S. Alexandrescu, A. Korshunov, S. Lai, S. Dabiri, S. Patil et al., Epithelioid glioblastomas and anaplastic epithelioid pleomorphic xanthoastrocytomas?same entity or first cousins? Brain Pathol, 2015.
DOI : 10.1111/bpa.12295

J. Biegel, Molecular genetics of atypical teratoid/rhabdoid tumors, Neurosurgical Focus, vol.20, issue.1, p.11, 2006.
DOI : 10.3171/foc.2006.20.1.12

C. Bouvier, P. Metellus, A. De-paula, A. Vasiljevic, A. Jouvet et al., Solitary Fibrous Tumors and Hemangiopericytomas of the Meninges: Overlapping Pathological Features and Common Prognostic Factors Suggest the Same Spectrum of Tumors, Brain Pathology, vol.34, issue.4, pp.511-521, 2012.
DOI : 10.1111/j.1750-3639.2011.00552.x

A. Broniscer, O. Chamdine, S. Hwang, T. Lin, S. Pounds et al., Gliomatosis cerebri in children shares molecular characteristics with other pediatric gliomas, Acta Neuropathologica, vol.45, issue.2, pp.299-307, 2016.
DOI : 10.1007/s00401-015-1532-y

A. Broniscer, R. Tatevossian, N. Sabin, P. Klimo, . Jr et al., Clinical, radiological, histological and molecular characteristics of paediatric epithelioid glioblastoma, Neuropathology and Applied Neurobiology, vol.17, issue.3, pp.327-336, 2014.
DOI : 10.1111/nan.12093

C. Genome-atlas-research, . Network, D. Brat, R. Verhaak, K. Aldape et al., Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas, N Engl J Med, vol.372, pp.2481-249810, 1056.

L. Chen, Z. Voronovich, K. Clark, I. Hands, J. Mannas et al., Predicting the likelihood of an isocitrate dehydrogenase 1 or 2 mutation in diagnoses of infiltrative glioma, Neuro-Oncology, vol.16, issue.11, pp.1478-1483, 2014.
DOI : 10.1093/neuonc/nou097

J. Chmielecki, A. Crago, M. Rosenberg, O. Connor, R. Walker et al., Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors, Nature Genetics, vol.2, issue.2, pp.131-132, 2013.
DOI : 10.1038/nature11154

D. Ellison, J. Dalton, M. Kocak, S. Nicholson, C. Fraga et al., Medulloblastoma: clinicopathological correlates of SHH, WNT, and non-SHH/WNT molecular subgroups, Acta Neuropathologica, vol.58, issue.3, pp.381-396, 2011.
DOI : 10.1007/s00401-011-0800-8

D. Ellison, M. Kocak, D. Figarella-branger, G. Felice, C. G. Pietsch et al., Histopathological grading of pediatric ependymoma: reproducibility and clinical relevance in European trial cohorts, Journal of Negative Results in BioMedicine, vol.8, issue.1, pp.7-10, 2011.
DOI : 10.1016/j.ccr.2005.09.001

C. Giannini, B. Scheithauer, A. Weaver, P. Burger, J. Kros et al., Oligodendrogliomas: Reproducibility and Prognostic Value of Histologic Diagnosis and Grading, Journal of Neuropathology & Experimental Neurology, vol.60, issue.3, pp.248-262, 2001.
DOI : 10.1093/jnen/60.3.248

M. Hasselblatt, S. Gesk, F. Oyen, S. Rossi, E. Viscardi et al., Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression, The American Journal of Surgical Pathology, vol.35, issue.6, pp.933-935, 2011.
DOI : 10.1097/PAS.0b013e3182196a39

U. Herrlinger, D. Jones, M. Glas, E. Hattingen, D. Gramatzki et al., Gliomatosis cerebri: no evidence for a separate brain tumor entity, Acta Neuropathologica, vol.16, issue.2, 2015.
DOI : 10.1007/s00401-015-1495-z

J. Huse, E. Diamond, L. Wang, and M. Rosenblum, Mixed glioma with molecular features of composite oligodendroglioma and astrocytoma: a true ???oligoastrocytoma????, Acta Neuropathologica, vol.126, issue.1, pp.151-153, 2015.
DOI : 10.1007/s00401-014-1359-y

J. Huse, M. Edgar, J. Halliday, I. Mikolaenko, E. Lavi et al., Multinodular and Vacuolating Neuronal Tumors of the Cerebrum: 10 Cases of a Distinctive Seizure-Associated Lesion, Brain Pathology, vol.57, issue.5, pp.515-524, 2013.
DOI : 10.1111/bpa.12035

C. Ida, F. Rodriguez, P. Burger, A. Caron, S. Jenkins et al., Pleomorphic Xanthoastrocytoma: Natural History and Long-Term Follow-Up, Brain Pathology, vol.45, issue.5, 2014.
DOI : 10.1111/bpa.12217
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400218

