Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Birchmeier, Walter Prof. Dr. (1) Gotthardt, Michael Prof. Dr. (1) Grossmann, Katja Dr. (1) Heuser, Arnd Dr. (1) Hübner, Norbert Prof. Dr. (6) Hummel, Oliver (2) Lee, Young-Ae Prof. Dr. (10) Maatz, Henrike Dr. (1) Patone, Giannino Dr. (1) Perrot, Andreas (1) Radke, Michael Dr. (1) Sperling, Silke Prof. Dr. (1) (-) Klaassen, Sabine Prof. Dr. med. (10) (-) Marenholz, Ingo Dr. (5) (-) Saar, Kathrin Dr. (2) 2001 (1) 2002 (1) 2003 (1) (-) 2004 (2) 2005 (1) 2006 (5) 2007 (2) 2008 (3) 2009 (4) 2010 (2) 2011 (4) (-) 2012 (5) (-) 2013 (9) 2014 (4) 2015 (9) 2016 (3) 2017 (4) 2018 (5) 2019 (6) 2020 (5) 2021 (7) 2022 (13) 2023 (9) AG Müller/Dechend (ECRC) (1) Animal Phenotyping (2) Cardiac MRI (1) Genetics and Genomics of Cardiovascular Diseases (16) (-) Genetics of Congenital Heart Disease (10) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (6) Molecular Physiology of Somatic Sensation (1) Nephrology and Inflammatory Vascular Diseases (1) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (6) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Translational Cardiology and Functional Genomics (1) 16 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Marenholz, Ingo Dr.Saar, Kathrin Dr.Genetics of Congenital Heart DiseaseOut-patient Clinic for Pediatric Allergology and Atopic Dermatitis200420122013 Sort: Result score Newest to oldest Oldest to newest 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 April 01, 2013 / Clin Exp Allergy Genome-wide association study of body mass index in 23 000 individuals with and without asthma E. Melén R. Granell M. Kogevinas D. Strachan J.R. Gonzalez M. Wjst D. Jarvis M. Ege C. Braun-Fahrländer J. Genuneit E. Horak E. Bouzigon F. Demenais F. Kauffmann V. Siroux S. Michel A. von Berg A. Heinzmann M. Kabesch N.M. Probst-Hensch I. Curjuric M. Imboden T. Rochat J. Henderson J.A.C. Sterne W.L. McArdle J. Hui A.L. James A. William Musk L.J. Palmer A. Becker A.L. Kozyrskyj M. Chan-Young J.E. Park A. Leung D. Daley M.B. Freidin I.A. Deev L.M. Ogorodova V.P. Puzyrev J.C. Celedón J.M. Brehm M.M. Cloutier G. Canino E. Acosta-Pérez M. Soto-Quiros L. Avila A. Bergstroem J. Magnusson C. Söderhäll I. Kull S. Scholtens H. Marike Boezen G.H. Koppelman A.H. Wijga I. Marenholz J. Esparza-Gordillo S. Lau Y.A. Lee M. Standl C.M. Tiesler C. Flexeder J. Heinrich R.A. Myers C. Ober D.L. Nicolae M. Farrall A. Kumar M.F. Moffatt W.O. Cookson J. Lasky-Su January 27, 2012 / BMC Med Genet Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis S. Knuppel J. Esparza-Gordillo I. Marenholz H. Holzhutter A. Bauerfeind A. Ruether S. Weidinger Y.A. Lee K. Rohde March 01, 2013 / Neth Heart J Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7 K. van Engelen A.V. Postma J.B.A. van de Meerakker J.W. Roos-Hesselink A.T.J.M. Helderman-van den Enden H.W. Vliegen T. Rahman M.J.H. Baars J.W. Sels U. Bauer T. Pickardt S.R. Sperling A.F.M. Moorman B. Keavney J. Goodship S. Klaassen B.J. Mulder May 01, 2012 / Nat Med RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing W. Guo S. Schafer M.L. Greaser M.H. Radke M. Liss T. Govindarajan H. Maatz H. Schulz S.E. Lincoln A.M. Parrish V. Dauksaite P. Vakeel S. Klaassen B. Gerull L. Thierfelder V. Regitz-Zagrosek T.A. Hacker K.W. Saupe G.W. Dec P.T. Ellinor C.A. MacRae B. Spallek R. Fischer A. Perrot C. Ozcelik K. Saar