Genes, Chromosomes and Cancer, 1045-2257

Journal

More filtering options
  1. Article
  2. Most gene fusions in cancer are stochastic events

    Bertil Johansson, Fredrik Mertens, Schyman, T., Jonas Björk, Nils Mandahl & Felix Mitelman, 2019 Sep, In : Genes Chromosomes and Cancer. 58, 9, p. 607-611 5 p.

    Research output: Contribution to journalArticle

  3. Cancer chromosome breakpoints cluster in gene-rich genomic regions

    Felix Mitelman, Bertil Johansson, Fredrik Mertens, Schyman, T. & Nils Mandahl, 2019, In : Genes Chromosomes and Cancer. 58, 3, p. 149-154

    Research output: Contribution to journalArticle

  4. Telomere length, telomerase reverse transcriptase promoter mutations, and melanoma risk

    Rachakonda, S., Kong, H., Srinivas, N., Garcia-Casado, Z., Requena, C., Mahdi Fallah, Heidenreich, B., Planelles, D., Traves, V., Schadendorf, D., Nagore, E. & Kumar, R., 2018 Nov, In : Genes, Chromosomes and Cancer. 57, 11, p. 564-572 9 p.

    Research output: Contribution to journalArticle

  5. Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases

    Bekers, E. M., Groenen, P. J. T. A., Verdijk, M. A. J., Raaijmakers-van Geloof, W. L., Roepman, P., Vink, R., Gilhuijs, N. D. B., van Gorp, J. M., Bovée, J. V. M. G., Creytens, D. H., Flanagan, A. M., Suurmeijer, A. J. H., Mentzel, T., Elsa Arbajian & Flucke, U., 2017 Oct 1, In : Genes Chromosomes and Cancer. 56, 10, p. 750-757 8 p.

    Research output: Contribution to journalArticle

  6. Trisomy 8 in pediatric acute myeloid leukemia: A NOPHO-AML study

    Laursen, A. C. L., Sandahl, J. D., Kjeldsen, E., Abrahamsson, J., Asdahl, P., Ha, S. Y., Heldrup, J., Jahnukainen, K., Jónsson, Ó. G., Lausen, B., Palle, J., Zeller, B., Forestier, E. & Hasle, H., 2016 Sep 1, In : Genes Chromosomes and Cancer. 55, 9, p. 719-726 8 p.

    Research output: Contribution to journalArticle

  7. A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients

    Dirse, V., Bertasiute, A., Gineikiene, E., Zvirblis, T., Dambrauskiene, R., Gerbutavicius, R., Juozaityte, E., Malciute, L., Kajsa Paulsson & Griskevicius, L., 2015, In : Genes, Chromosomes and Cancer. 54, 5, p. 326-333

    Research output: Contribution to journalArticle

  8. Metabolic gene variants associated with chromosomal aberrations in healthy humans.

    Kari Hemminki, Frank, C., Asta Försti, Musak, L., Kazimirova, A., Barancokova, M., Horska, A., Vymetalkova, V., Smerhovsky, Z., Naccarati, A., Soucek, P., Vodickova, L., Buchancova, J., Smolkova, B., Dusinska, M. & Vodicka, P., 2015, In : Genes, Chromosomes and Cancer. 54, 4, p. 260-266

    Research output: Contribution to journalArticle

  9. Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.

    Macchia, G., Karolin Hansén Nord, Zoli, M., Purgato, S., D'Addabbo, P., Whelan, C. W., Carbone, L., Perini, G., Fredrik Mertens, Rocchi, M. & Storlazzi, C. T., 2015, In : Genes, Chromosomes and Cancer. 54, 3, p. 156-167

    Research output: Contribution to journalArticle

  10. Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas

    Joseph, C. G., Hwang, H., Jiao, Y., Wood, L. D., Kinde, I., Wu, J., Nils Mandahl, Luo, J., Hruban, R. H., Diaz Jr, L. A., He, T-C., Vogelstein, B., Kinzler, K. W., Fredrik Mertens & Papadopoulos, N., 2014, In : Genes, Chromosomes and Cancer. 53, 1, p. 15-24

    Research output: Contribution to journalArticle

  11. Ploidy and clinical characteristics of childhood acute myeloid leukemia: A NOPHO-AML study

    Sandahl, J. D., Kjeldsen, E., Abrahamsson, J., Ha, S-Y., Heldrup, J., Jahnukainen, K., Jonsson, O. G., Lausen, B., Palle, J., Zeller, B., Forestier, E. & Hasle, H., 2014, In : Genes, Chromosomes and Cancer. 53, 8, p. 667-675

    Research output: Contribution to journalArticle

  12. Amplification of 2p as a genomic marker for transformation in lymphoma

    Anna Kwiecinska, Ichimura, K., Berglund, M., Dinets, A., Sulaiman, L., Collins, V. P., Larsson, C., Anna Porwit & Lagercrantz, S. B., 2014, In : Genes Chromosomes and Cancer. 53, 9, p. 750-768 19 p.

