Clinical utility gene card for: Long-QT syndrome

por Beckmann, Britt M., Scheiper-Welling, Stefanie, Wilde, Arthur A. M., Kääb, Stefan, Schulze-Bahr, Eric, Kauferstein, Silke
Publicado 2021

Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony

por Martens, Eimo, Sinner, Moritz F., Siebermair, Johannes, Raufhake, Carsten, Beckmann, Britt M., Veith, Stefan, Düvel, Dieter, Steinbeck, Gerhard, Kääb, Stefan
Publicado 2014

Variant interpretation in molecular autopsy: a useful dilemma

por Scheiper-Welling, Stefanie, Tabunscik, Monika, Gross, Theresa E., Jenewein, Tina, Beckmann, Britt M., Niess, Constanze, Gradhand, Elise, Wunder, Cora, Schneider, Peter M., Rothschild, Markus A., Verhoff, Marcel A., Kauferstein, Silke
Publicado 2022

Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade

por Schinner, Camilla, Xu, Lifen, Franz, Henriette, Zimmermann, Aude, Wanuske, Marie-Therès, Rathod, Maitreyi, Hanns, Pauline, Geier, Florian, Pelczar, Pawel, Liang, Yan, Lorenz, Vera, Stüdle, Chiara, Maly, Piotr I., Kauferstein, Silke, Beckmann, Britt M., Sheikh, Farah, Kuster, Gabriela M., Spindler, Volker
Publicado 2022

Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation

por Ellinor, Patrick T., Lunetta, Kathryn L., Glazer, Nicole L., Pfeufer, Arne, Alonso, Alvaro, Chung, Mina K., Sinner, Moritz F., de Bakker, Paul I. W., Mueller, Martina, Lubitz, Steven A., Fox, Ervin, Darbar, Dawood, Smith, Nicholas L., Smith, Jonathan D., Schnabel, Renate B., Soliman, Elsayed Z., Rice, Kenneth M., Van Wagoner, David R., Beckmann, Britt-M., van Noord, Charlotte, Wang, Ke, Ehret, Georg B., Rotter, Jerome I., Hazen, Stanley L., Steinbeck, Gerhard, Smith, Albert V., Launer, Lenore J., Harris, Tamara B., Makino, Seiko, Nelis, Mari, Milan, David J., Perz, Siegfried, Esko, Tõnu, Köttgen, Anna, Moebus, Susanne, Newton-Cheh, Christopher, Li, Man, Möhlenkamp, Stefan, Wang, Thomas J., Kao, W.H. Linda, Vasan, Ramachandran S., Nöthen, Markus M., MacRae, Calum A., Stricker, Bruno H. Ch., Hofman, Albert, Uitterlinden, André G., Levy, Daniel, Boerwinkle, Eric, Metspalu, Andres, Topol, Eric J., Chakravarti, Aravinda, Gudnason, Vilmundur, Psaty, Bruce M., Roden, Dan M., Meitinger, Thomas, Wichmann, H.-Erich, Witteman, Jacqueline C.M., Barnard, John, Arking, Dan E., Benjamin, Emelia J., Heckbert, Susan R., Kääb, Stefan
Publicado 2010

Genome-wide association study of PR interval

por Pfeufer, Arne, van Noord, Charlotte, Marciante, Kristin D., Arking, Dan E., Larson, Martin G., Smith, Albert Vernon, Tarasov, Kirill V., Müller, Martina, Sotoodehnia, Nona, Sinner, Moritz F., Verwoert, Germaine C., Li, Man, Kao, W.H. Linda, Köttgen, Anna, Coresh, Josef, Bis, Joshua C., Psaty, Bruce M., Rice, Kenneth, Rotter, Jerome I., Rivadeneira, Fernando, Hofman, Albert, Kors, Jan A., Stricker, Bruno H.C., Uitterlinden, André G., van Duijn, Cornelia M., Beckmann, Britt M., Sauter, Wiebke, Gieger, Christian, Lubitz, Steven A., Newton-Cheh, Christopher, Wang, Thomas J., Magnani, Jared W., Schnabel, Renate B., Chung, Mina K., Barnard, John, Smith, Jonathan D., Van Wagoner, David R., Vasan, Ramachandran S., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Launer, Lenore J., Najjar, Samer S., Lakatta, Edward, Schlessinger, David, Uda, Manuela, Abecasis, Gonçalo R., Müller-Myhsok, Bertram, Ehret, Georg B., Boerwinkle, Eric, Chakravarti, Aravinda, Soliman, Elsayed Z., Lunetta, Kathryn L., Perz, Siegfried, Wichmann, H.-Erich, Meitinger, Thomas, Levy, Daniel, Gudnason, Vilmundur, Ellinor, Patrick T., Sanna, Serena, Kääb, Stefan, Witteman, Jacqueline C.M., Alonso, Alvaro, Benjamin, Emelia J., Heckbert, Susan R.
Publicado 2010

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

por 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, 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, Lathrop, Mark, 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, Makita, Naomasa, 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, Probst, Vincent, Horie, Minoru, Wilde, Arthur A., Tanck, Michael W.T., Bezzina, Connie R.
Publicado 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

por 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, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M., Bézieau, Stéphane, 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., Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen 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, Raphaël P., Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, 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, van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, 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, van den Berg, Maarten P., Olesen, Morten S., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, 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, Bezzina, Connie R.
Publicado 2020