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Integrated genomic characterization of endometrial carcinoma. Nature, 2013/05/02, Volume 497, Issue 7447, p.67-73, (2013)
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Punctuated evolution of prostate cancer genomes. Cell, 2013/04/25, Volume 153, Issue 3, p.666-77, (2013)
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Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell, 2013/02/14, Volume 152, Issue 4, p.714-26, (2013)
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Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nature biotechnology, 2013/02/10, (2013)
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Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors. Nature genetics, 2013/02/01, Volume 45, Issue 2, p.131-2, (2013)
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The genetic landscape of high-risk neuroblastoma. Nature genetics, 2013/01/20, (2013)
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Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature, 2012/12/13, Volume 492, Issue 7428, p.290, (2012)
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Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing. Cell, 2012/09/14, Volume 150, Issue 6, p.1107-20, (2012)
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Comprehensive genomic characterization of squamous cell lung cancers. Nature, 2012/09/09, (2012)
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Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2. Proceedings of the National Academy of Sciences of the United States of America, 2012/09/04, Volume 109, Issue 36, p.14476-81, (2012)
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Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations. Nature, 2012/08/02, Volume 488, Issue 7409, p.106-10, (2012)
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A landscape of driver mutations in melanoma. Cell, 2012/07/20, Volume 150, Issue 2, p.251-63, (2012)
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Sequence analysis of mutations and translocations across breast cancer subtypes. Nature, 2012/06/20, Volume 486, Issue 7403, p.405-9, (2012)
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Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer. Nature genetics, 2012/05/20, Volume 44, Issue 6, p.685-9, (2012)
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Melanoma genome sequencing reveals frequent PREX2 mutations. Nature, 2012/05/09, Volume 485, Issue 7399, p.502-6, (2012)
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Absolute quantification of somatic DNA alterations in human cancer. Nature biotechnology, 2012/04/29, (2012)
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The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature, 2012/03/28, Volume 483, Issue 7391, p.603-7, (2012)
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High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. Cancer discovery, 2012/01/01, Volume 2, Issue 1, p.82-93, (2012)
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SF3B1 and other novel cancer genes in chronic lymphocytic leukemia. The New England journal of medicine, 2011/12/29, Volume 365, Issue 26, p.2497-506, (2011)
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Glioblastoma-Derived Epidermal Growth Factor Receptor Carboxyl-Terminal Deletion Mutants Are Transforming and Are Sensitive to EGFR-Directed Therapies. Cancer research, 2011/12/15, Volume 71, Issue 24, p.7587-96, (2011)
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Amplification of CRKL Induces Transformation and Epidermal Growth Factor Receptor Inhibitor Resistance in Human Non-Small Cell Lung Cancers. Cancer discovery, 2011/12/01, Volume 1, Issue 7, p.608-25, (2011)
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Genomic analysis identifies association of Fusobacterium with colorectal carcinoma. Genome research, 2011/10/18, (2011)
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Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion. Nature genetics, 2011/09/04, Volume 43, Issue 10, p.964-8, (2011)
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The mutational landscape of head and neck squamous cell carcinoma. Science (New York, N.Y.), 2011/08/26, Volume 333, Issue 6046, p.1157-60, (2011)
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Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011/08/01, Volume 29, Issue 22, p.3085-96, (2011)
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Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer. Proceedings of the National Academy of Sciences of the United States of America, 2011/07/26, Volume 108, Issue 30, p.12372-7, (2011)
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Integrative genomic analysis of medulloblastoma identifies a molecular subgroup that drives poor clinical outcome. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011/04/10, Volume 29, Issue 11, p.1424-30, (2011)
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Predicting relapse in patients with medulloblastoma by integrating evidence from clinical and genomic features. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011/04/10, Volume 29, Issue 11, p.1415-23, (2011)
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Initial genome sequencing and analysis of multiple myeloma. Nature, 2011/03/24, Volume 471, Issue 7339, p.467-72, (2011)
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The genomic complexity of primary human prostate cancer. Nature, 2011/02/10, Volume 470, Issue 7333, p.214-20, (2011)
