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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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Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity. Nature genetics, 2013/04/26, Volume 45, Issue 5, p.478-86, (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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Comprehensive genomic characterization of squamous cell lung cancers. Nature, 2012/09/09, (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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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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Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing. Proceedings of the National Academy of Sciences of the United States of America, 2012/03/06, Volume 109, Issue 10, p.3879-84, (2012)
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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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The genomic complexity of primary human prostate cancer. Nature, 2011/02/10, Volume 470, Issue 7333, p.214-20, (2011)
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