QT interval prolongation and risk for cardiac events in genotyped LQTS-index children by Wedekind, H., Burde, D., Zumhagen, S., Debus, V., Burkhardtsmaier, G., Mönnig, G., Breithardt, G., Schulze-Bahr, E.

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Totally subcutaneous cardioverter-defibrillator (S-ICD®) : recent experience and future perspectives by Köbe, J, Zumhagen, S, Reinke, F, Schulze-Bahr, E, Eckardt, L

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Whole exome sequencing (WES) in a patient with a cardiac conduction defect and ventricular arrhythmias by Friedrich, C., Rinne, S., Zumhagen, S., Netter, M., Stallmeyer, B., Schulze-Bahr, E., Decher, N.

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Prediction of variant pathogenicity in congenital LQT syndrome: Performance analyses of 7 programs using 354 validated variants by Stallmeyer, B., Schlegelberger, T., Zumhagen, S., Friedrich, C., Seebohm, G., Schulze-Bahr, E.

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Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: A long-term follow-up by Mönnig, Gerold, Köbe, Julia, Löher, Andreas, Wasmer, Kristina, Milberg, Peter, Zellerhoff, Stephan, Pott, Christian, Zumhagen, Sven, Radu, Razvan, Scheld, Hans H., Haverkamp, Wilhelm, Schulze-Bahr, Eric, Eckardt, Lars

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Monogene kardiale Ionenkanalerkrankungen by Zumhagen, S., Friedrich, C., Stallmeyer, B., Ising, J., Seebohm, G., Schulze-Bahr, E.

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Restrictions for ICD patients in daily life by Köbe, Julia, Gradaus, Rainer, Zumhagen, Sven, Böcker, Dirk

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Komplett subkutaner Kardioverter-Defibrillator (S-ICD®): Aktuelle Erfahrungen und Ausblick by Köbe, J., Zumhagen, S., Reinke, F., Schulze-Bahr, E., Eckardt, L.

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Monogene kardiale Ionenkanalerkrankungen by Zumhagen, S., Friedrich, C., Stallmeyer, B., Ising, J., Seebohm, G., Schulze-Bahr, E.

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Totally subcutaneous cardioverter-defibrillator (S-ICD®) : recent experience and future perspectives by Köbe, J, Zumhagen, S, Reinke, F, Schulze-Bahr, E, Eckardt, L

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EKG-Quiz by Bauersachs, J., Borggrefe, M., Eckardt, L., Ehlermann, P., Engberding, R., Frommeyer, G., Fabritz, L., Friedrich, C., Gerecke, B., Herrera-Siklody, C., Katus, H. A., Kirchhof, P., McKenna, W. J., Oswald, H., Paul, M., Parade, U., Pott, C., Rüb, N., Schimpf, R., Seebohm, G., Schulze-Bahr, E., Sen-Chowdhry, Srijita, Stallmeyer, B., Strotmann, C., Tomé Esteban, M. T., Veltmann, C., Waltenberger, J., Wichter, T., Wolpert, C., Zumhagen, S.

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A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction by Stallmeyer, Birgit, Kuß, Johanna, Kotthoff, Stefan, Zumhagen, Sven, Vowinkel, Kirsty, Rinné, Susanne, Matschke, Lina A, Friedrich, Corinna, Schulze-Bahr, Ellen, Rust, Stephan, Seebohm, Guiscard, Decher, Niels, Schulze-Bahr, Eric

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Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia by Decher, Niels, Ortiz‐Bonnin, Beatriz, Friedrich, Corinna, Schewe, Marcus, Kiper, Aytug K, Rinné, Susanne, Seemann, Gunnar, Peyronnet, Rémi, Zumhagen, Sven, Bustos, Daniel, Kockskämper, Jens, Kohl, Peter, Just, Steffen, González, Wendy, Baukrowitz, Thomas, Stallmeyer, Birgit, Schulze‐Bahr, Eric

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T peak –T end interval and T peak –T end /QT ratio in patients with Brugada syndrome by Zumhagen, Sven, Zeidler, Eva Maria, Stallmeyer, Birgit, Ernsting, Marko, Eckardt, Lars, Schulze-Bahr, Eric

