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 en Europace (2014)

Not all Beta-Blockers are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events under Metoprolol

por Chockalingam, Priya, Crotti, Lia, Girardengo, Giulia, Johnson, Jonathan N., Harris, Katy M., van der Heijden, Jeroen F., Hauer, Richard N.W., Beckmann, Britt M., Spazzolini, Carla, Rordorf, Roberto, Rydberg, Annika, Clur, Sally-Ann B., Fischer, Markus, van den Heuvel, Freek, Kääb, Stefan, Blom, Nico A., Ackerman, Michael J., Schwartz, Peter J., Wilde, Arthur A.M.
Publicado 2012

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

por Kolder, Iris C.R.M., Tanck, Michael W.T., Postema, Pieter G., Barc, Julien, Sinner, Moritz F., Zumhagen, Sven, Husemann, Anja, Stallmeyer, Birgit, Koopmann, Tamara T., Hofman, Nynke, Pfeufer, Arne, Lichtner, Peter, Meitinger, Thomas, Beckmann, Britt M., Myerburg, Robert J., Bishopric, Nanette H., Roden, Dan M., Kääb, Stefan, Wilde, Arthur A.M., Schott, Jean-Jacques, Schulze-Bahr, Eric, Bezzina, Connie R.
Publicado en Circ Cardiovasc Genet (2015)

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

por Kääb, Stefan, Darbar, Dawood, van Noord, Charlotte, Dupuis, Josée, Pfeufer, Arne, Newton-Cheh, Christopher, Schnabel, Renate, Makino, Seiko, Sinner, Moritz F., Kannankeril, Prince J., Beckmann, Britt M., Choudry, Subbarao, Donahue, Brian S., Heeringa, Jan, Perz, Siegfried, Lunetta, Kathryn L., Larson, Martin G., Levy, Daniel, MacRae, Calum A., Ruskin, Jeremy N., Wacker, Annette, Schömig, Albert, Wichmann, H.-Erich, Steinbeck, Gerhard, Meitinger, Thomas, Uitterlinden, André G., Witteman, Jacqueline C.M., Roden, Dan M., Benjamin, Emelia J., Ellinor, Patrick T.
Publicado 2009

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

por Bezzina, Connie R., Barc, Julien, Mizusawa, Yuka, Remme, Carol Ann, Gourraud, Jean-Baptiste, Simonet, Floriane, Verkerk, Arie O., Schwartz, Peter J., Crotti, Lia, Dagradi, Federica, Guicheney, Pascale, Fressart, Véronique, Leenhardt, Antoine, Antzelevitch, Charles, Bartkowiak, Susan, Schulze-Bahr, Eric, Zumhagen, Sven, Behr, Elijah R., Bastiaenen, Rachel, Tfelt-Hansen, Jacob, Olesen, Morten Salling, Kääb, Stefan, Beckmann, Britt M., Weeke, Peter, Watanabe, Hiroshi, Endo, Naoto, Minamino, Tohru, Horie, Minoru, Ohno, Seiko, Hasegawa, Kanae, Makita, Naomasa, Nogami, Akihiko, Shimizu, Wataru, Aiba, Takeshi, Froguel, Philippe, Balkau, Beverley, Lantieri, Olivier, Torchio, Margherita, Wiese, Cornelia, Weber, David, Wolswinkel, Rianne, Coronel, Ruben, Boukens, Bas J., Bézieau, Stéphane, Charpentier, Eric, Chatel, Stéphanie, Despres, Aurore, Gros, Françoise, Kyndt, Florence, Lecointe, Simon, Lindenbaum, Pierre, Portero, Vincent, Violleau, Jade, Gessler, Manfred, Tan, Hanno L., Roden, Dan M., Christoffels, Vincent M., Le Marec, Hervé, Wilde, Arthur A, Probst, Vincent, Schott, Jean-Jacques, Dina, Christian, Redon, Richard
Publicado 2013

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 en Circulation (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 en Genet Med (2020)