Silvia Viaggi

6PUBLICATIONS
23CO-AUTHORS
Radiation therapyNeurogeneticsHaematologyDevelopmental genetics (incl. sex determination)Molecular targets
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Journal

Publications (6)

|Jun 12, 2026
45A ncRNA Expression Leads to Chromosomal Instability and Cytoskeletal Dynamics Impairment by Modulating GTSE1/p53/AurB Subcellular Localization.

|Oct 29, 2025
A New Variant in the NALCN Channel Is Responsible for Cerebellar Ataxia and Cognitive Impairment.

Rute Luísa Cabrita Pinto, Roberto Fancellu, Tiziana Benzi Markushi

|Aug 14, 2025
Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia.

Gianluca Dell'Orso, Tommaso Passarella, Serena Cappato

|Apr 28, 2023
Exome Analysis Reveals Novel Missense and Deletion Variants in the <i>CC2D2A</i> Gene as Causative of Joubert Syndrome.

Rute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale

|Nov 02, 2019
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma.

Francesca Piaggio, Veronica Tozzo, Cinzia Bernardi

|Apr 25, 2018
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma.

Serena Patrone, Irena Maric, Mariangela Rutigliani

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Frequent Collaborators

3 joint publications

Domenico Coviello

2 joint publications

Rute Luísa Cabrita Pinto

2 joint publications

Giuseppina Conteduca

2 joint publications

Barbara Testa