22849

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21987465

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/21987465

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrence of Congenital Heart Defects in Families

1 reference

https://pubmed.ncbi.nlm.nih.gov/21987465

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/BDRA.22849

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

ResearchGate publication ID

0 references

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