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| 36916248 | Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study. | Neuro Oncol | 2023 |
| 36437415 | Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification. | Acta Neuropathol | 2023 |
| 37727849 | Embryonal tumor with multilayered rosettes: Overview of diagnosis and therapy. | Neurooncol Adv | 2023 |
| 37644658 | Cortical laminar necrosis mimicking leptomeningeal recurrence in a child with medulloblastoma and epilepsy. | | 2023 |
| 37557958 | Translating metagenomics into clinical practice for complex paediatric neurological presentations. | J Infect | 2023 |
| 37549682 | National UK guidelines for the management of paediatric craniopharyngioma. | | 2023 |
| 36964296 | Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature. | NPJ Precis Oncol | 2023 |
| 36786841 | Correction to: Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification. | Acta Neuropathol | 2023 |
| 35018471 | SIOP Ependymoma I: Final results, long-term follow-up, and molecular analysis of the trial cohort-A BIOMECA Consortium Study. | Neuro Oncol | 2022 |
| 35512371 | Causes of Sudden Unexpected Death in Childhood: Autopsy Findings from a Specialist Centre. | Pediatr Dev Pathol | 2022 |
| 35438562 | MRI Radiogenomics of Pediatric Medulloblastoma: A Multicenter Study. | Radiology | 2022 |
| 36070143 | Epigenetic profiling reveals a subset of pediatric-type glioneuronal tumors characterized by oncogenic gene fusions involving several targetable kinases. | Acta Neuropathol | 2022 |
| 35869291 | 2021 WHO classification of tumours of the central nervous system: a review for the neuroradiologist. | Neuroradiology | 2022 |
| 35926460 | Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development. | Cell Rep | 2022 |
| 34272868 | Emergence and maintenance of actionable genetic drivers at medulloblastoma relapse. | Neuro Oncol | 2022 |
| 34921008 | A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era. | Cancer Discov | 2022 |
| 34737188 | DIPG Harbors Alterations Targetable by MEK Inhibitors, with Acquired Resistance Mechanisms Overcome by Combinatorial Inhibition. | Cancer Discovery | 2022 |
| 35040226 | Developmental delay and progressive seizures in 2-month-old child with diffuse MRI abnormalities. | Brain Pathology | 2022 |
| 34980502 | Clinical outcomes, Kadish-INSICA staging and therapeutic targeting of somatostatin receptor 2 in olfactory neuroblastoma. | Eur J Cancer | 2022 |
| 34850171 | Radiomic signatures of posterior fossa ependymoma: Molecular subgroups and risk profiles. | Neuro Oncol | 2022 |
| 33325069 | A case series of Diffuse Glioneuronal Tumours with Oligodendroglioma-like features and Nuclear Clusters (DGONC). | Neuropathol Appl Neurobiol | 2021 |
| 34077956 | Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study. | Neuro Oncol | 2021 |
| 33797808 | Identifying cellular signalling molecules in developmental disorders of the brain: Evidence from focal cortical dysplasia and tuberous sclerosis. | Neuropathol Appl Neurobiol | 2021 |
| 33534137 | A rare case of paediatric astroblastoma with concomitant MN1-GTSE1 and EWSR1-PATZ1 gene fusions altering management. | Neuropathol Appl Neurobiol | 2021 |
| 34058334 | Quantitative MRI susceptibility mapping reveals cortical signatures of changes in iron, calcium and zinc in malformations of cortical development in children with drug-resistant epilepsy. | NeuroImage | 2021 |
| 34056100 | Diagnosing Mitochondrial Disorders Remains Challenging in the Omics Era. | Neurol Genet | 2021 |
| 33577116 | Acute flaccid myelitis caused by enterovirus D68 unmasking primary intracranial tumour in a previously healthy child. | Journal of Paediatrics and Child Health | 2021 |
| 33949696 | Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial. | Epilepsia | 2021 |
| 34214482 | Management of children and young people with idiopathic pituitary stalk thickening, central diabetes insipidus, or both: a national clinical practice consensus guideline. | | 2021 |
| 33664107 | A Diagnostic Algorithm for Posterior Fossa Tumors in Children: A Validation Study. | AJNR Am J Neuroradiol | 2021 |
| 33826763 | Advanced molecular pathology for rare tumours: A national feasibility study and model for centralised medulloblastoma diagnostics. | Neuropathol Appl Neurobiol | 2021 |
| 33977272 | MRI-based radiomics for prognosis of pediatric diffuse intrinsic pontine glioma: an international study. | Neurooncol Adv | 2021 |
| 32705327 | Spectrum of neuroimaging findings post-proton beam therapy in a large pediatric cohort. | Child's Nervous System | 2021 |
| 33247381 | Constitutional mismatch repair deficiency (CMMRD) presenting with high-grade glioma, multiple developmental venous anomalies and malformations of cortical development-a multidisciplinary/multicentre approach and neuroimaging clues to clinching the diagnos | Child's Nervous System | 2021 |
| 33130881 | A subset of pediatric-type thalamic gliomas share a distinct DNA methylation profile, H3K27me3 loss and frequent alteration of EGFR. | Neuro Oncol | 2021 |
| 32779246 | The molecular landscape and associated clinical experience in infant medulloblastoma: prognostic significance of second-generation subtypes. | Neuropathol Appl Neurobiol | 2021 |
| 31306337 | Challenges in the Diagnosis of Medulloblastoma Recurrence at an Unusual Site in a Patient With Prader-Willi Syndrome. | Journal of Pediatric Hematology/Oncology | 2020 |
| 32125720 | CTNNB1 mutations are clonal in adamantinomatous craniopharyngioma. | Neuropathology and Applied Neurobiology | 2020 |
| 32065673 | MRI profiling of focal cortical dysplasia using multi-compartment diffusion models. | Epilepsia | 2020 |
| 31786093 | DNA methylation-based profiling for paediatric CNS tumour diagnosis and treatment: a population-based study. | Lancet Child Adolesc Health | 2020 |
| 32238360 | Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes. | Cancer Discov | 2020 |
| 32057098 | Methylation-based algorithms for diagnosis: experience from neuro-oncology. | Journal of Pathology | 2020 |
| 31563982 | Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course. | Acta Neuropathol | 2020 |
| 32155661 | Novel therapeutic targets in epilepsy: oxidative stress and iron metabolism. | Neuropathol Appl Neurobiol | 2020 |
| 32637631 | Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene. | Neurol Genet | 2020 |
| 32859926 | Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity. | Nat Commun | 2020 |
| 32954524 | Free virtual issue: Novel paradigms for inborn errors with muscular and central neuropathology. | Journal of Inherited Metabolic Disease | 2020 |
| 32619987 | The utility of brain biopsy in pediatric cryptogenic neurological disease. | Journal of Neurosurgery: Pediatrics | 2020 |
| 33222802 | Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study. | Lancet Child Adolesc Health | 2020 |
| 32614133 | A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups. | Pediatr Blood Cancer | 2020 |