Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (1) Gotthardt, Michael Prof. Dr. (6) Hübner, Norbert Prof. Dr. (2) Hummel, Oliver (1) Kirchner, Marieluise Dr. (1) Lee, Young-Ae Prof. Dr. (1) Marenholz, Ingo Dr. (1) Radke, Michael Dr. (2) Rajewsky, Nikolaus Prof. Dr. (1) Selbach, Matthias Prof. Dr. (1) Sperling, Silke Prof. Dr. (1) (-) Klaassen, Sabine Prof. Dr. med. (3) (-) Landthaler, Markus Prof. Dr. (1) (-) Maatz, Henrike Dr. (1) 2001 (1) 2002 (1) 2003 (1) 2004 (2) 2006 (3) 2008 (3) 2009 (1) 2010 (1) 2011 (2) 2013 (5) (-) 2014 (4) 2016 (3) 2017 (1) 2018 (2) 2019 (5) 2020 (1) 2021 (6) 2022 (12) 2023 (7) Endocrinology, Diabetes and Nutritional Medicine (1) Genetics and Genomics of Cardiovascular Diseases (6) (-) Genetics of Congenital Heart Disease (3) Mathematical Modelling of Cellular Processes (1) Myology (1) Protein Production and Characterization (1) Proteome Dynamics (1) Proteomics and Metabolomics (1) RNA Biology and Posttranscriptional Regulation (8) Structural Biology of Membrane-Associated Processes (1) Systems Biology of Gene Regulatory Elements (2) (-) Translational Cardiology and Functional Genomics (1) 4 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Landthaler, Markus Prof. Dr.Maatz, Henrike Dr.Genetics of Congenital Heart DiseaseTranslational Cardiology and Functional Genomics2014 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 January 06, 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling April 03, 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles August 01, 2014 / J Clin Invest RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing H. Maatz M. Jens M. Liss S. Schafer M. Heinig M. Kirchner E. Adami C. Rintisch V. Dauksaite M.H. Radke M. Selbach P.J.R. Barton S.A. Cook N. Rajewsky M. Gotthardt M. Landthaler N. Hubner
January 06, 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling
April 03, 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles
August 01, 2014 / J Clin Invest RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing H. Maatz M. Jens M. Liss S. Schafer M. Heinig M. Kirchner E. Adami C. Rintisch V. Dauksaite M.H. Radke M. Selbach P.J.R. Barton S.A. Cook N. Rajewsky M. Gotthardt M. Landthaler N. Hubner