about
Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from ScandinaviaIntersection of systematic review methodology with the NIH reproducibility initiativeFolate and one-carbon metabolism gene polymorphisms and their associations with oral facial cleftsEvaluation of the association between persistent organic pollutants (POPs) and diabetes in epidemiological studies: a national toxicology program workshop reviewGenetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.Systematic review and evidence integration for literature-based environmental health science assessmentsMaternal alcohol consumption, alcohol metabolism genes, and the risk of oral clefts: a population-based case-control study in Norway, 1996-2001.Standardizing global gene expression analysis between laboratories and across platforms.Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway.Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.Candidate gene analysis in human neural tube defects.Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia.How credible are the study results? Evaluating and applying internal validity tools to literature-based assessments of environmental health hazards.Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study.Safe use of high intakes of folic acid: research challenges and paths forward.The quest for the elusive causative SNP.Apolipoprotein E alleles and sensorineural hearing loss.Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.Forest Plot Viewer: a new graphing tool.Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15
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Abee Lowman Boyles
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0000-0002-8711-2077