Sven Zumhagen
Publications by Year
Research Areas
Cardiac electrophysiology and arrhythmias, Ion channel regulation and function, Cardiac pacing and defibrillation studies, Cardiac Arrhythmias and Treatments, ECG Monitoring and Analysis
Most-Cited Works
- → An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing(2009)755 cited
- → Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death(2013)542 cited
- → Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances(2011)166 cited
- → A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes(2011)164 cited
- → Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome(2020)135 cited
- → Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls(2020)102 cited
- → Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome(2015)92 cited
- → Sodium permeable and “hypersensitive” TREK ‐1 channels cause ventricular tachycardia(2017)73 cited
- → Gain‐of‐function mutation in TASK ‐4 channels and severe cardiac conduction disorder(2014)69 cited
- → Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes(2013)66 cited