RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing von Guo, Wei, Schafer, Sebastian, Greaser, Marion L, Radke, Michael H, Liss, Martin, Govindarajan, Thirupugal, Maatz, Henrike, Schulz, Herbert, Li, Shijun, Parrish, Amanda M, Dauksaite, Vita, Vakeel, Padmanabhan, Klaassen, Sabine, Gerull, Brenda, Thierfelder, Ludwig, Regitz-Zagrosek, Vera, Hacker, Timothy A, Saupe, Kurt W, Dec, G William, Ellinor, Patrick T, MacRae, Calum A, Spallek, Bastian, Fischer, Robert, Perrot, Andreas, Özcelik, Cemil, Saar, Kathrin, Hubner, Norbert, Gotthardt, Michael

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Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy von Arndt, Anne-Karin, Schafer, Sebastian, Drenckhahn, Jorg-Detlef, Sabeh, M. Khaled, Plovie, Eva R., Caliebe, Almuth, Klopocki, Eva, Musso, Gabriel, Werdich, Andreas A., Kalwa, Hermann, Heinig, Matthias, Padera, Robert F., Wassilew, Katharina, Bluhm, Julia, Harnack, Christine, Martitz, Janine, Barton, Paul J., Greutmann, Matthias, Berger, Felix, Hubner, Norbert, Siebert, Reiner, Kramer, Hans-Heiner, Cook, Stuart A., MacRae, Calum A., Klaassen, Sabine

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Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction von KLAASSEN, Sabine, PROBST, Susanne, GRAMLICH, Michael, DRENCKHAHN, Jörg-Detlef, HEUSER, Amd, BERGER, Felix, JENNI, Rolf, THIERFELDER, Ludwig, OECHSLIN, Erwin, GERULL, Brenda, KRINGS, Gregor, SCHULER, Pia, GREUTMANN, Matthias, HURLIMANN, David, YEGITBASI, Mustafa, PONS, Lucia

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Loss of murine Gfi1 causes neutropenia and induces osteoporosis depending on the pathogen load and systemic inflammation von Geissler, Sven, Textor, Martin, Stumpp, Sabine, Seitz, Sebastian, Lekaj, Anja, Brunk, Sabrina, Klaassen, Sabine, Schinke, Thorsten, Klein, Christoph, Mundlos, Stefan, Kornak, Uwe, Kühnisch, Jirko

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Nationwide Registry-Based Analysis of Infective Endocarditis Risk After Pulmonary Valve Replacement von Stammnitz, Clara, Huscher, Dörte, Bauer, Ulrike M M, Urban, Aleksandra, Nordmeyer, Johannes, Schubert, Stephan, Photiadis, Joachim, Berger, Felix, Klaassen, Sabine

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Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene von Poller, Wolfgang, Haas, Jan, Klingel, Karin, Kuehnisch, Jirko, Gast, Martina, Kaya, Ziya, Escher, Felicitas, Kayvanpour, Elham, Degener, Franziska, Opgen-Rhein, Bernd, Berger, Felix, Mochmann, Hans-Christian, Skurk, Carsten, Heidecker, Bettina, Schultheiss, Heinz-Peter, Monserrat, Lorenzo, Meder, Benjamin, Landmesser, Ulf, Klaassen, Sabine

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Predictors of Adverse Outcome in Adolescents and Adults With Isolated Left Ventricular Noncompaction von Greutmann, Matthias, MD, Mah, May Ling, MD, Silversides, Candice K., MD, Klaassen, Sabine, MD, Attenhofer Jost, Christine H., MD, Jenni, Rolf, MD, MSEE, Oechslin, Erwin N., MD

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Left Ventricular Noncompaction in Children: The Role of Genetics, Morphology, and Function for Outcome von Klaassen, Sabine, Kühnisch, Jirko, Schultze-Berndt, Alina, Seidel, Franziska

