Published in Cleft Palate Craniofac J on September 01, 2004
Association of generalized aggressive periodontitis and ectrodactyly-ectodermal dysplasia-cleft syndrome. Indian J Hum Genet (2012) 0.84
LADD syndrome with glaucoma is caused by a novel gene. Mol Vis (2017) 0.75
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet (2002) 6.29
Maternal periconceptional vitamins: interactions with selected factors and congenital anomalies? Epidemiology (2002) 1.93
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects. BMC Med Genet (2009) 1.74
Maternal smoking and environmental tobacco smoke exposure and the risk of orofacial clefts. Epidemiology (2007) 1.67
NAT2 variation and idiopathic talipes equinovarus (clubfoot). Am J Med Genet A (2007) 1.57
Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004. Am J Med Genet A (2009) 1.55
Schizencephaly: heterogeneous etiologies in a population of 4 million California births. Am J Med Genet A (2005) 1.55
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Hum Mol Genet (2009) 1.55
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects. Am J Med Genet A (2013) 1.48
Diacylglycerol kinase K variants impact hypospadias in a California study population. J Urol (2012) 1.43
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome. Am J Hum Genet (2012) 1.39
Maternal corticosteroid use and orofacial clefts. Am J Obstet Gynecol (2007) 1.34
Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis. Birth Defects Res A Clin Mol Teratol (2006) 1.25
Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab (2003) 1.25
Patterns of infantile hemangiomas: new clues to hemangioma pathogenesis and embryonic facial development. Pediatrics (2006) 1.24
Comprehensive EMX2 genotyping of a large schizencephaly case series. Am J Med Genet A (2007) 1.22
Integration of DNA sample collection into a multi-site birth defects case-control study. Teratology (2002) 1.22
Association between a leukotriene C4 synthase gene promoter polymorphism and coronary artery calcium in young women: the Muscatine Study. Arterioscler Thromb Vasc Biol (2006) 1.19
Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes. Am J Med Genet A (2005) 1.18
Environmental and genetic contributors to hypospadias: a review of the epidemiologic evidence. Birth Defects Res A Clin Mol Teratol (2012) 1.17
Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida. Am J Med Genet (2002) 1.17
Maternal periconceptional smoking and alcohol consumption and risk for select congenital anomalies. Birth Defects Res A Clin Mol Teratol (2008) 1.15
Maternal reproductive and demographic characteristics as risk factors for hypospadias. Paediatr Perinat Epidemiol (2007) 1.13
Embryonic development of folate binding protein-1 (Folbp1) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation. Dev Dyn (2004) 1.10
Maternal stressful life events and risks of birth defects. Epidemiology (2007) 1.06
Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts? Am J Med Genet A (2005) 1.04
Endothelial nitric oxide synthase (NOS3) genetic variants, maternal smoking, vitamin use, and risk of human orofacial clefts. Am J Epidemiol (2005) 1.04
Maternal progestin intake and risk of hypospadias. Arch Pediatr Adolesc Med (2005) 1.04
Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997. Am J Med Genet A (2005) 1.04
Autoantibodies to folate receptor during pregnancy and neural tube defect risk. J Reprod Immunol (2008) 1.03
Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome. Am J Med Genet A (2007) 1.01
Maternal occupational exposure to polycyclic aromatic hydrocarbons and risk of neural tube defect-affected pregnancies. Birth Defects Res A Clin Mol Teratol (2012) 1.00
Fetal constraint as a potential risk factor for craniosynostosis. Am J Med Genet A (2010) 1.00
Associations between polymorphisms within the thymidylate synthase gene and spina bifida. Birth Defects Res A Clin Mol Teratol (2003) 0.99
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects. Am J Epidemiol (2003) 0.98
A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis. PLoS One (2011) 0.96
Maternal and infant gene-folate interactions and the risk of neural tube defects. Am J Med Genet A (2012) 0.95
Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft. Am J Med Genet A (2008) 0.94
Maternal occupational chemical exposures and biotransformation genotypes as risk factors for selected congenital anomalies. Am J Epidemiol (2003) 0.93
Gene-nutrient interactions: importance of folates and retinoids during early embryogenesis. Toxicol Appl Pharmacol (2004) 0.92
Hypospadias and residential proximity to pesticide applications. Pediatrics (2013) 0.91
Craniosynostosis and nutrient intake during pregnancy. Birth Defects Res A Clin Mol Teratol (2010) 0.88
