Arrhythmic Risk in Carriers of Predicted Deleterious Rare Variants in Dilated and Arrhythmogenic Cardiomyopathy Genes
In dilated (DCM) and arrhythmogenic cardiomyopathies (ACM), monogenic variants in causative genes are key prognostic factors. In the general population, the clinical role of these variants remains debated.
Authors
- Giulia Barbati (ORCID: https://orcid.org/0000-0001-8942-5686)
- Maria Perotto (ORCID: https://orcid.org/0000-0001-8252-2934)
- Martina Setti (ORCID: https://orcid.org/0000-0002-3618-2833)
- Ilaria Gandin (ORCID: https://orcid.org/0000-0003-3196-2491)
- Matteo Dal Ferro (ORCID: https://orcid.org/0000-0002-2310-0448)
- Andrea Mario Vergani (ORCID: https://orcid.org/0000-0003-3378-4406)
- Michela Carlotta Massi (ORCID: https://orcid.org/0000-0001-5393-8180)
- Francesca Ieva (ORCID: https://orcid.org/0000-0003-0165-1983)
- Alessia Paldino (ORCID: https://orcid.org/0000-0002-5823-3777)
- Marco Merlo
- Emanuele Di Angelantonio
- Gianfranco Sinagra
Institutions
- University of Verona (IT)
- University of Trieste (IT)
- Human Technopole (IT)
- Azienda Sanitaria Universitaria Integrata di Trieste (IT)
- Politecnico di Milano (IT)
Publication Details
- Journal
- JACC Advances
- Published
- 2026-07-28
- DOI
- https://doi.org/10.1016/j.jacadv.2026.103066
- Primary Topic
- Cardiovascular Effects of Exercise
- Type
- article
- Field-Weighted Citation Impact
- 0.00