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RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy von Al-Wakeel-Marquard, Nadya, Degener, Franziska, Herbst, Christopher, Kühnisch, Jirko, Dartsch, Josephine, Schmitt, Boris, Kuehne, Titus, Messroghli, Daniel, Berger, Felix, Klaassen, Sabine

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Severe heart failure in the setting of inflammatory cardiomyopathy with likely pathogenic titin variant von Mueller, Melina, Zwinger, Lilli, Klaassen, Sabine, Poller, Wolfgang, Monserrat Iglesias, Lorenzo, Pablo Ochoa, Juan, Klingel, Karin, Landmesser, Ulf, Heidecker, Bettina

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Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot von Bansal, Vikas, Dorn, Cornelia, Grunert, Marcel, Klaassen, Sabine, Hetzer, Roland, Berger, Felix, Sperling, Silke R

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Left Ventricular Noncompaction: Phenotype in an Integrated Model of Cardiomyopathy? von Oechslin, Erwin, Klaassen, Sabine

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Stress-induced dilated cardiomyopathy in a knock-in mouse model mimicking human titin-based disease von Gramlich, Michael, Michely, Beate, Krohne, Christian, Heuser, Arnd, Erdmann, Bettina, Klaassen, Sabine, Hudson, Bryan, Magarin, Manuela, Kirchner, Florian, Todiras, Mihail, Granzier, Henk, Labeit, Siegfried, Thierfelder, Ludwig, Gerull, Brenda

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Midwall Fibrosis and Cardiac Mechanics: Rigid Body Rotation Is a Novel Marker of Disease Severity in Pediatric Primary Dilated Cardiomyopathy von Al-Wakeel-Marquard, Nadya, Seidel, Franziska, Kühnisch, Jirko, Kuehne, Titus, Berger, Felix, Messroghli, Daniel R, Klaassen, Sabine

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Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy von Warnecke, Nele, Ulmer, Bärbel M., Laufer, Sandra D., Shibamiya, Aya, Krämer, Elisabeth, Neuber, Christiane, Hanke, Sophia, Behrens, Charlotta, Loos, Malte, Münch, Julia, Kühnisch, Jirko, Klaassen, Sabine, Eschenhagen, Thomas, Patten-Hamel, Monica, Carrier, Lucie, Mearini, Giulia

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Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis—Further Impact of Heterozygous Immune Disorder Gene Variants? von Seidel, Franziska, Laser, Kai Thorsten, Klingel, Karin, Dartsch, Josephine, Theisen, Simon, Pickardt, Thomas, Holtgrewe, Manuel, Gärtner, Anna, Berger, Felix, Beule, Dieter, Milting, Hendrik, Schubert, Stephan, Klaassen, Sabine, Kühnisch, Jirko

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Reduced Systolic Function and Not Genetic Variants Determine Outcome in Pediatric and Adult Left Ventricular Noncompaction Cardiomyopathy von Schultze-Berndt, Alina, Kuehnisch, Jirko, Herbst, Christopher, Seidel, Franziska, Al-Wakeel-Marquard, Nadya, Dartsch, Josephine, Theisen, Simon, Knirsch, Walter, Jenni, Rolf, Greutmann, Matthias, Oechslin, Erwin, Berger, Felix, Klaassen, Sabine

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Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients von Sasse-Klaassen, Sabine, Gerull, Brenda, Oechslin, Erwin, Jenni, Rolf, Thierfelder, Ludwig

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Left Ventricular Noncompaction von Oechslin, Erwin, Klaassen, Sabine

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Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy von Schulze-Bahr, Eric, Ellinor, Patrick T, McDermott, Deborah A, Birchmeier, Walter, Sasse-Klaassen, Sabine, Gerull, Brenda, Markowitz, Steve M, Lerman, Bruce B, MacRae, Calum A, Thierfelder, Ludwig, Dietz, Rainer, Basson, Craig T, Wichter, Thomas, Paul, Matthias, Heuser, Arnd, Peters, Stefan, Grossmann, Katja S, Michely, Beate, Breithardt, Günter

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