Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome von Ripperger, Tim, Schlegelberger, Brigitte

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MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies von 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

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

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Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity von 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

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

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Genetic tumor risk syndromes : Human genetic aspects for radiologists von Ripperger, Tim

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Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A von Golas, Monika M., Auber, Bernd, Ripperger, Tim, Pabst, Brigitte, Schmidt, Gunnar, Morlot, Michel, Diebold, Uta, Steinemann, Doris, Schlegelberger, Brigitte, Morlot, Susanne

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

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Constitutional mismatch repair deficiency and childhood leukemia/lymphoma – report on a novel biallelic MSH6 mutation von RIPPERGER, Tim, BEGER, Carmela, RAHNER, Nils, SYKORA, Karl W, BOCKMEYER, Clemens L, LEHMANN, Ulrich, KREIPE, Hans H, SCHLEGELBERGER, Brigitte

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

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

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Tentative clinical diagnosis of Lujan-Fryns syndrome-A conglomeration of different genetic entities? von Hackmann, Karl, Rump, Andreas, Haas, Stefan A., Lemke, Johannes R., Fryns, Jean-Pierre, Tzschach, Andreas, Wieczorek, Dagmar, Albrecht, Beate, Kuechler, Alma, Ripperger, Tim, Kobelt, Albrecht, Oexle, Konrad, Tinschert, Sigrid, Schrock, Evelin, Kalscheuer, Vera M., Di Donato, Nataliya

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

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Genetische Tumorrisikosyndrome: Humangenetische Aspekte für Radiologen von Ripperger, Tim

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Breast cancer susceptibility: current knowledge and implications for genetic counselling von RIPPERGER, Tim, GADZICKI, Dorothea, MEINDL, Alfons, SCHIEGELBERGER, Brigitte

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Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms von Tesi, Bianca, Davidsson, Josef, Voss, Matthias, Rahikkala, Elisa, Holmes, Tim D., Chiang, Samuel C.C., Komulainen-Ebrahim, Jonna, Gorcenco, Sorina, Rundberg Nilsson, Alexandra, Ripperger, Tim, Kokkonen, Hannaleena, Bryder, David, Fioretos, Thoas, Henter, Jan-Inge, Möttönen, Merja, Niinimäki, Riitta, Nilsson, Lars, Pronk, Cornelis Jan, Puschmann, Andreas, Qian, Hong, Uusimaa, Johanna, Moilanen, Jukka, Tedgård, Ulf, Cammenga, Jörg, Bryceson, Yenan T.

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Beyond Pathogenic IRUNX1/I Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies von Förster, Alisa, Decker, Melanie, Schlegelberger, Brigitte, Ripperger, Tim

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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 (Feb, 1... von Ripperger, Tim, Evans, D. Gareth, Malkin, David, Kratz, Christian P.

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

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Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer von Kratz, Christian P, Smirnov, Dmitrii, Autry, Robert, Jäger, Natalie, Waszak, Sebastian M, Großhennig, Anika, Berutti, Riccardo, Wendorff, Mareike, Hainaut, Pierre, Pfister, Stefan M, Prokisch, Holger, Ripperger, Tim, Malkin, David

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