Faith Pangilinan

Faith Pangilinan

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Faith Pangilinan

Faith Pangilinan

Publications by authors named "Faith Pangilinan"

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39Publications

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Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.

Mol Genet Metab Rep 2019 Dec 11;21:100518. Epub 2019 Oct 11.

Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.

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http://dx.doi.org/10.1016/j.ymgmr.2019.100518DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796782PMC
December 2019

Mice lacking the transcobalamin-vitamin B12 receptor, CD320, suffer from anemia and reproductive deficits when fed vitamin B12-deficient diet.

Hum Mol Genet 2018 10;27(20):3627-3640

Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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https://academic.oup.com/hmg/article/27/20/3627/5067847
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http://dx.doi.org/10.1093/hmg/ddy267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168973PMC
October 2018

The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites.

Mol Genet Metab Rep 2018 Sep 11;16:20-22. Epub 2018 Jun 11.

Department of Clinical Medicine, School of Medicine, Trinity College Dublin 2, Ireland.

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http://dx.doi.org/10.1016/j.ymgmr.2018.05.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034155PMC
September 2018

Genetic Risk Factors for Folate-Responsive Neural Tube Defects.

Annu Rev Nutr 2017 08 19;37:269-291. Epub 2017 Jun 19.

Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892; email: ,

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http://dx.doi.org/10.1146/annurev-nutr-071714-034235DOI Listing
August 2017

Association of a transcobalamin II genetic variant with falsely low results for the holotranscobalamin immunoassay.

Eur J Clin Invest 2016 May 15;46(5):434-9. Epub 2016 Apr 15.

Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.

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http://dx.doi.org/10.1111/eci.12617DOI Listing
May 2016

Association of Transcobalamin II (TCN2) and Transcobalamin II-Receptor (TCblR) Genetic Variations With Cobalamin Deficiency Parameters in Elderly Women.

Biol Res Nurs 2015 Jul 5;17(4):444-54. Epub 2015 Feb 5.

Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA

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http://journals.sagepub.com/doi/ 10.1177/1099800415569506
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http://dx.doi.org/10.1177/1099800415569506DOI Listing
July 2015

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.

BMC Med Genet 2014 Oct 8;15:102. Epub 2014 Oct 8.

Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Room 5306, 50 South Drive, Bethesda, MD, 20892-8004, USA.

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http://dx.doi.org/10.1186/s12881-014-0102-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411759PMC
October 2014

Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

Am J Med Genet A 2011 Jan 10;155A(1):14-21. Epub 2010 Dec 10.

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892-7510, USA.

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http://dx.doi.org/10.1002/ajmg.a.33755DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503244PMC
January 2011

Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.

Birth Defects Res A Clin Mol Teratol 2010 Feb;88(2):84-93

Division of Epidemiology, Statistics, and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/bdra.20639DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503531PMC
February 2010

Uncoupling protein 2 polymorphisms as risk factors for NTDs.

Birth Defects Res A Clin Mol Teratol 2009 Feb;85(2):156-60

Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, 50 South Drive, Bethesda, MD 20892-8004, USA.

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http://dx.doi.org/10.1002/bdra.20520DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724655PMC
February 2009

Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.

Birth Defects Res A Clin Mol Teratol 2008 Sep;82(9):636-43

Division of Epidemiology, Statistics and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://doi.wiley.com/10.1002/bdra.20491
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http://dx.doi.org/10.1002/bdra.20491DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670560PMC
September 2008

The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels.

Mol Genet Metab 2006 Jul 18;88(3):290-4. Epub 2006 Apr 18.

School of Biochemistry and Immunology, Trinity College Dublin, Ireland.

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http://dx.doi.org/10.1016/j.ymgme.2006.02.011DOI Listing
July 2006

Reduced folate carrier polymorphisms and neural tube defect risk.

Mol Genet Metab 2006 Apr 15;87(4):364-9. Epub 2005 Dec 15.

Department of Biochemistry, Trinity College Dublin, Ireland.

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http://dx.doi.org/10.1016/j.ymgme.2005.09.024DOI Listing
April 2006

Screening for new MTHFR polymorphisms and NTD risk.

Am J Med Genet A 2005 Oct;138A(2):99-106

Department of Biochemistry, Trinity College Dublin, Dublin, Ireland.

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http://dx.doi.org/10.1002/ajmg.a.30846DOI Listing
October 2005

Folate-related genes and omphalocele.

Am J Med Genet A 2005 Jul;136(1):8-11

Division of Epidemiology, Statistics and Prevention Research, NICHD, NIH, DHHS, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1002/ajmg.a.30772DOI Listing
July 2005

Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.

Birth Defects Res A Clin Mol Teratol 2005 Apr;73(4):239-44

Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1002/bdra.20122DOI Listing
April 2005