Area of research
Cardiology and Cardiovascular Medicine · Surgery
Research interest
Research interests include Cardiomyopathy and Myosin Studies, Viral Infections and Immunology Research, Coronary Interventions and Diagnostics, and Cardiovascular Effects of Exercise.
Integration of genetic testing into diagnostic pathways for cardiomyopathies: a clinical consensus statement by the ESC Council on Cardiovascular Genomics
Independent role of atherosclerotic plaque composition and extension in predicting the risk of cardiac events: a CLIMA substudy
Management of Adults With Anomalous Aortic Origin of the Coronary Arteries
The contribution of amyloid deposition in the aortic valve to calcification and aortic stenosis
Risk of Arrhythmic Death in Patients With Nonischemic Cardiomyopathy
Risk of Type B Dissection in Marfan Syndrome
Author Correction: Optical coherence tomography in coronary atherosclerosis assessment and intervention
2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension
Optical coherence tomography in coronary atherosclerosis assessment and intervention
Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
Dalla regressione alla stabilizzazione: l’evoluzione della placca aterosclerotica coronarica secondo le nuove evidenze
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
POPDC2 a novel susceptibility gene for conduction disorders
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23
Heart Failure in Cardiomyopathies: A Position Paper from the Heart Failure Association of the European Society of Cardiology
European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Cardiac Phenotypes in Hereditary Muscle Disorders
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Contemporary genetic testing in inherited cardiac disease
Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking
Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' Collaboration
Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients
Atlas of the clinical genetics of human dilated cardiomyopathy
The MOGE(S) Classification of Cardiomyopathy for Clinicians
Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases