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Andreas Perrot
Andreas Perrot
Charité - Universitätsmedizin Berlin, Experimental & Clinical Research Center
Verified email at charite.de
Title
Cited by
Cited by
Year
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
W Guo, S Schafer, ML Greaser, MH Radke, M Liss, T Govindarajan, ...
Nature medicine 18 (5), 766-773, 2012
5832012
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
P Charron, M Arad, E Arbustini, C Basso, Z Bilinska, P Elliott, T Helio, ...
European heart journal 31 (22), 2715-2726, 2010
5642010
Risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers: a European cohort study
IAW van Rijsingen, E Arbustini, PM Elliott, J Mogensen, ...
Journal of the American College of Cardiology 59 (5), 493-500, 2012
5472012
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy
C Geier, A Perrot, C Özcelik, P Binner, D Counsell, K Hoffmann, B Pilz, ...
Circulation 107 (10), 1390-1395, 2003
3142003
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy
B Hoffmann, H Schmidt-Traub, A Perrot, KJ Osterziel, R Geßner
Human mutation 17 (6), 524, 2001
1942001
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy
C Geier, K Gehmlich, E Ehler, S Hassfeld, A Perrot, K Hayess, N Cardim, ...
Human molecular genetics 17 (18), 2753-2765, 2008
1772008
Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overload
AN Panek, MG Posch, N Alenina, SK Ghadge, B Erdmann, E Popova, ...
PloS one 4 (8), e6743, 2009
1532009
Gender‐specific differences in major cardiac events and mortality in lamin A/C mutation carriers
IAW van Rijsingen, EA Nannenberg, E Arbustini, PM Elliott, J Mogensen, ...
European journal of heart failure 15 (4), 376-384, 2013
1522013
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects
MG Posch, M Gramlich, M Sunde, KR Schmitt, SHY Lee, S Richter, ...
Journal of medical genetics 47 (4), 230-235, 2010
1512010
Calcineurin in human heart hypertrophy
O Ritter, S Hack, K Schuh, N Röthlein, A Perrot, KJ Osterziel, HD Schulte, ...
Circulation 105 (19), 2265-2269, 2002
1232002
Mutations in GATA4, NKX2. 5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects
MG Posch, A Perrot, K Schmitt, S Mittelhaus, EM Esenwein, B Stiller, ...
American journal of medical genetics Part A 146 (2), 251-253, 2008
1182008
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy
S Fokstuen, R Lyle, A Munoz, C Gehrig, R Lerch, A Perrot, KJ Osterziel, ...
Human mutation 29 (6), 879-885, 2008
1132008
Expression profiling of human idiopathic dilated cardiomyopathy
R Grzeskowiak, H Witt, M Drungowski, R Thermann, S Hennig, A Perrot, ...
Cardiovascular research 59 (2), 400-411, 2003
1112003
Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy
R Roncarati, C Viviani Anselmi, P Krawitz, G Lattanzi, Y Von Kodolitsch, ...
European Journal of Human Genetics 21 (10), 1105-1111, 2013
1072013
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
M Jung, I Poepping, A Perrot, AE Ellmer, TF Wienker, R Dietz, A Reis, ...
The American Journal of Human Genetics 65 (4), 1068-1077, 1999
1051999
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy
ZT Kabaeva, A Perrot, B Wolter, R Dietz, N Cardim, JM Correia, ...
European Journal of Human Genetics 10 (11), 741-748, 2002
1042002
Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes
MG Posch, A Perrot, C Geier, LH Boldt, G Schmidt, HB Lehmkuhl, ...
Heart Rhythm 6 (4), 480-486, 2009
1002009
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects
MG Posch, S Waldmuller, M Müller, T Scheffold, D Fournier, ...
PloS one 6 (12), e28872, 2011
992011
Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance
B Seebohm, F Matinmehr, J Köhler, A Francino, F Navarro-Lopez, ...
Biophysical journal 97 (3), 806-824, 2009
992009
Severe DCM phenotype of patient harboring RBM20 mutation S635A can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes
K Streckfuss-Bömeke, M Tiburcy, A Fomin, X Luo, W Li, C Fischer, ...
Journal of molecular and cellular cardiology 113, 9-21, 2017
972017
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