Detalhe da pesquisa
1.
DNA methylation-based classification of central nervous system tumours.
Nature
; 555(7697): 469-474, 2018 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29539639
2.
Simultaneous Nbs1 and p53 inactivation in neural progenitors triggers high-grade gliomas.
Neuropathol Appl Neurobiol
; 49(4): e12915, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37296499
3.
Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA): a molecularly distinct brain tumor type with recurrent NTRK gene fusions.
Acta Neuropathol
; 145(5): 667-680, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36933012
4.
Survey of NF1 inactivation by surrogate immunohistochemistry in ovarian carcinomas.
Gynecol Oncol
; 178: 80-88, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37820398
5.
Updates on the WHO diagnosis of IDH-mutant glioma.
J Neurooncol
; 162(3): 461-469, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36717507
6.
Anaplastic ganglioglioma-A diagnosis comprising several distinct tumour types.
Neuropathol Appl Neurobiol
; 48(7): e12847, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35977725
7.
Oligosarcomas, IDH-mutant are distinct and aggressive.
Acta Neuropathol
; 143(2): 263-281, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34967922
8.
Molecular matched targeted therapies for primary brain tumors-a single center retrospective analysis.
J Neurooncol
; 159(2): 243-259, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35864412
9.
Accurate calling of KIAA1549-BRAF fusions from DNA of human brain tumours using methylation array-based copy number and gene panel sequencing data.
Neuropathol Appl Neurobiol
; 47(3): 406-414, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33336421
10.
Molecular characterisation of sporadic endolymphatic sac tumours and comparison to von Hippel-Lindau disease-related tumours.
Neuropathol Appl Neurobiol
; 47(6): 756-767, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34091929
11.
Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1.
Acta Neuropathol
; 141(2): 281-290, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33319313
12.
Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis.
Acta Neuropathol
; 141(1): 85-100, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33216206
13.
Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors.
Acta Neuropathol
; 142(5): 827-839, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34355256
14.
Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1.
Acta Neuropathol
; 142(1): 179-189, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33876327
15.
Infratentorial IDH-mutant astrocytoma is a distinct subtype.
Acta Neuropathol
; 140(4): 569-581, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32776277
16.
Molecular characterization of CNS paragangliomas identifies cauda equina paragangliomas as a distinct tumor entity.
Acta Neuropathol
; 140(6): 893-906, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32926213
17.
Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course.
Acta Neuropathol
; 139(1): 193-209, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31563982
18.
Routine RNA sequencing of formalin-fixed paraffin-embedded specimens in neuropathology diagnostics identifies diagnostically and therapeutically relevant gene fusions.
Acta Neuropathol
; 138(5): 827-835, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31278449
19.
MYCN amplification drives an aggressive form of spinal ependymoma.
Acta Neuropathol
; 138(6): 1075-1089, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31414211
20.
Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1.
Acta Neuropathol
; 138(3): 497-504, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31250151