(Q33606720)

28 July 2017

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

1 reference

28 July 2017

1 reference

Philip J Lupo

1

0 references

Elizabeth Goldmuntz

series ordinal

2

object named as

Elizabeth Goldmuntz

1 reference

28 July 2017

Laura E Mitchell

3

1 reference

PubMed ID

20111745

28 July 2017

language of work or name

1 reference

12 January 2010

1 reference

Journal of Biomedicine and Biotechnology

28 July 2017

1 reference

28 July 2017

2010

1 reference

28 July 2017

630940

1 reference

Creative Commons Attribution 3.0 Unported

28 July 2017

start time

1 January 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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=2810479

118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart 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=2810479

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Influence of the cystathionine beta-synthase 844ins68 and methylenetetrahydrofolate reductase 677C>T polymorphisms on folate and homocysteine concentrations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

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.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Common genetic polymorphisms affect the human requirement for the nutrient choline

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Racial and temporal variations in the prevalence of heart 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=2810479

Gene-environment and gene-gene interaction in the determination of plasma homocysteine levels in healthy middle-aged men.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Allowing for missing parents in genetic studies of case-parent triads

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Case-only design to measure gene-gene interaction.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

21 June 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Linkage disequilibrium at the cystathionine β synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Polymorphisms in the transcobalamin gene: association with plasma homocysteine in healthy individuals and vascular disease patients.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810479

Case-Only Design to Measure Gene-Gene Interaction

30 October 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2010%2F630940

Role of MTHFR (677, 1298) haplotype in the risk of developing secondary leukemia after treatment of breast cancer and hematological malignancies

21 January 2018

1 reference

12 December 2020

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies

1 reference

12 December 2020

Population stratification bias in the case-only study for gene-environment interactions

1 reference

12 December 2020

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

1 reference

12 December 2020

A common 844INS68 insertion variant in the cystathionine beta-synthase gene

1 reference

12 December 2020

A novel polymorphism in the MCP-1 gene regulatory region that influences MCP-1 expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Evaluation of offspring and maternal genetic effects on disease risk using a family-based approach: the "pent" design

1 reference

12 December 2020

Identifiers

DOI

10.1155/2010/630940

1 reference

release_tsc2ig6vkjedhfphkbjclzowjm

28 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tsc2ig6vkjedhfphkbjclzowjm

24 November 2022

mapped directly with Wikidata item

PMCID

2810479

1 reference

28 July 2017

1 reference

PubMed ID

20111745