review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1002/PATH.4813 |
P698 | PubMed publication ID | 27701736 |
P50 | author | Cheng-Hsuan Chiang | Q56335411 |
P2093 | author name string | David W Ellison | |
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Cross-Species Genomics Identifies TAF12, NFYC, and RAD54L as Choroid Plexus Carcinoma Oncogenes | Q35692614 | ||
Pilomyxoid Astrocytoma (PMA) Shows Significant Differences in Gene Expression vs. Pilocytic Astrocytoma (PA) and Variable Tendency Toward Maturation to PA. | Q35752324 | ||
Chromosomal imbalances in choroid plexus tumors | Q35788860 | ||
Malignant and benign ganglioglioma: a pathological and molecular study | Q35800003 | ||
A case of solitary subependymal giant cell astrocytoma: two somatic hits of TSC2 in the tumor, without evidence of somatic mosaicism | Q35836708 | ||
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A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers | Q36129157 | ||
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Epithelioid GBMs show a high percentage of BRAF V600E mutation. | Q36175648 | ||
Medulloblastoma: clinicopathological correlates of SHH, WNT, and non-SHH/WNT molecular subgroups | Q36460209 | ||
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Pediatric glioma-associated KIAA1549:BRAF expression regulates neuroglial cell growth in a cell type-specific and mTOR-dependent manner. | Q36464991 | ||
Definition of Disease-Risk Stratification Groups in Childhood Medulloblastoma Using Combined Clinical, Pathologic, and Molecular Variables | Q36476670 | ||
BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas | Q36532504 | ||
The pilomyxoid astrocytoma and its relationship to pilocytic astrocytoma: report of a case and a critical review of the entity | Q36540545 | ||
Gorlin syndrome and desmoplastic medulloblastoma: Report of 3 cases with unfavorable clinical course and novel mutations | Q36612342 | ||
Gangliogliomas: a clinicopathological study of 25 cases and review of the literature | Q36746001 | ||
TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal | Q36762656 | ||
Optic pathway gliomas in neurofibromatosis-1: controversies and recommendations. | Q36771546 | ||
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas | Q36780903 | ||
The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression | Q36850449 | ||
Classification and grading of low-grade astrocytic tumors in children | Q36862370 | ||
Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology. | Q36900873 | ||
Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma | Q36929844 | ||
Evaluation of histone 3 lysine 27 trimethylation (H3K27me3) and enhancer of Zest 2 (EZH2) in pediatric glial and glioneuronal tumors shows decreased H3K27me3 in H3F3A K27M mutant glioblastomas | Q36981245 | ||
Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas | Q37055286 | ||
Novel oncogenic PDGFRA mutations in pediatric high-grade gliomas | Q37238690 | ||
Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors | Q37289800 | ||
Integrative genomic analysis of medulloblastoma identifies a molecular subgroup that drives poor clinical outcome | Q28298987 | ||
Exome sequencing identifies BRAF mutations in papillary craniopharyngiomas | Q28305680 | ||
JMJD1C, a JmjC domain-containing protein, is required for long-term maintenance of male germ cells in mice | Q28587091 | ||
Super-enhancers in the control of cell identity and disease | Q28661442 | ||
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma | Q29616862 | ||
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms | Q29618586 | ||
Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations | Q30040534 | ||
CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2007-2011. | Q30402063 | ||
Nevoid basal cell carcinoma syndrome: relation with desmoplastic medulloblastoma in infancy. A population-based study and review of the literature | Q30968980 | ||
A prognostic gene expression signature in infratentorial ependymoma | Q33581494 | ||
Clinical, radiological, histological and molecular characteristics of paediatric epithelioid glioblastoma | Q33702910 | ||
C11orf95-RELA fusions drive oncogenic NF-κB signalling in ependymoma | Q33730977 | ||
The genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade glioma | Q33751426 | ||
Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene | Q33772206 | ||
Exome sequencing identifies somatic gain-of-function PPM1D mutations in brainstem gliomas | Q33813999 | ||
BRAF V600E mutations are common in pleomorphic xanthoastrocytoma: diagnostic and therapeutic implications | Q33867475 | ||
Embryonal tumor with abundant neuropil and true rosettes (ETANTR), ependymoblastoma, and medulloepithelioma share molecular similarity and comprise a single clinicopathological entity | Q33917715 | ||
Integrated molecular genetic profiling of pediatric high-grade gliomas reveals key differences with the adult disease | Q33990951 | ||
Cross-species genomics matches driver mutations and cell compartments to model ependymoma | Q34031780 | ||
Delineation of two clinically and molecularly distinct subgroups of posterior fossa ependymoma | Q34132926 | ||
Activating mutations in BRAF characterize a spectrum of pediatric low-grade gliomas | Q34132964 | ||
CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entity | Q34157312 | ||
Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas | Q34167499 | ||
Mesenchymal transition and PDGFRA amplification/mutation are key distinct oncogenic events in pediatric diffuse intrinsic pontine gliomas | Q34184430 | ||
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy | Q34240198 | ||
Choroid plexus papilloma in a girl with hypomelanosis of Ito. | Q34336841 | ||
Genomic analysis of diffuse pediatric low-grade gliomas identifies recurrent oncogenic truncating rearrangements in the transcription factor MYBL1 | Q34342166 | ||
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma | Q34354839 | ||
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma | Q34362028 | ||
Radial glia cells are candidate stem cells of ependymoma | Q34459796 | ||
