Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Gerlach, Kerstin (1) Gotthardt, Michael Prof. Dr. (1) Hammes-Lewin, Annette Dr. (2) Höpken, Uta Elisabeth PD Dr. (1) Maatz, Henrike Dr. (1) Perrot, Andreas (1) Rehm, Armin Dr. (1) Schmidt-Krüger, Vanessa Dr. (4) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (9) Wolf, Jana Prof. Dr. (1) (-) Hübner, Norbert Prof. Dr. (2) (-) Klaassen, Sabine Prof. Dr. med. (4) (-) Radke, Michael Dr. (1) (-) Saar, Kathrin Dr. (1) 2002 (1) 2003 (1) 2004 (3) 2005 (1) 2006 (3) 2008 (2) 2009 (1) 2010 (1) 2011 (2) (-) 2012 (5) 2013 (4) 2014 (3) 2015 (3) 2016 (3) 2017 (1) 2018 (1) 2020 (1) 2021 (6) 2022 (11) 2023 (8) Genetics and Genomics of Cardiovascular Diseases (9) (-) Genetics of Congenital Heart Disease (4) (-) Molecular Cardiovascular Research (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (1) Molecular Physiology of Somatic Sensation (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (1) Translational Cardiology and Functional Genomics (1) 5 Results: Active Filter: Hübner, Norbert Prof. Dr.Klaassen, Sabine Prof. Dr. med.Radke, Michael Dr.Saar, Kathrin Dr.Genetics of Congenital Heart DiseaseMolecular Cardiovascular Research2012 Sort: Result score Newest to oldest Oldest to newest March 01, 2012 / Arch Neurol Identification of Alzheimer disease risk genotype that predicts efficiency of SORL1 expression in the brain S. Caglayan A. Bauerfeind V. Schmidt A.S. Carlo T. Prabakaran N. Huebner T.E. Willnow 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 06, 2012 / PLoS Genet Rare copy number variants contribute to congenital left-sided heart disease M.P. Hitz L.P. Lemieux-Perreault C. Marshall Y. Feroz-Zada R. Davies S.W. Yang A.C. Lionel G. D'Amours E. Lemyre R. Cullum J.L. Bigras M. Thibeault P. Chetaille A. Montpetit P. Khairy B. Overduin S. Klaassen P. Hoodless P. Awadalla J. Hussin Y. Idaghdour M. Nemer A.F. Stewart C. Boerkoel S.W. Scherer A. Richter M.P. Dube G. Andelfinger
March 01, 2012 / Arch Neurol Identification of Alzheimer disease risk genotype that predicts efficiency of SORL1 expression in the brain S. Caglayan A. Bauerfeind V. Schmidt A.S. Carlo T. Prabakaran N. Huebner T.E. Willnow
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 06, 2012 / PLoS Genet Rare copy number variants contribute to congenital left-sided heart disease M.P. Hitz L.P. Lemieux-Perreault C. Marshall Y. Feroz-Zada R. Davies S.W. Yang A.C. Lionel G. D'Amours E. Lemyre R. Cullum J.L. Bigras M. Thibeault P. Chetaille A. Montpetit P. Khairy B. Overduin S. Klaassen P. Hoodless P. Awadalla J. Hussin Y. Idaghdour M. Nemer A.F. Stewart C. Boerkoel S.W. Scherer A. Richter M.P. Dube G. Andelfinger