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(28) de la Rosa, Kathrin Dr. (1) Diebolder, Christoph Dr. (1) Diecke, Sebastian Dr. (3) Di Virgilio, Michela Prof. Dr. (2) Dörr, Jan Rafael (1) Fälber, Katja Dr. (2) Falcke, Martin Prof. Dr. (5) Falk, Kirsten Dr. (4) Fielitz, Jens Dr. (4) Fischer, Christian (3) Forslund, Sofia Dr. (2) Frahm-Barske, Silke Dr. (1) Gargiulo, Gaetano Dr. (2) Gorski, Stan Dr. (2) Gösele, Claudia Dr. (1) Gotthardt, Michael Prof. Dr. (6) Gouti, Mina Dr. (1) Graf, Robin Dr. (1) Grobe, Jenny (1) Grossmann, Katja Dr. (3) Grosswendt, Stefanie Dr. (1) Haas, Simon Dr. rer. nat. (1) Haase, Nadine Dr. (1) Hammes-Lewin, Annette Dr. (2) Hänig, Christian (1) Haucke, Volker Professor (4) Heinemann, Udo Prof. Dr. (21) Henssen, Anton Prof. Dr. med. (1) Herse, Florian PD Dr. (7) Heuser, Arnd Dr. (3) Hinz, Michael Dr. (1) Hofstätter, Maria (3) Höpken, Uta Elisabeth PD Dr. (4) Hörnberg, Hanna Dr. (2) Hübner, Norbert Prof. Dr. (33) Hummel, Oliver (3) Infante Duarte, Carmen (5) Ittermann, Bernd Dr. (1) Ivics, Zoltan Dr. (16) Izsvak, Zsuzsanna Dr. (16) Janke, Jürgen Dr. (7) Janz, Martin Dr. (6) Jarosch, Ernst Dr. (3) Jentsch, Thomas Prof. Dr. (35) Jung, Simone (1) Junker, Jan Philipp Prof. Dr. (2) Jüttner, Rene Dr. (2) Kainmüller, Dagmar Prof. Dr. (2) Kaminski, Michael Dr. (1) Kammertöns, Thomas Dr. (6) Keller, Ulrich Dr. med. 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(31) Perrot, Andreas (14) Pezzutto, Antonio Prof. Dr. (10) Piazza, Ilaria Dr. (1) Pilz, Bernhard Dr. (3) Pischon, Tobias Prof. Dr. (29) Pombo, Ana Prof. Dr. (8) Popova, Elena Dr. (5) Potente, Michael Prof. Dr. (4) Poulet, James Prof. Dr. (3) Preibisch, Stephan Dr. (2) Prigione, Alessandro Prof. Dr. (4) Qadri, Fatimunnisa Dr. (4) Quedenau, Claudia (1) Quensel, Christina Dr. (1) Rademann, Joerg Prof. Dr. (1) Rahn, Hans-Peter Dr. (3) Rajewsky, Klaus Prof. Dr. (5) Rajewsky, Nikolaus Prof. Dr. (12) Rathjen, Fritz Prof. Dr. (7) Rehm, Armin Dr. (2) Rocks, Oliver Dr. (12) Rosenthal, Walter Prof. Dr. (6) Roske, Yvette Dr. (3) Rousselle, Anthony (2) Rybak-Wolf, Agnieszka Dr. (1) Saar, Kathrin Dr. (10) Sander, Maike Prof. Dr. (10) Schäfer, Gesa Dr. (1) Scheidereit, Claus Prof. Dr. (15) Schiattarella, Gabriele G. Dr. (5) Schlag, Peter M. 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(7) (-) Luganskaja, Tatjana (1) (-) Sperling, Silke Prof. Dr. (5) Angiogenese & Metabolismus (1) Animal Phenotyping (3) Genetik und Genomik von Herz- Kreislauferkrankungen (1) Genetik von Angeborenen Herzerkrankungen (7) Integrative Vaskuläre Biologie (13) 1996 (1) (-) 1997 (1) 1999 (4) 2000 (6) (-) 2001 (2) 2002 (5) 2003 (6) 2004 (9) 2005 (7) (-) 2006 (9) 2007 (7) 2008 (17) 2009 (9) 2010 (7) 2011 (15) 2012 (8) (-) 2013 (13) 2014 (14) 2015 (16) 2016 (23) 2017 (13) 2018 (13) 2019 (18) 2020 (9) 2021 (15) 2022 (21) 2023 (13) 2024 (1) 25 Ergebnisse: Active Filter: Gerhardt, Holger Prof. Dr.Klaassen, Sabine Prof. Dr. med.Luganskaja, TatjanaSperling, Silke Prof. Dr.1997200120062013 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 11. Juli 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 01. August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney 01. März 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 01. Januar 2006 / Genome Inform A new statistical model to select target sequences bound by transcription factors U.J. Pape S. Grossmann S. Hammer S. Sperling M. Vingron 01. Januar 2006 / Methods Mol Med Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot S. Sperling 01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner 01. Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder 01. August 2006 / Hum Hered Concordant association of lipid gene variation with a combined HDL/LDL-cholesterol phenotype in two European populations A. Bauerfeind H. Knoblauch M.C. Costanza T. Luganskaja M.R. Toliat P. Nuernberg F.C. Luft J.G. Reich A. Morabia 04. Juli 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae 01. Dezember 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
11. Juli 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
01. August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney
01. März 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
01. Januar 2006 / Genome Inform A new statistical model to select target sequences bound by transcription factors U.J. Pape S. Grossmann S. Hammer S. Sperling M. Vingron
01. Januar 2006 / Methods Mol Med Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot S. Sperling
01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner
01. Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder
01. August 2006 / Hum Hered Concordant association of lipid gene variation with a combined HDL/LDL-cholesterol phenotype in two European populations A. Bauerfeind H. Knoblauch M.C. Costanza T. Luganskaja M.R. Toliat P. Nuernberg F.C. Luft J.G. Reich A. Morabia
04. Juli 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae
01. Dezember 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull