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1. Full Text Erratum: Comprehensive genomic characterization of squamous cell lung cancers (Nature (2012) 489 (519-525) DOI:10.1038/nature11404)
Nature, ISSN 0028-0836, 11/2012, Volume 491, Issue 7423, p. 288
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2. Full Text Erratum: Integrated genomic characterization of endometrial carcinoma (Nature (2013) 497 (67-73) Doi:10.1038/nature12113)
Nature, ISSN 0028-0836, 2013, Volume 500, Issue 7461, p. 242
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3. Full Text Corrigendum: Comprehensive genomic characterization defines human glioblastoma genes and core pathways
by Network, The Cancer Genome Atlas Research
Nature, ISSN 0028-0836, 02/2013, Volume 494, Issue 7438, p. 506
CORRIGENDUM doi:10.1038/nature11903 The Cancer Genome Atlas Research Network Nature 455, 1061-1068 (2008); doi:10.1038/nature07385 In this Article, we reported... 
Genomes | Mutation | Genes | Deoxyribonucleic acid--DNA | Cancer
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4. Full Text Erratum: Corrigendum: Comprehensive genomic characterization defines human glioblastoma genes and core pathways
by Network, The Cancer Genome Atlas Research
Nature, ISSN 0028-0836, 02/2013, Volume 494, Issue 7438, pp. 506 - 506
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5. Full Text Erratum: Integrated genomic analyses of ovarian carcinoma
by Network, The Cancer Genome Atlas Research
Nature, ISSN 0028-0836, 10/2012, Volume 490, Issue 7419, pp. 292 - 292
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6. Full Text Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia
by Ley, Timothy J and Miller, Christopher and Ding, Li and Raphael, Benjamin J and Mungall, Andrew J and Robertson, Gordon and Hoadley, Katherine and Triche Jr, Timothy J and Laird, Peter W and Baty, Jack D and Fulton, Lucinda L and Fulton, Robert and Heath, Sharon E and Kalicki-Veizer, Joelle and Kandoth, Cyriac and Klco, Jeffery M and Koboldt, Daniel C and Kanchi, Krishna-Latha and Kulkarni, Shashikant and Lamprecht, Tamara L and Larson, David E and Lin, G and Lu, Charles and McLellan, Michael D and McMichael, Joshua F and Payton, Jacqueline and Schmidt, Heather and Spencer, David H and Tomasson, Michael H and Wallis, John W and Wartman, Lukas D and Watson, Mark A and Welch, John and Wendl, Michael C and Ally, Adrian and Balasundaram, Miruna and Birol, Inanc and Butterfield, Yaron and Chiu, Readman and Chu, Andy and Chuah, Eric and Chun, Hye-Jung and Corbett, Richard and Dhalla, Noreen and Guin, Ranabir and He, An and Hirst, Carrie and Hirst, Martin and Holt, Robert A and Jones, Steven and Karsan, Aly and Lee, Darlene and Li, Haiyan I and Marra, Marco A and Mayo, Michael and Moore, Richard A and Mungall, Karen and Parker, Jeremy and Pleasance, Erin and Plettner, Patrick and Schein, Jacquie and Stoll, Dominik and Swanson, Lucas and Tam, Angela and Thiessen, Nina and Varhol, Richard and Wye, Natasja and Zhao, Yongjun and Gabriel, Stacey and Getz, Gad and Sougnez, Carrie and Zou, Lihua and Leiserson, Mark D. M and Vandin, Fabio and Wu, Hsin-Ta and Applebaum, Frederick and Baylin, Stephen B and Akbani, Rehan and Broom, Bradley M and Chen, Ken and Motter, Thomas C and Nguyen, Khanh and Weinstein, John N and Zhang, Nianziang and Ferguson, Martin L and Adams, Christopher and Black, Aaron and Bowen, Jay and Gastier-Foster, Julie and Grossman, Thomas and Lichtenberg, Tara and Wise, Lisa and Davidsen, Tanja and Demchok, John A and Mills Shaw, Kenna R and Sheth, Margi and Sofia, Heidi J and Yang, Liming and Downing, James R and Eley, Greg and ... and The Cancer Genome Atlas Research Network and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network
The New England Journal of Medicine, ISSN 0028-4793, 05/2013, Volume 368, Issue 22, pp. 2059 - 2074
More than 25% of patients with AML carry no mutations in genes known to be associated with leukemia. Analyses of genomes, transcriptomes, and methylomes of AML... 
MEDICINE, GENERAL & INTERNAL | COPY NUMBER ALTERATIONS | HYPERMETHYLATION | EVOLUTION | GENE | TRANSCRIPTION | MONOSOMAL KARYOTYPE | EXPRESSION PROFILES | MUTATIONS | MICRORNA EXPRESSION | CANCER | Gene Expression | Epigenomics | Humans | Middle Aged | Gene Fusion | Male | DNA Methylation | CpG Islands | Adult | Female | MicroRNAs - genetics | Mutation | Genome, Human | Sequence Analysis, DNA - methods | Leukemia, Myeloid, Acute - classification | Leukemia, Myeloid, Acute - genetics | Gene mutations | Research | Chromatin | Phenotypes | Myeloid leukemia | Pathogenesis | MiRNA | Genomes | Algorithms | Consolidation | Classification | DNA methylation | Tumor suppressor genes | Cohesin | Acute myeloid leukemia | DNA sequencing
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7. Full Text Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas
by Brat, Daniel J and Verhaak, Roel G. W and Aldape, Kenneth D and Yung, W. K. Alfred and Salama, Sofie R and Cooper, Lee A. D and Rheinbay, Esther and Miller, C. Ryan and Vitucci, Mark and Morozova, Olena and Robertson, A. Gordon and Noushmehr, Houtan and Laird, Peter W and Cherniack, Andrew D and Akbani, Rehan and Huse, Jason T and Ciriello, Giovanni and Poisson, Laila M and Barnholtz-Sloan, Jill S and Berger, Mitchel S and Brennan, Cameron and Colen, Rivka R and Colman, Howard and Flanders, Adam E and Giannini, Caterina and Grifford, Mia and Iavarone, Antonio and Jain, Rajan and Joseph, Isaac and Kim, Jaegil and Kasaian, Katayoon and Mikkelsen, Tom and Murray, Bradley A and O'Neill, Brian Patrick and Pachter, Lior and Parsons, Donald W and Sougnez, Carrie and Sulman, Erik P and Vandenberg, Scott R and Van Meir, Erwin G and Von Deimling, Andreas and Zhang, Hailei and Crain, Daniel and Lau, Kevin and Mallery, David and Morris, Scott and Paulauskis, Joseph and Penny, Robert and Shelton, Troy and Sherman, Mark and Yena, Peggy and Black, Aaron and Bowen, Jay and Dicostanzo, Katie and Gastier-Foster, Julie and Leraas, Kristen M and Lichtenberg, Tara M and Pierson, Christopher R and Ramirez, Nilsa C and Taylor, Cynthia and Weaver, Stephanie and Wise, Lisa and Zmuda, Erik and Davidsen, Tanja and Demchok, John A and Eley, Greg and Ferguson, Martin L and Hutter, Carolyn M and Shaw, Kenna R. Mills and Ozenberger, Bradley A and Sheth, Margi and Sofia, Heidi J and Tarnuzzer, Roy and Wang, Zhining and Yang, Liming and Zenklusen, Jean Claude and Ayala, Brenda and Baboud, Julien and Chudamani, Sudha and Jensen, Mark A and Liu, Jia and Pihl, Todd and Raman, Rohini and Wan, Yunhu and Wu, Ye and Ally, Adrian and Auman, J. Todd and Balasundaram, Miruna and Balu, Saianand and Baylin, Stephen B and Beroukhim, Rameen and Bootwalla, Moiz S and Bowlby, Reanne and Bristow, Christopher A and Brooks, Denise and Butterfield, Yaron and Carlsen, Rebecca and Carter, Scott and Chin, Lynda and Chu, Andy and ... and The Cancer Genome Atlas Research Network and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network
The New England Journal of Medicine, ISSN 0028-4793, 06/2015, Volume 372, Issue 26, pp. 2481 - 2498
The Cancer Genome Atlas consortium analyzed 293 lower-grade gliomas obtained from adult patients. The integration of genomic and clinical data shows that... 
MOLECULAR-GENETICS | MEDICINE, GENERAL & INTERNAL | TERT PROMOTER MUTATIONS | OLIGODENDROGLIOMA | LANDSCAPE | IDH1 | CLASSIFICATION | TUMORS | CHEMOTHERAPY | FREQUENT ATRX | 1P/19Q LOSS | Glioma - mortality | Signal Transduction | Humans | Middle Aged | Kaplan-Meier Estimate | Proportional Hazards Models | Male | Sequence Analysis, DNA | Glioma - metabolism | Glioma - genetics | Chromosomes, Human, Pair 19 | Genes, p53 | Chromosomes, Human, Pair 1 | Neoplasm Grading | Glioblastoma - genetics | Adolescent | Adult | Female | Aged | DNA, Neoplasm - analysis | Mutation | Cluster Analysis | Usage | Gene mutations | Gliomas | Analysis | Exome sequencing | Genetic aspects | Diagnosis | Research | Risk factors | Genomic analysis | Nucleotide sequence | Copy number | p53 Protein | Genomics | Glioblastoma | MiRNA | Gene expression | Glioma | DNA methylation | Cancer | Tumors | Statistical analysis | Brain cancer | Genomes | Cancer therapies | Consent | Medical prognosis | MicroRNAs | Classification | Deoxyribonucleic acid--DNA
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8. Full Text Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma
by Linehan, W. Marston and Spellman, Paul T and Ricketts, Christopher J and Creighton, Chad J and Fei, Suzanne S and Davis, Caleb and Wheeler, David A and Murray, Bradley A and Schmidt, Laura and Vocke, Cathy D and Peto, Myron and Al Mamun, Abu Amar M and Shinbrot, Eve and Sethi, Anurag and Brooks, Samira and Rathmell, W. Kimryn and Brooks, Angela N and Hoadley, Katherine A and Robertson, A. Gordon and Brooks, Denise and Bowlby, Reanne and Sadeghi, Sara and Shen, Hui and Weisenberger, Daniel J and Bootwalla, Moiz and Baylin, Stephen B and Laird, Peter W and Cherniack, Andrew D and Saksena, Gordon and Haake, Scott and Li, Jun and Liang, Han and Lu, Yiling and Mills, Gordon B and Akbani, Rehan and Leiserson, Mark D.M and Raphael, Benjamin J and Anur, Pavana and Bottaro, Donald and Albiges, Laurence and Barnabas, Nandita and Choueiri, Toni K and Czerniak, Bogdan and Godwin, Andrew K and Hakimi, A. Ari and Ho, Thai H and Hsieh, James and Ittmann, Michael and Kim, William Y and Krishnan, Bhavani and Merino, Maria J and Shaw, Kenna R. Mills and Reuter, Victor E and Reznik, Ed and Shelley, Carl S and Shuch, Brian and Signoretti, Sabina and Srinivasan, Ramaprasad and Tamboli, Pheroze and Thomas, George and Tickoo, Satish and Burnett, Kenneth and Crain, Daniel and Gardner, Johanna and Lau, Kevin and Mallery, David and Morris, Scott and Paulauskis, Joseph D and Penny, Robert J and Shelton, Candace and Shelton, W. Troy and Sherman, Mark and Thompson, Eric and Yena, Peggy and Avedon, Melissa T and Bowen, Jay and Gastier-Foster, Julie M and Gerken, Mark and Leraas, Kristen M and Lichtenberg, Tara M and Ramirez, Nilsa C and Santos, Tracie and Wise, Lisa and Zmuda, Erik and Demchok, John A and Felau, Ina and Hutter, Carolyn M and Sheth, Margi and Sofia, Heidi J and Tarnuzzer, Roy and Wang, Zhining and Yang, Liming and Zenklusen, Jean C and Zhang, Jiashan and Ayala, Brenda and Baboud, Julien and Chudamani, Sudha and Liu, Jia and Lolla, Laxmi and Naresh, Rashi and ... and The Cancer Genome Atlas Research Network and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network
The New England Journal of Medicine, ISSN 0028-4793, 01/2016, Volume 374, Issue 2, pp. 135 - 145
Papillary renal-cell carcinomas account for 15 to 20% of kidney cancers. Type 1, which is often multifocal and more indolent, was associated with mutations in... 