    Research output: Contribution to journalArticle

  13. Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

    Mohajeri, A., Tayebwa, J., Collin, A., Nilsson, J., Magnusson, L., Fredrik Vult von Steyern, Brosjö, O., Domanski, H., Larsson, O., Sciot, R., Debiec-Rychter, M., Hornick, J. L., Nils Mandahl, Karolin Hansén Nord & GCC Klinisk genetik, F. M., 2013, In : Genes, Chromosomes and Cancer. 52, 10, p. 873-886

    Research output: Contribution to journalArticle

  14. Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer

    Partanen, L., Johan Staaf, Tanner, M., Tuominen, V. J., Åke Borg & Isola, J., 2012, In : Genes, Chromosomes and Cancer. 51, 9, p. 832-840

    Research output: Contribution to journalArticle

  15. Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data

    Wang, L., Motoi, T., Khanin, R., Olshen, A., Fredrik Mertens, Bridge, J., Dal Cin, P., Antonescu, C. R., Singer, S., Hameed, M., Bovee, J. V. M. G., Hogendoorn, P. C. W., Socci, N. & Ladanyi, M., 2012, In : Genes, Chromosomes and Cancer. 51, 2, p. 127-139

    Research output: Contribution to journalArticle

  16. Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis

    Molenaar, J. J., Koster, J., Ebus, M. E., van Sluis, P., Westerhout, E. M., de Preter, K., David Gisselsson Nord, Ingrid Øra, Speleman, F., Caron, H. N. & Versteeg, R., 2012, In : Genes, Chromosomes and Cancer. 51, 1, p. 10-19

    Research output: Contribution to journalArticle

  17. Telomere length and LINE1 methylation is associated with chromosomal aberrations in peripheral blood.

    Li, H., Hilmarsen, H. T., Hossain, M. B., Jonas Björk, Hansteen, I-L., Maria Albin, Furu Skjelbred, C. & Karin Broberg Palmgren, 2012, In : Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  18. Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.

    Jin, Y., Möller, E., Karolin Hansén Nord, Nils Mandahl, Fredrik Vult von Steyern, Domanski, H., Mariño-Enríquez, A., Magnusson, L., Nilsson, J., Sciot, R., Fletcher, C. D. M., Debiec-Rychter, M. & Fredrik Mertens, 2012, In : Genes, Chromosomes and Cancer. 51, 5, p. 510-520

    Research output: Contribution to journalArticle

  19. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.

    Lundin, C., Lars Hjorth, Behrendtz, M., Nordgren, A., Palmqvist, L., Andersen, M. K., Biloglav, A., Forestier, E., Kajsa Paulsson & Bertil Johansson, 2012, In : Genes, Chromosomes and Cancer. 51, p. 196-206

    Research output: Contribution to journalArticle

  20. Fusion Gene Microarray Reveals Cancer Type-Specificity Among Fusion Genes

    Lovf, M., Thomassen, G. O. S., Bakken, A. C., Celestino, R., Thoas Fioretos, Lind, G. E., Lothe, R. A. & Skotheim, R. I., 2011, In : Genes, Chromosomes and Cancer. 50, 5, p. 348-357

    Research output: Contribution to journalArticle

  21. Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.

    Bartuma, H., Karolin Hansén Nord, Macchia, G., Isaksson, M., Nilsson, J., Domanski, H., Nils Mandahl & Fredrik Mertens, 2011, In : Genes, Chromosomes and Cancer. 50, p. 619-632

    Research output: Contribution to journalArticle

  22. High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.

    Halldórsdóttir, A. M., Sander, B., Göransson, H., Isaksson, A., Kimby, E., Mansouri, M., Rosenquist, R. & Hans Ehrencrona, 2011, In : Genes, Chromosomes and Cancer. 50, 2, p. 113-121

    Research output: Contribution to journalArticle

  23. Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.