N. Hubner M. Gotthardt January 15, 2012 / Am J Cardiol Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction M. Greutmann M.L. Mah C.K. Silversides S. Klaassen C.H. Attenhofer Jost R. Jenni E.N. Oechslin December 01, 2012 / Eur Radiol Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies M. Grothoff M. Pachowsky J. Hoffmann M. Posch S. Klaassen L. Lehmkuhl M. Gutberlet September 01, 2013 / Int J Cardiol Left ventricular non-compaction: prevalence in congenital heart disease B.E. Stähli C. Gebhard P. Biaggi S. Klaassen E. Valsangiacomo Buechel C.H. Attenhofer Jost R. Jenni F.C. Tanner M. Greutmann July 11, 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen Pagination Current page 1 Page 2 Next page Next › Last page Last »
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
April 01, 2013 / Clin Exp Allergy Genome-wide association study of body mass index in 23 000 individuals with and without asthma E. Melén R. Granell M. Kogevinas D. Strachan J.R. Gonzalez M. Wjst D. Jarvis M. Ege C. Braun-Fahrländer J. Genuneit E. Horak E. Bouzigon F. Demenais F. Kauffmann V. Siroux S. Michel A. von Berg A. Heinzmann M. Kabesch N.M. Probst-Hensch I. Curjuric M. Imboden T. Rochat J. Henderson J.A.C. Sterne W.L. McArdle J. Hui A.L. James A. William Musk L.J. Palmer A. Becker A.L. Kozyrskyj M. Chan-Young J.E. Park A. Leung D. Daley M.B. Freidin I.A. Deev L.M. Ogorodova V.P. Puzyrev J.C. Celedón J.M. Brehm M.M. Cloutier G. Canino E. Acosta-Pérez M. Soto-Quiros L. Avila A. Bergstroem J. Magnusson C. Söderhäll I. Kull S. Scholtens H. Marike Boezen G.H. Koppelman A.H. Wijga I. Marenholz J. Esparza-Gordillo S. Lau Y.A. Lee M. Standl C.M. Tiesler C. Flexeder J. Heinrich R.A. Myers C. Ober D.L. Nicolae M. Farrall A. Kumar M.F. Moffatt W.O. Cookson J. Lasky-Su
January 27, 2012 / BMC Med Genet Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis S. Knuppel J. Esparza-Gordillo I. Marenholz H. Holzhutter A. Bauerfeind A. Ruether S. Weidinger Y.A. Lee K. Rohde
March 01, 2013 / Neth Heart J Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7 K. van Engelen A.V. Postma J.B.A. van de Meerakker J.W. Roos-Hesselink A.T.J.M. Helderman-van den Enden H.W. Vliegen T. Rahman M.J.H. Baars J.W. Sels U. Bauer T. Pickardt S.R. Sperling A.F.M. Moorman B. Keavney J. Goodship S. Klaassen B.J. Mulder
May 01, 2012 / Nat Med RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing W. Guo S. Schafer M.L. Greaser M.H. Radke M. Liss T. Govindarajan H. Maatz H. Schulz S.E. Lincoln A.M. Parrish V. Dauksaite P. Vakeel S. Klaassen B. Gerull L. Thierfelder V. Regitz-Zagrosek T.A. Hacker K.W. Saupe G.W. Dec P.T. Ellinor C.A. MacRae B. Spallek R. Fischer A. Perrot C. Ozcelik K. Saar N. Hubner M. Gotthardt
January 15, 2012 / Am J Cardiol Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction M. Greutmann M.L. Mah C.K. Silversides S. Klaassen C.H. Attenhofer Jost R. Jenni E.N. Oechslin
December 01, 2012 / Eur Radiol Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies M. Grothoff M. Pachowsky J. Hoffmann M. Posch S. Klaassen L. Lehmkuhl M. Gutberlet
September 01, 2013 / Int J Cardiol Left ventricular non-compaction: prevalence in congenital heart disease B.E. Stähli C. Gebhard P. Biaggi S. Klaassen E. Valsangiacomo Buechel C.H. Attenhofer Jost R. Jenni F.C. Tanner M. Greutmann
July 11, 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen