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Genes|July 27, 2024
Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada SyndromeMaria d'Apolito, Francesco Santoro, Alessandra Ranaldi, et al.
Clinical Chemistry|November 26, 2002
Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technologyRosa Santacroce, Antonia Ratti, Francesco Caroli, et al.
Haematologica|April 5, 2008
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotypeMaurizio Margaglione, Giancarlo Castaman, Massimo Morfini, et al.
Journal of Cardiovascular Electrophysiology|June 23, 2025
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene MutationFrancesco Santoro, Maria D'Apolito, Ilaria Ragnatela, et al.
Genes|September 28, 2024
Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann-Steiner SyndromeIghli di Bari, Caterina Ceccarini, Maria Curcetti, et al.
BMJ Open|November 25, 2016
Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocolIoana Cotlarciuc, Thomas Marjot, Muhammad S Khan, et al.
European Stroke Journal|April 6, 2023
Age of onset of cerebral venous thrombosis: the BEAST studyRedoy Ranjan, Gie Ken-Dror, Ida Martinelli, et al.
Neurology|May 17, 2024
Gene-Gene Interaction Between Factor-XI and ABO Genes in Cerebral Venous Thrombosis: The BEAST StudyGie Ken-Dror, Ida Martinelli, Elvira Grandone, et al.
European Journal of Neurology|April 22, 2024
Coma in adult cerebral venous thrombosis: The BEAST studyRedoy Ranjan, Gie Ken-Dror, Ida Martinelli, et al.
Annals of Neurology|August 30, 2021
Genome-Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous ThrombosisGie Ken-Dror, Ioana Cotlarciuc, Ida Martinelli, et al.
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