Veröffentlichungen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Beule, Dieter Dr. (1) Böhmert, Laura (1) Dartsch, Josephine (3) dos Santos Periquito, Joao (2) Eigentler, Thomas Wilhelm (2) Hübner, Norbert Prof. Dr. (1) Jordan, Petya Dr. (1) Kettenmann, Helmut Prof. Dr. (2) Ku, Min-Chi Dr. (3) Kuehnisch, Jirko Dr. (3) Millward, Jason Dr. (3) Niendorf, Thoralf Prof. Dr. (36) Özerdem, Celal (1) Paul, Friedemann Prof. Dr. med. (3) Prinz, Christian (2) Purfürst, Bettina Dr. (1) Qadri, Fatimunnisa Dr. (1) Reimann, Henning Dr. (1) Schulz-Menger, Jeanette Prof. Dr. (7) Sperling, Silke Prof. Dr. (1) Waiczies, Helmar Dr. (10) Waiczies, Sonia Dr. (12) Winter, Lukas Dr. (5) Wolf, Susanne Dr. (2) (-) Klaassen, Sabine PD Dr.med. (8) (-) Ramos Delgado, Paula (2) Bioinformatics (4) Bioinformatik der Genregulation (3) Epigenetische Regulation und Chromatinstruktur (1) Experimentelle Genetik von Herz- Kreislauferkrankungen (2) (-) Experimentelle Ultrahochfeld-MR (2) (-) Genetik von Angeborenen Herzerkrankungen (8) Genregulation und Zelltypspezifizierung in C. elegans (1) Hypertonie-vermittelter Endorganschaden (2) Hypertonie bedingte Endorganschäden (2) Pluripotent Stem Cells (1) Proteomics (1) RNA Biologie und Posttranscriptionale Regulation (1) Systembiologie von Gen-regulatorischen Elementen (1) 2002 (1) 2003 (1) 2004 (2) 2006 (3) 2008 (2) 2009 (1) 2011 (2) 2012 (4) (-) 2013 (4) 2014 (3) 2015 (3) 2016 (2) 2017 (1) 2018 (1) (-) 2019 (6) 2020 (5) 2021 (5) 10 Ergebnisse: Active Filter: Klaassen, Sabine PD Dr.med.Ramos Delgado, PaulaExperimentelle Ultrahochfeld-MRGenetik von Angeborenen Herzerkrankungen20132019 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Dezember 2019 in Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen 06. August 2019 in J Am Heart Assoc RIKADA study reveals risk factors in pediatric primary cardiomyopathy N. Al-Wakeel-Marquard F. Degener C. Herbst J. Kühnisch J. Dartsch B. Schmitt T. Kuehne D. Messroghli F. Berger S. Klaassen 01. August 2019 in Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull 01. April 2019 in J Am Coll Cardiol Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy? E. Oechslin S. Klaassen 01. Februar 2019 in Magn Reson Mat Phys Biol Med Fluorine-19 MRI at 21.1 T: enhanced spin-lattice relaxation of perfluoro-15-crown-5-ether and sensitivity as demonstrated in ex vivo murine neuroinflammation S. Waiczies J.T. Rosenberg A. Kuehne L. Starke P.R. Delgado J. Millward C. Prinz J. dos Santos Periquito A. Pohlmann H. Waiczies T. Niendorf 01. Februar 2019 in Magn Reson Mat Phys Biol Med Toward (19)F magnetic resonance thermometry: spin-lattice and spin-spin-relaxation times and temperature dependence of fluorinated drugs at 9.4 T C. Prinz P.R. Delgado T.W. Eigentler L. Starke T. Niendorf S. Waiczies 01. September 2013 in 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 01. August 2013 in 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 11. Juli 2013 in 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. März 2013 in 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. Dezember 2019 in Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen
06. August 2019 in J Am Heart Assoc RIKADA study reveals risk factors in pediatric primary cardiomyopathy N. Al-Wakeel-Marquard F. Degener C. Herbst J. Kühnisch J. Dartsch B. Schmitt T. Kuehne D. Messroghli F. Berger S. Klaassen
01. August 2019 in Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull
01. April 2019 in J Am Coll Cardiol Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy? E. Oechslin S. Klaassen
01. Februar 2019 in Magn Reson Mat Phys Biol Med Fluorine-19 MRI at 21.1 T: enhanced spin-lattice relaxation of perfluoro-15-crown-5-ether and sensitivity as demonstrated in ex vivo murine neuroinflammation S. Waiczies J.T. Rosenberg A. Kuehne L. Starke P.R. Delgado J. Millward C. Prinz J. dos Santos Periquito A. Pohlmann H. Waiczies T. Niendorf
01. Februar 2019 in Magn Reson Mat Phys Biol Med Toward (19)F magnetic resonance thermometry: spin-lattice and spin-spin-relaxation times and temperature dependence of fluorinated drugs at 9.4 T C. Prinz P.R. Delgado T.W. Eigentler L. Starke T. Niendorf S. Waiczies
01. September 2013 in 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
01. August 2013 in 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
11. Juli 2013 in 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. März 2013 in 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
