Marina Raffaele di Barletta

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Gisèle Bonne, Marina Raffaele di Barletta, Shaïda Varnous et al. · Nature Genetics · 1999 · 1.3K citations

Life Sciences, Genetics, Molecular Genetics +7

A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the <i>KCNJ2</i> Gene

Silvia G. Priori, Sandeep V. Pandit, Ilaria Rivolta et al. · Circulation Research · 2005 · 624 citations · Full text

Life Sciences, Cardiology, Genetics +17

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi et al. · The American Journal of Human Genetics · 2000 · 411 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor

Marina Cerrone, Barbara Colombi, Massimo Santoro et al. · Circulation Research · 2005 · 282 citations · Full text

Medicine, Cardiology, Genetics +17

Clinical Phenotype and Functional Characterization of <i>CASQ2</i> Mutations Associated With Catecholaminergic Polymorphic Ventricular Tachycardia

Marina Raffaele di Barletta, Serge Viatchenko‐Karpinski, Alessandra Nori et al. · Circulation · 2006 · 204 citations

Medicine, Cardiology, Genetics +17