Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies

por Brozou, Triantafyllia, Yasin, Layal, Brandes, Danielle, Picard, Daniel, Walter, Carolin, Varghese, Julian, Dugas, Martin, Fischer, Ute, Borkhardt, Arndt, Haas, Oskar A.
Publicado 2023

Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer

por Wagener, Rabea, Taeubner, Julia, Walter, Carolin, Yasin, Layal, Alzoubi, Deya, Bartenhagen, Christoph, Attarbaschi, Andishe, Classen, Carl-Friedrich, Kontny, Udo, Hauer, Julia, Fischer, Ute, Dugas, Martin, Kuhlen, Michaela, Borkhardt, Arndt, Brozou, Triantafyllia
Publicado 2021

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia

por Brandes, Danielle, Yasin, Layal, Nebral, Karin, Ebler, Jana, Schinnerl, Dagmar, Picard, Daniel, Bergmann, Anke K., Alam, Jubayer, Köhrer, Stefan, Haas, Oskar A., Attarbaschi, Andishe, Marschall, Tobias, Stanulla, Martin, Borkhardt, Arndt, Brozou, Triantafyllia, Fischer, Ute, Wagener, Rabea
Publicado 2023