Area of research
Rheumatology · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Folate and B Vitamins Research, Pharmacological Effects and Toxicity Studies, Prenatal Screening and Diagnostics, and Epigenetics and DNA Methylation.
The contribution of de novo coding mutations to meningomyelocele
Risk of meningomyelocele mediated by the common 22q11.2 deletion
Transcriptomic analysis reveals the anti-cancer effect of gestational mesenchymal stem cell secretome
Excess folic acid intake increases DNA de novo point mutations
Whole-exome sequencing study of hypospadias
Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndrome
Additional file 7 of Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndrome
Additional file 5 of Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndrome
Additional file 6 of Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndrome
Additional file 3 of Transcriptomic analysis of stem cells from chorionic villi uncovers the impact of chromosomes 2, 6 and 22 in the clinical manifestations of Down syndrome
Gene Environment Interactions in the Etiology of Neural Tube Defects
Actuation enhances patterning in human neural tube organoids
Two-Year-Old Cognitive Outcomes in Children of Pregnant Women With Epilepsy in the Maternal Outcomes and Neurodevelopmental Effects of Antiepileptic Drugs Study
Unraveling the complex genetics of neural tube defects: From biological models to human genomics and back
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children
Knowledge gaps in understanding the metabolic and clinical effects of excess folates/folic acid: a summary, and perspectives, from an NIH workshop
Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects
Fetal loss and malformations in the MONEAD study of pregnant women with epilepsy
The antagonism of folate receptor by dolutegravir
The TFAP2A–IRF6–GRHL3 genetic pathway is conserved in neurulation
Overview on neural tube defects: From development to physical characteristics
Formate rescues neural tube defects caused by mutations in <i>Slc25a32</i>
Threshold for neural tube defect risk by accumulated singleton loss-of-function variants
Genetic analysis of Wnt/PCP genes in neural tube defects
Metabolome-wide association study of anti-epileptic drug treatment during pregnancy
Serum homocysteine, arsenic methylation, and arsenic-induced skin lesion incidence in Bangladesh: A one-carbon metabolism candidate gene study
MicroRNA-197 controls ADAM10 expression to mediate MeCP2’s role in the differentiation of neuronal progenitors
Teratogenicity of valproic acid and its constitutional isomer, amide derivative valnoctamide in mice
Disruption of the ATXN1–CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans