Candidate driver genes in focal chromosomal aberrations of stage II colon cancer
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H. Grabsch | M. Cuesta | B. Ylstra | G. Meijer | R. Brosens | J. Haan | B. Carvalho | F. Rustenburg | P. Quirke | Alexander F Engel | N. Maughan | M. Flens | A. Engel
[1] O. Beahrs. The American Joint Committee on Cancer. , 1984, Bulletin of the American College of Surgeons.
[2] B. Vogelstein,et al. A genetic model for colorectal tumorigenesis , 1990, Cell.
[3] L. Sobin,et al. TNM classification of malignant tumors, fifth edition (1997) , 1997, Cancer.
[4] M M Weiss,et al. Comparative genomic hybridisation. , 1999, Molecular pathology : MP.
[5] Christian A. Rees,et al. Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[6] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[7] Terry Speed,et al. Normalization of cDNA microarray data. , 2003, Methods.
[8] N. Carter,et al. Array Comparative Genomic Hybridization Analysis of Colorectal Cancer Cell Lines and Primary Carcinomas , 2004, Cancer Research.
[9] T. Hubbard,et al. A census of human cancer genes , 2004, Nature Reviews Cancer.
[10] Terrence S. Furey,et al. The UCSC Table Browser data retrieval tool , 2004, Nucleic Acids Res..
[11] E. Birney,et al. A survey of homozygous deletions in human cancer genomes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[12] D. Pinkel,et al. Array comparative genomic hybridization and its applications in cancer , 2005, Nature Genetics.
[13] Terrence S. Furey,et al. The UCSC Genome Browser Database: update 2006 , 2005, Nucleic Acids Res..
[14] G. Thomas,et al. Retention of chromosome arm 5q in stage II colon cancers identifies 83% of liver metastasis occurrences , 2006, Genes, chromosomes & cancer.
[15] B. Ylstra,et al. BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH) , 2006, Nucleic acids research.
[16] R. Lothe,et al. The order of genetic events associated with colorectal cancer progression inferred from meta‐analysis of copy number changes , 2006, Genes, chromosomes & cancer.
[17] D. Albertson,et al. Gene amplification in cancer. , 2006, Trends in genetics : TIG.
[18] Wessel N. van Wieringen,et al. CGHcall: Calling aberrations for array CGH tumor profiles. , 2008 .
[19] Derek Y. Chiang,et al. Characterizing the cancer genome in lung adenocarcinoma , 2007, Nature.
[20] A. Sparks,et al. The Genomic Landscapes of Human Breast and Colorectal Cancers , 2007, Science.
[21] H. Grabsch,et al. DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification , 2007, Cellular oncology : the official journal of the International Society for Cellular Oncology.
[22] E. Kay,et al. Formalin‐fixed paraffin‐embedded clinical tissues show spurious copy number changes in array‐CGH profiles , 2007, Clinical genetics.
[23] David Haussler,et al. The UCSC genome browser database: update 2007 , 2006, Nucleic Acids Res..
[24] Gordon K. Smyth,et al. A comparison of background correction methods for two-colour microarrays , 2007, Bioinform..
[25] D. Busam,et al. An Integrated Genomic Analysis of Human Glioblastoma Multiforme , 2008, Science.
[26] Sjoerd J. Vosse,et al. Across array comparative genomic hybridization: A strategy to reduce reference channel hybridizations , 2008, Genes, chromosomes & cancer.
[27] G. Parmigiani,et al. Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers , 2008, Proceedings of the National Academy of Sciences.
[28] E. Schröck,et al. Multiple putative oncogenes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression , 2008, Gut.
[29] C. Caldas,et al. Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies. , 2008, Seminars in radiation oncology.
[30] G. Parmigiani,et al. Core Signaling Pathways in Human Pancreatic Cancers Revealed by Global Genomic Analyses , 2008, Science.
[31] Toshihide Ueno,et al. Chromosome copy number analysis in screening for prognosis‐related genomic regions in colorectal carcinoma , 2008, Cancer science.
[32] B. Ylstra,et al. DNA copy number profiles of primary tumors as predictors of response to chemotherapy in advanced colorectal cancer. , 2009, Annals of oncology : official journal of the European Society for Medical Oncology.
[33] Yong-shu He,et al. [Structural variation in the human genome]. , 2009, Yi chuan = Hereditas.
[34] Brad T. Sherman,et al. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists , 2008, Nucleic acids research.
[35] Derek Y. Chiang,et al. The landscape of somatic copy-number alteration across human cancers , 2010, Nature.
[36] Henry Z. Montes,et al. TNM Classification of Malignant Tumors, 7th edition , 2010 .