| Year |
Citation |
Score |
| 2024 |
Barkauskas R, Jenewein T, Scheiper-Welling S, Wilmes V, Niess C, Petzel-Witt S, Reitz A, Gradhand E, Falagkari A, Papathanasiou M, Wakili R, Leistner DM, Vasseur J, Göbel J, Storf H, ... ... Beckmann BM, et al. From rare events to systematic data collection: the RESCUED registry for sudden cardiac death in the young in Germany. Clinical Research in Cardiology : Official Journal of the German Cardiac Society. PMID 38748206 DOI: 10.1007/s00392-024-02460-z |
0.322 |
|
| 2023 |
Yeruva S, Stangner K, Jungwirth A, Hiermaier M, Shoykhet M, Kugelmann D, Hertl M, Egami S, Ishii N, Koga H, Hashimoto T, Weis M, Beckmann BM, Biller R, Schüttler D, et al. Correction: Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion. Cellular and Molecular Life Sciences : Cmls. 80: 296. PMID 37728633 DOI: 10.1007/s00018-023-04942-1 |
0.414 |
|
| 2023 |
Neumann B, Vink AS, Hermans BJM, Lieve KVV, Cömert D, Beckmann BM, Clur SB, Blom NA, Delhaas T, Wilde AAM, Kääb S, Postema PG, Sinner MF. Manual versus Automatic Assessment of the QT-Interval and QTc. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. PMID 37470430 DOI: 10.1093/europace/euad213 |
0.494 |
|
| 2023 |
Yeruva S, Stangner K, Jungwirth A, Hiermaier M, Shoykhet M, Kugelmann D, Hertl M, Egami S, Ishii N, Koga H, Hashimoto T, Weis M, Beckmann BM, Biller R, Schüttler D, et al. Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion. Cellular and Molecular Life Sciences : Cmls. 80: 203. PMID 37450050 DOI: 10.1007/s00018-023-04853-1 |
0.535 |
|
| 2023 |
Rinné S, Oertli A, Nagel C, Tomsits P, Jenewein T, Kääb S, Kauferstein S, Loewe A, Beckmann BM, Decher N. Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome Variants. International Journal of Molecular Sciences. 24. PMID 36674868 DOI: 10.3390/ijms24021350 |
0.57 |
|
| 2022 |
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, ... ... Beckmann BM, et al. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics. PMID 35474365 DOI: 10.1038/s41588-022-01079-y |
0.47 |
|
| 2022 |
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, ... ... Beckmann BM, et al. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics. PMID 35210625 DOI: 10.1038/s41588-021-01007-6 |
0.551 |
|
| 2021 |
Oertli A, Rinné S, Moss R, Kääb S, Seemann G, Beckmann BM, Decher N. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness. International Journal of Molecular Sciences. 22. PMID 33498651 DOI: 10.3390/ijms22031112 |
0.539 |
|
| 2020 |
Scheiper-Welling S, Zuccolini P, Rauh O, Beckmann BM, Geisen C, Moroni A, Thiel G, Kauferstein S. Characterization of an N-terminal Na1.5 channel variant - a potential risk factor for arrhythmias and sudden death? Bmc Medical Genetics. 21: 227. PMID 33213388 DOI: 10.1186/s12881-020-01170-3 |
0.366 |
|
| 2020 |
Siebermair J, Lehner S, Sattler SM, Rizas KD, Beckmann BM, Becker A, Schiller J, Metz C, Zacherl M, Vonderlin N, Rassaf T, Dobrev D, Rischpler C, Kääb S, Hacker M, et al. Left-ventricular innervation assessed by I-SPECT/CT is associated with cardiac events in inherited arrhythmia syndromes. International Journal of Cardiology. PMID 32201099 DOI: 10.1016/J.Ijcard.2020.03.013 |
0.577 |
|
| 2019 |
Crotti L, Spazzolini C, Tester DJ, Ghidoni A, Baruteau AE, Beckmann BM, Behr ER, Bennett JS, Bezzina CR, Bhuiyan ZA, Celiker A, Cerrone M, Dagradi F, De Ferrari GM, Etheridge SP, et al. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry. European Heart Journal. PMID 31170290 DOI: 10.1093/Eurheartj/Ehz311 |
0.325 |
|
| 2018 |
Scheiper S, Ramos-Luis E, Blanco-Verea A, Niess C, Beckmann BM, Schmidt U, Kettner M, Geisen C, Verhoff MA, Brion M, Kauferstein S. Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses. Forensic Science International. 293: 70-76. PMID 30415094 DOI: 10.1016/J.Forsciint.2018.09.034 |
0.393 |
|
| 2017 |
Scheiper S, Hertel B, Beckmann BM, Kääb S, Thiel G, Kauferstein S. Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients. Bmc Medical Genetics. 18: 113. PMID 29017447 DOI: 10.1186/S12881-017-0472-X |
0.549 |
|
| 2017 |
Kauferstein S, Herz N, Scheiper S, Biel S, Jenewein T, Kunis M, Erkapic D, Beckmann BM, Neumann T. Relevance of molecular testing in patients with a family history of sudden death. Forensic Science International. 276: 18-23. PMID 28472724 DOI: 10.1016/J.Forsciint.2017.04.001 |
0.44 |
|
| 2017 |
Beckmann B, Curta A, Kääb S. Genetische Arrhythmiesyndrome – Teil 2 Kardiologie Up2date. 13: 23-44. DOI: 10.1055/S-0042-122794 |
0.424 |
|
| 2016 |
Ortiz-Bonnin B, Rinné S, Moss R, Streit AK, Scharf M, Richter K, Stöber A, Pfeufer A, Seemann G, Kääb S, Beckmann BM, Decher N. Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations. Pflugers Archiv : European Journal of Physiology. PMID 27287068 DOI: 10.1007/S00424-016-1844-3 |
0.598 |
|
| 2016 |
Siebermair J, Sinner MF, Beckmann BM, Laubender RP, Martens E, Sattler S, Fichtner S, Estner HL, Kääb S, Wakili R. 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. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 18: 718-25. PMID 26759124 DOI: 10.1093/Europace/Euv301 |
0.539 |
|
| 2016 |
Tülümen E, Schulze-Bahr E, Zumhagen S, Stallmeyer B, Seebohm G, Beckmann BM, Kääb S, Rudic B, Liebe V, Wolpert C, Herrera-Siklody C, Veltmann C, Schimpf R, Borggrefe M. Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 18: 1587-1592. PMID 26705564 DOI: 10.1093/Europace/Euv357 |
0.62 |
|
| 2016 |
Reithmann C, Beckmann BM, Kääb S. Purkinje-related ventricular fibrillation associated with a homozygous H558R polymorphism in the sodium channel SCN5A gene. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 18: 896. PMID 26084969 DOI: 10.1093/Europace/Euv134 |
0.589 |
|
| 2016 |
Beckmann B, Kääb S. Genetische Arrhythmiesyndrome ohne strukturelle Herzerkrankung Kardiologie Up2date. 12: 63-75. DOI: 10.1055/S-0042-102278 |
0.439 |
|
| 2014 |
Arking DE, Pulit SL, Crotti L, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Gudbjartsson DF, Noseworthy PA, Eijgelsheim M, ... ... Beckmann BM, et al. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature Genetics. 46: 826-36. PMID 24952745 DOI: 10.1038/Ng.3014 |
0.549 |
|
| 2014 |
Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, et al. Novel calmodulin mutations associated with congenital arrhythmia susceptibility. Circulation. Cardiovascular Genetics. 7: 466-74. PMID 24917665 DOI: 10.1161/Circgenetics.113.000459 |
0.557 |
|
| 2013 |
Beckmann BM, Wilde AA, Kääb S. Clinical utility gene card for: long-QT syndrome (types 1-13). European Journal of Human Genetics : Ejhg. 21. PMID 23511927 DOI: 10.1038/Ejhg.2013.28 |
0.449 |
|
| 2013 |
Crotti L, Johnson CN, Graf E, De Ferrari GM, Cuneo BF, Ovadia M, Papagiannis J, Feldkamp MD, Rathi SG, Kunic JD, Pedrazzini M, Wieland T, Lichtner P, Beckmann BM, Clark T, et al. Calmodulin mutations associated with recurrent cardiac arrest in infants. Circulation. 127: 1009-17. PMID 23388215 DOI: 10.1161/Circulationaha.112.001216 |
0.513 |
|
| 2012 |
Beckmann BM, Kääb S. [Genetic testing in hereditary arrythmia syndromes today and in the future]. Herzschrittmachertherapie & Elektrophysiologie. 23: 161-6. PMID 22993117 DOI: 10.1007/S00399-012-0230-X |
0.535 |
|
| 2012 |
Sinner MF, Porthan K, Noseworthy PA, Havulinna AS, Tikkanen JT, Müller-Nurasyid M, Peloso G, Ulivi S, Beckmann BM, Brockhaus AC, Cooper RR, Gasparini P, Hengstenberg C, Hwang SJ, Iorio A, et al. A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 9: 1627-34. PMID 22683750 DOI: 10.1016/J.Hrthm.2012.06.008 |
0.488 |
|
| 2012 |
Kääb S, Crawford DC, Sinner MF, Behr ER, Kannankeril PJ, Wilde AA, Bezzina CR, Schulze-Bahr E, Guicheney P, Bishopric NH, Myerburg RJ, Schott JJ, Pfeufer A, Beckmann BM, Martens E, et al. A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. Circulation. Cardiovascular Genetics. 5: 91-9. PMID 22100668 DOI: 10.1161/Circgenetics.111.960930 |
0.474 |
|
| 2012 |
Reithmann C, Fiek M, Beckmann BM, Kääb S. Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongation. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 14: 299-300. PMID 21908450 DOI: 10.1093/Europace/Eur278 |
0.593 |
|
| 2011 |
