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Author Details

Erin R Bonner
2001
16
10
PMIDPaper TitleJournal TitlePublished Year
37318058PNOC015: Repeated convection-enhanced delivery of MTX110 (aqueous panobinostat) in children with newly diagnosed diffuse intrinsic pontine glioma.Neuro Oncol2023
37640703Pan-cancer atlas of somatic core and linker histone mutations.NPJ Genom Med2023
35157764Imipridones affect tumor bioenergetics and promote cell lineage differentiation in diffuse midline gliomas.Neuro Oncol2022
35703183Mass cytometry detects H3.3K27M-specific vaccine responses in diffuse midline glioma.J Clin Invest2022
36068285Circulating tumor DNA sequencing provides comprehensive mutation profiling for pediatric central nervous system tumors.NPJ Precis Oncol2022
35852795Upfront Biology-Guided Therapy in Diffuse Intrinsic Pontine Glioma: Therapeutic, Molecular, and Biomarker Outcomes from PNOC003.Clin Cancer Res2022
33272983Mesenchymal Stem Cells Successfully Deliver Oncolytic Virotherapy to Diffuse Intrinsic Pontine Glioma.Clin Cancer Res2021
33658570Standardization of the liquid biopsy for pediatric diffuse midline glioma using ddPCR.Sci Rep2021
33336683Mechanisms of imipridones in targeting mitochondrial metabolism in cancer cells.Neuro Oncol2021
32817593Mass cytometry detects H3.3K27M-specific vaccine responses in diffuse midline glioma.J Clin Invest2020
32438648Addition of Multimodal Immunotherapy to Combination Treatment Strategies for Children with DIPG: A Single Institution Experience.Medicines (Basel)2020
31233019Detection and Monitoring of Tumor Associated Circulating DNA in Patient Biofluids.J Vis Exp2019
30588509Liquid biopsy for pediatric central nervous system tumors.NPJ Precis Oncol2018
12481986Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.Neurogenetics2002
12210356Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defects.American Journal of Medical Genetics2002
11354831Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.Neurogenetics2001
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