The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects-Reference-Cited by-同舟云学术

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The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects

Published:2009-04 Issue:4 Volume:85 Page:285-294
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defect Res A

Author:

Molloy Anne M.,Brody Lawrence C.,Mills James L.,Scott John M.,Kirke Peadar N.

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference129 articles.

1. Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects;Afman;Mol Genet Metab,2003

2. The H475Y polymorphism in the glutamate carboxypeptidase II gene increases plasma folate without affecting the risk for neural tube defects in humans;Afman;J Nutr,2003

3. Non-Latin European descent could be a requirement for association of NTDs and MTHFR variant 677C > T: a meta-analysis;Amorim;Am J Med Genet A,2007

4. Genome studies: genetics by numbers;Baker;Nature,2008

5. Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population;Barber;Mol Genet Metab,2000

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4. Folate Pathway Gene Single Nucleotide Polymorphisms and Neural Tube Defects: A Systematic Review and Meta-Analysis;Journal of Personalized Medicine;2022-09-29

5. Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study;BMC Pregnancy and Childbirth;2022-01-31

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