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Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity

Nature communications, 2020-08, Vol.11 (1), p.4324-4324, Article 4324

2020

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Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (28), p.11482-11487

2011

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Stem cell senescence drives age-attenuated induction of pituitary tumours in mouse models of paediatric craniopharyngioma

Nature communications, 2017-11, Vol.8 (1), p.1819-14, Article 1819

2017

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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 (Orlando, Fla.), 2021-09, Vol.238, p.118102-118102, Article 118102

2021

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DNA methylation‐based classification of glioneuronal tumours synergises with histology and radiology to refine accurate molecular stratification

Neuropathology and applied neurobiology, 2023-04, Vol.49 (2), p.e12894-n/a

2023

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A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease

PloS one, 2016-01, Vol.11 (1), p.e0145500

2016

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Homeostatic and tumourigenic activity of SOX2+ pituitary stem cells is controlled by the LATS/YAP/TAZ cascade

eLife, 2019-03, Vol.8

2019

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Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

NeuroImage clinical, 2017-01, Vol.15, p.95-105

2017

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Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature

NPJ precision oncology, 2023-03, Vol.7 (1), p.30-30, Article 30

2023

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Essential Role for Hematopoietic Prostaglandin D2 Synthase in the Control of Delayed Type Hypersensitivity

Proceedings of the National Academy of Sciences - PNAS, 2006-03, Vol.103 (13), p.5179-5184

2006

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Genotype‐phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery

Brain pathology (Zurich, Switzerland), 2019-07, Vol.29 (4), p.473-484

2019

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Methylation‐based algorithms for diagnosis: experience from neuro‐oncology

The Journal of pathology, 2020-04, Vol.250 (5), p.510-517

2020

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Human Coronavirus OC43 Associated with Fatal Encephalitis

The New England journal of medicine, 2016-08, Vol.375 (5), p.497-498

2016

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Free virtual issue: Novel paradigms for inborn errors with muscular and central neuropathology

Journal of inherited metabolic disease, 2020-09, Vol.43 (5), p.903-903

2020

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2021 WHO classification of tumours of the central nervous system: a review for the neuroradiologist

Neuroradiology, 2022-10, Vol.64 (10), p.1919-1950

2022

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International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods

Epilepsia (Copenhagen), 2013-07, Vol.54 (7), p.1315-1329

2013

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Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

The Journal of clinical investigation, 2018-04, Vol.128 (4), p.1496-1508

2018

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A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era

Cancer discovery, 2022-02, Vol.12 (2), p.331-355

2022

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Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation

Journal of allergy and clinical immunology, 2019-09, Vol.144 (3), p.863-866.e5

2019

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Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study

Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity

Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans

Stem cell senescence drives age-attenuated induction of pituitary tumours in mouse models of paediatric craniopharyngioma

Combined MYC and P53 Defects Emerge at Medulloblastoma Relapse and Define Rapidly Progressive, Therapeutically Targetable Disease

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

DNA methylation‐based classification of glioneuronal tumours synergises with histology and radiology to refine accurate molecular stratification

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease

Homeostatic and tumourigenic activity of SOX2+ pituitary stem cells is controlled by the LATS/YAP/TAZ cascade

Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature

Essential Role for Hematopoietic Prostaglandin D2 Synthase in the Control of Delayed Type Hypersensitivity

Genotype‐phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery

Methylation‐based algorithms for diagnosis: experience from neuro‐oncology

Human Coronavirus OC43 Associated with Fatal Encephalitis

Molecular, Pathological, Radiological, and Immune Profiling of Non-brainstem Pediatric High-Grade Glioma from the HERBY Phase II Randomized Trial

Free virtual issue: Novel paradigms for inborn errors with muscular and central neuropathology

2021 WHO classification of tumours of the central nervous system: a review for the neuroradiologist

International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era

The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission

A subset of pediatric-type thalamic gliomas share a distinct DNA methylation profile, H3K27me3 loss and frequent alteration of EGFR

Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation

Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial

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