% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Pajtler:127266,
author = {K. Pajtler$^*$ and H. Witt$^*$ and M. Sill$^*$ and D.
Jones$^*$ and V. Hovestadt$^*$ and F. Kratochwil$^*$ and K.
Wani and R. Tatevossian and C. Punchihewa and P. Johann$^*$
and J. Reimand and H.-J. Warnatz and M. Ryzhova and S. Mack
and V. Ramaswamy and D. Capper$^*$ and L. Schweizer$^*$ and
L. Sieber$^*$ and A. Wittmann$^*$ and Z. Huang$^*$ and P.
van Sluis and R. Volckmann and J. Koster and R. Versteeg and
D. Fults and H. Toledano and S. Avigad and L. M. Hoffman and
A. M. Donson and N. Foreman and E. Hewer and K. Zitterbart
and M. Gilbert and T. S. Armstrong and N. Gupta and J. C.
Allen and M. A. Karajannis and D. Zagzag and M. Hasselblatt
and A. E. Kulozik and O. Witt$^*$ and V. P. Collins and K.
von Hoff and S. Rutkowski and T. Pietsch and G. Bader and
M.-L. Yaspo and A. von Deimling$^*$ and P. Lichter$^*$ and
M. D. Taylor and R. Gilbertson and D. W. Ellison and K.
Aldape and A. Korshunov$^*$ and M. Kool$^*$ and S.
Pfister$^*$},
title = {{M}olecular {C}lassification of {E}pendymal {T}umors across
{A}ll {CNS} {C}ompartments, {H}istopathological {G}rades,
and {A}ge {G}roups.},
journal = {Cancer cell},
volume = {27},
number = {5},
issn = {1535-6108},
address = {Cambridge, Mass.},
publisher = {Cell Press},
reportid = {DKFZ-2017-03291},
pages = {728 - 743},
year = {2015},
abstract = {Ependymal tumors across age groups are currently classified
and graded solely by histopathology. It is, however,
commonly accepted that this classification scheme has
limited clinical utility based on its lack of
reproducibility in predicting patients' outcome. We aimed at
establishing a uniform molecular classification using DNA
methylation profiling. Nine molecular subgroups were
identified in a large cohort of 500 tumors, 3 in each
anatomical compartment of the CNS, spine, posterior fossa,
supratentorial. Two supratentorial subgroups are
characterized by prototypic fusion genes involving RELA and
YAP1, respectively. Regarding clinical associations, the
molecular classification proposed herein outperforms the
current histopathological classification and thus might
serve as a basis for the next World Health Organization
classification of CNS tumors.},
keywords = {Adaptor Proteins, Signal Transducing (NLM Chemicals) /
Phosphoproteins (NLM Chemicals) / YAP1 (Yes-associated)
protein, human (NLM Chemicals)},
cin = {B062 / C060 / B060 / G380 / G340 / L101},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)C060-20160331 /
I:(DE-He78)B060-20160331 / I:(DE-He78)G380-20160331 /
I:(DE-He78)G340-20160331 / I:(DE-He78)L101-20160331},
pnm = {312 - Functional and structural genomics (POF3-312)},
pid = {G:(DE-HGF)POF3-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:25965575},
pmc = {pmc:PMC4712639},
doi = {10.1016/j.ccell.2015.04.002},
url = {https://inrepo02.dkfz.de/record/127266},
}