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| Approaches to catheter ablation for persistent atrial fibrillation A Verma, C Jiang, TR Betts, J Chen, I Deisenhofer, R Mantovan, L Macle, ... New England Journal of Medicine 372 (19), 1812-1822, 2015 | 2132 | 2015 |
| Dopamine agonists and the risk of cardiac-valve regurgitation R Schade, F Andersohn, S Suissa, W Haverkamp, E Garbe New England Journal of Medicine 356 (1), 29-38, 2007 | 882 | 2007 |
| Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II SG Priori, J Barhanin, RNW Hauer, W Haverkamp, HJ Jongsma, ... Circulation 99 (4), 518-528, 1999 | 663 | 1999 |
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| KCNE1 mutations cause Jervell and Lange-Nielsen syndrome E Schulze-Bahr, Q Wang, H Wedekind, W Haverkamp, Q Chen, Y Sun, ... Nature genetics 17 (3), 267-268, 1997 | 592 | 1997 |
| The potential for QT prolongation and pro-arrhythmia by non-anti-arrhythmic drugs: clinical and regulatory implications: report on a Policy Conference of the European Society … W Haverkamp, G Breithardt, AJ Camm, MJ Janse, MR Rosen, ... Cardiovascular research 47 (2), 219-233, 2000 | 483 | 2000 |
| Efficacy of antiarrhythmic drugs in patients with arrhythmogenic right ventricular disease. Results in patients with inducible and noninducible ventricular tachycardia. T Wichter, M Borggrefe, W Haverkamp, X Chen, G Breithardt Circulation 86 (1), 29-37, 1992 | 458 | 1992 |
| Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients JPP Smits, L Eckardt, V Probst, CR Bezzina, JJ Schott, CA Remme, ... Journal of the American College of Cardiology 40 (2), 350-356, 2002 | 453 | 2002 |
| Anterior-posterior versus anterior-lateral electrode positions for external cardioversion of atrial fibrillation: a randomised trial P Kirchhof, L Eckardt, P Loh, K Weber, RJ Fischer, KH Seidl, D Böcker, ... The Lancet 360 (9342), 1275-1279, 2002 | 374 | 2002 |
| Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients ADC Paulussen, RAHJ Gilissen, M Armstrong, PA Doevendans, ... Journal of molecular medicine 82, 182-188, 2004 | 328 | 2004 |
| Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: Different incidences in familial and sporadic disease E Schulze‐Bahr, L Eckardt, G Breithardt, K Seidl, T Wichter, C Wolpert, ... Human mutation 21 (6), 651-652, 2003 | 290 | 2003 |
| Potential usefulness and clinical relevance of adding left atrial strain to left atrial volume index in the detection of left ventricular diastolic dysfunction DA Morris, E Belyavskiy, R Aravind-Kumar, M Kropf, A Frydas, ... JACC: Cardiovascular Imaging 11 (10), 1405-1415, 2018 | 286 | 2018 |
| Peripheral artery occlusive disease in chronic phase chronic myeloid leukemia patients treated with nilotinib or imatinib TD Kim, D Rea, M Schwarz, P Grille, FE Nicolini, G Rosti, L Levato, ... Leukemia 27 (6), 1316-1321, 2013 | 284 | 2013 |
| Divergent proarrhythmic potential of macrolide antibiotics despite similar QT prolongation: fast phase 3 repolarization prevents early afterdepolarizations and torsade de pointes P Milberg, L Eckardt, HJ Bruns, J Biertz, S Ramtin, N Reinsch, D Fleischer, ... Journal of Pharmacology and Experimental Therapeutics 303 (1), 218-225, 2002 | 283 | 2002 |
| Normal values and clinical relevance of left atrial myocardial function analysed by speckle-tracking echocardiography: multicentre study DA Morris, M Takeuchi, M Krisper, C Köhncke, T Bekfani, T Carstensen, ... European Heart Journal-Cardiovascular Imaging 16 (4), 364-372, 2015 | 257 | 2015 |
| The ajmaline challenge in Brugada syndrome: diagnostic impact, safety, and recommended protocol S Rolf, HJ Bruns, T Wichter, P Kirchhof, M Ribbing, K Wasmer, M Paul, ... European Heart Journal 24 (12), 1104-1112, 2003 | 253 | 2003 |
| Dilated cardiomyopathy in mice deficient for the lysosomal cysteine peptidase cathepsin L J Stypmann, K Gläser, W Roth, DJ Tobin, I Petermann, R Matthias, ... Proceedings of the National Academy of Sciences 99 (9), 6234-6239, 2002 | 243 | 2002 |
| De Novo Mutation in the SCN5A Gene Associated With Early Onset of Sudden Infant Death H Wedekind, JPP Smits, E Schulze-Bahr, R Arnold, MW Veldkamp, ... Circulation 104 (10), 1158-1164, 2001 | 231 | 2001 |
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