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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

R. Verhaak, K. Hoadley, E. Purdom, V. Wang, Y. Qi, M. Wilkerson, C. Miller, L. Ding, T. Golub, J. Mesirov, G. Alexe, M. Lawrence, M. O'Kelly, P. Tamayo, B. Weir, S. Gabriel, W. Winckler, S. Gupta, L. Jakkula, H. Feiler, J. Hodgson, C. James, J. Sarkaria, C. Brennan, A. Kahn, P. Spellman, R. Wilson, T. Speed, J. Gray, M. Meyerson, G. Getz, C. Perou, D. Hayes, and Cancer Genome Atlas Research Network. Cancer Cell, 17 (1): 98-110 (January 2010)
DOI: 10.1016/j.ccr.2009.12.020

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Markus P J Mergens

Adrian P J Schulte

Johannes P J Maassen

Armin J -P Bogs

Wolfram J P Karges

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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1R. Verhaak, K. Hoadley, E. Purdom, V. Wang, Y. Qi, M. Wilkerson, C. Miller, L. Ding, T. Golub, J. Mesirov and 24 other author(s). Cancer Cell, 17 (1): 98-110 (January 2010)Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profilesA. Subramanian, P. Tamayo, V. Mootha, S. Mukherjee, B. Ebert, M. Gillette, A. Paulovich, S. Pomeroy, T. Golub, E. Lander and 1 other author(s). Proc Natl Acad Sci U S A, 102 (43): 15545-15550 (October 2005)Initial sequencing and analysis of the human genomeE. Lander, L. Linton, B. Birren, C. Nusbaum, M. Zody, J. Baldwin, K. Devon, K. Dewar, M. Doyle, W. FitzHugh and 247 other author(s). Nature, 409 (6822): 860-921 (February 2001)Subclass mapping: identifying common subtypes in independent disease data setsY. Hoshida, J. Brunet, P. Tamayo, T. Golub, and J. Mesirov. (2007)Initial sequencing and analysis of the human genomeE. Lander, L. Linton, B. Birren, C. Nusbaum, M. Zody, J. Baldwin, K. Devon, K. Dewar, M. Doyle, W. FitzHugh and 246 other author(s). Nature, (February 2001)Initial sequencing and comparative analysis of the mouse genomeR. Waterston, K. Lindblad-Toh, E. Birney, J. Rogers, J. Abril, P. Agarwal, R. Agarwala, R. Ainscough, M. Alexandersson, P. An and 212 other author(s). Nature, (December 2002)The GenePattern Notebook EnvironmentM. Reich, T. Tabor, T. Liefeld, H. Thorvaldsdóttir, B. Hill, P. Tamayo, and J. Mesirov. Cell Syst, 5 (2): 149-151 (August 2017)Molecular classification of cancer: class discovery and class prediction by gene expression monitoringR. Golub, K. Slonim, P. Tamayo, C. Huard, M. Gaasenbeek, P. Mesirov, H. Coller, L. Loh, R. Downing, a. Caligiuri and 2 other author(s). Science, (1999)Molecular classification of cancer: class discovery and class prediction by gene expression monitoringT. Golub, D. Slonim, P. Tamayo, C. Huard, M. Gaasenbeek, J. Mesirov, H. Coller, M. Loh, J. Downing, M. Caligiuri and 2 other author(s). Science, 286 (5439): 531-537 (October 1999)Integrative genomics viewer.J. Robinson, H. Thorvaldsdóttir, W. Winckler, M. Guttman, E. Lander, G. Getz, and J. Mesirov. Nat Biotechnol, 29 (1): 24-6 (2011)

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Disambiguation of "Mesirov, J P"

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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

Please choose a person to relate this publication to

Markus P J Mergens

Adrian P J Schulte

Johannes P J Maassen

Armin J -P Bogs

Wolfram J P Karges

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Mesirov, J P"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1

Please choose a person to relate this publication to

Markus P J Mergens

Adrian P J Schulte

Johannes P J Maassen

Armin J -P Bogs

Wolfram J P Karges

Other publications of authors with the same name

Disambiguation

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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1