Search Results - Tim Ripperger

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  1. 1

    Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency by Tim Ripperger, Marcel Tauscher, Detlef Haase, Frank Griesinger, Brigitte Schlegelberger, Doris Steinemann

    Published in Haematologica (2011-12-01)
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  2. 2

    Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH by Georgi Manukjan, Marcel Tauscher, Tim Ripperger, Adrian Schwarzer, Brigitte Schlegelberger, Doris Steinemann

    Published in BioTechniques (2012-10-01)
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  3. 3

    SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES by Alisa Förster, Melanie Decker, Yvonne L. Behrens, Gudrun Göhring, Brigitte Schlegelberger, Tim Ripperger

    Published in EJC Paediatric Oncology (2023-12-01)
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  4. 4

    FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES by Melanie Decker, Förster Alisa, Prüne Alina, Anne Seebacher, Alena Wittstock, Thomas Illig, Brigitte Schlegelberger, Tim Ripperger

    Published in EJC Paediatric Oncology (2023-12-01)
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  5. 5

    GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia by Georgi Manukjan, Tim Ripperger, Letizia Venturini, Michael Stadler, Gudrun Göhring, Axel Schambach, Brigitte Schlegelberger, Doris Steinemann

    Published in Stem Cell Research (2016-05-01)
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  6. 6

    Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation by Tim Ripperger, Carmela Beger, Nils Rahner, Karl W. Sykora, Clemens L. Bockmeyer, Ulrich Lehmann, Hans H. Kreipe, Brigitte Schlegelberger

    Published in Haematologica (2010-05-01)
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  7. 7

    Progressive Immunodeficiency with Gradual Depletion of B and CD4<sup>+</sup> T Cells in Immunodeficiency, Centromeric Instability and Facial Anomalies Syndrome 2 (ICF2) by Georgios Sogkas, Natalia Dubrowinskaja, Anke K. Bergmann, Jana Lentes, Tim Ripperger, Mykola Fedchenko, Diana Ernst, Alexandra Jablonka, Robert Geffers, Ulrich Baumann, Reinhold E. Schmidt, Faranaz Atschekzei

    Published in Diseases (2019-04-01)
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  8. 8

    MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies by Tim Ripperger, Winfried Hofmann, Jan C. Koch, Katayoon Shirneshan, Detlef Haase, Gerald Wulf, Peter R. Issing, Matthias Karnebogen, Gunnar Schmidt, Bernd Auber, Brigitte Schlegelberger, Thomas Illig, Birgit Zirn, Doris Steinemann

    Published in Haematologica (2018-02-01)
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  9. 9

    Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle cell lymphomas by Tim Ripperger, Nils von Neuhoff, Kathrin Kamphues, Makito Emura, Ulrich Lehmann, Marcel Tauscher, Margit Schraders, Patricia Groenen, Britta Skawran, Cornelia Rudolph, Evelyne Callet-Bauchu, Johan H.J.M. van Krieken, Brigitte Schlegelberger, Doris Steinemann

    Published in Haematologica (2007-04-01)
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  10. 10

    Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence by Judith Penkert, Andre Märtens, Martin Seifert, Bernd Auber, Katja Derlin, Ursula Hille-Betz, Philipp Hörmann, Norman Klopp, Jana Prokein, Lisa Schlicker, Frank Wacker, Hannah Wallaschek, Brigitte Schlegelberger, Karsten Hiller, Karsten Hiller, Tim Ripperger, Thomas Illig, Thomas Illig

    Published in Frontiers in Oncology (2021-04-01)
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  11. 11

    Model of care for individuals with rare cancer predisposition syndromes in Germany by Valentina Härter, Birte Sänger, Josephine C. Gieseke, Tanja Gerasimov, Beatrice Hoffmann, Carolin Huisinga, Anja Karow, Lucas J. Müntnich, Natalie E. Palmaers, Stefanie Paquet, Judith Penkert, Diane M. Renz, Tim Ripperger, Farina J. Silchmüller, Christina M. Dutzmann, Christian P. Kratz

    Published in The Lancet Regional Health. Europe (2025-09-01)
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  12. 12

    Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy) by Martijn P. T. Ernst, Jurjen Versluis, Peter J. M. Valk, Marc Bierings, Rienk Y. J. Tamminga, Louise H. Hooimeijer, Konstanze Döhner, Paolo Gresele, Kiran Tawana, Saskia M. C. Langemeijer, Bert A. Van der Reijden, Helena Podgornik, Matjaz Sever, Tor H. A. Tvedt, Tom Vulliamy, Jude Fitzgibbon, Inderjeet Dokal, Panagiotis Baliakas, José M. Bastida, Christian Pohlkamp, Torsten Haferlach, Lise Larcher, Jean Soulier, Roger E. G. Schutgens, Kathleen Freson, Nicolas Duployez, Bob Löwenberg, Katrin Ericson, Jörg Cammenga, Tim Ripperger, Marc H. G. P. Raaijmakers

    Published in HemaSphere (2025-01-01)
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  13. 13

    The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy by Claire C. Homan, Sarah L. King-Smith, David M. Lawrence, Peer Arts, Jinghua Feng, James Andrews, Mark Armstrong, Thuong Ha, Julia Dobbins, Michael W. Drazer, Kai Yu, Csaba Bödör, Alan Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Remi Favier, Stefan Fröhling, Jude Fitzgibbon, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V. Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslova, Hugh Rienhoff, Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Velloso, Benedict Yan, Paul Liu, Lucy A. Godley, Andreas W. Schreiber, Christopher N. Hahn, Hamish S. Scott, Anna L. Brown

    Published in Haematologica (2021-07-01)
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