Craniosynostosis and maternal smoking. Birth Defects Res A Clin Mol Teratol (2008) 0.88
Screening for novel PAX3 polymorphisms and risks of spina bifida. Birth Defects Res A Clin Mol Teratol (2007) 0.88
Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida. Am J Med Genet A (2006) 0.87
Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects. Mol Genet Metab (2004) 0.87
Maternal periconceptional alcohol consumption and risk for conotruncal heart defects. Birth Defects Res A Clin Mol Teratol (2003) 0.86
Hypospadias and genes related to genital tubercle and early urethral development. J Urol (2013) 0.85
CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population. BMC Med (2006) 0.85
Periconceptional nutrient intakes and risks of conotruncal heart defects. Birth Defects Res A Clin Mol Teratol (2010) 0.85
Candidate gene polymorphisms do not differ between newborns with stroke and normal controls. Stroke (2006) 0.84
Hypospadias and maternal exposures to cigarette smoke. Paediatr Perinat Epidemiol (2005) 0.84
Maternal occupational exposure to polycyclic aromatic hydrocarbons and risk of oral cleft-affected pregnancies. Cleft Palate Craniofac J (2012) 0.84
Thymidylate synthase polymorphisms and risks of human orofacial clefts. Birth Defects Res A Clin Mol Teratol (2013) 0.83
Planar cell polarity pathway genes and risk for spina bifida. Am J Med Genet A (2010) 0.83
Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida. Birth Defects Res A Clin Mol Teratol (2003) 0.83
Congenital malformations in births with orofacial clefts among 3.6 million California births, 1983-1997. Am J Med Genet A (2004) 0.83
Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory response, and blood pressure regulation. Am J Med Genet A (2006) 0.83
Autosomal recessive frontotemporal pachygyria. Am J Med Genet A (2004) 0.83
Maternal smoking during early pregnancy, GSTP1 and EPHX1 variants, and risk of isolated orofacial clefts. Cleft Palate Craniofac J (2007) 0.83
A known functional polymorphism (Ile120Val) of the human PCMT1 gene and risk of spina bifida. Mol Genet Metab (2005) 0.82
Evaluation of the Cited2 gene and risk for spina bifida and congenital heart defects. Am J Med Genet A (2004) 0.82
Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defects. Am J Med Genet A (2012) 0.81
Association between CFL1 gene polymorphisms and spina bifida risk in a California population. BMC Med Genet (2007) 0.81
Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects. Am J Med Genet A (2004) 0.81
Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense? Genet Test (2002) 0.80
Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects. Birth Defects Res A Clin Mol Teratol (2003) 0.80
Limb deficiency defects, MSX1, and exposure to tobacco smoke. Am J Med Genet A (2004) 0.79
Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study. BMC Med Genet (2010) 0.79
Corticosteroid use and risk of orofacial clefts. Birth Defects Res A Clin Mol Teratol (2014) 0.79
One-carbon metabolite levels in mid-pregnancy and risks of conotruncal heart defects. Birth Defects Res A Clin Mol Teratol (2014) 0.79
Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes. Birth Defects Res A Clin Mol Teratol (2010) 0.79
Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. Am J Med Genet A (2009) 0.78
Genes encoding catalytic subunits of protein kinase A and risk of spina bifida. Birth Defects Res A Clin Mol Teratol (2005) 0.78
Gene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis. Food Nutr Bull (2008) 0.78
Association between 49 infant gene polymorphisms and preterm delivery. Am J Med Genet A (2007) 0.77
Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida. Teratology (2002) 0.76
Thymidylate synthase polymorphisms and risk of conotruncal heart defects. Am J Med Genet A (2012) 0.76
Lack of association between ZIC2 and ZIC3 genes and the risk of neural tube defects (NTDs) in Hispanic populations. Am J Med Genet A (2003) 0.76
Nicotinamide N-methyl transferase (NNMT) gene polymorphisms and risk for spina bifida. Birth Defects Res A Clin Mol Teratol (2008) 0.76
Genetic variation in the proto-oncogene SKI and risk for orofacial clefting. Mol Genet Metab (2005) 0.75
Is Sonic hedgehog (SHH) a candidate gene for spina bifida? A pilot study. Am J Med Genet A (2003) 0.75
Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly. Am J Med Genet (2002) 0.75
Nutrient intakes in women and risks of anophthalmia and microphthalmia in their offspring. Birth Defects Res A Clin Mol Teratol (2007) 0.75
Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: a case control study of genetic factors. Am J Med Genet A (2013) 0.75
The READIT assay as a method for genotyping NAT1*10 polymorphisms. Genet Test (2002) 0.75