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Trends in Genetics : TIG|April 13, 2026
A new era for the dark genomeMerel Stemerdink, Dalila Capasso, Munevver Burcu CicekdalBMC Genomics|April 18, 2023
Definition of the transcriptional units of inherited retinal disease genes by meta-analysis of human retinal transcriptome dataKarla Alejandra Ruiz-Ceja, Dalila Capasso, Michele Pinelli, et al.Journal of Cellular and Molecular Medicine|February 28, 2020
Association of PARP1 polymorphisms with response to chemotherapy in patients with high-risk neuroblastomaMarianna Avitabile, Vito Alessandro Lasorsa, Sueva Cantalupo, et al.HGG Advances|April 19, 2025
Targeted long-read cDNA sequencing reveals novel splice-altering pathogenic variants causing retinal dystrophiesDalila Capasso, Roberta Zeuli, Gavin Arno, et al.HGG Advances|May 31, 2024
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patientsRoberta Zeuli, Marianthi Karali, Suzanne E de Bruijn, et al.Cellular and Molecular Life Sciences : CMLS|July 7, 2026
Retina-specific long non-coding RNAs associated with inherited retinal disease genesEmma Delanote, Karla Alejandra Ruiz-Ceja, Alfredo Dueñas Rey, et al.Pageof 1