FUMARATE | MEDICINE, GENERAL & INTERNAL | MET PROTOONCOGENE | GENETIC-BASIS | GERMLINE | HEREDITARY | NRF2 | PHENOTYPE | MUTATIONS | EXPRESSION | KIDNEY CANCER | Proto-Oncogene Proteins c-met - metabolism | RNA, Neoplasm - chemistry | Carcinoma, Papillary - genetics | Kidney Neoplasms - genetics | Humans | Kidney Neoplasms - metabolism | CpG Islands - physiology | Carcinoma, Papillary - metabolism | Proto-Oncogene Proteins c-met - genetics | DNA Methylation | Phenotype | Sequence Analysis, RNA | NF-E2-Related Factor 2 - metabolism | NF-E2-Related Factor 2 - genetics | RNA, Messenger - chemistry | Signal Transduction - physiology | Mutation | Proto-Oncogene Proteins c-met - chemistry | MicroRNAs - chemistry | Care and treatment | Histology | Carcinoma, Renal cell | Research | Gene mutations | Analysis | Phenotypes | Carcinoma | Cell survival | MiRNA | mRNA | Genomes | Antioxidants | Fumarate hydratase | Kidney cancer | DNA methylation | Molecular biology | Chromosomes | Clear cell-type renal cell carcinoma | DNA sequencing | CpG islands | Tumors
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9. Full Text Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer
by Bolton, Kelly L and Chenevix- Trench, Georgia and Goh, Cindy and Sadetzki, Siegal and Ramus, Susan J and Karlan, Beth Y and Lambrechts, Diether and Despierre, Evelyn and Barrowdale, Daniel and McGuffog, Lesley and Healey, Sue and Easton, Douglas F and Sinilnikova, Olga and Benítez, Javier and García, María J and Neuhausen, Susan and Gail, Mitchell H and Hartge, Patricia and Peock, Susan and Frost, Debra and Evans, D. Gareth and Eeles, Rosalind and Godwin, Andrew K and Daly, Mary B and Kwong, Ava and Ma, Edmond S. K and Lázaro, Conxi and Blanco, Ignacio and Montagna, Marco and D'Andrea, Emma and Nicoletto, Maria Ornella and Johnatty, Sharon E and Kjær, Susanne Krüger and Jensen, Allan and Høgdall, Estrid and Goode, Ellen L and Fridley, Brooke L and Loud, Jennifer T and Greene, Mark H and Mai, Phuong L and Chetrit, Angela and Lubin, Flora and Hirsh-Yechezkel, Galit and Glendon, Gord and Andrulis, Irene L and Toland, Amanda E and Senter, Leigha and Gore, Martin E and Gourley, Charlie and Michie, Caroline O and Song, Honglin and Tyrer, Jonathan and Whittemore, Alice S and McGuire, Valerie and Sieh, Weiva and Kristoffersson, Ulf and Olsson, Håkan and Borg, Åke and Levine, Douglas A and Steele, Linda and Beattie, Mary S and Chan, Salina and Nussbaum, Robert L and Moysich, Kirsten B and Gross, Jenny and Cass, Ilana and Walsh, Christine and Li, Andrew J and Leuchter, Ronald and Gordon, Ora and Garcia-Closas, Montserrat and Gayther, Simon A and Chanock, Stephen J and Antoniou, Antonis C and Pharoah, Paul D. P and EMBRACE, kConFab Investigators, and The Cancer Genome Atlas Research Network, for the and KConFab Investigators and Canc Genome Atlas Res Network and EMBRACE and Cancer Genome Atlas Research Network and kConFab Investigators and Onkologi och Patologi, MV and Lund University and Division of Clinical Genetics and Oncology and Pathology, MV and Avdelningen för klinisk genetik and EpiHealth: Epidemiology for Health and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation and Lunds universitet
JAMA, ISSN 0098-7484, 01/2012, Volume 307, Issue 4, pp. 382 - 389
CONTEXT Approximately 10% of women with invasive epithelial ovarian cancer (EOC) carry deleterious germline mutations in BRCA1 or BRCA2. A recent article... 
