Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation.

The continuing challenge of understanding, preventing, and treating neural tube defects. Science (2013) 1.86

Neural tube defects. Annu Rev Neurosci (2014) 1.69

How to form and close the brain: insight into the mechanism of cranial neural tube closure in mammals. Cell Mol Life Sci (2012) 0.92

Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice. Nat Commun (2015) 0.91

No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generations. Mamm Genome (2013) 0.82

When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome. Philos Trans R Soc Lond B Biol Sci (2017) 0.81

Modeling anterior development in mice: diet as modulator of risk for neural tube defects. Am J Med Genet C Semin Med Genet (2013) 0.81

Spina bifida. Nat Rev Dis Prim (2015) 0.77

Blastopathies and microcephaly in a Chornobyl impacted region of Ukraine. Congenit Anom (Kyoto) (2014) 0.76

Maternal and infant factors associated with infancy-onset hydrocephalus in Washington State. Pediatr Neurol (2014) 0.75

Comment on changes in sex ratio in neural tube defects since food fortification with folic acid: re "hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural tube fold elevation". Birth Defects Res A Clin Mol Teratol (2012) 0.75

Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse. J Virol (2003) 2.33

Mouse genetic models of cleft lip with or without cleft palate. Birth Defects Res A Clin Mol Teratol (2008) 1.41

Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Birth Defects Res A Clin Mol Teratol (2006) 1.39

Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Birth Defects Res A Clin Mol Teratol (2005) 1.21

A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects. Birth Defects Res A Clin Mol Teratol (2012) 1.12

A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci. Birth Defects Res A Clin Mol Teratol (2004) 1.07

The clf2 gene has an epigenetic role in the multifactorial etiology of cleft lip and palate in the A/WySn mouse strain. Birth Defects Res A Clin Mol Teratol (2011) 0.80

Why take an HIV test? Concerns, benefits, and strategies to promote HIV testing among low-income heterosexual African American young adults. Health Educ Behav (2011) 0.80

Accelerated embryonic development associated with increased risk of neural tube defects induced by maternal diet in offspring of SELH/Bc mice. Birth Defects Res A Clin Mol Teratol (2008) 0.79

The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Genomics (2005) 0.78

Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. Birth Defects Res A Clin Mol Teratol (2014) 0.76