1. Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring
   Mengting Sun et al, 2021, BMC Cardiovascular Disorders CrossRef
2. A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate
   Lin Liu et al, 2017, Journal of Craniofacial Surgery CrossRef
3. Association Between MTHFR Polymorphisms and Congenital Heart Disease: A Meta-analysis based on 9,329 cases and 15,076 controls
   Chao Xuan et al, 2014, Scientific Reports CrossRef
4. MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies
   Di Yu et al, 2017, Italian Journal of Pediatrics CrossRef
5. Interactions between genetic and lifestyle factors on cardiometabolic disease-related outcomes in Latin American and Caribbean populations: A systematic review
   Ramatu Wuni et al, 2023, Frontiers in Nutrition CrossRef
6. Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population
   Sumbal Sarwar et al, 2022, Italian Journal of Pediatrics CrossRef
7. Study on Maternal SNPs of MTHFR Gene and HCY Level Related to Congenital Heart Diseases
   Hui Shi et al, 2021, Pediatric Cardiology CrossRef
8. A Common Polymorphism in the MTHFD1 Gene Is a Modulator of Risk of Congenital Heart Disease
   Nataša Karas Kuželički et al, 2022, Journal of Cardiovascular Development and Disease CrossRef
9. Relationship of MTHFD1 G1958A and CBS 844ins68 polymorphism with congenital heart defects in North Indian population (Jammu and Kashmir): A case-control study
   Ankush Bala et al, 2023, Indian Journal of Medical Sciences CrossRef
10. Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study
    Xinli Song et al, 2022, BMC Pregnancy and Childbirth CrossRef
11. Association of Maternal Dietary Habits and MTHFD1 Gene Polymorphisms With Ventricular Septal Defects in Offspring: A Case-Control Study
    Xinli Song et al, 2022, Frontiers in Pediatrics CrossRef
12. The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population
    Teena Koshy et al, 2015, Pediatric Cardiology CrossRef