Результаты поиска - Britt-Maria Beckmann

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  1. 1
    Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony

    Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony по Eimo Martens, Moritz F. Sinner, Johannes Siebermair, Carsten Raufhake, Britt Maria Beckmann, Stella Veith, D. Duvel, Gerhard Steinbeck, S. Kaab

    Опубликовано 2014
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    Artigo
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  2. 2
    Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study

    Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study по Martin Hinterseer, Morten B. Thomsen, Britt-Maria Beckmann, Arne Pfeufer, Rainer Schimpf, H.‐Erich Wichmann, G. Steinbeck, MA Vos, Stefan Kääb

    Опубликовано 2007
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  3. 3
    Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow-up over 20 years

    Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow... по Johannes Siebermair, Moritz F. Sinner, Britt-Maria Beckmann, Rüdiger P. Laubender, Eimo Martens, Stefan M. Sattler, Stephanie Fichtner, Heidi Estner, Stefan Kääb, Reza Wakili

    Опубликовано 2016
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    Artigo
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  4. 4
    Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

    Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? по Nynke Hofman, A. A. M. Wilde, Stefan Kääb, Irene M. van Langen, Michael W.T. Tanck, Marcel M.A.M. Mannens, Martin Hinterseer, Britt Maria Beckmann, Hanno L. Tan

    Опубликовано 2006
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    Artigo
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  5. 5
    The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)

    The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG) по Moritz F. Sinner, Arne Pfeufer, Mahmut Akyol, Britt-Maria Beckmann, Martin Hinterseer, Annette Wacker, Siegfried Perz, Wiebke Sauter, Thomas Illig, Michael Näbauer, Claus Schmitt, Hans Wichmann, Albert Schömig, Gerhard Steinbeck, Thomas Meitinger, Stefan Kääb

    Опубликовано 2008
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    Artigo
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  6. 6
    Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA)

    Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA) по Moritz F. Sinner, Wibke Reinhard, Martina Müller‐Nurasyid, Britt-Maria Beckmann, Eimo Martens, Siegfried Perz, Arne Pfeufer, Janina Winogradow, Klaus Stark, Christa Meisinger, H.‐Erich Wichmann, Annette Peters, Günter A.J. Riegger, Gerhard Steinbeck, Christian Hengstenberg, Stefan Kääb

    Опубликовано 2010
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    Artigo
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  7. 7
    Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade

    Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade по Camilla Schinner, Lifen Xu, Henriette Franz, Aude Zimmermann, Marie‐Therès Wanuske, Maitreyi Rathod, Pauline Hanns, Florian Geier, Paweł Pelczar, Yan Liang, Vera Lorenz, Chiara Stüdle, I. Piotr Maly, Silke Kauferstein, Britt Maria Beckmann, Farah Sheikh, Gabriela M. Kuster, Volker Spindler

    Опубликовано 2022
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    Artigo
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  8. 8
    Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2

    Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2 по Priya Chockalingam, Lia Crotti, Giulia Girardengo, Jonathan N. Johnson, Katy M. Harris, Jeroen F. van der Heijden, Richard N.W. Hauer, Britt Maria Beckmann, Carla Spazzolini, Roberto Rordorf, Annika Rydberg, Sally-Ann B. Clur, Markus Fischer, Freek van den Heuvel, Stefan Kääb, Nico A. Blom, Michael J. Ackerman, Peter J. Schwartz, Arthur A.M. Wilde

    Опубликовано 2012
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    Artigo
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  9. 9
    Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

    Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants по Lia Crotti, Christopher N. Johnson, Elisabeth Graf, Gaetano Maria De Ferrari, Bettina F. Cuneo, Marc Ovadia, John Papagiannis, Michael D. Feldkamp, Subodh Rathi, Jennifer D. Kunic, Matteo Pedrazzini, Thomas Wieland, Peter Lichtner, Britt Maria Beckmann, Travis Clark, Christian M. Shaffer, D. Woodrow Benson, Stefan Kääb, Thomas Meitinger, Tim M. Strom, Walter Chazin, Peter J. Schwartz, Alfred L. George

    Опубликовано 2013
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    Artigo
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  10. 10
    Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

    Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2 по I. Kolder, Michael W.T. Tanck, Pieter G. Postema, Julien Barc, Moritz F. Sinner, Sven Zumhagen, Anja Husemann, Birgit Stallmeyer, Tamara T. Koopmann, Nynke Hofman, Arne Pfeufer, Peter Lichtner, Thomas Meitinger, Britt Maria Beckmann, Robert J. Myerburg, Nanette H. Bishopric, Dan M. Roden, Stefan Kääb, Arthur A.M. Wilde, Jean‐Jacques Schott, Eric Schulze‐Bahr, Connie R. Bezzina

    Опубликовано 2015
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  11. 11
    Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

    Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation по Stefan Kääb, Dawood Darbar, Charlotte van Noord, Josée Dupuis, Arne Pfeufer, Chris Newton-Cheh, Renate B. Schnabel, S Makino, Moritz F. Sinner, Prince J. Kannankeril, Britt Maria Beckmann, Subbarao Choudry, Brian S. Donahue, Jan Heeringa, Siegfried Perz, Kathryn L. Lunetta, Martin G. Larson, Daniel Levy, Calum A. MacRae, Jeremy N. Ruskin, A. Wacker, Albert Schömig, H.‐Erich Wichmann, Gerhard Steinbeck, Thomas Meitinger, André G. Uitterlinden, Jacqueline C.M. Witteman, D M Roden, Emelia J. Benjamin, Patrick T. Ellinor

    Опубликовано 2008
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  12. 12
    Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

    Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility по Naomasa Makita, Nobue Yagihara, Lia Crotti, Christopher N. Johnson, Britt Maria Beckmann, Michelle S. Roh, Daichi Shigemizu, Peter Lichtner, Taisuke Ishikawa, Takeshi Aiba, Tessa Homfray, Elijah R. Behr, Didier Klug, Isabelle Denjoy, Elisa Mastantuono, Daniel Theisen, Tatsuhiko Tsunoda, Wataru Satake, Tatsushi Toda, Hidewaki Nakagawa, Yukiomi Tsuji, Takeshi Tsuchiya, Hirokazu Yamamoto, Yoshihiro Miyamoto, Naoto Endo, Akinori Kimura, Kouichi Ozaki, Hideki Motomura, Kenji Suda, Toshihiro Tanaka, Peter J. Schwartz, Thomas Meitinger, Stefan Kääb, Pascale Guicheney, Wataru Shimizu, Zahurul A. Bhuiyan, Hiroshi Watanabe, Walter Chazin, Alfred L. George

    Опубликовано 2014
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  13. 13
    A Large Candidate Gene Survey Identifies the <i>KCNE1</i> D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

    A Large Candidate Gene Survey Identifies the <i>KCNE1</i> D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes по Stefan Kääb, Dana C. Crawford, Moritz F. Sinner, Elijah R. Behr, Prince J. Kannankeril, Arthur A.M. Wilde, Connie R. Bezzina, Eric Schulze‐Bahr, Pascale Guicheney, Nanette H. Bishopric, Robert J. Myerburg, Jean‐Jacques Schott, Arne Pfeufer, Britt Maria Beckmann, Eimo Martens, Taifang Zhang, Birgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, Abdennasser Bardai, Isabelle C. Van Gelder, Yalda Jamshidi, Chrysoula Dalageorgou, Vanessa Marshall, Steve Jeffery, Saad Shakir, A. John Camm, Gerhard Steinbeck, Siegfried Perz, Peter Lichtner, Thomas Meitinger, Annette Peters, H-Erich Wichmann, Christiana D. Ingram, Yuki Bradford, Shannon Carter, Kris Norris, Marylyn D. Ritchie, Alfred L. George, Dan M. Roden

    Опубликовано 2011
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    Artigo
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  14. 14
    A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern

    A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern по Moritz F. Sinner, Kimmo Porthan, Peter A. Noseworthy, Aki S. Havulinna, Jani T. Tikkanen, Martina Müller‐Nurasyid, Gina M. Peloso, Sheila Ulivi, Britt Maria Beckmann, Anne Catharina Brockhaus, Rebecca R. Cooper, Paolo Gasparini, Christian Hengstenberg, Shih-Jen Hwang, Alfonso Iorio, Juhani Junttila, Norman Klopp, Mika Kähönen, Maarit A. Laaksonen, Terho Lehtimäki, Peter Lichtner, Leo‐Pekka Lyytikäinen, Eimo Martens, Christa Meisinger, Thomas Meitinger, Faisal M. Merchant, Markku S. Nieminen, Annette Peters, Arto Pietilä, Siegfried Perz, Lasse Oikarinen, Olli T. Raitakari, Wibke Reinhard, Kaisa Silander, Barbara Thorand, H-Erich Wichmann, Gianfranco Sinagra, Jorma Viikari, Christopher J. O’Donnell, Patrick T. Ellinor, Heikki V. Huikuri, Stefan Kääb, Christopher Newton‐Cheh, Veikko Salomaa

