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Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.

T. Rausch, D. Jones, M. Zapatka, A. Stütz, T. Zichner, J. Weischenfeldt, N. Jäger, M. Remke, D. Shih, P. Northcott, E. Pfaff, J. Tica, Q. Wang, L. Massimi, H. Witt, S. Bender, S. Pleier, H. Cin, C. Hawkins, C. Beck, A. von Deimling, V. Hans, B. Brors, R. Eils, W. Scheurlen, J. Blake, V. Benes, A. Kulozik, O. Witt, D. Martin, C. Zhang, R. Porat, D. Merino, J. Wasserman, N. Jabado, A. Fontebasso, L. Bullinger, F. Rücker, K. Döhner, H. Döhner, J. Koster, J. Molenaar, R. Versteeg, M. Kool, U. Tabori, D. Malkin, A. Korshunov, M. Taylor, P. Lichter, S. Pfister, and J. Korbel. Cell, 148 (1-2): 59--71 (January 2012)
DOI: 10.1016/j.cell.2011.12.013

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Hendrik Rogier

Dietmar Rogier

Hermann Rogier

Rogier Blokland

Eduard Rogier

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Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.T. Rausch, D. Jones, M. Zapatka, A. Stütz, T. Zichner, J. Weischenfeldt, N. Jäger, M. Remke, D. Shih, P. Northcott and 41 other author(s). Cell, 148 (1-2): 59--71 (January 2012)Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.D. Jones, B. Hutter, N. Jäger, A. Korshunov, M. Kool, H. Warnatz, T. Zichner, S. Lambert, M. Ryzhova, D. Quang and 66 other author(s). Nat Genet, 45 (8): 927--932 (August 2013)Hypermutation of the inactive X chromosome is a frequent event in cancer.N. Jäger, M. Schlesner, D. Jones, S. Raffel, J. Mallm, K. Junge, D. Weichenhan, T. Bauer, N. Ishaque, M. Kool and 26 other author(s). Cell, 155 (3): 567--581 (October 2013)Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.P. Northcott, C. Lee, T. Zichner, A. Stütz, S. Erkek, D. Kawauchi, D. Shih, V. Hovestadt, M. Zapatka, D. Sturm and 69 other author(s). Nature, 511 (7510): 428--434 (July 2014)Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome.A. Cornero, M. Acquaviva, P. Fardin, R. Versteeg, A. Schramm, A. Eva, M. Bosco, F. Blengio, S. Barzaghi, and L. Varesio. BMC Bioinform., 13 (S-4): S13 (2012)Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing.V. Hovestadt, D. Jones, S. Picelli, W. Wang, M. Kool, P. Northcott, M. Sultan, K. Stachurski, M. Ryzhova, H. Warnatz and 35 other author(s). Nature, 510 (7506): 537--541 (June 2014)Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition.M. Kool, D. Jones, N. Jäger, P. Northcott, T. Pugh, V. Hovestadt, R. Piro, L. Esparza, S. Markant, M. Remke and 67 other author(s). Cancer Cell, 25 (3): 393--405 (March 2014)

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Disambiguation of "Versteeg, Rogier"

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Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.

Please choose a person to relate this publication to

Hendrik Rogier

Dietmar Rogier

Hermann Rogier

Rogier Blokland

Eduard Rogier

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Versteeg, Rogier"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.

Please choose a person to relate this publication to

Hendrik Rogier

Dietmar Rogier

Hermann Rogier

Rogier Blokland

Eduard Rogier

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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history of this post
URL
DOI
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Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.