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Paper Details

Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics.
Acta Neuropathol
3
2023
AT, AT/, AT/RT, AT/RT-MYC, AT/RT-SHH, AT/RT-SMARCA4, AT/RT-TYR, Atypical teratoid/rhabdoid tumors, RNA, RT, RT-SHH, SMARCA4, SMARCB1, atypical teratoid/rhabdoid tumors, chromosome 10, chromosome 1q, malignant brain tumors, patients, primary, primary tumors, tumor, tumors
Author NameAffiliation
Pascal D JohannSwabian Children's Cancer Center Augsburg, Germany and Bavarian Cancer Research Center (BZKF)
Pascal D JohannGerman Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK)
Pascal D JohannHopp Children's Cancer Center (KiTZ)
Michael BockmayrUniversity Medical Center Hamburg-Eppendorf
Michael BockmayrResearch Institute Children's Cancer Center Hamburg
Michael BockmayrUniversity Medical Center Hamburg-Eppendorf
Christine HaberlerInstitute of Neurology, Medical University of Vienna
Christine HaberlerComprehensive Cancer Center, Medical University of Vienna
Reiner SiebertInstitute of Human Genetics, Ulm University & Ulm University Medical Center
Marcel KoolHopp Children's Cancer Center (KiTZ)
Marcel KoolPrincess Maxima Center for Pediatric Oncology
Marcel KoolGerman Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK)
Marcel KoolHopp Children's Cancer Center (KiTZ)
Marcel KoolGerman Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK)
Marcel KoolPrincess Maxima Center for Pediatric Oncology
Michael C FrühwaldSwabian Children's Cancer Center Augsburg, Germany and Bavarian Cancer Research Center (BZKF)
Ulrich Sch??llerUniversity Medical Center Hamburg-Eppendorf
Ulrich Sch??llerResearch Institute Children's Cancer Center Hamburg
Ulrich Sch??llerInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf
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