Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2
Chockalingam, Priya, MBBS, PhD, Crotti, Lia, MD, PhD, Girardengo, Giulia, MD, Johnson, Jonathan N., MD, Harris, Katy M., MS, RN, van der Heijden, Jeroen F., MD, PhD, Hauer, Richard N.W., MD, PhD, Beckmann, Britt M., MD, Spazzolini, Carla, DVM, MS, Rordorf, Roberto, MD, Rydberg, Annika, MD, PhD, Clur, Sally-Ann B., MBBCh, MSc (Med), PhD, Fischer, Markus, MD, van den Heuvel, Freek, MD, PhD, Kääb, Stefan, MD, PhD, Blom, Nico A., MD, PhD, Ackerman, Michael J., MD, PhD, Schwartz, Peter J., MD, Wilde, Arthur A.M., MD, PhD
Published in Journal of the American College of Cardiology (13.11.2012)
Published in Journal of the American College of Cardiology (13.11.2012)
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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, Borggrefe, Martin, Schimpf, Rainer, 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
Published in Nature genetics (01.09.2013)
Published in Nature genetics (01.09.2013)
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Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade
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
Published in Circulation (New York, N.Y.) (22.11.2022)
Published in Circulation (New York, N.Y.) (22.11.2022)
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Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol
CHOCKALINGAM, Priya, CROTTI, Lia, RYDBERG, Annika, CLUR, Sally-Ann B, FISCHER, Markus, DEN HEUVEL, Freek Van, KAAB, Stefan, BLOM, Nico A, ACKERMAN, Michael J, SCHWARTZ, Peter J, WILDE, Arthur A. M, GIRARDENGO, Giulia, JOHNSON, Jonathan N, HARRIS, Katy M, DER HEIJDEN, Jeroen F. Van, HAUER, Richard N. W, BECKMANN, Britt M, SPAZZOLINI, Carla, RORDORF, Roberto
Published in Journal of the American College of Cardiology (13.11.2012)
Published in Journal of the American College of Cardiology (13.11.2012)
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Clinical utility gene card for: Long-QT syndrome
Beckmann, Britt M, Scheiper-Welling, Stefanie, Wilde, Arthur A M, Kääb, Stefan, Schulze-Bahr, Eric, Kauferstein, Silke
Published in European journal of human genetics : EJHG (01.12.2021)
Published in European journal of human genetics : EJHG (01.12.2021)
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Variant interpretation in molecular autopsy: a useful dilemma
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
Published in International journal of legal medicine (01.03.2022)
Published in International journal of legal medicine (01.03.2022)
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Torsades de Pointes: A Rare Complication of an Extra-Adrenal Pheochromocytoma
Methe, Heiko, Hinterseer, Martin, Wilbert-Lampen, Ute, Beckmann, Britt M, Steinbeck, Gerhard, Kääb, Stefan
Published in Hypertension research (01.12.2007)
Published in Hypertension research (01.12.2007)
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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
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.
Published in European heart journal (01.04.2009)
Published in European heart journal (01.04.2009)
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Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony
Martens, Eimo, Sinner, Moritz F, Siebermair, Johannes, Raufhake, Carsten, Beckmann, Britt M, Veith, Stefan, Düvel, Dieter, Steinbeck, Gerhard, Kääb, Stefan
Published in Europace (London, England) (01.12.2014)
Published in Europace (London, England) (01.12.2014)
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Journal Article
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2
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
Published in Circulation. Cardiovascular genetics (01.06.2015)
Published in Circulation. Cardiovascular genetics (01.06.2015)
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Journal Article
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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, Veronique, Leenhardt, Antoine, Antzelevitch, Charles, Bartkowiak, Susan, Schulze-Bahr, Eric, Zumhagen, Sven, Behr, Elijah R, Bastiaenen, Rachel, Tfelt-Hansen, Jacob, Olesen, Morten Salling, Kaeaeb, 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, Bezieau, Stephane, Charpentier, Eric, Chatel, Stephanie, Despres, Aurore, Gros, Francoise, Kyndt, Florence, Lecointe, Simon, et. al
Published in Nature genetics (01.11.2013)
Published in Nature genetics (01.11.2013)
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Baseline values and sotalol-induced changes of ventricular repolarization duration, heterogeneity, and instability in patients with a history of drug-induced torsades de pointes
