Alpha 2.0
Login Register
» Articles » PMID: 11186937

Comorbidity of 5,10-methylenetetrahydrofolate Reductase and Methionine Synthase Gene Polymorphisms and Risk for Neural Tube Defects

Overview
Journal J Med Genet
Specialty Genetics
Date 2001 Feb 24
PMID 11186937
Citations 7
Authors
G L Johanning
T Tamura
K E Johnston
K D Wenstrom
Affiliations
Soon will be listed here.
Citing Articles

Folate Pathway Gene Single Nucleotide Polymorphisms and Neural Tube Defects: A Systematic Review and Meta-Analysis.

AlMekkawi A, Aljardali M, Daadaa H, Lane A, Worner A, Karim M J Pers Med. 2022; 12(10).

PMID: 36294748 PMC: 9605131. DOI: 10.3390/jpm12101609.

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.

Pangilinan F, Molloy A, Mills J, Troendle J, Parle-McDermott A, Kay D BMC Med Genet. 2014; 15:102.

PMID: 25293959 PMC: 4411759. DOI: 10.1186/s12881-014-0102-9.

Neural tube defects, folic acid and methylation.

Imbard A, Benoist J, Blom H Int J Environ Res Public Health. 2013; 10(9):4352-89.

PMID: 24048206 PMC: 3799525. DOI: 10.3390/ijerph10094352.

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

Molloy A, Brody L, Mills J, Scott J, Kirke P Birth Defects Res A Clin Mol Teratol. 2009; 85(4):285-94.

PMID: 19235830 PMC: 6129971. DOI: 10.1002/bdra.20566.

Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.

Driscoll D, Boland T, Emanuel B, Kirschner R, LaRossa D, Manson J Cleft Palate Craniofac J. 2006; 43(4):435-41.

PMID: 16854201 PMC: 2818507. DOI: 10.1597/05-070.1.