    Опубликовано 2012
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  15. 15
    Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

    Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry по Lia Crotti, Carla Spazzolini, David J. Tester, Alice Ghidoni, Alban‐Elouen Baruteau, Britt Maria Beckmann, Elijah R. Behr, Jeffrey S. Bennett, Connie R. Bezzina, Zahurul A. Bhuiyan, Alpay Çeliker, Marina Cerrone, Federica Dagradi, Gaetano Maria De Ferrari, Susan P. Etheridge, Meena Fatah, Pablo García‐Pavía, Saleh Alghamdi, Robert M. Hamilton, Zuhair N. Al‐Hassnan, Minoru Horie, Juan Jiménez‐Jáimez, Ronald J. Kanter, Juan Pablo Kaski, Maria‐Christina Kotta, Najim Lahrouchi, Naomasa Makita, Gabrielle Norrish, Hans Henrik Odland, Seiko Ohno, John Papagiannis, Gianfranco Parati, Nicole Sekarski, Kristian Tveten, Matteo Vatta, Gregory Webster, Arthur A.M. Wilde, Julianne Wojciak, Alfred L. George, Michael J. Ackerman, Peter J. Schwartz

    Опубликовано 2019
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  16. 16
    Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

    Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death по Connie R. Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean‐Baptiste Gourraud, Floriane Simonet, Arie O. Verkerk, Peter J. Schwartz, Lia Crotti, Federica Dagradi, Pascale Guicheney, Véronique Fressart, Antoine Leenhardt, Charles Antzelevitch, S. Bartkowiak, Martin Borggrefe, Rainer Schimpf, Eric Schulze‐Bahr, Sven Zumhagen, Elijah R. Behr, Rachel Bastiaenen, Jacob Tfelt‐Hansen, Morten S. Olesen, Stefan Kääb, Britt Maria Beckmann, Peter Weeke, Hiroshi Watanabe, Naoto Endo, Tohru Minamino, Minoru Horie, Seiko Ohno, Kanae Hasegawa, Naomasa Makita, Akihiko Nogami, Wataru Shimizu, Takeshi Aiba, Philippe Froguel, Beverley Balkau, Olivier Lantieri, Margherita Torchio, Cornelia Wiese, David Weber, Rianne Wolswinkel, Ruben Coronel, Bastiaan J. Boukens, Stéphane Bézieau, Éric Charpentier, Stéphanie Chatel, Aurore Després, F Gros, Florence Kyndt, Simon Lecointe, Pierre Lindenbaum, Vincent Portero, Jade Violleau, Manfred Gessler, Hanno L. Tan, Dan M. Roden, Vincent M. Christoffels, Hervé Le Marec, Arthur A.M. Wilde, Vincent Probst, Jean‐Jacques Schott, Christian Dina, Richard Redon

    Опубликовано 2013
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  17. 17
    Genome-wide association study of PR interval

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

    Опубликовано 2010
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  18. 18
    Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

    Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility по Julien Barc, Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet, Sean J. Jurgens, Manon Baudic, Michele Nicastro, F Potet, Joost A. Offerhaus, Roddy Walsh, Seung Hoan Choi, Arie O. Verkerk, Yuka Mizusawa, Soraya Anys, Damien Minois, Marine Arnaud, Josselin Duchâteau, Yanushi D. Wijeyeratne, Alison Muir, Michael Papadakis, Silvia Castelletti, Margherita Torchio, Cristina Gil, Javier Lacunza, Daniela Giachino, Natascia Cerrato, Raphaël P. Martins, Òscar Campuzano, Sonia Van Dooren, Aurélie Thollet, Florence Kyndt, Andrea Mazzanti, Nicolas Clémenty, Arnaud Bisson, Anniek Corveleyn, Birgit Stallmeyer, Sven Dittmann, Johan Saenen, Antoine Noël, Shohreh Honarbakhsh, Boris Rudic, Halim Marzak, Matthew Rowe, Claire Federspiel, Sophie Le Page, Leslie Placide, Antoine Milhem, Hector Barajas‐Martínez, Britt Maria Beckmann, Ingrid P.C. Krapels, Johannes Steinfurt, Bo Gregers Winkel, Reza Jabbari, M. Benjamin Shoemaker, Bas J. Boukens, Doris Škorić‐Milosavljević, Hennie Bikker, Federico Manevy, Peter Lichtner, Marta Ribasés, Thomas Meitinger, Martina Müller‐Nurasyid, Konstantin Strauch, Annette Peters, Holger Schulz, Lars Schwettmann, Reiner Leidl, Margit Heier, Jan H. Veldink, Leonard H. van den Berg, Philip Van Damme, Daniele Cusi, Chiara Lanzani, Sidwell Rigade, Éric Charpentier, Estelle Baron, Stéphanie Bonnaud, Simon Lecointe, Audrey Donnart, Hervé Le Marec, Stéphanie Chatel, Matilde Karakachoff, Stéphane Bézieau, Barry London, Jacob Tfelt‐Hansen, Dan M. Roden, Katja E. Odening, Marina Cerrone, Larry A. Chinitz, Paul G.A. Volders, Maarten P. van den Berg, Gabriel Laurent, Laurence Faivre, Charles Antzelevitch, Stefan Kääb, Alain Al Arnaout, Jean‐Marc Dupuis, Jean‐Luc Pasquié

    Опубликовано 2022
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  19. 19
    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls по Roddy Walsh, Najim Lahrouchi, Rafik Tadros, Florence Kyndt, Charlotte Glinge, Pieter G. Postema, Ahmad S. Amin, Eline A. Nannenberg, James S. Ware, Nicola Whiffin, Francesco Mazzarotto, Doris Škorić‐Milosavljević, Christian Krijger, Elena Arbelo, Dominique Babuty, Hector Barajas‐Martínez, Britt Maria Beckmann, Stéphane Bézieau, J Martijn Bos, Jeroen Breckpot, Òscar Campuzano, Silvia Castelletti, Candan Celen, Sebastian Clauß, Anniek Corveleyn, Lia Crotti, Federica Dagradi, Carlo de Asmundis, Isabelle Denjoy, Sven Dittmann, Patrick T. Ellinor, Cristina Gil, Carla Giustetto, Jean‐Baptiste Gourraud, Daisuke Hazeki, Minoru Horie, Taisuke Ishikawa, Hideki Itoh, Yoshiaki Kaneko, Jørgen K. Kanters, Hiroki Kimoto, Maria‐Christina Kotta, Ingrid P.C. Krapels, Masahiko Kurabayashi, Julieta Lazarte, Antoine Leenhardt, Bart Loeys, Catarina Lundin, Takeru Makiyama, Jacques Mansourati, Raphaël P. Martins, Andrea Mazzanti, Stellan Mörner, Carlo Napolitano, Kimie Ohkubo, Michael Papadakis, Boris Rudic, María Sabater‐Molina, Fréderic Sacher, Hatice Şahin, Geòrgia Sarquella-Brugada, Regina Sebastiano, Sanjay Sharma, Mary N. Sheppard, Keiko Shimamoto, M. Benjamin Shoemaker, Birgit Stallmeyer, Johannes Steinfurt, Yuji Tanaka, David J. Tester, Keisuke Usuda, Paul A. van der Zwaag, Sonia Van Dooren, Lut Van Laer, Annika Winbo, Bo Gregers Winkel, Kenichiro Yamagata, Sven Zumhagen, Paul G.A. Volders, Steven A. Lubitz, Charles Antzelevitch, Pyotr G. Platonov, Katja E. Odening, Dan M. Roden, Jason D. Roberts, Jonathan R. Skinner, Jacob Tfelt‐Hansen, Maarten P. van den Berg, Morten S. Olesen, Pier D. Lambiase, Martin Borggrefe, Kenshi Hayashi, Annika Rydberg, Tadashi Nakajima, Masao Yoshinaga, Johan Saenen, Stefan Kääb, Pedro Brugada, Tomas Robyns, Daniela Giachino

    Опубликовано 2020
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