- Works count
- 1,461
- Citation count
- 22,510
- H-index
- 47
- i10-index
- 106
Research interests
Publications
2023 ESC Guidelines for the management of cardiomyopathies
European Heart Journal · 2023 · https://doi.org/10.1093/eurheartj/ehad194
Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial
The Lancet · 2020 · https://doi.org/10.1016/s0140-6736(20)31792-x
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene
Circulation Heart Failure · 2020 · 10.1161/circheartfailure.119.006832
Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)
JAMA Cardiology · 2019 · https://doi.org/10.1001/jamacardio.2019.2861
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
Journal of the American College of Cardiology · 2018 · 10.1016/j.jacc.2018.08.2181
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
Journal of the American College of Cardiology · 2018 · 10.1016/j.jacc.2018.08.2181
International External Validation Study of the 2014 European Society of Cardiology Guidelines on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (EVIDENCE-HCM)
Circulation · 2017 · https://doi.org/10.1161/circulationaha.117.030437
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
European Heart Journal · 2016 · https://doi.org/10.1093/eurheartj/ehv727
Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
European Heart Journal · 2014 · https://doi.org/10.1093/eurheartj/ehu217
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
European Heart Journal · 2014 · https://doi.org/10.1093/eurheartj/ehu284
Atlas of the clinical genetics of human dilated cardiomyopathy
European Heart Journal · 2014 · https://doi.org/10.1093/eurheartj/ehu301
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
European Heart Journal · 2013 · https://doi.org/10.1093/eurheartj/eht210
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
Journal of the American College of Cardiology · 2012 · https://doi.org/10.1016/j.jacc.2011.08.078
Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases
European Heart Journal · 2012 · https://doi.org/10.1093/eurheartj/ehs397
Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype
Journal of the American College of Cardiology · 2007 · https://doi.org/10.1016/j.jacc.2007.02.061
Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy
European Heart Journal · 2006 · https://doi.org/10.1093/eurheartj/ehl041
Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy
Circulation · 2005 · https://doi.org/10.1161/circulationaha.104.532234
Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome
Journal of the American College of Cardiology · 2005 · 10.1016/j.jacc.2004.11.053
Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy
Heart · 2005 · 10.1136/hrt.2003.031161
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy
Journal of the American College of Cardiology · 2004 · https://doi.org/10.1016/j.jacc.2004.08.027
Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy
The Lancet · 2004 · 10.1016/s0140-6736(04)15468-8
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations
Journal of Clinical Investigation · 2003 · https://doi.org/10.1172/jci16336
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations
Journal of Clinical Investigation · 2003 · https://doi.org/10.1172/jci200316336
α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
Journal of Clinical Investigation · 1999 · https://doi.org/10.1172/jci6460
Current projects
No projects listed.