Even heterozygous loss of CDKN2A/B greatly accelerates recurrence in aggressive meningioma. Read more about Even heterozygous loss of CDKN2A/B greatly accelerates recurrence in aggressive meningioma.
Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas. Read more about Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas.
Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification. Read more about Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions. Read more about Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions.
Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1. Read more about Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1.
Intratumor and informatic heterogeneity influence meningioma molecular classification. Read more about Intratumor and informatic heterogeneity influence meningioma molecular classification.
High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13. Read more about High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13.
Activating NTRK2 and ALK receptor tyrosine kinase fusions extend the molecular spectrum of pleomorphic xanthoastrocytomas of early childhood: a diagnostic overlap with infant-type hemispheric glioma. Read more about Activating NTRK2 and ALK receptor tyrosine kinase fusions extend the molecular spectrum of pleomorphic xanthoastrocytomas of early childhood: a diagnostic overlap with infant-type hemispheric glioma.
EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma. Read more about EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma.
Genetic and epigenetic characterization of posterior pituitary tumors. Read more about Genetic and epigenetic characterization of posterior pituitary tumors.
