Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome-Reference-Cited by-同舟云学术

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome

Published:2010-08-17 Issue:6 Volume:34 Page:613-623
ISSN:0741-0395
Container-title:Genetic Epidemiology
language:en
Short-container-title:Genet. Epidemiol.

Author:

Locke Adam E.,Dooley Kenneth J.,Tinker Stuart W.,Cheong Soo Yeon,Feingold Eleanor,Allen Emily G.,Freeman Sallie B.,Torfs Claudine P.,Cua Clifford L.,Epstein Michael P.,Wu Michael C.,Lin Xihong,Capone George,Sherman Stephanie L.,Bean Lora J.H.

Publisher

Wiley

Subject

Genetics (clinical),Epidemiology

Reference52 articles.

1. Folic acid supplementation and the occurrence of congenital heart defects, orofacial clefts, multiple births, and miscarriage;Bailey;Am J Clin Nutr,2005

2. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

3. Do multivitamin or folic acid supplements reduce the risk for congenital heart defects? Evidence and gaps;Botto;Am J Med Genet A,2003

4. Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts;Boyles;Am J Med Genet A,2008

5. Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study;Boyles;Genet Epidemiol,2009

Cited by 65 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies;Current Problems in Cardiology;2024-09

2. Congenital Heart Disease and Genetic Changes in Folate/Methionine Cycles;Genes;2024-07-02

3. Human Genetics of Atrioventricular Septal Defect;Advances in Experimental Medicine and Biology;2024

4. Association of C677T and A1298C polymorphisms of the MTHFR gene with maternal risk for Down syndrome: A meta-analysis of case-control studies;Mutation Research/Reviews in Mutation Research;2023-07

5. Gene-dosage imbalance due to trisomic HSA21 and genotype–phenotype association in Down syndrome;Genetics and Neurobiology of Down Syndrome;2022