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Clinical Genetics|November 30, 2024
WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and MacrocephalyLudovico Graziani, Miriam Lucia Carriero, Valentina Ferradini, et al.
International Journal of Molecular Sciences|September 28, 2021
Genetic and Epigenetic Factors of Takotsubo Syndrome: A Systematic ReviewValentina Ferradini, Davide Vacca, Beatrice Belmonte, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 22, 2017
Targeted Next Generation Sequencing in patients with Myotonia CongenitaValentina Ferradini, Marco Cassone, Sara Nuovo, et al.
American Journal of Medical Genetics. Part A|February 22, 2023
A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser-Winter syndromeLudovico Graziani, Giacomo Cinnirella, Valentina Ferradini, et al.
Minerva Cardiology and Angiology|February 27, 2023
Spontaneous coronary artery dissection: review, case report and analysis of COVID-19-related casesJoseph Cosma, Alessandro Russo, Valentina Ferradini, et al.
Journal of Cardiovascular Development and Disease|July 25, 2025
The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and ChannelopathiesValerio Caputo, Virginia Veronica Visconti, Enrica Marchionni, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 11, 2016
Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada SyndromeRuggiero Mango, Andrea Luchetti, Raffaele Sangiuolo, et al.
Frontiers in Pediatrics|January 26, 2023
Case Report: Crossing a rugged road in a primary immune regulatory disorderMayla Sgrulletti, Cristina Cifaldi, Silvia Di Cesare, et al.
Genes|June 2, 2021
Variants in <i>MHY7</i> Gene Cause Arrhythmogenic CardiomyopathyValentina Ferradini, Luca Parca, Annamaria Martino, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 2019
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experienceLiliana Mannucci, Serena Luciano, Leila B Salehi, et al.
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