Anna M. Di Blasio
Milan, Italy
Last Updated: 09/26/2026
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Found 69 publications
Autosomal recessive retinopathy (ARRP) associated with a novel variant in NR2E3 gene.
Journal: Ophthalmic genetics
Published: July 10, 2026
Correction: Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID‑19 infection: insights from a genome‑wide DNA methylation study.
Journal: Clinical epigenetics
Published: November 15, 2024
Genetic Characterization of 191 Probands with Inherited Retinal Dystrophy by Targeted NGS Analysis.
Journal: Genes
Published: May 10, 2024
Optic Neuropathy AFG3L2 Related in a Patient Affected by Congenital Stationary Night Blindness.
Journal: Case reports in ophthalmological medicine
Published: May 07, 2024
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation study.
Journal: Clinical epigenetics
Published: April 05, 2024
A promising eco-sustainable wound dressing based on cellulose extracted from Spartium junceum L. and impregnated with Glycyrrhiza glabra L extract: Design, production and biological properties.
Journal: International journal of biological macromolecules
Published: November 29, 2023
Altered Lipid Moieties and Carbonyls in a Wistar Rat Dietary Model of Subclinical Fatty Liver: Potential Sex-Specific Biomarkers of Early Fatty Liver Disease?
Journal: Antioxidants (Basel, Switzerland)
Published: August 22, 2023
Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome.
Journal: European journal of medical research
Published: July 13, 2022
Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients.
Journal: Biomolecules
Published: June 22, 2022
Sex Dimorphism in the Metabolome of Metabolic Syndrome in Morbidly Obese Individuals.
Journal: Metabolites
Published: April 15, 2022
Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and incomplete Congenital Stationary Night Blindness.
Journal: Experimental eye research
Published: February 21, 2022
Last Updated: 09/26/2026