Stefan Kaab
Affiliations: | Cardiology | LMU Munich, München, Bayern, Germany |
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Sign in to add trainee| Aline D. Scherff | grad student | 2019- | LMU Munich |
| Britt-Maria Beckmann | research scientist | LMU Munich |
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| Yeruva S, Stangner K, Jungwirth A, et al. (2023) 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 |
| Neumann B, Vink AS, Hermans BJM, et al. (2023) 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 |
| Yeruva S, Stangner K, Jungwirth A, et al. (2023) Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion. Cellular and Molecular Life Sciences : Cmls. 80: 203 |
| Rinné S, Oertli A, Nagel C, et al. (2023) Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome Variants. International Journal of Molecular Sciences. 24 |
| Young WJ, Lahrouchi N, Isaacs A, et al. (2022) Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. Nature Communications. 13: 5144 |
| Barc J, Tadros R, Glinge C, et al. (2022) 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 |
| Barc J, Tadros R, Glinge C, et al. (2022) Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics |
| Oertli A, Rinné S, Moss R, et al. (2021) Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness. International Journal of Molecular Sciences. 22 |
| Brado J, Hochadel M, Senges J, et al. (2021) Outcomes of ablation in Wolff-Parkinson-White-syndrome: Data from the German Ablation Registry. International Journal of Cardiology. 323: 106-112 |
| Walsh R, Lahrouchi N, Tadros R, et al. (2020) Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in Medicine : Official Journal of the American College of Medical Genetics |