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International Journal of Molecular Sciences|December 30, 2020
New Omics-Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?Luigi Donato, Concetta Scimone, Simona Alibrandi, et al.
American Journal of Physiology. Cell Physiology|September 12, 2022
Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAsConcetta Scimone, Luigi Donato, Simona Alibrandi, et al.
Biology|April 26, 2025
Mechanotransduction in Development: A Focus on AngiogenesisSimona Alibrandi, Carmela Rinaldi, Sergio Lucio Vinci, et al.
World Journal of Stem Cells|August 7, 2023
Human retinal secretome: A cross-link between mesenchymal and retinal cellsLuigi Donato, Concetta Scimone, Simona Alibrandi, et al.
RNA Biology|June 30, 2022
Editome landscape of CCM-derived endothelial cellsConcetta Scimone, Simona Alibrandi, Luigi Donato, et al.
International Journal of Molecular Sciences|April 3, 2021
Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular ModelingLuigi Donato, Ebtesam Mohamed Abdalla, Concetta Scimone, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 12, 2026
Circulating lncRNAs Remark Expression Profile of Cerebrovascular Malformation Endothelial CellsDomenico Mordà, Luigi Donato, Simona Alibrandi, et al.
Heliyon|May 3, 2024
Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degenerationLuigi Donato, Concetta Scimone, Simona Alibrandi, et al.
Progress in Retinal and Eye Research|September 25, 2025
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneityDomenico Mordà, Simona Alibrandi, Concetta Scimone, et al.
Thrombosis Research|December 19, 2025
Combined exome and RNA-seq analysis in patients with rare non-syndromic inherited brain arteriovenous malformation suggests a novel function for PTPN13 in arterial specificationSimona Alibrandi, Domenico Mordà, Antonino Germanò, et al.
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