Search Results - Ripperger, Tim

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  1. 1
    Correspondence (letter to the editor): Supplemental Human Genetics Point of View

    Correspondence (letter to the editor): Supplemental Human Genetics Point of View by Ripperger, Tim, Illig, Thomas, Schlegelberger, Brigitte

    Published 2019
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  2. 2
    Breast cancer susceptibility: current knowledge and implications for genetic counselling

    Breast cancer susceptibility: current knowledge and implications for genetic counselling by Ripperger, Tim, Gadzicki, Dorothea, Meindl, Alfons, Schlegelberger, Brigitte

    Published 2009
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  3. 3
    Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies

    Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies by Förster, Alisa, Decker, Melanie, Schlegelberger, Brigitte, Ripperger, Tim

    Published 2022
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  4. 4
    Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer

    Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer by Ripperger, Tim, Evans, D Gareth, Malkin, David, Kratz, Christian P.

    Published 2021
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  5. 5
    Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer

    Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with... by Ripperger, Tim, Evans, D. Gareth, Malkin, David, Kratz, Christian P.

    Published 2021
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  6. 6
    Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire

    Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire by Schwermer, Miriam, Behnert, Astrid, Dörgeloh, Beate, Ripperger, Tim, Kratz, Christian P.

    Published 2021
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  7. 7
    Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency

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

    Published 2011
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  8. 8
    Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies

    Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies by Ripperger, Tim, Tawana, Kiran, Kratz, Christian, Schlegelberger, Brigitte, Fitzgibbon, Jude, Steinemann, Doris

    Published 2016
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  9. 9
    On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancer

    On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancer by Penkert, Judith, Ripperger, Tim, Schieck, Maximilian, Schlegelberger, Brigitte, Steinemann, Doris, Illig, Thomas

    Published 2016
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  10. 10
    PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1

    PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1 by Vogt, Julia, Wernstedt, Annekatrin, Ripperger, Tim, Pabst, Brigitte, Zschocke, Johannes, Kratz, Christian, Wimmer, Katharina

    Published 2016
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  11. 11
    Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation

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

    Published 2010
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  12. 12
    GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

    GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families by Schubert, Stephanie, Ripperger, Tim, Rood, Melanie, Petkidis, Anthony, Hofmann, Winfried, Frye-Boukhriss, Hildegard, Tauscher, Marcel, Auber, Bernd, Hille-Betz, Ursula, Illig, Thomas, Schlegelberger, Brigitte, Steinemann, Doris

    Published 2017
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  13. 13
    Progressive Immunodeficiency with Gradual Depletion of B and CD4(+) T Cells in Immunodeficiency, Centromeric Instability and Facial Anomalies Syndrome 2 (ICF2)

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

    Published 2019
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  14. 14
    A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency

    A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency by Wimmer, Katharina, Beilken, Andreas, Nustede, Rainer, Ripperger, Tim, Lamottke, Britta, Ure, Benno, Steinmann, Diana, Reineke-Plaass, Tanja, Lehmann, Ulrich, Zschocke, Johannes, Valle, Laura, Fauth, Christine, Kratz, Christian P.

    Published 2016
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  15. 15
    MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies

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

    Published 2018
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  16. 16
    Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

    Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity by Penkert, Judith, Schmidt, Gunnar, Hofmann, Winfried, Schubert, Stephanie, Schieck, Maximilian, Auber, Bernd, Ripperger, Tim, Hackmann, Karl, Sturm, Marc, Prokisch, Holger, Hille-Betz, Ursula, Mark, Dorothea, Illig, Thomas, Schlegelberger, Brigitte, Steinemann, Doris

    Published 2018
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  17. 17
    Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence

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

    Published 2021
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  18. 18
    Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies

    Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies by Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim

    Published 2021
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  19. 19
    Validation and clinical application of transactivation assays for RUNX1 variant classification

    Validation and clinical application of transactivation assays for RUNX1 variant classification by Decker, Melanie, Agarwal, Anupriya, Benneche, Andreas, Churpek, Jane, Duployez, Nicolas, Duvall, Adam, Ernst, Martijn P. T., Förster, Alisa, Høberg-Vetti, Hildegunn, Hofmann, Inga, Nash, Michelle, Raaijmakers, Marc H. G. P., Tvedt, Tor H. A., Vlachos, Adrianna, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim

    Published 2022
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  20. 20
    Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome

    Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome by Winter, Greta, Kirschner-Schwabe, Renate, Groeneveld-Krentz, Stefanie, Escherich, Gabriele, Möricke, Anja, von Stackelberg, Arend, Stanulla, Martin, Bailey, Simon, Richter, Lisa, Steinemann, Doris, Ripperger, Tim, Escudero, Adela, Farah, Roula, Lohi, Olli, Wadt, Karin, Jongmans, Marjolijn, van Engelen, Nienke, Eckert, Cornelia, Kratz, Christian Peter

    Published 2021
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