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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome by Tadros, Rafik, Mizusawa, Yuka, Postema, Pieter G., Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L., Mazzanti, Andrea, Beckmann, Britt M., Shimamoto, Keiko, Diamant, Ulla-Britt, Wijeyeratne, Yanushi D., Kucho, Yu, Robyns, Tomas, Ishikawa, Taisuke, Arbelo, Elena, Christiansen, Michael, Winbo, Annika, Jabbari, Reza, Steinfurt, Johannes, Rudic, Boris, Loeys, Bart, Shoemaker, M. Ben, Weeke, Peter E., Pfeiffer, Ryan, Davies, Brianna, Andorin, Antoine, Hofman, Nynke, Dagradi, Federica, Pedrazzini, Matteo, Tester, David J., Bos, J. Martijn, Sarquella-Brugada, Georgia, Campuzano, Óscar, Platonov, Pyotr G., Stallmeyer, Birgit, Zumhagen, Sven, Nannenberg, Eline A., Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Andersen, Peter M., Müller-Nurasyid, Martina, Cusi, Daniele, Barlassina, Cristina, Galan, Pilar, Munter, Markus, Werge, Thomas, Ribasés, Marta, Aung, Tin, Khor, Chiea C., Ozaki, Mineo, Lichtner, Peter, Meitinger, Thomas, van Tintelen, J. Peter, Hoedemaekers, Yvonne, Denjoy, Isabelle, Leenhardt, Antoine, Napolitano, Carlo, Shimizu, Wataru, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Krahn, Andrew D., Antzelevitch, Charles, Roden, Dan M., Saenen, Johan, Borggrefe, Martin, Odening, Katja E., Ellinor, Patrick T., Tfelt-Hansen, Jacob, Skinner, Jonathan R., van den Berg, Maarten P., Olesen, Morten Salling, Brugada, Josep, Brugada, Ramón, Breckpot, Jeroen, Yoshinaga, Masao, Behr, Elijah R., Rydberg, Annika, Aiba, Takeshi, Kääb, Stefan, Priori, Silvia G., Guicheney, Pascale, Tan, Hanno L., Newton-Cheh, Christopher, Ackerman, Michael J., Schwartz, Peter J., Schulze-Bahr, Eric, Horie, Minoru, Wilde, Arthur A., Tanck, Michael W.T., Bezzina, Connie R.

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Gain‐of‐function mutation in TASK‐4 channels and severe cardiac conduction disorder by Friedrich, Corinna, Rinné, Susanne, Zumhagen, Sven, Kiper, Aytug K, Silbernagel, Nicole, Netter, Michael F, Stallmeyer, Birgit, Schulze‐Bahr, Eric, Decher, Niels

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Changes in Corneal Densitometry in Patients with Fuchs Endothelial Dystrophy after Endothelial Keratoplasty by Alnawaiseh, Maged, Rosentreter, André, Prokosch, Verena, Eveslage, Maria, Eter, Nicole, Zumhagen, Lars

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Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes by Behr, Elijah R, Ritchie, Marylyn D, Tanaka, Toshihiro, Kääb, Stefan, Crawford, Dana C, Nicoletti, Paola, Floratos, Aris, Sinner, Moritz F, Kannankeril, Prince J, Wilde, Arthur A M, Bezzina, Connie R, Schulze-Bahr, Eric, Zumhagen, Sven, Guicheney, Pascale, Bishopric, Nanette H, Marshall, Vanessa, Shakir, Saad, Dalageorgou, Chrysoula, Bevan, Steve, Jamshidi, Yalda, Bastiaenen, Rachel, Myerburg, Robert J, Schott, Jean-Jacques, Camm, A John, Steinbeck, Gerhard, Norris, Kris, Altman, Russ B, Tatonetti, Nicholas P, Jeffery, Steve, Kubo, Michiaki, Nakamura, Yusuke, Shen, Yufeng, George, Jr, Alfred L, Roden, Dan M

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Our Toil Respite Only: Woolf, Diamond, and the Difficulty of Reality by Zumhagen-Yekplé, Karen

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Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome by Wemhöner, Konstantin, Friedrich, Corinna, Stallmeyer, Birgit, Coffey, Alison J, Grace, Andrew, Zumhagen, Sven, Seebohm, Guiscard, Ortiz-Bonnin, Beatriz, Rinné, Susanne, Sachse, Frank B, Schulze-Bahr, Eric, Decher, Niels

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