Beckmann BM, Pfeufer A, Kääb S. Inherited cardiac arrhythmias: diagnosis, treatment, and prevention. Deutsches Arzteblatt International. 108: 623-33; quiz 634. PMID 21977220 DOI: 10.3238/Arztebl.2011.0623 |
0.581 |
|
| 2011 |
Sinner MF, Lubitz SA, Pfeufer A, Makino S, Beckmann BM, Lunetta KL, Steinbeck G, Perz S, Rahman R, Sonni A, Greenberg SM, Furie KL, Wichmann HE, Meitinger T, Peters A, et al. Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 403-9. PMID 21056700 DOI: 10.1016/J.Hrthm.2010.11.003 |
0.537 |
|
| 2010 |
Sinner MF, Reinhard W, Müller M, Beckmann BM, Martens E, Perz S, Pfeufer A, Winogradow J, Stark K, Meisinger C, Wichmann HE, Peters A, Riegger GA, Steinbeck G, Hengstenberg C, et al. Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA). Plos Medicine. 7: e1000314. PMID 20668657 DOI: 10.1371/Journal.Pmed.1000314 |
0.567 |
|
| 2010 |
Hinterseer M, Beckmann BM, Thomsen MB, Pfeufer A, Ulbrich M, Sinner MF, Perz S, Wichmann HE, Lengyel C, Schimpf R, Maier SK, Varró A, Vos MA, Steinbeck G, Kääb S. Usefulness of short-term variability of QT intervals as a predictor for electrical remodeling and proarrhythmia in patients with nonischemic heart failure. The American Journal of Cardiology. 106: 216-20. PMID 20599006 DOI: 10.1016/J.Amjcard.2010.02.033 |
0.582 |
|
| 2010 |
Beckmann BM, Holinski-Feder E, Walter MC, Haserück N, Reithmann C, Hinterseer M, Wilde AA, Kääb S. Laminopathy presenting as familial atrial fibrillation. International Journal of Cardiology. 145: 394-396. PMID 20472316 DOI: 10.1016/J.Ijcard.2010.04.024 |
0.458 |
|
| 2009 |
Sinner MF, Pfeufer A, Perz S, Schulze-Bahr E, Mönnig G, Eckardt L, Beckmann BM, Wichmann HE, Breithardt G, Steinbeck G, Fabritz L, Kääb S, Kirchhof P. Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 11: 1338-44. PMID 19654127 DOI: 10.1093/Europace/Eup205 |
0.521 |
|
| 2009 |
Hinterseer M, Beckmann BM, Thomsen MB, Pfeufer A, Dalla Pozza R, Loeff M, Netz H, Steinbeck G, Vos MA, Kääb S. Relation of increased short-term variability of QT interval to congenital long-QT syndrome. The American Journal of Cardiology. 103: 1244-8. PMID 19406266 DOI: 10.1016/J.Amjcard.2009.01.011 |
0.554 |
|
| 2009 |
Zellerhoff S, Pistulli R, Mönnig G, Hinterseer M, Beckmann BM, Köbe J, Steinbeck G, Kääb S, Haverkamp W, Fabritz L, Gradaus R, Breithardt G, Schulze-Bahr E, Böcker D, Kirchhof P. Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study. Journal of Cardiovascular Electrophysiology. 20: 401-7. PMID 19017345 DOI: 10.1111/J.1540-8167.2008.01339.X |
0.618 |
|
| 2009 |
Götz O, Beckmann B, Kääb S, Hinterseer M. 12-Kanal-EKG bei Brugada-Syndrom Notfall & Rettungsmedizin. 12: 37-39. DOI: 10.1007/S10049-008-1115-8 |
0.556 |
|
| 2008 |
Sinner MF, Pfeufer A, Akyol M, Beckmann BM, Hinterseer M, Wacker A, Perz S, Sauter W, Illig T, Näbauer M, Schmitt C, Wichmann HE, Schömig A, Steinbeck G, Meitinger T, et al. 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). European Heart Journal. 29: 907-14. PMID 18222980 DOI: 10.1093/Eurheartj/Ehm619 |
0.591 |
|
| 2008 |
Hinterseer M, Thomsen MB, Beckmann BM, Pfeufer A, Schimpf R, Wichmann HE, Steinbeck G, Vos MA, Kaab S. Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study. European Heart Journal. 29: 185-90. PMID 18156612 DOI: 10.1093/Eurheartj/Ehm586 |
0.569 |
|
| 2007 |
Vollmar C, Feddersen B, Beckmann BM, Kääb S, Noachtar S. Seizures on hearing the alarm clock. Lancet (London, England). 370: 2172. PMID 18156040 DOI: 10.1016/S0140-6736(07)61913-8 |
0.375 |
|
| 2007 |
Hofman N, Wilde AA, Kääb S, van Langen IM, Tanck MW, Mannens MM, Hinterseer M, Beckmann BM, Tan HL. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? European Heart Journal. 28: 575-80. PMID 17090615 DOI: 10.1093/Eurheartj/Ehl355 |
0.526 |
|
| 2006 |
Hinterseer M, Beckmann B, Thomsen MB, Pfeufer A, Perz S, Wichmann HE, Steinbeck G, Vos MA, Kääb S. P5-30: Beat-to-beat variability of QT intervals is increased in drug-induced and congenital long-QT syndromes Heart Rhythm. 3. DOI: 10.1016/J.Hrthm.2006.02.808 |
0.353 |
|
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