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Birth Defects Research. Part A, Clinical and Molecular Teratology|November 26, 2009
Testing reported associations of genetic risk factors for oral clefts in a large Irish study populationTonia C Carter, Anne M Molloy, Faith Pangilinan, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2008
Folate-related gene polymorphisms as risk factors for cleft lip and cleft palateJames L Mills, Anne M Molloy, Anne Parle-McDermott, et al.
BMC Medical Genetics|October 9, 2014
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
The Journal of Nutrition|May 15, 2015
Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy AdultsTonia C Carter, Faith Pangilinan, Anne M Molloy, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 23, 2005
Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish populationDeborah A Swanson, Faith Pangilinan, James L Mills, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral cleftsJulia E VanderMeer, Tonia C Carter, Faith Pangilinan, et al.
American Journal of Medical Genetics. Part A|February 2, 2022
Probing the functional consequence and clinical relevance of CD320 p.E88del, a variant in the transcobalamin receptor geneFaith Pangilinan, David Watkins, David Bernard, et al.
American Journal of Human Genetics|May 3, 2016
A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of CobalaminAnne M Molloy, Faith Pangilinan, James L Mills, et al.
BMC Medical Genetics|August 4, 2012
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defectsFaith Pangilinan, Anne M Molloy, James L Mills, et al.
American Journal of Medical Genetics. Part A|August 6, 2021
Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 childrenGeorgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, et al.
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