Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Laura Cleary
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
Genetics
Related publications
Impact of the MTHFR C677T Polymorphism on Risk of Neural Tube Defects: Case-Control Study
BMJ
Recurrence Risk of Neural Tube Defects.
Journal of Medical Genetics
Genetics
The Etiology of Neural Tube Defects
Homocysteine Metabolism: From Basic Science to Clinical Medicine
Analysis of the MTHFD1 Promoter and Risk of Neural Tube Defects
Human Genetics
Genetics
Association of the Maternal MTHFR C677T Polymorphism With Susceptibility to Neural Tube Defects in Offsprings: Evidence From 25 Case-Control Studies
PLoS ONE
Multidisciplinary
Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphism (G894T) as a Risk Factor for Obesity in the Egyptian Population
Asian Journal of Chemical Sciences
Maternal Serum Neurone Specific Enolase in the Diagnosis of Anencephaly and Other Neural Tube Defects
Annals of Clinical Biochemistry
Medicine
Clinical Biochemistry
A Randomised Trial of Low Dose Folic Acid to Prevent Neural Tube Defects. The Irish Vitamin Study Group.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Preventing Neural Tube Defects in Europe: Population Based Study
British Medical Journal
Medicine