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Inhibitor-sensitive FGFR1 amplification in human non-small cell lung cancer. PloS one, 2011/01/01, Volume 6, Issue 6, p.e20351, (2011)
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Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy. Nature genetics, 2010/08/01, Volume 42, Issue 8, p.715-21, (2010)
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Integrative analysis of the melanoma transcriptome. Genome research, 2010/04/01, Volume 20, Issue 4, p.413-27, (2010)
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The landscape of somatic copy-number alteration across human cancers. Nature, 2010/02/18, Volume 463, Issue 7283, p.899-905, (2010)
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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. Cancer cell, 2010/01/19, Volume 17, Issue 1, p.98-110, (2010)
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Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1. Nature, 2009/11/05, Volume 462, Issue 7269, p.108-12, (2009)
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Lin28 promotes transformation and is associated with advanced human malignancies. Nature genetics, 2009/07/01, Volume 41, Issue 7, p.843-8, (2009)
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Integrated genomic profiling of endometrial carcinoma associates aggressive tumors with indicators of PI3 kinase activation. Proceedings of the National Academy of Sciences of the United States of America, 2009/03/24, Volume 106, Issue 12, p.4834-9, (2009)
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High-resolution mapping of copy-number alterations with massively parallel sequencing. Nature methods, 2009/01/01, Volume 6, Issue 1, p.99-103, (2009)
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Highly parallel identification of essential genes in cancer cells. Proceedings of the National Academy of Sciences of the United States of America, 2008/12/23, Volume 105, Issue 51, p.20380-5, (2008)
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Somatic mutations affect key pathways in lung adenocarcinoma. Nature, 2008/10/23, Volume 455, Issue 7216, p.1069-75, (2008)
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Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature, 2008/10/16, Volume 455, Issue 7215, p.975-8, (2008)
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Drug-sensitive FGFR2 mutations in endometrial carcinoma. Proceedings of the National Academy of Sciences of the United States of America, 2008/06/24, Volume 105, Issue 25, p.8713-7, (2008)
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Modeling genomic diversity and tumor dependency in malignant melanoma. Cancer research, 2008/02/01, Volume 68, Issue 3, p.664-73, (2008)
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Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma. Proceedings of the National Academy of Sciences of the United States of America, 2007/12/11, Volume 104, Issue 50, p.20007-12, (2007)
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Characterizing the cancer genome in lung adenocarcinoma. Nature, 2007/12/06, Volume 450, Issue 7171, p.893-8, (2007)
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Comment on "The consensus coding sequences of human breast and colorectal cancers". Science (New York, N.Y.), 2007/09/14, Volume 317, Issue 5844, p.1500, (2007)
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Integrative genomic approaches identify IKBKE as a breast cancer oncogene. Cell, 2007/06/15, Volume 129, Issue 6, p.1065-79, (2007)
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High-throughput oncogene mutation profiling in human cancer. Nature genetics, 2007/03/01, Volume 39, Issue 3, p.347-51, (2007)
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Epidermal growth factor receptor activation in glioblastoma through novel missense mutations in the extracellular domain. PLoS medicine, 2006/12/01, Volume 3, Issue 12, p.e485, (2006)
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Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants. PLoS medicine, 2005/11/01, Volume 2, Issue 11, p.e313, (2005)
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Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer cell, 2005/04/01, Volume 7, Issue 4, p.387-97, (2005)
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EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science (New York, N.Y.), 2004/06/04, Volume 304, Issue 5676, p.1497-500, (2004)
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High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines. Oncogene, 2004/04/08, Volume 23, Issue 15, p.2716-26, (2004)
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Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses Proceedings of the National Academy of Sciences of the United States of America, 2001/11/20/, Volume 98, Issue 24, p.13790 - 5, (2001)
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Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses Proceedings of the National Academy of Sciences of the United States of America, 2001/11/20/, Volume 98, Issue 24, p.13790 - 5, (2001)
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Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays Nature Biotechnology, 2000/09//, Volume 18, Issue 9, p.1001 - 5, (2000)
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- Showing 1-58 of 58 Results




