Brent Alan Orr
Affiliations: | 2007 | University of Illinois, Urbana-Champaign, Urbana-Champaign, IL |
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"Brent Orr"Mean distance: 15.82 (cluster 19) | S | N | B | C | P |
Parents
Sign in to add mentorEdward J. Roy | grad student | 2007 | UIUC | |
(Engineering and characterization of a single chain antibody specific for murine CD28.) |
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Publications
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Carey SS, Huang J, Myers JR, et al. (2024) Outcomes for children with recurrent/refractory atypical teratoid rhabdoid tumor: A single-institution study with molecular correlation. Pediatric Blood & Cancer. e31208 |
Vizcaino MA, Giannini C, Lalich D, et al. (2024) Ganglioglioma with anaplastic/high-grade transformation: Histopathologic, molecular, and epigenetic characterization of 3 cases. Journal of Neuropathology and Experimental Neurology |
Patel AG, Ashenberg O, Collins NB, et al. (2024) A spatial cell atlas of neuroblastoma reveals developmental, epigenetic and spatial axis of tumor heterogeneity. Biorxiv : the Preprint Server For Biology |
Okonechnikov K, Joshi P, Sepp M, et al. (2023) Mapping pediatric brain tumors to their origins in the developing cerebellum. Neuro-Oncology |
Madsen PJ, Hollawell ML, Santi M, et al. (2023) Diffuse leptomeningeal glioneuronal tumor in a child masquerading as an intramedullary spinal pilocytic astrocytoma. Neuro-Oncology Advances. 5: vdad049 |
Howden K, McDonald PJ, Kazina C, et al. (2022) Sustained and durable response with Alisertib monotherapy in the treatment of relapsed Atypical Teratoid Rhabdoid Tumor (ATRT). Neuro-Oncology Advances. 4: vdac090 |
Upadhyaya SA, Campagne O, Billups CA, et al. (2022) Phase II study of alisertib as a single agent for treating recurrent or progressive atypical teratoid/rhabdoid tumor. Neuro-Oncology |
Arunachalam S, Szlachta K, Brady SW, et al. (2022) Convergent evolution and multi-wave clonal invasion in H3 K27-altered diffuse midline gliomas treated with a PDGFR inhibitor. Acta Neuropathologica Communications. 10: 80 |
Newman S, Nakitandwe J, Kesserwan CA, et al. (2021) Genomes for Kids: The scope of pathogenic mutations in pediatric cancer revealed by comprehensive DNA and RNA sequencing. Cancer Discovery |
Doucet-O'Hare TT, DiSanza BL, DeMarino C, et al. (2021) SMARCB1 deletion in atypical teratoid rhabdoid tumors results in human endogenous retrovirus K (HML-2) expression. Scientific Reports. 11: 12893 |