N. Joseph, J. Phillips, S. Dahiya, M. Felicella, T. Tihan et al., Diagnostic implications of IDH1-R132H and OLIG2 expression patterns in rare and challenging glioblastoma variants, Modern Pathology, vol.29, issue.3, pp.315-326, 2013.
DOI : 10.1111/j.1750-3639.2003.tb00018.x

A. Judkins, Immunohistochemistry of INI1 Expression: A New Tool for Old Challenges in CNS and Soft Tissue Pathology, Advances in Anatomic Pathology, vol.14, issue.5, pp.335-339, 2007.
DOI : 10.1097/PAP.0b013e3180ca8b08

D. Khuong-quang, P. Buczkowicz, P. Rakopoulos, X. Liu, A. Fontebasso et al., K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas, Acta Neuropathologica, vol.28, issue.3, pp.439-447, 2012.
DOI : 10.1007/s00401-012-0998-0

P. Killela, C. Pirozzi, P. Healy, Z. Reitman, E. Lipp et al., promoter define clinically distinct subgroups of adult malignant gliomas, Oncotarget, vol.5, issue.6, pp.1515-1525, 2014.
DOI : 10.18632/oncotarget.1765

B. Kleinschmidt-demasters, D. Aisner, D. Birks, and N. Foreman, Epithelioid GBMs Show a High Percentage of BRAF V600E Mutation, The American Journal of Surgical Pathology, vol.37, issue.5, pp.685-698, 2013.
DOI : 10.1097/PAS.0b013e31827f9c5e

B. Kleinschmidt-demasters, D. Aisner, and N. Foreman, BRAF VE1 Immunoreactivity Patterns in Epithelioid Glioblastomas Positive for BRAF V600E Mutation, The American Journal of Surgical Pathology, vol.39, issue.4, pp.528-540, 2015.
DOI : 10.1097/PAS.0000000000000363

B. Kleinschmidt-demasters, A. Alassiri, D. Birks, K. Newell, W. Moore et al., Epithelioid Versus Rhabdoid Glioblastomas Are Distinguished by Monosomy 22 and Immunohistochemical Expression of INI-1 but not Claudin 6, The American Journal of Surgical Pathology, vol.34, issue.3, pp.341-354669, 2010.
DOI : 10.1097/PAS.0b013e3181ce107b

D. Louis, The next step in brain tumor classification: ???Let us now praise famous men?????? or molecules?, Acta Neuropathologica, vol.124, issue.6, pp.761-762, 2012.
DOI : 10.1007/s00401-012-1067-4

D. Louis, H. Ohgaki, O. Wiestler, and W. Cavenee, World Health Organization histological classification of tumours of the central nervous system, International Agency for Research on Cancer, 2007.

D. Louis, H. Ohgaki, O. Wiestler, and W. Cavenee, World Health Organization Histological Classification of Tumours of the Central Nervous System, International Agency for Research on Cancer, 2016.

D. Louis, A. Perry, P. Burger, D. Ellison, G. Reifenberger et al., International Society of Neuropathology-Haarlem Consensus Guidelines for Nervous System Tumor Classification and Grading, Brain Pathology, vol.24, issue.5, pp.429-435, 2014.
DOI : 10.1111/bpa.12171

N. Nonoguchi, T. Ohta, J. Oh, Y. Kim, P. Kleihues et al., TERT promoter mutations in primary and secondary glioblastomas, Acta Neuropathologica, vol.360, issue.8, pp.931-937, 2013.
DOI : 10.1007/s00401-013-1163-0

H. Ohgaki and P. Kleihues, The Definition of Primary and Secondary Glioblastoma, Clinical Cancer Research, vol.19, issue.4, pp.764-772, 2013.
DOI : 10.1158/1078-0432.CCR-12-3002

H. Ohgaki and P. Kleihues, Population-Based Studies on Incidence, Survival Rates, and Genetic Alterations in Astrocytic and Oligodendroglial Gliomas, Journal of Neuropathology & Experimental Neurology, vol.64, issue.6, pp.479-489, 2005.
DOI : 10.1093/jnen/64.6.479

A. Olar, K. Wani, K. Alfaro-munoz, L. Heathcock, H. Van-thuijl et al., IDH mutation status and role of WHO grade and mitotic index in overall survival in grade II???III diffuse gliomas, Acta Neuropathologica, vol.14, issue.12, pp.585-596, 2015.
DOI : 10.1007/s00401-015-1398-z

M. Parker, K. Mohankumar, C. Punchihewa, R. Weinlich, J. Dalton et al., C11orf95???RELA fusions drive oncogenic NF-??B signalling in ependymoma, Nature, vol.19, issue.7489, pp.451-45510, 1038.
DOI : 10.1016/j.cell.2013.02.023

A. Perry, C. Miller, M. Gujrati, B. Scheithauer, S. Zambrano et al., Malignant Gliomas with Primitive Neuroectodermal Tumor-like Components: A Clinicopathologic and Genetic Study of 53 Cases, Brain Pathology, vol.20, issue.1, pp.81-90, 2009.
DOI : 10.1111/j.1750-3639.2008.00167.x

