Sabine Klaassen

Sabine Klaassen

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Sabine Klaassen

Sabine Klaassen

Publications by authors named "Sabine Klaassen"

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Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.

Clin Genet 2019 Sep 30. Epub 2019 Sep 30.

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Experimental and Clinical Research Center (ECRC), a joint cooperation between the Charité Medical Faculty and the Max-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.

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http://dx.doi.org/10.1111/cge.13645DOI Listing
September 2019

Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype.

Hum Mutat 2019 Aug 24;40(8):1101-1114. Epub 2019 Apr 24.

Comprehensive Heart Failure Center (CHFC) and Department of Medicine I, University and University Hospital Würzburg, Würzburg, Germany.

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http://dx.doi.org/10.1002/humu.23757DOI Listing
August 2019

RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.

J Am Heart Assoc 2019 Aug 23;8(15):e012531. Epub 2019 Jul 23.

DZHK (German Centre for Cardiovascular Research), partner site Berlin Berlin Germany.

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http://dx.doi.org/10.1161/JAHA.119.012531DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761660PMC
August 2019

Left Ventricular Noncompaction: Phenotype in an Integrated Model of Cardiomyopathy?

J Am Coll Cardiol 2019 Apr;73(13):1612-1615

Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Pediatric Cardiology and Experimental and Clinical Research Center, a joint cooperation between the Charité Medical Faculty and the Max-Delbrück-Center for Molecular Medicine, Berlin, Germany; DZHK (German Centre for Cardiovascular Research), partner site Berlin, Berlin, Germany.

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http://dx.doi.org/10.1016/j.jacc.2018.11.064DOI Listing
April 2019

Loss of murine Gfi1 causes neutropenia and induces osteoporosis depending on the pathogen load and systemic inflammation.

PLoS One 2018 7;13(6):e0198510. Epub 2018 Jun 7.

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Medical Genetics and Human Genetics, Berlin, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0198510PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991660PMC
December 2018

The progressive ankylosis protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface.

Hum Mol Genet 2016 09 27;25(17):3836-3848. Epub 2016 Jul 27.

Institute for Medical and Human Genetics, Charité - Universitätsmedizin Berlin, Germany

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http://dx.doi.org/10.1093/hmg/ddw230DOI Listing
September 2016

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Nat Genet 2016 09 1;48(9):1060-5. Epub 2016 Aug 1.

Wellcome Trust Sanger Institute, Cambridge, UK.

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http://dx.doi.org/10.1038/ng.3627DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988037PMC
September 2016

[Molecular diagnosis for cardiovascular diseases].

Dtsch Med Wochenschr 2015 Oct 7;140(20):1538. Epub 2015 Oct 7.

Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum und Technische Universität München, Deutsches Zentrum für Herz- und Kreislaufforschung (DZHK), Munich Heart Alliance, München.

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http://dx.doi.org/10.1055/s-0041-106132DOI Listing
October 2015

Malformations of the Left Ventricle: What Comes First: Form or Function?

Authors:
Sabine Klaassen

Circ Cardiovasc Genet 2015 Aug;8(4):537-40

From the Department of Pediatric Cardiology, Charité-University Medicine Berlin & Experimental and Clinical Research Center, a joint cooperation between the Charité Medical Faculty and the Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.

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http://dx.doi.org/10.1161/CIRCGENETICS.115.001189DOI Listing
August 2015

Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.

PLoS One 2014 6;9(1):e85375. Epub 2014 Jan 6.

Department of Cardiovascular Genetics, Experimental and Clinical Research Center, Charité - Universitätsmedizin Berlin and Max Delbrück Center (MDC) for Molecular Medicine, Berlin, Germany ; Department of Biology, Chemistry, and Pharmacy, Free University of Berlin, Berlin, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085375PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882271PMC
September 2014

Reponse to De Leeuw and Houge.

Am J Hum Genet 2014 Jan;94(1):154-5

Experimental and Clinical Research Center, Charité Medical Faculty and Max Delbrück Center for Molecular Medicine, 13125 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2013.11.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882908PMC
January 2014

Left ventricular non-compaction: prevalence in congenital heart disease.

Int J Cardiol 2013 Sep 15;167(6):2477-81. Epub 2012 Jun 15.

Cardiology, Cardiovascular Center, University Hospital Zürich, Zürich, Switzerland.

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http://dx.doi.org/10.1016/j.ijcard.2012.05.095DOI Listing
September 2013

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.

Am J Med Genet C Semin Med Genet 2013 Aug 21;163C(3):178-84. Epub 2013 Jun 21.

Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.c.31365DOI Listing
August 2013

Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies.

Eur Radiol 2012 Dec 10;22(12):2699-709. Epub 2012 Jul 10.

Department of Diagnostic and Interventional Radiology, University of Leipzig - Heart Center, Strümpellstr. 39, 04289, Leipzig, Germany.

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http://dx.doi.org/10.1007/s00330-012-2554-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486997PMC
December 2012

Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction.

Am J Cardiol 2012 Jan 28;109(2):276-81. Epub 2011 Oct 28.

Division of Cardiology, University Hospital, Zurich, Switzerland.

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http://dx.doi.org/10.1016/j.amjcard.2011.08.043DOI Listing
January 2012

Mutations in the sarcomere gene MYH7 in Ebstein anomaly.

Circ Cardiovasc Genet 2011 Feb 2;4(1):43-50. Epub 2010 Dec 2.

Heart Failure Research Center, the Department of Anatomy, Embryology and Physiology, Academic Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1161/CIRCGENETICS.110.957985DOI Listing
February 2011