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. (1) Dartsch, Josephine (3) Gotthardt, Michael Prof. Dr. (1) Heuser, Arnd Dr. (1) Hübner, Norbert Prof. Dr. (3) Hummel, Oliver (1) Lee, Young-Ae Prof. Dr. (7) Marenholz, Ingo Dr. (2) Patone, Giannino Dr. (1) Perrot, Andreas (1) Radke, Michael Dr. (1) (-) Klaassen, Sabine Prof. Dr. med. (11) (-) Maatz, Henrike Dr. (1) (-) Saar, Kathrin Dr. (2) 2001 (1) 2002 (1) 2003 (1) 2004 (2) 2006 (3) (-) 2008 (3) 2009 (1) 2010 (1) 2011 (2) (-) 2012 (4) 2013 (5) 2014 (3) 2015 (4) 2016 (3) 2017 (1) 2018 (1) (-) 2019 (5) 2020 (1) 2021 (6) 2023 (7) AG Müller/Dechend (ECRC) (2) Animal Phenotyping (2) Bioinformatics and Omics Data Science (4) Computational Regulatory Genomics (3) Epigenetic Regulation and Chromatin Architecture (1) Genetics and Genomics of Cardiovascular Diseases (12) (-) Genetics of Congenital Heart Disease (11) Hypertension-caused End-Organ Damage (2) Hypertension-Mediated End-Organ Damage (2) Mobile DNA (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (1) Molecular Physiology of Somatic Sensation (1) Nephrology and Inflammatory Vascular Diseases (1) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (1) Pluripotent Stem Cells (1) Proteomics (1) RNA Biology and Posttranscriptional Regulation (1) Systems Biology of Gene Regulatory Elements (1) Translational Bioinformatics (1) Translational Cardiology and Functional Genomics (1) 12 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Maatz, Henrike Dr.Saar, Kathrin Dr.Genetics of Congenital Heart DiseaseOut-patient Clinic for Pediatric Allergology and Atopic Dermatitis200820122019 Sort: Result score Newest to oldest Oldest to newest April 01, 2019 / J Am Coll Cardiol Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy? E. Oechslin S. Klaassen 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 Pagination First page « First Previous page ‹ Previous Page 1 Current page 2
April 01, 2019 / J Am Coll Cardiol Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy? E. Oechslin S. Klaassen
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