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Effects of Folate and Vitamin B12 Deficiencies During Pregnancy on Fetal, Infant, and Child Development

Food and nutrition bulletin, 2008-06, Vol.29 (2_suppl1), p.S101-S111

2008

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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Proceedings of the National Academy of Sciences - PNAS, 2013-01, Vol.110 (2), p.588-593

2013

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Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects

BMC medical genetics, 2012-08, Vol.13 (1), p.62-62, Article 62

2012

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group

American journal of human genetics, 2002-11, Vol.71 (5), p.1207-1215

2002

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Lack of Association between Folate-Receptor Autoantibodies and Neural-Tube Defects

The New England journal of medicine, 2009-07, Vol.361 (2), p.152-160

2009

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Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery

The American journal of clinical nutrition, 2005-10, Vol.82 (4), p.836-842

2005

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Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification

Pediatrics (Evanston), 2009-03, Vol.123 (3), p.917-923

2009

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

American journal of medical genetics. Part A, 2011-01, Vol.155A (1), p.14-21

2011

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Minimum effective dose of folic acid for food fortification to prevent neural-tube defects

The Lancet (British edition), 1997-12, Vol.350 (9092), p.1666-1669

1997

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Maternal folate, vitamin B12 and homocysteine levels in pregnancies affected by congenital malformations other than neural tube defects

Birth defects research. A Clinical and molecular teratology, 2011-07, Vol.91 (7), p.610-615

2011

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The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population

American journal of medical genetics. Part A, 2007-06, Vol.143A (11), p.1174-1180

2007

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Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects

The American journal of clinical nutrition, 2014-10, Vol.100 (4), p.1069-1074

2014

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Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association

Molecular genetics and metabolism, 2005-07, Vol.85 (3), p.220-227

2005

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Reduced folate carrier polymorphisms and neural tube defect risk

Molecular genetics and metabolism, 2006-04, Vol.87 (4), p.364-369

2006

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Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study

BMJ, 2004-06, Vol.328 (7455), p.1535-1536

2004

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Do high blood folate concentrations exacerbate metabolic abnormalities in people with low vitamin B-12 status?

The American journal of clinical nutrition, 2011-08, Vol.94 (2), p.495-500

2011

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The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2009-04, Vol.85 (4), p.285-294

2009

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common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency

Human mutation, 2009-12, Vol.30 (12), p.1650-1656

2009

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Survival and disability in a cohort of neural tube defect births in Dublin, Ireland

Birth defects research. A Clinical and molecular teratology, 2008-10, Vol.82 (10), p.701-709

2008

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Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

Journal of human genetics, 2003-04, Vol.48 (4), p.190-193

2003

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Folate levels and neural tube defects. Implications for prevention

JAMA : the journal of the American Medical Association, 1995-12, Vol.274 (21), p.1698

1995

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Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

European journal of human genetics : EJHG, 2006-06, Vol.14 (6), p.768-772

2006

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

Birth defects research. A Clinical and molecular teratology, 2010-02, Vol.88 (2), p.84-93

2010

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

Birth defects research. A Clinical and molecular teratology, 2008-09, Vol.82 (9), p.636-643

2008

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Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts

American journal of medical genetics. Part A, 2016-04, Vol.170A (4), p.1007-1016

2016

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Effects of Folate and Vitamin B12 Deficiencies During Pregnancy on Fetal, Infant, and Child Development

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects

A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group

Lack of Association between Folate-Receptor Autoantibodies and Neural-Tube Defects

Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery

Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification

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

Minimum effective dose of folic acid for food fortification to prevent neural-tube defects

Maternal folate, vitamin B12 and homocysteine levels in pregnancies affected by congenital malformations other than neural tube defects

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population

Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association

Reduced folate carrier polymorphisms and neural tube defect risk

Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study

Do high blood folate concentrations exacerbate metabolic abnormalities in people with low vitamin B-12 status?

The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects

common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency

Survival and disability in a cohort of neural tube defect births in Dublin, Ireland

Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

Folate levels and neural tube defects. Implications for prevention

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

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

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

Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts

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