Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population

25 Mar 2019

Abstract excerpt

Genetic polymorphisms of folate pathway genes have been reported to be associated with congenital heart diseases (CHDs); however, the results remain conflicting. We conducted a family-based case-control study, which included160 CHD case-parent triads and 208 control-parent triads to explore the association of 18 genetic variants of seven folate metabolism-related genes with the risk of CHDs. The MTR C allele of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiovascular Issues in Pregnancy
Share to Congenital Heart Disease Studies
Share to Folate and B Vitamins Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30911047
DOI: 10.1038/s41598-019-41641-z

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese populationPMID 30911047Read ↗

Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study.Semantic proximity Read ↗

Association of maternal folic acid supplementation and offspring MTRR gene polymorphism with congenital heart disease: a hospital-based case-control study in Han populationSemantic proximity Read ↗

Association of maternal folic acid supplementation and offspring MTRR gene polymorphism with congenital heart disease: a hospital-based case-control study in Han population.Semantic proximity Read ↗

Congenital heart disease and folate pathway gene polymorphisms: findings from a North Indian cohort.Semantic proximity Read ↗

Congenital Heart Disease and Genetic Changes in Folate/Methionine Cycles.Semantic proximity Read ↗

[Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].Semantic proximity Read ↗

Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population.Semantic proximity Read ↗

Periconception Red Blood Cell Folate and Offspring Congenital Heart DiseaseSemantic proximity Read ↗

Association of Maternal Folate Intake and Offspring MTHFD1 and MTHFD2 Genes with Congenital Heart DiseaseSemantic proximity Read ↗

[Association between maternal reduced folate carrier gene polymorphisms and congenital heart disease in offspring: a case-control study].Semantic proximity Read ↗

Association between maternal MTHFR and MTRR gene polymorphisms and the risk of congenital heart disease in newbornsSemantic proximity Read ↗

The Roles of Reduced Folate Carrier-1 (RFC1) A80G (rs1051266) Polymorphism in Congenital Heart Disease: A Meta-Analysis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.