"De novo replication repair deficient glioblastoma, IDH-wildtype" is a distinct glioblastoma subtype in adults that may benefit from immune checkpoint blockade. Read more about "De novo replication repair deficient glioblastoma, IDH-wildtype" is a distinct glioblastoma subtype in adults that may benefit from immune checkpoint blockade.
Somatic mosaic SOX10 indel mutations underlie a form of segmental schwannomatosis. Read more about Somatic mosaic SOX10 indel mutations underlie a form of segmental schwannomatosis.
Correction: Increased mRNA expression of CDKN2A is a transcriptomic marker of clinically aggressive meningiomas. Read more about Correction: Increased mRNA expression of CDKN2A is a transcriptomic marker of clinically aggressive meningiomas.
Increased mRNA expression of CDKN2A is a transcriptomic marker of clinically aggressive meningiomas. Read more about Increased mRNA expression of CDKN2A is a transcriptomic marker of clinically aggressive meningiomas.
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. Read more about 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.
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.
Expanded analysis of high-grade astrocytoma with piloid features identifies an epigenetically and clinically distinct subtype associated with neurofibromatosis type 1. Read more about Expanded analysis of high-grade astrocytoma with piloid features identifies an epigenetically and clinically distinct subtype associated with neurofibromatosis type 1.
Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions. Read more about Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions.
