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Stefan Kääb
Stefan Kääb
Professor of Medicine and Cardiology, Ludwig-Maximilians University, Department of Medicine 1
Verified email at med.lmu.de
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Cited by
Cited by
Year
Five-year outcomes with PCI guided by fractional flow reserve
P Xaplanteris, S Fournier, NHJ Pijls, WF Fearon, E Barbato, PAL Tonino, ...
New England Journal of Medicine 379 (3), 250-259, 2018
8132018
Simple risk model predicts incidence of atrial fibrillation in a racially and geographically diverse population: the CHARGE‐AF consortium
A Alonso, BP Krijthe, T Aspelund, KA Stepas, MJ Pencina, CB Moser, ...
Journal of the American Heart Association 2 (2), e000102, 2013
7862013
Recent advances in the molecular pathophysiology of atrial fibrillation
R Wakili, N Voigt, S Kääb, D Dobrev, S Nattel
The Journal of clinical investigation 121 (8), 2955-2968, 2011
7242011
Ionic mechanism of action potential prolongation in ventricular myocytes from dogs with pacing-induced heart failure
S Kääb, HB Nuss, N Chiamvimonvat, B O’Rourke, PH Pak, DA Kass, ...
Circulation research 78 (2), 262-273, 1996
7121996
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ...
Nature genetics 44 (6), 670-675, 2012
6692012
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
DE Arking, A Pfeufer, W Post, WHL Kao, C Newton-Cheh, M Ikeda, K West, ...
Nature genetics 38 (6), 644-651, 2006
6172006
Multi-ethnic genome-wide association study for atrial fibrillation
C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ...
Nature genetics 50 (9), 1225-1233, 2018
5942018
Mechanisms of altered excitation-contraction coupling in canine tachycardia-induced heart failure, I: experimental studies
B O’Rourke, DA Kass, GF Tomaselli, S Kääb, R Tunin, E Marbán
Circulation research 84 (5), 562-570, 1999
5881999
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
H Watanabe, TT Koopmann, S Le Scouarnec, T Yang, CR Ingram, ...
The Journal of clinical investigation 118 (6), 2260-2268, 2008
5742008
Guided de-escalation of antiplatelet treatment in patients with acute coronary syndrome undergoing percutaneous coronary intervention (TROPICAL-ACS): a randomised, open-label …
D Sibbing, D Aradi, C Jacobshagen, L Gross, D Trenk, T Geisler, M Orban, ...
The Lancet 390 (10104), 1747-1757, 2017
5602017
Common variants in KCNN3 are associated with lone atrial fibrillation
PT Ellinor, KL Lunetta, NL Glazer, A Pfeufer, A Alonso, MK Chung, ...
Nature genetics 42 (3), 240-244, 2010
5472010
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ...
Nature genetics 45 (9), 1044-1049, 2013
5342013
Molecular basis of transient outward potassium current downregulation in human heart failure: a decrease in Kv4. 3 mRNA correlates with a reduction in current density
S Kaab, J Dixon, J Duc, D Ashen, M Nabauer, DJ Beuckelmann, ...
Circulation 98 (14), 1383-1393, 1998
5321998
Immunothrombotic dysregulation in COVID-19 pneumonia is associated with respiratory failure and coagulopathy
L Nicolai, A Leunig, S Brambs, R Kaiser, T Weinberger, M Weigand, ...
Circulation 142 (12), 1176-1189, 2020
5272020
Risk stratification for sudden cardiac death: current status and challenges for the future
HJJ Wellens, PJ Schwartz, FW Lindemans, AE Buxton, JJ Goldberger, ...
European heart journal 35 (25), 1642-1651, 2014
5142014
Genome-wide association study of PR interval
A Pfeufer, C Van Noord, KD Marciante, DE Arking, MG Larson, AV Smith, ...
Nature genetics 42 (2), 153-159, 2010
4912010
Worldwide experience with a totally subcutaneous implantable defibrillator: early results from the EFFORTLESS S-ICD Registry
PD Lambiase, C Barr, DAMJ Theuns, R Knops, P Neuzil, JB Johansen, ...
European heart journal 35 (25), 1657-1665, 2014
4732014
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
A Pfeufer, S Sanna, DE Arking, M Müller, V Gateva, C Fuchsberger, ...
Nature genetics 41 (4), 407-414, 2009
4562009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
EJ Benjamin, KM Rice, DE Arking, A Pfeufer, C Van Noord, AV Smith, ...
Nature genetics 41 (8), 879-881, 2009
4472009
Calmodulin mutations associated with recurrent cardiac arrest in infants
L Crotti, CN Johnson, E Graf, GM De Ferrari, BF Cuneo, M Ovadia, ...
Circulation 127 (9), 1009-1017, 2013
4102013
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