    Lundberg, G., Sehic, D., Länsberg, J-K., Ingrid Øra, Attila Frigyesi, Castel, V., Navarro, S., Piqueras, M., Martinsson, T., Noguera, R. & David Gisselsson Nord, 2011, In : Genes, Chromosomes and Cancer. 50, 4, p. 250-262

    Research output: Contribution to journalArticle

  24. Polymorphisms in the Transforming Growth Factor Beta 1 Pathway in Relation to Colorectal Cancer Progression

    Foersti, A., Li, X., Wagner, K., Tavelin, B., Enquist, K., Palmqvist, R., Altieri, A., Hallmans, G., Kari Hemminki & Lenner, P., 2010, In : Genes, Chromosomes and Cancer. 49, 3, p. 270-281

    Research output: Contribution to journalArticle

  25. Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations

    Gorunova, L., Fredrik Vult von Steyern, Storlazzi, T., Bjerkehagen, B., Folleras, G., Heim, S., Nils Mandahl & Fredrik Mertens, 2009, In : Genes, Chromosomes and Cancer. 48, 7, p. 583-602

    Research output: Contribution to journalArticle

  26. t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma

    Brandal, P., Panagopoulos, I., Bjerkehagen, B. & Heim, S., 2009, In : Genes, Chromosomes and Cancer. 48, 12, p. 1051-1056

    Research output: Contribution to journalArticle

  27. Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors

    Trombetta, D., Fredrik Mertens, Lonoce, A., D'Addabbo, P., Rennstam, K., Nils Mandahl & Storlazzi, C. T., 2009, In : Genes, Chromosomes and Cancer. 48, 11, p. 993-1001

    Research output: Contribution to journalArticle

  28. No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies

    da Costa, C. E. T., Szuhai, K., van Eijk, R., Hoogeboom, M., Sciot, R., Fredrik Mertens, Bjorgvinsdottir, H., Debiec-Rychter, M., de Krijger, R. R., Hogendoorn, P. C. W., Egeler, R. M. & Annels, N. E., 2009, In : Genes, Chromosomes and Cancer. 48, 3, p. 239-249

    Research output: Contribution to journalArticle

  29. High hyperdiploid childhood acute lymphoblastic leukemia.

    Kajsa Paulsson & Bertil Johansson, 2009, In : Genes, Chromosomes and Cancer. 48, p. 637-660

    Research output: Contribution to journalArticle

  30. Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.

    Karrman, K., Forestier, E., Heyman, M., K Andersen, M., Autio, K., Blennow, E., Borgström, G., Hans Ehrencrona, Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kerndrup, G., Nordgren, A., Palmqvist, L. & Bertil Johansson, 2009, In : Genes, Chromosomes and Cancer. 48, 9, p. 795-805

    Research output: Contribution to journalArticle

  31. Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma

    Brandal, P., Panagopoulos, I., Bjerkehagen, B., Gorunova, L., Skjeldal, S., Micci, F. & Heim, S., 2008, In : Genes, Chromosomes and Cancer. 47, 7, p. 558-564

    Research output: Contribution to journalArticle

  32. Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-A comparative study of four differently designed, high resolution microarray platforms.

    Rebeqa Gunnarsson, Johan Staaf, Jansson, M., Ottesen, A. M., Göransson, H., Liljedahl, U., Ralfkiær, U., Mansouri, M., Buhl, A. M., Smedby, K. E., Hjalgrim, H., Syvänen, A-C., Åke Borg, Isaksson, A., Jurlander, J., Gunnar Juliusson & Rosenquist, R., 2008, In : Genes, Chromosomes and Cancer. 47, 8, p. 697-711

    Research output: Contribution to journalArticle

  33. Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors

    Möller, E., Nils Mandahl, Fredrik Mertens & Panagopoulos, I., 2008, In : Genes, Chromosomes and Cancer. 47, 1, p. 21-25

    Research output: Contribution to journalArticle

  34. Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia

    Kajsa Paulsson, Biloglav, A., Strömbeck, B., Nilsson, F., Heldrup, J., Behrendtz, M., Forestier, E., Anna Andersson, Thoas Fioretos & Bertil Johansson, 2008, In : Genes, Chromosomes and Cancer. 47, 1, p. 26-33

    Research output: Contribution to journalArticle

Previous 1 2 3 Next