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Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies

2021 . Decker, Melanie | Lammens, Tim | Ferster, Alina | Erlacher, Miriam | Yoshimi, Ayami | Niemeyer, Charlotte | Ernst, Martijn P. T. | Raaijmakers, Marc H. G. P. | Duployez, Nicolas | Flaum, Andreas | Steinemann, Doris | Schlegelberger, Brigitte | Illig, Thomas | Ripperger, Tim

Reconstructing clonal evolution in relapsed and non-relapsed Burkitt lymphoma

2020 . Reutter, Katrin | Sandmann, Sarah | Rohde, Jonas | Müller, Stephanie | Wöste, Marius | Khanam, Tasneem | Michgehl, Ulf | Klapper, Wolfram | Wößmann, Wilhelm | Seggewiß, Jochen | Lenz, Georg | Dugas, Martin | Burkhardt, Birgit

Validation and refinement of the revised 2017 European LeukemiaNet genetic risk stratification of acute myeloid leukemia

In cis TP53 and RAD51C pathogenic variants may predispose to sebaceous gland carcinomas

2020 . Le Duc, Diana | Hentschel, Julia | Neuser, Sonja | Stiller, Mathias | Meier, Carolin | Jäger, Elisabeth | Abou Jamra, Rami | Platzer, Konrad | Monecke, Astrid | Ziemer, Mirjana | Markovic, Aleksander | Bläker, Hendrik | Lemke, Johannes

Evaluation of current genetic testing reports in German-speaking countries with regard to secondary use and future electronic implementation

2020 . Radke, Teja Falk | Patton, Simon J. | Pantazoglou, Elisabeth | Sass, Julian | Thun, Sylvia