“Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis”

MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases

(2013) Haidy E. Zidan et al.   GENE

Genetic Variants in the Folate Pathway and the Risk of Neural Tube Defects: A Meta-Analysis of the Published Literature

(2013) Ti Zhang et al.   PLoS One

The importance of rapid aneuploidy screening and prenatal diagnosis in the detection of numerical chromosomal abnormalities

(2013) Ghada M Elsayed et al.   SpringerPlus

Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: A meta-analysis

(2012) Shengrong Ouyang et al.   GENE

MTHFR 677T variant contributes to diabetic nephropathy risk in Caucasian individuals with type 2 diabetes: A meta-analysis

(2012) Sheng Yang et al.   METABOLISM-CLINICAL AND EXPERIMENTAL

Association of the Maternal MTHFR C677T Polymorphism with Susceptibility to Neural Tube Defects in Offsprings: Evidence from 25 Case-Control Studies

(2012) Lifeng Yan et al.   PLoS One

Effect on risk of anencephaly of gene–nutrient interactions between methylenetetrahydrofolate reductase C677T polymorphism and maternal folate, vitamin B12 and homocysteine profile

(2012) Marina Lacasaña et al.   PUBLIC HEALTH NUTRITION

Association Between Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR) C677T and Risk of Myocardial Infarction: A Meta-analysis for 8,140 Cases and 10,522 Controls

(2011) Chao Xuan et al.   ARCHIVES OF MEDICAL RESEARCH

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India

(2011) Koumudi Godbole et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Folate supplementation, MTHFR gene polymorphism and neural tube defects: a community based case control study in North India

(2011) Roumi Deb et al.   METABOLIC BRAIN DISEASE

Meta-analysis of MTHFR gene variants in schizophrenia, bipolar disorder and unipolar depressive disorder: Evidence for a common genetic vulnerability?

(2010) Odette L.J. Peerbooms et al.   BRAIN BEHAVIOR AND IMMUNITY

C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects

(2010) M.O. Erdogan et al.   GENETICS AND MOLECULAR RESEARCH

Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects

(2010) Poomagame Narasimhamurthy Harisha et al.   Journal of Neurosurgery-Pediatrics

Polymorphisms of 5,10-Methylenetetrahydrofolate Reductase and Cystathionine β-Synthase Genes as a Risk Factor for Neural Tube Defects in Sétif, Algeria

(2010) Bakhouche Houcher et al.   PEDIATRIC NEUROSURGERY

Mutation Analysis of the PVRL1 Gene in Caucasians with Nonsyndromic Cleft Lip/Palate

(2009) Mehmet A. Sözen et al.   Genetic Testing and Molecular Biomarkers

Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India

(2009) Shaik Mohammad Naushad et al.   JOURNAL OF PERINATAL MEDICINE

Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: A multicenter case–control study

(2008) Mirande Candito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Thrombophilia-associated gene mutations in women with pregnancies complicated by fetal neural tube defects

(2008) Seyit Temel Ceyhan et al.   INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS

Correlation of polymorphism ofMTHFRs andRFC-1 genes with neural tube defects in China

(2007) Yali Shang et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY