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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 4
2022
Schinner, Camilla; Xu, Lifen; Franz, Henriette; Zimmermann, Aude; Wanuske, Marie-Theres; Rathod, Maitreyi; Hanns, Pauline; Geier, Florian; Pelczar, Pawel; Liang, Yan; Lorenz, Vera; Studle, Chiara; Maly, Piotr I.; Kauferstein, Silke; Beckmann, Britt M.; Sheikh, Farah; Kuster, Gabriela M. und Spindler, Volker
(2022):
Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-alpha V beta 6/TGF-beta Signaling Cascade.
In: Circulation, Bd. 146, Nr. 21: S. 1610-1626
2021
Beckmann, Britt M.; Scheiper-Welling, Stefanie; Wilde, Arthur A. M.; Kaab, Stefan; Schulze-Bahr, Eric und Kauferstein, Silke
(2021):
Clinical utility gene card for: Long-QT syndrome.
In: European Journal of Human Genetics, Bd. 29, Nr. 12: S. 1825-1832
2020
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G.; Amin, Ahmad S.; Nannenberg, Eline A.; Ware, James S.; Whiffin, Nicola; Mazzarotto, Francesco; Skoric-Milosavljevic, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M.; Bezieau, Stephane; Bos, J. Martijn; Breckpot, Jeroen; Campuzano, Oscar; Castelletti, Silvia; Celen, Candan; Clauss, Sebastian; Corveleyn, Anniek; Crotti, Lia; Dagradi, Federica; De Asmundis, Carlo; Denjoy, Isabelle; Dittmann, Sven; Ellinor, Patrick T.; Ortuno, Cristina Gil; Giustetto, Carla; Gourraud, Jean-Baptiste; Hazeki, Daisuke; Horie, Minoru; Ishikawa, Taisuke; Itoh, Hideki; Kaneko, Yoshiaki; Kanters, Jorgen K.; Kimoto, Hiroki; Kotta, Maria-Christina; Krapels, Ingrid P. C.; Kurabayashi, Masahiko; Lazarte, Julieta; Leenhardt, Antoine; Loeys, Bart L.; Lundin, Catarina; Makiyama, Takeru; Mansourati, Jacques; Martins, Raphael P.; Mazzanti, Andrea; Morner, Stellan; Napolitano, Carlo; Ohkubo, Kimie; Papadakis, Michael; Rudic, Boris; Molina, Maria Sabater; Sacher, Frederic; Sahin, Hatice; Sarquella-Brugada, Georgia; Sebastiano, Regina; Sharma, Sanjay; Sheppard, Mary N.; Shimamoto, Keiko; Shoemaker, M. Benjamin; Stallmeyer, Birgit; Steinfurt, Johannes; Tanaka, Yuji; Tester, David J.; Usuda, Keisuke; Zwaag, Paul A. van der; Dooren, Sonia van; Laer, Lut van; Winbo, Annika; Winkel, Bo G.; Yamagata, Kenichiro; Zumhagen, Sven; Volders, Paul G. A.; Lubitz, Steven A.; Antzelevitch, Charles; Platonov, Pyotr G.; Odening, Katja E.; Roden, Dan M.; Roberts, Jason D.; Skinner, Jonathan R.; Tfelt-Hansen, Jacob; Berg, Maarten P. van den; Olesen, Morten S.; Lambiase, Pier D.; Borggrefe, Martin; Hayashi, Kenshi; Rydberg, Annika; Nakajima, Tadashi; Yoshinaga, Masao; Saenen, Johan B.; Kaeaeb, Stefan; Brugada, Pedro; Robyns, Tomas; Giachino, Daniela F.; Ackerman, Michael J.; Brugada, Ramon; Brugada, Josep; Gimeno, Juan R.; Hasdemir, Can; Guicheney, Pascale; Priori, Silvia G.; Schulze-Bahr, Eric; Makita, Naomasa; Schwartz, Peter J.; Shimizu, Wataru; Aiba, Takeshi; Schott, Jean-Jacques; Redon, Richard; Ohno, Seiko; Probst, Vincent; Behr, Elijah R.; Barc, Julien und Bezzina, Connie R.
(2020):
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
In: Genetics in Medicine, Bd. 23, Nr. 1: S. 47-58
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; 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; Lubitz, Steven A.; 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, Oscar; Platonov, Pyotr G.; Stallmeyer, Birgit; Zumhagen, Sven; Nannenberg, Eline A.; Veldink, Jan H.; Berg, Leonard H. van den; Al-Chalabi, Ammar; Shaw, Christopher E.; Shaw, Pamela J.; Morrison, Karen E.; Andersen, Peter M.; Müller-Nurasyid, Martina; Cusi, Daniele; Barlassina, Cristina; Galan, Pilar; Lathrop, Mark; Munter, Markus; Werge, Thomas; Ribases, Marta; Aung, Tin; Khor, Chiea C.; Ozaki, Mineo; Lichtner, Peter; Meitinger, Thomas; Tintelen, J. Peter van; 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.; Berg, Maarten P. van den; Olesen, Morten Salling; Brugada, Josep; Brugada, Ramon; Makita, Naomasa; Breckpot, Jeroen; Yoshinaga, Masao; Behr, Elijah R.; Rydberg, Annika; Aiba, Takeshi; Kaeaeb, Stefan; Priori, Silvia G.; Guicheney, Pascale; Tan, Hanno L.; Newton-Cheh, Christopher; Ackerman, Michael J.; Schwartz, Peter J.; Schulze-Bahr, Eric; Probst, Vincent; Horie, Minoru; Wilde, Arthur A.; Tanck, Michael W. T. und Bezzina, Connie R.
(2020):
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
In: Circulation, Bd. 142, Nr. 4: S. 324-338