Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Bernert, Carola (1) Beule, Dieter Dr. (1) Bock-Bierbaum, Tobias Dr. (2) Daumke, Oliver Prof. Dr. (23) Di Virgilio, Michela Prof. Dr. (1) Fälber, Katja Dr. (5) Franke, Vedran Dr. (1) Grossmann, Katja Dr. (1) Hammes-Lewin, Annette Dr. (1) Haucke, Volker Professor (1) Heinemann, Udo Prof. Dr. (2) Heuser, Arnd Dr. (3) Hübner, Norbert Prof. Dr. (1) Kolesnichenko, Marina Dr. (1) Kudryashev, Mikhail Prof. Dr. (1) Kunz, Severine Dr. (2) Lahmann, Ines Dr. (1) Mathas, Stephan Dr. (1) Müller, Dominik Prof. Dr. (1) Noel, Jeffrey Dr. (8) Panakova, Daniela Dr. (1) Patone, Giannino Dr. (1) Rocks, Oliver Dr. (2) Roske, Yvette Dr. (2) Saha, Tannishtha (1) Scheidereit, Claus Prof. Dr. (1) Schlegel, Jeanette (1) Selbach, Matthias Prof. Dr. (3) Wanker, Erich Prof. Dr. (1) Witt, Marie Dr. (2) Zühlke, Kerstin Dr. (2) (-) Coralluzzo, Violeta (1) (-) Dartsch, Josephine (3) (-) Klaassen, Sabine Prof. Dr. med. (11) (-) Klußmann, Enno PD Dr. (2) (-) Pilz, Bernhard Dr. (1) 2002 (1) 2003 (1) 2004 (2) (-) 2006 (3) 2008 (2) 2009 (1) 2011 (2) 2012 (4) 2013 (4) 2014 (3) 2015 (3) (-) 2016 (5) 2017 (1) 2018 (2) (-) 2019 (6) 2020 (1) 2021 (6) 2022 (11) 2023 (7) AG Müller/Dechend (ECRC) (16) Anchored Signalling (29) Animal Phenotyping (4) Cardiac MRI (1) Cellular Neurosciences (1) Experimental Ultrahigh-Field MR (3) (-) Genetics of Congenital Heart Disease (11) Genome Diversification & Integrity (1) Host-microbiome factors in cardiovascular disease (2) Hypertension-caused End-Organ Damage (16) Hypertension-Mediated End-Organ Damage (16) Integrative Vascular Biology (1) Magnetic Resonance (3) Molecular Biology of Peptide Hormones (1) Molecular Pathways in Cortical Development (1) Proteome Dynamics (1) Proteomics and Metabolomics (1) (-) Structural Biology of Membrane-Associated Processes (3) Translational Bioinformatics (1) 14 Results: Active Filter: Coralluzzo, VioletaDartsch, JosephineKlaassen, Sabine Prof. Dr. med.Klußmann, Enno PD Dr.Pilz, Bernhard Dr.Genetics of Congenital Heart DiseaseStructural Biology of Membrane-Associated Processes200620162019 Sort: Result score Newest to oldest Oldest to newest December 01, 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull June 01, 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder July 04, 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae November 28, 2019 / Card Vasc Biol The genetic landscape of cardiomyopathies B. Gerull S. Klaassen A. Brodehl December 02, 2016 Left ventricular noncompaction Y.M. Hoedemaekers S. Klaassen October 07, 2016 / Nat Commun Bimodal antagonism of PKA signalling by ARHGAP36 R.L. Eccles M.T. Czajkowski C. Barth P.M. Müller E. McShane S. Grunwald P. Beaudette N. Mecklenburg R. Volkmer K. Zühlke G. Dittmar M. Selbach A. Hammes O. Daumke E. Klussmann S. Urbé O. Rocks August 06, 2019 / Cell Rep 53BP1 supports immunoglobulin class switch recombination independently of its DNA double-strand break end protection function D. Sundaravinayagam A. Rahjouei M. Andreani D. Tupiņa S. Balasubramanian T. Saha V. Delgado-Benito V. Coralluzzo O. Daumke M. Di Virgilio August 06, 2019 / J Am Heart Assoc RIKADA study reveals risk factors in pediatric primary cardiomyopathy N. Al-Wakeel-Marquard F. Degener C. Herbst J. Kühnisch J. Dartsch B. Schmitt T. Kuehne D. Messroghli F. Berger S. Klaassen December 01, 2019 / Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen August 01, 2019 / Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull Pagination Current page 1 Page 2 Next page Next › Last page Last »
December 01, 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull
June 01, 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder
July 04, 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae
November 28, 2019 / Card Vasc Biol The genetic landscape of cardiomyopathies B. Gerull S. Klaassen A. Brodehl
October 07, 2016 / Nat Commun Bimodal antagonism of PKA signalling by ARHGAP36 R.L. Eccles M.T. Czajkowski C. Barth P.M. Müller E. McShane S. Grunwald P. Beaudette N. Mecklenburg R. Volkmer K. Zühlke G. Dittmar M. Selbach A. Hammes O. Daumke E. Klussmann S. Urbé O. Rocks
August 06, 2019 / Cell Rep 53BP1 supports immunoglobulin class switch recombination independently of its DNA double-strand break end protection function D. Sundaravinayagam A. Rahjouei M. Andreani D. Tupiņa S. Balasubramanian T. Saha V. Delgado-Benito V. Coralluzzo O. Daumke M. Di Virgilio
August 06, 2019 / J Am Heart Assoc RIKADA study reveals risk factors in pediatric primary cardiomyopathy N. Al-Wakeel-Marquard F. Degener C. Herbst J. Kühnisch J. Dartsch B. Schmitt T. Kuehne D. Messroghli F. Berger S. Klaassen
December 01, 2019 / Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen
August 01, 2019 / Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull