Mutations within FGFR1 are associated with superior outcome in a series of 83 diffuse midline gliomas with H3F3A K27M mutations

Identification of prognostic markers in diffuse midline gliomas H3K27M‐mutant

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Recurrent non-canonical histone H3 mutations in spinal cord diffuse gliomas

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K27M midline gliomas display malignant progression by imaging and histology

(2017) F. J. Vettermann et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Targeted detection of genetic alterations reveal the prognostic impact of H3K27M and MAPK pathway aberrations in paediatric thalamic glioma

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Diffuse Midline Gliomas with Histone H3-K27M Mutation: A Series of 47 Cases Assessing the Spectrum of Morphologic Variation and Associated Genetic Alterations

(2015) David A. Solomon et al.   BRAIN PATHOLOGY

Evidence forBRAFV600E andH3F3AK27M double mutations in paediatric glial and glioneuronal tumours

(2015) Anh Tuan Nguyen et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

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

(2014) Adam M Fontebasso et al.   NATURE GENETICS

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

(2013) David T W Jones et al.   NATURE GENETICS

Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

(2012) Jeremy Schwartzentruber et al.   NATURE