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Electrophoresis|August 11, 2023
Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site levelDomenica Megalizzi, Giulia Trastulli, Valerio Caputo, et al.Cells|September 9, 2022
Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHDValerio Caputo, Domenica Megalizzi, Carlo Fabrizio, et al.Genes|April 27, 2024
Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder ManagementStefania Zampatti, Cristina Peconi, Domenica Megalizzi, et al.Genes|September 28, 2024
<i>RHO</i> Variants and Autosomal Dominant Retinitis Pigmentosa: Insights from the Italian Genetic LandscapeGiulia Trastulli, Domenica Megalizzi, Giulia Calvino, et al.Genes|January 25, 2025
AI-Powered Neurogenetics: Supporting Patient's Evaluation with ChatbotStefania Zampatti, Juliette Farro, Cristina Peconi, et al.Diagnostics (Basel, Switzerland)|January 25, 2025
Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample MonitoringGiulia Trastulli, Giulia Calvino, Bruno Papasergi, et al.International Journal of Molecular Sciences|October 26, 2024
Deciphering the Complexity of FSHD: A Multimodal Approach as a Model for Rare DisordersDomenica Megalizzi, Giulia Trastulli, Luca Colantoni, et al.Genes|January 8, 2025
Federated Learning: Breaking Down Barriers in Global Genomic ResearchGiulia Calvino, Cristina Peconi, Claudia Strafella, et al.Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.Journal of Personalized Medicine|July 27, 2022
WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic FactorsCarlo Fabrizio, Andrea Termine, Valerio Caputo, et al.Pageof 2