| In vitro Modeling of Ryanodine Receptor 2 Dysfunction Using Human Induced Pluripotent Stem Cells A Fatima, G Xu, K Shao, S Papadopoulos, M Lehmann, JJ Arnáiz-Cot, ... Cellular Physiology and Biochemistry 28 (4), 579-592, 2011 | 227 | 2011 |
| The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients A Fatima, S Kaifeng, S Dittmann, G Xu, MK Gupta, M Linke, U Zechner, ... PloS one 8 (12), e83005, 2013 | 102 | 2013 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility Nature Genetics, 2022 | 91 | 2022 |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 77 | 2021 |
| Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction … CC Veerman, I Mengarelli, EM Lodder, G Kosmidis, M Bellin, M Zhang, ... Journal of the American Heart Association 6 (7), e005135, 2017 | 67 | 2017 |
| Arrhythmogenic right ventricular cardiomyopathy-associated desmosomal variants are rarely de novo: segregation and haplotype analysis of a multinational cohort FHM van Lint, B Murray, C Tichnell, R Zwart, N Amat, RH Lekanne Deprez, ... Circulation: Genomic and Precision Medicine 12 (8), e002467, 2019 | 58 | 2019 |
| TASK-1 and TASK-3 may form heterodimers in human atrial cardiomyocytes S Rinné, AK Kiper, G Schlichthörl, S Dittmann, MF Netter, SH Limberg, ... Journal of Molecular and Cellular Cardiology 81, 71-80, 2015 | 54 | 2015 |
| An international multicenter evaluation of type 5 long QT syndrome: a low penetrant primary arrhythmic condition JD Roberts, SY Asaki, A Mazzanti, JM Bos, I Tuleta, AR Muir, L Crotti, ... Circulation 141 (6), 429-439, 2020 | 49 | 2020 |
| Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy D Frank, AY Rangrez, C Friedrich, S Dittmann, B Stallmeyer, P Yadav, ... Circulation: Genomic and Precision Medicine 12 (8), e002491, 2019 | 49 | 2019 |
| An autoantibody profile detects Brugada syndrome and identifies abnormally expressed myocardial proteins D Chatterjee, M Pieroni, M Fatah, F Charpentier, KS Cunningham, ... European heart journal 41 (30), 2878-2890, 2020 | 48 | 2020 |
| Congenital heart diseases: the broken heart S Rickert-Sperling, R Kelly, DJ Driscoll Springer, 2015 | 34 | 2015 |
| Antiviral effect of Bosentan and Valsartan during coxsackievirus B3 infection of human endothelial cells C Funke, M Farr, B Werner, S Dittmann, K Überla, C Piper, K Niehaus, ... Journal of General Virology 91 (8), 1959-1970, 2010 | 25 | 2010 |
| POPDC2 a novel susceptibility gene for conduction disorders S Rinné, B Ortiz-Bonnin, B Stallmeyer, AK Kiper, L Fortmüller, ... Journal of Molecular and Cellular Cardiology 145, 74-83, 2020 | 23 | 2020 |
| Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for … B Fischer, S Dittmann, A Brodehl, A Unger, B Stallmeyer, M Paul, ... International Journal of Cardiology 329, 167-174, 2021 | 17 | 2021 |
| Effect of lovastatin on coxsackievirus B3 infection in human endothelial cells B Werner, S Dittmann, C Funke, K Überla, C Piper, K Niehaus, ... Inflammation Research 63, 267-276, 2014 | 17 | 2014 |
| Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome MK Christiansen, K Kjær-Sørensen, NC Clavsen, S Dittmann, MF Jensen, ... Heart Rhythm 20 (8), 1136-1143, 2023 | 12 | 2023 |
| Detection of patients with congenital and often concealed long-QT syndrome by novel deep learning models F Doldi, L Plagwitz, LP Hoffmann, B Rath, G Frommeyer, F Reinke, P Leitz, ... Journal of Personalized Medicine 12 (7), 1135, 2022 | 11 | 2022 |
| Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic … S Rinné, B Stallmeyer, A Pinggera, MF Netter, LA Matschke, S Dittmann, ... International Journal of Molecular Sciences 23 (22), 14215, 2022 | 7 | 2022 |
| Data on the role of cardiac α-actin (ACTC1) gene mutations on SRF-signaling AY Rangrez, L Kilian, K Stiebeling, S Dittmann, P Yadav, E Schulze-Bahr, ... Data in brief 28, 105071, 2020 | 6 | 2020 |
| Sudden unexpected cardiac death and postmortem identification of a novel RYR2 gene mutation N Mahlke, S Dittmann, E Schulze-Bahr, S Ritz-Timme, B Hartung International Journal of Legal Medicine 133, 1835-1838, 2019 | 6 | 2019 |
Niels DecherProfessor for PhysiologyVerified email at staff.uni-marburg.de
