Genetic Variants in the Folate Pathway and the Risk of Neural Tube Defects: A Meta-Analysis of the Published Literature

Overview of attention for article published in PLOS ONE, April 2013

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The contribution of de novo coding mutations to meningomyelocele

Preprint in medRxiv (March 2024)

Folate-deficiency induced acyl-CoA synthetase short-chain family member 2 increases lysine crotonylome involved in neural tube defects

Article in Frontiers in Molecular Neuroscience (January 2023)

Single Nucleotide Polymorphisms of MTHFR (rs1051266) and SLC19A1 (rs1801133) Associated to Genomic Ancestry in Cuban Healthy Population

Article in Current Pharmacogenomics and Personalized Medicine (January 2023)