| De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy B Klauke, S Kossmann, A Gaertner, K Brand, I Stork, A Brodehl, ... Human molecular genetics 19 (23), 4595-4607, 2010 | 213 | 2010 |
| Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy A Brodehl, RA Ferrier, SJ Hamilton, SC Greenway, MA Brundler, W Yu, ... Human mutation 37 (3), 269-279, 2016 | 183 | 2016 |
| Molecular insights into cardiomyopathies associated with desmin (DES) mutations A Brodehl, A Gaertner-Rommel, H Milting Biophysical reviews 10 (4), 983-1006, 2018 | 119 | 2018 |
| Novel desmin mutation p. Glu401Asp impairs filament formation, disrupts cell membrane integrity, and causes severe arrhythmogenic left ventricular cardiomyopathy/dysplasia FJ Bermúdez-Jiménez, V Carriel, A Brodehl, M Alaminos, A Campos, ... Circulation 137 (15), 1595-1610, 2018 | 98 | 2018 |
| The novel αB‐crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy A Brodehl, A Gaertner‐Rommel, B Klauke, SA Grewe, I Schirmer, ... Human mutation 38 (8), 947-952, 2017 | 76 | 2017 |
| Human induced pluripotent stem-cell-derived cardiomyocytes as models for genetic cardiomyopathies A Brodehl, H Ebbinghaus, MA Deutsch, J Gummert, A Gärtner, ... International journal of molecular sciences 20 (18), 4381, 2019 | 64 | 2019 |
| Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants A Brodehl, PN Hedde, M Dieding, A Fatima, V Walhorn, S Gayda, T Šarić, ... Journal of Biological Chemistry 287 (19), 16047-16057, 2012 | 64 | 2012 |
| Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling A Brodehl, DD Belke, L Garnett, K Martens, N Abdelfatah, M Rodriguez, ... PLoS One 12 (3), e0174019, 2017 | 63 | 2017 |
| The novel desmin mutant p. A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death A Brodehl, M Dieding, B Klauke, E Dec, S Madaan, T Huang, J Gargus, ... Circulation: Cardiovascular Genetics 6 (6), 615-623, 2013 | 61 | 2013 |
| Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect A Brodehl, SA Pour Hakimi, C Stanasiuk, S Ratnavadivel, D Hendig, ... Genes 10 (11), 918, 2019 | 59 | 2019 |
| Functional characterization of the novel DES mutation p. L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect A Brodehl, M Dieding, N Biere, A Unger, B Klauke, V Walhorn, J Gummert, ... Journal of molecular and cellular cardiology 91, 207-214, 2016 | 50 | 2016 |
| The genetic landscape of cardiomyopathies B Gerull, S Klaassen, A Brodehl Genetic causes of cardiac disease, 45-91, 2019 | 43 | 2019 |
| Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy A Brodehl, S Rezazadeh, T Williams, NM Munsie, D Liedtke, T Oh, ... Translational Research 208, 15-29, 2019 | 42 | 2019 |
| Heat shock protein 27 modification is increased in the human diabetic failing heart T Gawlowski, B Stratmann, I Stork, B Engelbrecht, A Brodehl, K Niehaus, ... Hormone and metabolic research 41 (08), 594-599, 2009 | 41 | 2009 |
| Insights into genetics and pathophysiology of arrhythmogenic cardiomyopathy B Gerull, A Brodehl Current Heart Failure Reports 18, 378-390, 2021 | 39 | 2021 |
| Genetic animal models for arrhythmogenic cardiomyopathy B Gerull, A Brodehl Frontiers in Physiology 11, 624, 2020 | 38 | 2020 |
| The novel desmin variant p. Leu115Ile is associated with a unique form of biventricular Arrhythmogenic Cardiomyopathy A Protonotarios, A Brodehl, A Asimaki, J Jager, E Quinn, C Stanasiuk, ... Canadian Journal of Cardiology 37 (6), 857-866, 2021 | 36 | 2021 |
| The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy O Kulikova, A Brodehl, A Kiseleva, R Myasnikov, A Meshkov, C Stanasiuk, ... Genes 12 (1), 121, 2021 | 35 | 2021 |
| Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20 A Gaertner, B Klauke, E Felski, A Kassner, A Brodehl, D Gerdes, ... Human Mutation 41 (11), 1931-1943, 2020 | 34 | 2020 |
| Desminopathy: novel desmin variants, a new cardiac phenotype, and further evidence for secondary mitochondrial dysfunction M Kubánek, T Schimerová, L Piherová, A Brodehl, A Krebsová, ... Journal of clinical medicine 9 (4), 937, 2020 | 33 | 2020 |
Dario AnselmettiProfessor for Biophysics at Bielefeld University在 physik.uni-bielefeld.de 的电子邮件经过验证
