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Signal Transduction and Targeted Therapy|July 13, 2026
RBM20 variants disrupt Ca<sup>2+</sup> handling and metabolism in dilated and non-compaction cardiomyopathy stem cell modelsSabine Rebs, Farbod Sedaghat-Hamedani, Elham Kayvanpour, et al.EMBO Molecular Medicine|November 16, 2017
Genomic structural variations lead to dysregulation of important coding and non-coding RNA species in dilated cardiomyopathyJan Haas, Stefan Mester, Alan Lai, et al.Circulation|March 25, 2024
Scrutinizing the Role of Venoarterial Extracorporeal Membrane Oxygenation: Has Clinical Practice Outpaced the Evidence?Enzo Lüsebrink, Leonhard Binzenhöfer, Daniel Hering, et al.EMBO Molecular Medicine|January 24, 2013
Alterations in cardiac DNA methylation in human dilated cardiomyopathyJan Haas, Karen S Frese, Yoon Jung Park, et al.Frontiers in Cardiovascular Medicine|March 29, 2024
A contemporary training concept in critical care cardiologyLeonhard Binzenhöfer, Nils Gade, Daniel Roden, et al.Journal of the American College of Cardiology|November 11, 2025
Danicamtiv, a Selective Agonist of Cardiac Myosin, for Dilated Cardiomyopathy: A Phase 2 Open-Label TrialNeal K Lakdawala, Ray E Hershberger, Pablo Garcia-Pavia, et al.International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.Circulation. Heart Failure|March 16, 2019
Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic CardiomyopathyVictoria N Parikh, Colleen Caleshu, Chloe Reuter, et al.Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.European Heart Journal|October 14, 2017
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathyFarbod Sedaghat-Hamedani, Jan Haas, Feng Zhu, et al.Pageof 25