A. Perry, S. Stafford, B. Scheithauer, V. Suman, and C. Lohse, Meningioma Grading, The American Journal of Surgical Pathology, vol.21, issue.12, pp.1455-1465, 1997.
DOI : 10.1097/00000478-199712000-00008

T. Pietsch, I. Wohlers, T. Goschzik, V. Dreschmann, D. Denkhaus et al., Supratentorial ependymomas of childhood carry C11orf95???RELA fusions leading to pathological activation of the NF-??B signaling pathway, Acta Neuropathologica, vol.12, issue.4, pp.609-611, 2014.
DOI : 10.1007/s00401-014-1264-4

L. Ramkissoon, P. Horowitz, J. Craig, S. Ramkissoon, B. Rich et al., Genomic analysis of diffuse pediatric low-grade gliomas identifies recurrent oncogenic truncating rearrangements in the transcription factor MYBL1, Proceedings of the National Academy of Sciences, vol.110, issue.20, pp.8188-8193, 2013.
DOI : 10.1073/pnas.1300252110

D. Reuss, A. Kratz, F. Sahm, D. Capper, D. Schrimpf et al., Adult IDH wild type astrocytomas biologically and clinically resolve into other tumor entities, Acta Neuropathologica, vol.226, issue.3, pp.10-1007, 2015.
DOI : 10.1007/s00401-015-1454-8

D. Reuss, F. Sahm, D. Schrimpf, B. Wiestler, D. Capper et al., ATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an ???integrated??? diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma, Acta Neuropathologica, vol.360, issue.1, pp.133-146, 2015.
DOI : 10.1007/s00401-014-1370-3

D. Robinson, Y. Wu, S. Kalyana-sundaram, X. Cao, R. Lonigro et al., Identification of recurrent NAB2-STAT6 gene fusions in solitary fibrous tumor by integrative sequencing, Nature Genetics, vol.13, issue.2, pp.180-185, 2013.
DOI : 10.1016/j.ccr.2010.03.018

F. Rodriguez, A. Perry, M. Rosenblum, S. Krawitz, K. Cohen et al., Disseminated oligodendroglial-like leptomeningeal tumor of childhood: a distinctive clinicopathologic entity, Acta Neuropathologica, vol.109, issue.5, pp.627-641, 2012.
DOI : 10.1007/s00401-012-1037-x

F. Rodriguez, M. Schniederjan, T. Nicolaides, T. Tihan, P. Burger et al., High rate of concurrent BRAF-KIAA1549 gene fusion and 1p deletion in disseminated oligodendroglioma-like leptomeningeal neoplasms (DOLN), Acta Neuropathologica, vol.110, issue.4, pp.609-610, 2015.
DOI : 10.1007/s00401-015-1400-9

F. Sahm, D. Reuss, C. Koelsche, D. Capper, J. Schittenhelm et al., Farewell to oligoastrocytoma: in situ molecular genetics favor classification as either oligodendroglioma or astrocytoma, Acta Neuropathologica, vol.360, issue.4, pp.551-559, 2014.
DOI : 10.1007/s00401-014-1326-7

L. Schweizer, C. Koelsche, F. Sahm, R. Piro, D. Capper et al., Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein, Acta Neuropathologica, vol.8, issue.5, pp.651-658, 2013.
DOI : 10.1007/s00401-013-1117-6

M. Taylor, P. Northcott, A. Korshunov, M. Remke, Y. Cho et al., Molecular subgroups of medulloblastoma: the current consensus, Acta Neuropathologica, vol.58, issue.2, pp.465-472297, 2012.
DOI : 10.1007/s00401-011-0922-z

B. Wiestler, D. Capper, M. Sill, D. Jones, V. Hovestadt et al., Integrated DNA methylation and copy-number profiling identify three clinically and biologically relevant groups of anaplastic glioma, Acta Neuropathologica, vol.360, issue.4, pp.561-571, 2014.
DOI : 10.1007/s00401-014-1315-x

P. Wilcox, C. Li, M. Lee, B. Shivalingam, J. Brennan et al., Oligoastrocytomas: throwing the baby out with the bathwater?, Acta Neuropathologica, vol.128, issue.4, pp.147-149, 2015.
DOI : 10.1007/s00401-014-1353-4

A. Woehrer, I. Slavc, T. Waldhoer, H. Heinzl, N. Zielonke et al., Incidence of atypical teratoid/rhabdoid tumors in children, Cancer, vol.16, issue.24, pp.5725-5732, 1996.
DOI : 10.1002/cncr.25540

G. Wu, A. Broniscer, T. Mceachron, C. Lu, B. Paugh et al., Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas, Nature Genetics, vol.44, issue.3, pp.251-253, 2012.
DOI : 10.1126/science.1164382

J. Zhang, G. Wu, C. Miller, R. Tatevossian, J. Dalton et al., Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas, Nature Genetics, vol.160, issue.6, pp.602-612, 2013.
DOI : 10.1200/JCO.2010.30.2810