BREAST-CANCER | CONSORTIUM | MEDICINE, GENERAL & INTERNAL | NONSENSE | POLYMERASE | SUSCEPTIBILITY GENE | RISK | LOW-GRADE | PROGESTERONE-RECEPTOR | CARCINOMA | CARRIERS | Ovarian Neoplasms - genetics | Prognosis | Humans | Middle Aged | Survival Analysis | Genes, BRCA2 | Germ-Line Mutation | Adult | Female | Aged | Genes, BRCA1 | Ovarian Neoplasms - mortality | Cancer patients | BRCA mutations | Causes of | Genetic aspects | Research | Health aspects | Ovarian cancer | Survival analysis | Medical research | Mutation | Womens health | Clinical Medicine | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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10. Full Text Spectrum of somatic mitochondrial mutations in five cancers
by Tatianna C. Larman and Steven R. DePalma and Angela G. Hadjipanayis and Alexei Protopopov and Jianhua Zhang and Stacey B. Gabriel and Lynda Chin and Christine E. Seidman and Raju Kucherlapati and J. G. Seidman and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network and The Cancer Genome Atlas Research Network
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2012, Volume 109, Issue 35, pp. 14087 - 14091
Somatic mtDNA mutations have been reported in some human tumors, but their spectrum in different malignancies and their role in cancer development remain... 
Somatic mutation | Dehydrogenases | Cellular metabolism | Mitochondrial DNA | Genomes | Kidney cells | Genetic mutation | Sequencing | Tumors | Cancer | Colon adenocarcinoma | Ovarian serous cystadenocarcinoma | Deleterious mutations | Acute myeloid leukemia | Rectal adenomcarcinoma | PROSTATE | colon adenocarcinoma | rectal adenomcarcinoma | MULTIDISCIPLINARY SCIENCES | deleterious mutations | TUMORS | GENOME | DEHYDROGENASE | acute myeloid leukemia | MTDNA | DISEASE | ovarian serous cystadenocarcinoma | GENERATION | CELL-METABOLISM | SELECTION | DNA MUTATIONS | Colonic Neoplasms - genetics | Colorectal Neoplasms - genetics | Genomics | Humans | Cystadenocarcinoma, Serous - genetics | Mutation, Missense - genetics | Ovarian Neoplasms - genetics | Genes, Mitochondrial - genetics | DNA, Mitochondrial - genetics | Gene Deletion | Female | Adenocarcinoma - genetics | Gene Expression Regulation, Neoplastic - genetics | Leukemia, Myeloid, Acute - genetics | Biological Sciences
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11. Full Text Integrated analyses of microRNAs demonstrate their widespread influence on gene expression in high-grade serous ovarian carcinoma
by Creighton, Chad J and Hernandez-Herrera, Anadulce and Jacobsen, Anders and Levine, Douglas A and Mankoo, Parminder and Schultz, Nikolaus and Du, Ying and Zhang, Yiqun and Larsson, Erik and Sheridan, Robert and Xiao, Weimin and Spellman, Paul T and Getz, Gad and Wheeler, David A and Perou, Charles M and Gibbs, Richard A and Sander, Chris and Hayes, D. Neil and Gunaratne, Preethi H and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network and The Cancer Genome Atlas Research Network
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e34546
Background: The Cancer Genome Atlas (TCGA) Network recently comprehensively catalogued the molecular aberrations in 487 high-grade serous ovarian cancers, with... 
MESSENGER-RNAS | PROFILES | SIGNATURES | 5'-UTR | BIOLOGY | SITES | 3'-UTR | TARGETS | HUMAN BREAST-TUMORS | CANCER | REVEALS | Neoplasms, Cystic, Mucinous, and Serous - pathology | Humans | Gene Expression Regulation, Neoplastic | Ovarian Neoplasms - pathology | Breast - metabolism | DNA Copy Number Variations | Neoplasms, Cystic, Mucinous, and Serous - genetics | Ovarian Neoplasms - genetics | Cell Line, Tumor | Female | MicroRNAs - genetics | 3' Untranslated Regions | Breast - pathology | Prognosis | Genes | Genomics | Genomes | Gene expression | Ovarian cancer | Surveys | Messenger RNA | MicroRNA | Methyltransferases | Analysis | Genetic aspects | Cancer | Ovarian carcinoma | Leukemia | Lung cancer | Biochemistry | Biology | Datasets | DNA methylation | Bioinformatics | Deoxyribonucleic acid--DNA | MiRNA | Medicine | Studies | Overexpression | Ribonucleic acids | Correlation analysis | MicroRNAs | Aberration | Web sites | Viability | Binding sites | Tumors | Deoxyribonucleic acid | DNA
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