Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Beule, Dieter Dr. (4) Birchmeier, Walter Prof. Dr. (1) Dartsch, Josephine (7) Fritsche, Raphaela Dr. (1) Gotthardt, Michael Prof. Dr. (1) Grossmann, Katja Dr. (2) Haucke, Volker Professor (1) Heuser, Arnd Dr. (7) Hübner, Norbert Prof. Dr. (3) Kirchner, Marieluise Dr. (1) Kirwan, Jennifer Dr. (1) Maatz, Henrike Dr. (1) Mertins, Philipp Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Perrot, Andreas (1) Pilz, Bernhard Dr. (1) Radke, Michael Dr. (1) Saar, Kathrin Dr. (1) Seidel, Franziska Dr. med. (12) Sperling, Silke Prof. Dr. (3) Todiras, Mihail (1) (-) Klaassen, Sabine Prof. Dr. med. (61) 2002 (1) 2003 (1) 2004 (2) 2006 (3) 2008 (2) 2009 (1) 2011 (2) 2012 (4) 2013 (4) 2014 (3) 2015 (3) 2016 (3) 2017 (1) 2018 (1) 2019 (5) 2020 (1) 2021 (6) 2022 (11) 2023 (7) Animal Phenotyping (8) Genetics and Genomics of Cardiovascular Diseases (3) (-) Genetics of Congenital Heart Disease (61) Molecular Biology of Peptide Hormones (1) Proteomics (1) Translational Bioinformatics (4) Translational Cardiology and Functional Genomics (1) 61 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Genetics of Congenital Heart Disease Sort: Result score Newest to oldest Oldest to newest January 02, 2014 / Am J Hum Genet Reponse to De Leeuw and Houge A.K. Arndt C.A. Macrae S. Klaassen June 01, 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder June 08, 2004 / Circulation Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15 S. Sasse-Klaassen S. Probst B. Gerull E. Oechslin P. Nuernberg A. Heuser R. Jenni H.C. Hennies L. Thierfelder November 01, 2004 / Nat Genet Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy B. Gerull A. Heuser T. Wichter M. Paul C.T. Basson D.A. McDermott B.B. Lerman S.M. Markowitz P.T. Ellinor C.A. MacRae S. Peters K.S. Grossmann J. Drenckhahn B. Michely S. Sasse-Klaassen W. Birchmeier R. Dietz G. Breithardt E. Schulze-Bahr L. Thierfelder February 01, 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder July 29, 2021 / PLoS Genet Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease E. Audain A. Wilsdon J. Breckpot J.M. Izarzugaza T.W. Fitzgerald A.K. Kahlert A. Sifrim F. Wünnemann Y. Perez-Riverol H. Abdul-Khaliq M. Bak A.S. Bassett W.D. Benson F. Berger I. Daehnert K. Devriendt S. Dittrich P.E. Daubeney V. Garg K. Hackmann K. Hoff P. Hofmann G. Dombrowsky T. Pickardt U. Bauer B.D. Keavney S. Klaassen H.H. Kramer C.R. Marshall D.M. Milewicz S. Lemaire J.S. Coselli M.E. Mitchell A. Tomita-Mitchell S.K. Prakash K. Stamm A.F.R. Stewart C.K. Silversides R. Siebert B. Stiller J.A. Rosenfeld I. Vater A.V. Postma A. Caliebe J.D. Brook G. Andelfinger M.E. Hurles B. Thienpont L.A. Larsen M.P. Hitz November 28, 2019 / Card Vasc Biol The genetic landscape of cardiomyopathies B. Gerull S. Klaassen A. Brodehl January 01, 2017 / Kardiologie up2date Myokarditis im Kindes- und Jugendalter S. Schubert D. Messroghli S. Klaassen F. Berger December 02, 2016 Left ventricular noncompaction Y.M. Hoedemaekers S. Klaassen August 01, 2021 / Stem Cell Res Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy N. Warnecke B.M. Ulmer S.D. Laufer A. Shibamiya E. Krämer C. Neuber S. Hanke C. Behrens M. Loos J. Münch J. Kühnisch S. Klaassen T. Eschenhagen M. Patten-Hamel L. Carrier G. Mearini Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
June 01, 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder
June 08, 2004 / Circulation Novel gene locus for autosomal dominant left ventricular noncompaction maps to chromosome 11p15 S. Sasse-Klaassen S. Probst B. Gerull E. Oechslin P. Nuernberg A. Heuser R. Jenni H.C. Hennies L. Thierfelder
November 01, 2004 / Nat Genet Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy B. Gerull A. Heuser T. Wichter M. Paul C.T. Basson D.A. McDermott B.B. Lerman S.M. Markowitz P.T. Ellinor C.A. MacRae S. Peters K.S. Grossmann J. Drenckhahn B. Michely S. Sasse-Klaassen W. Birchmeier R. Dietz G. Breithardt E. Schulze-Bahr L. Thierfelder
February 01, 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder
July 29, 2021 / PLoS Genet Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease E. Audain A. Wilsdon J. Breckpot J.M. Izarzugaza T.W. Fitzgerald A.K. Kahlert A. Sifrim F. Wünnemann Y. Perez-Riverol H. Abdul-Khaliq M. Bak A.S. Bassett W.D. Benson F. Berger I. Daehnert K. Devriendt S. Dittrich P.E. Daubeney V. Garg K. Hackmann K. Hoff P. Hofmann G. Dombrowsky T. Pickardt U. Bauer B.D. Keavney S. Klaassen H.H. Kramer C.R. Marshall D.M. Milewicz S. Lemaire J.S. Coselli M.E. Mitchell A. Tomita-Mitchell S.K. Prakash K. Stamm A.F.R. Stewart C.K. Silversides R. Siebert B. Stiller J.A. Rosenfeld I. Vater A.V. Postma A. Caliebe J.D. Brook G. Andelfinger M.E. Hurles B. Thienpont L.A. Larsen M.P. Hitz
November 28, 2019 / Card Vasc Biol The genetic landscape of cardiomyopathies B. Gerull S. Klaassen A. Brodehl
January 01, 2017 / Kardiologie up2date Myokarditis im Kindes- und Jugendalter S. Schubert D. Messroghli S. Klaassen F. Berger
August 01, 2021 / Stem Cell Res Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy N. Warnecke B.M. Ulmer S.D. Laufer A. Shibamiya E. Krämer C. Neuber S. Hanke C. Behrens M. Loos J. Münch J. Kühnisch S. Klaassen T. Eschenhagen M. Patten-Hamel L. Carrier G. Mearini