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Journal of Human Genetics|May 6, 2003
Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defectsAnne Parle-McDermott, James L Mills, Peadar N Kirke, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish populationFaith Pangilinan, Kerry Geiler, Jessica Dolle, et al.
American Journal of Medical Genetics. Part A|May 9, 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 populationAnne Parle-McDermott, Faith Pangilinan, James L Mills, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study populationTonia C Carter, Faith Pangilinan, James F Troendle, et al.
BMC Medicine|July 27, 2025
Associations of one-carbon metabolism, related B-vitamins and ApoE genotype with cognitive function in older adults: identification of a novel gene-nutrient interactionShane Gordon, Leane Hoey, Helene McNulty, et al.
The American Journal of Clinical Nutrition|October 20, 2018
The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish populationBarry Shane, Faith Pangilinan, James L Mills, et al.
Molecular Genetics and Metabolism|June 28, 2005
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk associationValerie B O'Leary, James L Mills, Faith Pangilinan, et al.
Molecular Genetics and Metabolism|June 18, 2003
Analysis of the human folate receptor beta gene for an association with neural tube defectsValerie B O'Leary, James L Mills, Peadar N Kirke, et al.
Molecular Genetics and Metabolism|December 5, 2003
Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defectsAnne Parle-McDermott, Edward J McManus, James L Mills, et al.
Human Molecular Genetics|October 18, 2017
The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylationAneliya Velkova, Jennifer E L Diaz, Faith Pangilinan, et al.
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