Sven Dittmann

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Niels DecherProfessor for PhysiologyZweryfikowany adres z staff.uni-marburg.de
Aytug K KiperPhilipps-University Marburg, Institute for Physiology and Pathophysiology, AG DecherZweryfikowany adres z staff.uni-marburg.de
Matthias LinkeInstitute of Human Genetics; Medical Center of the Johannes Gutenberg University MainzZweryfikowany adres z uni-mainz.de
Derk FrankUKSH, Campus Kiel, GermanyZweryfikowany adres z uksh.de
Ashraf Yusuf Rangrez, PhDGroup Leader, Heidelberg UniversityZweryfikowany adres z med.uni-heidelberg.de
Arie O. VerkerkAmsterdam UMC, University of Amsterdam, Amsterdam, The NetherlandsZweryfikowany adres z amsterdamumc.nl
Wolfgang A LinkeProfessor of Physiology, University of MünsterZweryfikowany adres z uni-muenster.de
J. Peter van Tintelenprofessor of clinical geneticsZweryfikowany adres z umcutrecht.nl
Paul van der ZwaagClinical Geneticist, University of Groningen, University Medical Center GroningenZweryfikowany adres z umcg.nl
J.D.H. JongbloedPrincipal Investigator, clinical laboratoy geneticist, Department of Genetics, University Medical Center Groningen, University oZweryfikowany adres z umcg.nl
Hugh CalkinsProfessor of Medicine, Johns Hopkins Medical InstitutionsZweryfikowany adres z jhmi.edu
H. WulfAnästhesistZweryfikowany adres z med.uni-marburg.de
Wolfram-Hubertus ZimmermannInstitute for Pharmacology and Toxicology, University Medical Center GöttingenZweryfikowany adres z med.uni-goettingen.de
Manoj Kumar GuptaJoslin Diabetes Center, Harvard Medical SchoolZweryfikowany adres z joslin.harvard.edu
Milena BellinLeiden University Medical centerZweryfikowany adres z lumc.nl
Boris GreberCatalent Cell & Gene TherapyZweryfikowany adres z catalent.com
Kaomei GuanProfessor of Stem Cell Research and Regenerative Pharmacology and ToxicologyZweryfikowany adres z tu-dresden.de
Cynthia A. James, PhD, CGCAssociate Professor and Genetic Counselor, Division of Cardiology, Johns Hopkins UniversityZweryfikowany adres z jhmi.edu
Robert HamiltonThe Hospital for Sick Children (SickKids)Zweryfikowany adres z sickkids.ca
Danna SpearsUniversity of TorontoZweryfikowany adres z uhn.ca

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Sven Dittmann

Universitätsklinikum Münster, Institut für Genetik von Herzerkrankungen

Zweryfikowany adres z ukmuenster.de - Strona główna

human genetics biochemistry stem cells PCR next generation sequencing


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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	226	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	104	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	102	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	82	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	68	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	60	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	56	2015
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	51	2020
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	50	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	50	2019
Congenital heart diseases: the broken heart S Rickert-Sperling, RG Kelly, DJ Driscoll Springer, 2015	35	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
A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers European Heart Journal, 2024	19	2024
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	18	2014
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
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	15	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	12	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	9	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	7	2020

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