References
- Botto, L.D. and Yang, Q., 2000. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. American journal of epidemiology, 151 (9), 862–877.
- Botto, L.D., et al., 1999. Neural-tube defects. New England journal of medicine, 341 (20), 1509–1519.
- Copp, A.J. and Greene, N.D.E., 2010. Genetics and development of neural tube defects. The journal of pathology, 220, 217–230.
- De Marco, P., et al., 2011. Human neural tube defects: genetic causes and prevention. Biofactors (Oxford, England), 37, 261–268.
- Deak, K.L., et al., 2008. Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects. Birth defects research: A, 82, 662–669.
- Doudney, K., et al., 2009. Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects. American journal of medical genetics: A, 149A, 1585–1589.
- Guilmatre, A. and Sharp, A.J., 2012. Parent of origin effects. Clinical genetics, 81, 201–209.
- Johnson, W.G., et al., 2004. New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): a risk factor for spina bifida acting in mothers during pregnancy? American journal of medical genetics: A, 124A, 339–345.
- Kalmbach, R.D., et al., 2008. A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate. Journal of nutrition, 138 (12), 2323–2327.
- Li, S., Cui, Y. and Romero, R., 2014. Entropy-based selection for maternal-fetal genotype incompatibility with application to preterm prelabor rupture of membranes. BMC genetics, 15 (1), 66.
- Li, S., et al., 2009. A regularized regression approach for dissecting genetic conflicts that increase disease risk in pregnancy. Statistical applications in genetics and molecular biology, 8 (1), 1–28.
- Li, Y.M. and Xiang, Y., 2017. Detecting disease association with rare variants in case-parents studies. Journal of human genetics, 62 (5), 549.
- Parle-McDermott, A., et al., 2007. The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population. American journal of medical genetics, A, 143A, 1174–1180.
- Safi, J., Joyeux, L., and Chalouhi, G.E., 2012. Periconceptional folate deficiency and implications in neural tube defects. Journal of pregnancy, 2012, Article ID 295083. doi: 10.1155/2012/295083
- Shields, D.C., et al., 1999. The “thermolabile” variant of methylenetetrahydrofolate reductase and neural tube defects: an evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. The American journal of human genetics, 64 (4), 1045–1055.
- Spielman, R.S., McGinnis, R.E., and Ewens, W.J., 1993. Transmission test for linkage disequilibrium: the insulin gene region and insulin dependent diabetes mellitus (IDDM). The American journal of human genetics, 52, 506–516.
- Stanislawska-Sachadyn, A., et al., 2008. An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Human genetics, 123, 289–295.
- Van der Linden, I.J., et al., 2007. Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida. Molecular genetics and metabolism, 91, 98–103.