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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, and D. Hayes. Cancer Cell, 17 (1): 98 - 110 (2010)
DOI: https://doi.org/10.1016/j.ccr.2009.12.020

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Katherine Lippert

Katherine Mayes

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Katherine MacLennan

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Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesK. Ellrott, M. Bailey, G. Saksena, K. Covington, C. Kandoth, C. Stewart, J. Hess, S. Ma, K. Chiotti, M. McLellan and 730 other author(s). Cell Systems, 6 (3): 271--281.e7 (March 2018)Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 PatientsA. Kahles, K. Lehmann, N. Toussaint, M. Hüser, S. Stark, T. Sachsenberg, O. Stegle, O. Kohlbacher, C. Sander, S. Caesar-Johnson and 725 other author(s). Cancer Cell, 34 (2): 211--224.e6 (August 2018)Bidimensional linked matrix factorization for pan-omics pan-cancer analysis.E. Lock, J. Park, and K. Hoadley. CoRR, (2020)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 23 other author(s). Cancer Cell, 17 (1): 98 - 110 (2010)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 23 other author(s). Cancer Cell, 17 (1): 98--110 (2010)Jackstraw inference for AJIVE data integration.X. Yang, K. Hoadley, J. Hannig, and J. Marron. Comput. Stat. Data Anal., (April 2023)A hierarchical spike-and-slab model for pan-cancer survival using pan-omic data.S. Samorodnitsky, K. Hoadley, and E. Lock. BMC Bioinform., 23 (1): 235 (2022)Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic PipelinesK. Ellrott, M. Bailey, G. Saksena, K. Covington, C. Kandoth, C. Stewart, J. Hess, S. Ma, K. Chiotti, M. McLellan and 730 other author(s). Cell Systems, 6 (3): 271--281.e7 (March 2018)Multiplatform Analysis of 12 Cancer Types Reveals Molecular Classification within and across Tissues of Origin.K. Hoadley, C. Yau, D. Wolf, A. Cherniack, D. Tamborero, S. Ng, M. Leiserson, B. Niu, M. McLellan, V. Uzunangelov and 23 other author(s). Cell, (August 2014)An approach for normalization and quality control for NanoString RNA expression data.A. Bhattacharya, A. Hamilton, H. Furberg, E. Pietzak, M. Purdue, M. Troester, K. Hoadley, and M. Love. Briefings Bioinform., (2021)

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Disambiguation of "Hoadley, Katherine A."

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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

Katherine Lippert

Katherine Mayes

Katherine Hester

Katherine Kämpchen

Katherine MacLennan

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Hoadley, Katherine A."

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

Katherine Lippert

Katherine Mayes

Katherine Hester

Katherine Kämpchen

Katherine MacLennan

Other publications of authors with the same name

Disambiguation

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URL
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Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1