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Episignature analysis of moderate effects and mosaics.
Oexle, Konrad; Zech, Michael; Stühn, Lara G; Siegert, Sandy; Brunet, Theresa; Schmidt, Wolfgang M; Wagner, Matias; Schmidt, Axel; Engels, Hartmut; Tilch, Erik; Monestier, Olivier; Destree, Anne; Hanker, Britta; Boesch, Sylvia; Jech, Robert; Berutti, Riccardo; Kaiser, Frank; Haslinger, Bernhard; Haack, Tobias B; Garavaglia, Barbara; Krawitz, Peter; Winkelmann, Juliane; Mirza-Schreiber, Nazanin.
Afiliação
  • Oexle K; Neurogenetic Systems Analysis Group, Institute of Neurogenomics, Helmholtz Munich, 85764, Neuherberg, Germany. konrad.oexle@helmholtz-muenchen.de.
  • Zech M; Institute of Neurogenomics,Helmholtz Munich, 85764, Neuherberg, Germany. konrad.oexle@helmholtz-muenchen.de.
  • Stühn LG; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675, Munich, Germany. konrad.oexle@helmholtz-muenchen.de.
  • Siegert S; Institute of Neurogenomics,Helmholtz Munich, 85764, Neuherberg, Germany.
  • Brunet T; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675, Munich, Germany.
  • Schmidt WM; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, 72076, Tübingen, Germany.
  • Wagner M; Centre for Rare Diseases, University of Tuebingen, 72076, Tuebingen, Germany.
  • Schmidt A; Department of Pediatric and Adolescent Medicine, Medical University of Vienna, 1090, Wien, Austria.
  • Engels H; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675, Munich, Germany.
  • Tilch E; Neuromuscular Research Department, Center for Anatomy and Cell Biology, Medical University of Vienna, 1090, Vienna, Austria.
  • Monestier O; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675, Munich, Germany.
  • Destree A; Institute of Human Genetics, School of Medicine, University Hospital Bonn, 53127, Bonn, Germany.
  • Hanker B; Institute of Human Genetics, School of Medicine, University Hospital Bonn, 53127, Bonn, Germany.
  • Boesch S; Neurogenetic Systems Analysis Group, Institute of Neurogenomics, Helmholtz Munich, 85764, Neuherberg, Germany.
  • Jech R; Institute of Neurogenomics,Helmholtz Munich, 85764, Neuherberg, Germany.
  • Berutti R; Centre de Génétique Humaine, Institut de Pathologie et de Génétique ASBL, 6041, Gosselies, Belgium.
  • Kaiser F; Centre de Génétique Humaine, Institut de Pathologie et de Génétique ASBL, 6041, Gosselies, Belgium.
  • Haslinger B; Institute of Human Genetics, Universitätsklinikum Schleswig-Holstein, 23538, Lübeck, Germany.
  • Haack TB; Department of Neurology, Medizinische Universität, 6020, Insbruck, Austria.
  • Garavaglia B; Department of Neurology, Charles University, 1st Faculty of Medicine and General University Hospital in Prague, 12108, Prague, Czech Republic.
  • Krawitz P; Institute of Neurogenomics,Helmholtz Munich, 85764, Neuherberg, Germany.
  • Winkelmann J; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675, Munich, Germany.
  • Mirza-Schreiber N; Institute of Human Genetics, Universitätsklinikum Essen, 45122, Essen, Germany.
Eur J Hum Genet ; 31(9): 1032-1039, 2023 09.
Article em En | MEDLINE | ID: mdl-37365401
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Metilação de DNA Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Metilação de DNA Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article