Farewell message from the Editor‐in‐Chief of Genes, Chromosomes & Cancer von Mitelman, Felix

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Modeling human cancer predisposition syndromes using CRISPR/Cas9 in human cell line models: Prepared for the special Issue for Genes Chromosomes and Cancer, dedicated on ‘Model Systems for Cancer in the Genomics and CRISPR Era’ von Draper, Garrett M., Panken, Daniel J., Largaespada, David A.

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Genes, Chromosomes and Cancer von Reith, A.

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Genes, chromosomes & cancer

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Genes, chromosomes, and cancer von Littlefield, John W.

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Genes, chromosomes and cancer. First meeting of the "Arbeitsgemeinschaft Molekular- und Zytogenetik (AEK)" of the Deutsche Krebsgesellschaft von Schwab, M

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Genes, chromosomes & cancer: A new forum for research in cancer genetics von Mitelman, Felix, Heim, Sverre, Rowley, Janet D., le Beau, Michelle M.

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Genes, chromosomes and cancer von Castillo, S

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Germline miRNA DNA variants and the risk of colorectal cancer by subtype von Lindor, Noralane M., Larson, Melissa C., DeRycke, Melissa S., McDonnell, Shannon K., Baheti, Saurabh, Fogarty, Zachary C., Win, Aung Ko, Potter, John D., Buchanan, Daniel D., Clendenning, Mark, Newcomb, Polly A., Casey, Graham, Gallinger, Steven, Le Marchand, Loïc, Hopper, John L., Jenkins, Mark A., Goode, Ellen L., Thibodeau, Stephen N.

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Cytogenetic and molecular profile of endometrial stromal sarcoma von Micci, Francesca, Gorunova, Ludmila, Agostini, Antonio, Johannessen, Lene E., Brunetti, Marta, Davidson, Ben, Heim, Sverre, Panagopoulos, Ioannis

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Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH von Selzer, Rebecca R., Richmond, Todd A., Pofahl, Nathan J., Green, Roland D., Eis, Peggy S., Nair, Prakash, Brothman, Arthur R., Stallings, Raymond L.

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Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene von Juhlin, C. Christofer, Stenman, Adam, Haglund, Felix, Clark, Victoria E., Brown, Taylor C., Baranoski, Jacob, Bilguvar, Kaya, Goh, Gerald, Welander, Jenny, Svahn, Fredrika, Rubinstein, Jill C., Caramuta, Stefano, Yasuno, Katsuhito, Günel, Murat, Bäckdahl, Martin, Gimm, Oliver, Söderkvist, Peter, Prasad, Manju L., Korah, Reju, Lifton, Richard P., Carling, Tobias

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A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myeloma von Boyle, Eileen M., Proszek, Paula Z., Kaiser, Martin F., Begum, Dil, Dahir, Nasrin, Savola, Suvi, Wardell, Christopher P., Leleu, Xavier, Ross, Fiona M., Chiecchio, Laura, Cook, Gordon, Drayson, Mark T., Owen, Richard G., Ashcroft, John M., Jackson, Graham H., Anthony Child, James, Davies, Faith E., Walker, Brian A., Morgan, Gareth J.

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Genomic and transcriptomic analysis of imatinib resistance in gastrointestinal stromal tumors von Takahashi, Tsuyoshi, Elzawahry, Asmaa, Mimaki, Sachiyo, Furukawa, Eisaku, Nakatsuka, Rie, Nakamura, Hiromi, Nishigaki, Takahiko, Serada, Satoshi, Naka, Tetsuji, Hirota, Seiichi, Shibata, Tatsuhiro, Tsuchihara, Katsuya, Nishida, Toshirou, Kato, Mamoru

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HRAS mutation prevalence and associated expression patterns in pheochromocytoma von Stenman, Adam, Welander, Jenny, Gustavsson, Ida, Brunaud, Laurent, Bäckdahl, Martin, Söderkvist, Peter, Gimm, Oliver, Juhlin, C. Christofer, Larsson, Catharina

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Detection of chromothripsis-like patterns with a custom array platform for chronic lymphocytic leukemia von Salaverria, Itziar, Martín-Garcia, David, López, Cristina, Clot, Guillem, García-Aragonés, Manel, Navarro, Alba, Delgado, Julio, Baumann, Tycho, Pinyol, Magda, Martin-Guerrero, Idoia, Carrió, Ana, Costa, Dolors, Queirós, Ana C., Jayne, Sandrine, Aymerich, Marta, Villamor, Neus, Colomer, Dolors, González, Marcos, López-Guillermo, Armando, Campo, Elías, Dyer, Martin J. S., Siebert, Reiner, Armengol, Lluís, Beà, Sílvia

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Genetic and chromosomal alterations in Kenyan Wilms Tumor von Lovvorn III, Harold N., Pierce, Janene, Libes, Jaime, Li, Bingshan, Wei, Qiang, Correa, Hernan, Gouffon, Julia, Clark, Peter E., Axt, Jason R., Hansen, Erik, Newton, Mark, O'Neill Jr, James A.

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GREM1 and POLE variants in hereditary colorectal cancer syndromes von Rohlin, Anna, Eiengård, Frida, Lundstam, Ulf, Zagoras, Theofanis, Nilsson, Staffan, Edsjö, Anders, Pedersen, Jan, Svensson, Janhenry, Skullman, Stefan, Karlsson, B. Göran, Björk, Jan, Nordling, Margareta

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Analysis of alternative lengthening of telomere markers in BRCA1 defective cells von Kargaran, Parisa K., Yasaei, Hemad, Anjomani-Virmouni, Sara, Mangiapane, Giovanna, Slijepcevic, Predrag

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Comprehensive exploration of novel chimeric transcripts in clear cell renal cell carcinomas using whole transcriptome analysis von Gotoh, Masahiro, Ichikawa, Hitoshi, Arai, Eri, Chiku, Suenori, Sakamoto, Hiromi, Fujimoto, Hiroyuki, Hiramoto, Masaki, Nammo, Takao, Yasuda, Kazuki, Yoshida, Teruhiko, Kanai, Yae

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