Couderc, Jean-Philippe, Kaab, Stefan, Hinterseer, Martin, McNitt, Scott, Xia, Xiaojuan, Fossa, Anthony, Beckmann, Britt M, Polonsky, Slava, Zareba, Wojciech
Published in Journal of clinical pharmacology (01.01.2009)
Published in Journal of clinical pharmacology (01.01.2009)
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Journal Article
Dual Inheritance of Sudden Death from Cardiovascular Causes
Beckmann, Britt M, Kääb, Stefan, Wilde, Arthur A.M
Published in The New England journal of medicine (08.05.2008)
Published in The New England journal of medicine (08.05.2008)
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The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study
Akyol, Mahmut, Jalilzadeh, Shapour, Sinner, Moritz F., Perz, Siegfried, Beckmann, Britt M., Gieger, Christian, Illig, Thomas, Wichmann, H.-Erich, Meitinger, Thomas, Kääb, Stefan, Pfeufer, Arne
Published in European heart journal (01.02.2007)
Published in European heart journal (01.02.2007)
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Journal Article
Common variants in KCNN3 are associated with lone atrial fibrillation
Topol, Eric J, Moebus, Susanne, Rice, Kenneth M, Smith, Jonathan D, Lunetta, Kathryn L, Uitterlinden, André G, Milan, David J, Schnabel, Renate B, Launer, Lenore J, Köttgen, Anna, Esko, Tõnu, Wang, Thomas J, Soliman, Elsayed Z, Gudnason, Vilmundur, Boerwinkle, Eric, Pfeufer, Arne, Barnard, John, Harris, Tamara B, Levy, Daniel, Ch Stricker, Bruno H, van Noord, Charlotte, Alonso, Alvaro, Linda Kao, W H, Van Wagoner, David R, Meitinger, Thomas, Chung, Mina K, Wichmann, H-Erich, Fox, Ervin, Steinbeck, Gerhard, Newton-Cheh, Christopher, de Bakker, Paul I W, Nelis, Mari, Beckmann, Britt-M, Mueller, Martina, MacRae, Calum A, Heckbert, Susan R, Möhlenkamp, Stefan, Kääb, Stefan, Smith, Albert V, Smith, Nicholas L, Glazer, Nicole L, Metspalu, Andres, Vasan, Ramachandran S, Li, Man, Lubitz, Steven A, Hazen, Stanley L, Psaty, Bruce M, Wang, Ke, Chakravarti, Aravinda, Ellinor, Patrick T, Sinner, Moritz F, Perz, Siegfried, Makino, Seiko, Benjamin, Emelia J, Ehret, Georg B, Hofman, Albert, Nöthen, Markus M, Roden, Dan M, Witteman, Jacqueline C M, Darbar, Dawood, Arking, Dan E, Rotter, Jerome I
Published in Nature Genetics (01.03.2010)
Published in Nature Genetics (01.03.2010)
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Corrigendum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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
Published in Nature genetics (01.11.2013)
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Published in Nature genetics (01.11.2013)
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Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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
Published in Nature genetics (29.10.2013)
Published in Nature genetics (29.10.2013)
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Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure
Hinterseer, Martin, MD, Beckmann, Britt-Maria, MD, Thomsen, Morten B., PhD, Pfeufer, Arne, MD, BSc, Ulbrich, Michael, MD, Sinner, Moritz F., MD, Perz, Siegfried, MSc, Wichmann, H.-Erich, MD, PhD, Lengyel, Csaba, MD, PhD, Schimpf, Rainer, MD, PhD, Maier, Sebastian K.G., MD, PhD, Varró, András, MD, PhD, Vos, Marc A., PhD, Steinbeck, Gerhard, MD, PhD, Kääb, Stefan, MD, PhD
Published in The American journal of cardiology (15.07.2010)
Published in The American journal of cardiology (15.07.2010)
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Journal Article
Relation of Increased Short-Term Variability of QT Interval to Congenital Long-QT Syndrome
Hinterseer, Martin, MD, Beckmann, Britt-Maria, MD, Thomsen, Morten B., PhD, Pfeufer, Arne, MD, Dalla Pozza, Robert, MD, Loeff, Markus, MD, Netz, Heinrich, MD, PhD, Steinbeck, Gerhard, MD, PhD, Vos, Marc A., PhD, Kääb, Stefan, MD, PhD
Published in The American journal of cardiology (01.05.2009)
Published in The American journal of cardiology (01.05.2009)
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Journal Article
Lack of replication in polymorphisms reported to be associated with atrial fibrillation
Sinner, Moritz F., MD, Lubitz, Steven A., MD, MPH, Pfeufer, Arne, MD, MSc, Makino, Seiko, MS, Beckmann, Britt-Maria, MD, Lunetta, Kathryn L., PhD, Steinbeck, Gerhard, MD, Perz, Siegfried, MSc, Rahman, Rosanna, PhD, Sonni, Akshata, BS, Greenberg, Steven M., MD, PhD, Furie, Karen L., MD, MPH, Wichmann, H.-Erich, MD, PhD, Meitinger, Thomas, MD, Peters, Annette, PhD, Benjamin, Emelia J., MD, ScM, Rosand, Jonathan, MD, MSc, Ellinor, Patrick T., MD, PhD, Kääb, Stefan, MD, PhD
Published in Heart rhythm (01.03.2011)
Published in Heart rhythm (01.03.2011)
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