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs | Q34515911 | ||
Pediatric astrocytomas with monomorphous pilomyxoid features and a less favorable outcome | Q34646450 | ||
Dysembryoplastic neuroepithelial tumor: a surgically curable tumor of young patients with intractable partial seizures. Report of thirty-nine cases | Q34685937 | ||
Temozolomide in the treatment of children with newly diagnosed diffuse intrinsic pontine gliomas: a report from the Children's Oncology Group | Q34722864 | ||
The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary | Q38829244 | ||
Histone H3.3. mutations drive pediatric glioblastoma through upregulation of MYCN. | Q39173934 | ||
Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma | Q39788891 | ||
Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours | Q41238200 | ||
Integrated analysis of pediatric glioblastoma reveals a subset of biologically favorable tumors with associated molecular prognostic markers | Q41264935 | ||
High rate of concurrent BRAF-KIAA1549 gene fusion and 1p deletion in disseminated oligodendroglioma-like leptomeningeal neoplasms (DOLN). | Q41494035 | ||
Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumors | Q41817349 | ||
Oncogenic RAF1 rearrangement and a novel BRAF mutation as alternatives to KIAA1549:BRAF fusion in activating the MAPK pathway in pilocytic astrocytoma | Q41888346 | ||
Alterations of BRAF and HIPK2 loci predominate in sporadic pilocytic astrocytoma | Q42636358 | ||
Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma | Q42812964 | ||
Epidemiology of central nervous system tumors in childhood and adolescence based on the new WHO classification | Q43569987 | ||
Dysembryoplastic neuroepithelial tumors share with pleomorphic xanthoastrocytomas and gangliogliomas BRAF(V600E) mutation and expression | Q43838170 | ||
Frequency, risk-factors and survival of children with atypical teratoid rhabdoid tumors (AT/RT) of the CNS diagnosed between 1988 and 2004, and registered to the German HIT database | Q43944813 | ||
Frequent gains at chromosome 7q34 involving BRAF in pilocytic astrocytoma | Q44739121 | ||
Genome-wide DNA copy number analysis of desmoplastic infantile astrocytomas and desmoplastic infantile gangliogliomas | Q44890960 | ||
Incidence patterns for ependymoma: a surveillance, epidemiology, and end results study. | Q45944762 | ||
Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups | Q46158282 | ||
Epithelioid Glioblastomas and Anaplastic Epithelioid Pleomorphic Xanthoastrocytomas--Same Entity or First Cousins? | Q46365183 | ||
Immunohistochemical analysis of hSNF5/INI1 in pediatric CNS neoplasms | Q47708980 | ||
Activation of the ERK/MAPK pathway: a signature genetic defect in posterior fossa pilocytic astrocytomas. | Q47992753 | ||
Ganglioglioma: a detailed histopathological and immunohistochemical analysis of 61 cases | Q48218230 | ||
Histological heterogeneity of dysembryoplastic neuroepithelial tumour: identification and differential diagnosis in a series of 74 cases | Q48219312 | ||
Nodule formation and desmoplasia in medulloblastomas-defining the nodular/desmoplastic variant and its biological behavior | Q48227672 | ||
Focal genomic amplification at 19q13.42 comprises a powerful diagnostic marker for embryonal tumors with ependymoblastic rosettes. | Q48229405 | ||
Outcome analysis of childhood pilocytic astrocytomas: a retrospective study of 148 cases at a single institution | Q48231129 | ||
Clinical and molecular characteristics of malignant transformation of low-grade glioma in children | Q48269415 | ||
Whole-genome profiling of pediatric diffuse intrinsic pontine gliomas highlights platelet-derived growth factor receptor alpha and poly (ADP-ribose) polymerase as potential therapeutic targets | Q48315065 | ||
Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma | Q48329991 | ||
Disseminated oligodendroglial-like leptomeningeal tumor of childhood: a distinctive clinicopathologic entity | Q48391103 | ||
Genetic alterations commonly found in diffusely infiltrating cerebral gliomas are rare or absent in pleomorphic xanthoastrocytomas | Q48425137 | ||
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas | Q48446962 | ||
Mutational and expression analysis of the NF1 gene argues against a role as tumor suppressor in sporadic pilocytic astrocytomas | Q48465073 | ||
IDH1 mutation in pediatric gliomas: has it a diagnostic and prognostic value? | Q48606060 | ||
Low-grade astrocytoma: a decade of experience at St. Jude Children's Research Hospital | Q48651367 | ||
Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR. | Q48820061 | ||
Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes | Q48872957 | ||
Clinico-pathological features of pilomyxoid astrocytoma of the optic pathway | Q49215584 | ||
Mutually exclusive mutations of KIT and RAS are associated with KIT mRNA expression and chromosomal instability in primary intracranial pure germinomas. | Q53071216 | ||
Spectrum of pilomyxoid astrocytomas: intermediate pilomyxoid tumors. | Q53287380 | ||
Defining the molecular landscape of ependymomas. | Q53510508 | ||
Supratentorial ependymomas of childhood carry C11orf95-RELA fusions leading to pathological activation of the NF-κB signaling pathway. | Q55461138 | ||
BRAF alterations are frequent in cerebellar low-grade astrocytomas with diffuse growth pattern. | Q55462093 | ||
Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH. | Q55466873 | ||
Analysis of p53 mutation and expression in pleomorphic xanthoastrocytoma. | Q55474092 | ||
Choroid plexus carcinomas are characterized by complex chromosomal alterations related to patient age and prognosis | Q58001730 | ||
Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression | Q58001757 | ||
P433 | issue | 2 | |
P304 | page(s) | 159-172 | |
P577 | publication date | 2016-11-10 | |
P1433 | published in | Journal of Pathology | Q400296 |
P1476 | title | Molecular pathology of paediatric central nervous system tumours | |
P478 | volume | 241 |
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