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Importance of gene-environment interactions in the etiology of selected birth defects

Clinical genetics, 2009-05, Vol.75 (5), p.409-423

2009

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In utero antiepileptic drug exposure: fetal death and malformations

Neurology, 2006-08, Vol.67 (3), p.407

2006

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De novo ALX4 variant detected in child with non-syndromic craniosynostosis

Brazilian journal of medical and biological research, 2021-01, Vol.54 (11), p.e11396-e11396

2021

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Association between inhibited binding of folic acid to folate receptor α in maternal serum and folate-related birth defects in Norway

Human reproduction (Oxford), 2011-08, Vol.26 (8), p.2232-2238

2011

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Cerebral folate deficiency with developmental delay, autism, and response to folinic acid

Neurology, 2005-03, Vol.64 (6), p.1088

2005

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Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

Nature genetics, 1999-10, Vol.23 (2), p.228-232

1999

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Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Journal of human genetics, 2002-06, Vol.47 (6), p.319-324

2002

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Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

American journal of epidemiology, 1998-07, Vol.148 (1), p.30-37

1998

Volltextzugriff (PDF)

Papers from the eighth international neural tube defects conference

Birth defects research. A Clinical and molecular teratology, 2014-08, Vol.100 (8), p.561-562

2014

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Teratology: General considerations and principles

Journal of allergy and clinical immunology, 1999-02, Vol.103 (2), p.S337-S342

Finnell, Richard H.

1999

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Polymorphisms in DNA repair genes as risk factors for spina bifida and orofacial clefts

American journal of medical genetics. Part A, 2005-06, Vol.135A (3), p.268-273

2005

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Protein-reactive metabolites of carbamazepine in mouse liver microsomes

Drug metabolism and disposition, 1996-05, Vol.24 (5), p.509

1996

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Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome

The New England journal of medicine, 1990-05, Vol.322 (22), p.1567-1572

1990

Volltextzugriff (PDF)

Maternal Smoking and the Risk of Orofacial Clefts: Susceptibility with NAT1 and NAT2 Polymorphisms

Epidemiology (Cambridge, Mass.), 2004-03, Vol.15 (2), p.150-156

2004

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Maternal Smoking, Genetic Variation of Glutathione S-Transferases, and Risk for Orofacial Clefts

Epidemiology (Cambridge, Mass.), 2005-09, Vol.16 (5), p.698-701

2005

Volltextzugriff (PDF)

Teratogenicity of carbamazepine-10, 11-epoxide and oxcarbazepine in the SWV mouse

The Journal of pharmacology and experimental therapeutics, 1996-12, Vol.279 (3), p.1237

1996

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Molecular basis of environmentally induced birth defects

Annual review of pharmacology and toxicology, 2002-01, Vol.42 (1), p.181-208

2002

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Stereoselective pharmacokinetics and pharmacodynamics of propylisopropyl acetamide, a CNS-active chiral amide analog of valproic acid

Pharmaceutical research, 1999-10, Vol.16 (10), p.1582-1588

1999

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Valproic acid-induced alterations in growth and neurotrophic factor

Reproductive toxicology (Elmsford, N.Y.), 2000, Vol.14 (1), p.1-11

2000

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Ethanol Decreases Glial Derived Neurotrophic Factor (GDNF) Protein Release but Not mRNA Expression and Increases GDNF-Stimulated Shc Phosphorylation in the Developing Cerebellum

Alcoholism, clinical and experimental research, 1999-10, Vol.23 (10), p.1691-1697

1999

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Identification of two putative novel folate receptor genes in humans and mouse

Gene, 2000-11, Vol.258 (1), p.117-125

2000

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Reduced folate carrier polymorphism (80A→G) and neural tube defects

European journal of human genetics : EJHG, 2003-03, Vol.11 (3), p.245-252

2003

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Gene–nutrient interactions: importance of folates and retinoids during early embryogenesis

Toxicology and applied pharmacology, 2004-07, Vol.198 (2), p.75-85

2004

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Microarray analysis of homocysteine‐responsive genes in cardiac neural crest cells in vitro

Developmental dynamics, 2007-04, Vol.236 (4), p.1044-1054

2007

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Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip

American journal of medical genetics, 1998-11, Vol.80 (3), p.196-198

1998

Volltextzugriff (PDF)

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Importance of gene-environment interactions in the etiology of selected birth defects

In utero antiepileptic drug exposure: fetal death and malformations

De novo ALX4 variant detected in child with non-syndromic craniosynostosis

Association between inhibited binding of folic acid to folate receptor α in maternal serum and folate-related birth defects in Norway

Cerebral folate deficiency with developmental delay, autism, and response to folinic acid

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

Papers from the eighth international neural tube defects conference

Teratology: General considerations and principles

Polymorphisms in DNA repair genes as risk factors for spina bifida and orofacial clefts

Protein-reactive metabolites of carbamazepine in mouse liver microsomes

Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome

Maternal Smoking and the Risk of Orofacial Clefts: Susceptibility with NAT1 and NAT2 Polymorphisms

Maternal Smoking, Genetic Variation of Glutathione S-Transferases, and Risk for Orofacial Clefts

Teratogenicity of carbamazepine-10, 11-epoxide and oxcarbazepine in the SWV mouse

Molecular basis of environmentally induced birth defects

Stereoselective pharmacokinetics and pharmacodynamics of propylisopropyl acetamide, a CNS-active chiral amide analog of valproic acid

Valproic acid-induced alterations in growth and neurotrophic factor

Ethanol Decreases Glial Derived Neurotrophic Factor (GDNF) Protein Release but Not mRNA Expression and Increases GDNF-Stimulated Shc Phosphorylation in the Developing Cerebellum

Identification of two putative novel folate receptor genes in humans and mouse

Reduced folate carrier polymorphism (80A→G) and neural tube defects

Gene–nutrient interactions: importance of folates and retinoids during early embryogenesis

Microarray analysis of homocysteine‐responsive genes in cardiac neural crest cells in vitro

Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip

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