Raffaella Cascella
Tirana, Albania
Last Updated: 09/26/2026
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Found 77 publications
High-Resolution Imaging of RPE Cellular Mosaic Over Drusen.
Journal: JAMA ophthalmology
Published: August 27, 2026
AI-Powered Neurogenetics: Supporting Patient's Evaluation with Chatbot.
Journal: Genes
Published: December 03, 2024
Federated Learning: Breaking Down Barriers in Global Genomic Research.
Journal: Genes
Published: December 02, 2024
Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample Monitoring.
Journal: Diagnostics (Basel, Switzerland)
Published: November 27, 2024
Deciphering the Complexity of FSHD: A Multimodal Approach as a Model for Rare Disorders.
Journal: International journal of molecular sciences
Published: July 31, 2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients.
Journal: Clinical epigenetics
Published: June 18, 2024
Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder Management.
Journal: Genes
Published: February 29, 2024
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families.
Journal: Clinical genetics
Published: October 04, 2023
A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy.
Journal: Genes
Published: July 24, 2023
Long-Term Structural and Functional Assessment of Doyne Honeycomb Retinal Dystrophy following Nanosecond 2RT Laser Treatment: A Case Series.
Journal: Case reports in ophthalmology
Published: June 29, 2023
Last Updated: 09/26/2026