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1. Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics

2. Transcriptional immunogenomic analysis reveals distinct immunological clusters in paediatric nervous system tumours

3. Relevance of Molecular Groups in Children with Newly Diagnosed Atypical Teratoid Rhabdoid Tumor: Results from Prospective St. Jude Multi-institutional Trials.

4. SMARCB1 loss interacts with neuronal differentiation state to block maturation and impact cell stability.

5. Refractory and relapsed paediatric ACC in the MET studies – A challenging situation necessitating novel diagnostic and therapeutic concepts

7. Human-Level Differentiation of Medulloblastoma from Pilocytic Astrocytoma: A Real-World Multicenter Pilot Study

8. ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

9. DNA methylation-based classification of sinonasal tumors

10. Single-cell transcriptomics identifies potential cells of origin of MYC rhabdoid tumors

11. Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumors

12. Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors

14. Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases

16. New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs.

17. Sarcoma classification by DNA methylation profiling

18. Clinical response to nivolumab in an INI1-deficient pediatric chordoma correlates with immunogenic recognition of brachyury

19. Locoregionally administered B7-H3-targeted CAR T cells for treatment of atypical teratoid/rhabdoid tumors

20. Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

21. Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups

22. Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma.

23. Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition

24. Rhabdoid tumors in patients conceived following ART: is there an association?

25. §§ 111b-111q

27. Embryonal tumor with multilayered rosettes located in the brainstem: Promising results after multimodal treatment including interstitial brachytherapy.

28. Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1

30. Supplementary Table from The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets

31. Data from The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets

32. Supplementary Figure from The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets

35. Data from A Novel Method for Rapid Molecular Subgrouping of Medulloblastoma

36. Supplementary Appendix from A Novel Method for Rapid Molecular Subgrouping of Medulloblastoma

37. Supplementary Figures from Relevance of Molecular Groups in Children with Newly Diagnosed Atypical Teratoid Rhabdoid Tumor: Results from Prospective St. Jude Multi-institutional Trials

38. Supplementary Tables from A Novel Method for Rapid Molecular Subgrouping of Medulloblastoma

41. Outcome for Pediatric Adreno-Cortical Tumors Is Best Predicted by the COG Stage and Five-Item Microscopic Score—Report from the German MET Studies

44. Transcriptional immunogenomic analysis reveals distinct immunological clusters in pediatric nervous system tumours

45. Active medulloblastoma enhancers reveal subgroup-specific cellular origins

46. NFB-13. Rhabdoid Tumor Predisposition Syndrome (RTPS) – Finding Evidence by systematic Analyses

47. ATRT-04. Clinical and (epi)genetic characterisation of patients with atypical teratoid/rhabdoid tumor (ATRT) and extracranial malignant rhabdoid tumor conceived following assisted reproduction technologies (ART)

48. ATRT-14. Malignant rhabdoid tumors of cranial nerves – ATRT or extracranial rhabdoid tumor?

49. ATRT-08. SMARCB1- and SMARCA4-deficient malignant brain tumors with complex copy number alterations andTP53 mutations may represent the first clinical manifestation of Li-Fraumeni syndrome

50. IMMU-04. Transcriptional analysis reveals distinct microenvironmental subgroups across pediatric nervous system tumors

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