Genes, Chromosomes and Cancer, 1045-2257

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  1. 2019
  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. Clonal evolution through genetic bottlenecks and telomere attrition: Potential threats to in vitro data reproducibility

    David Gisselsson, Lichtenzstejn, D., Kachko, P., Jenny Karlsson, Manor, E. & Mai, S., 2019, In : Genes Chromosomes and Cancer. 58, 7, p. 452-461

    Research output: Contribution to journalReview article

  5. 2018
  6. 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

  7. A field guide for cancer diagnostics using cell-free DNA: From principles to practice and clinical applications

    Volckmar, A. L., Sültmann, H., Riediger, A., Thoas Fioretos, Schirmacher, P., Endris, V., Stenzinger, A. & Dietz, S., 2018 Mar 1, In : Genes Chromosomes and Cancer. 57, 3, p. 123-139 17 p.

    Research output: Contribution to journalReview article

  8. 2017
  9. 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

  10. Pediatric T-cell acute lymphoblastic leukemia

    Karrman, K. & Bertil Johansson, 2017 Feb 1, In : Genes Chromosomes and Cancer. 56, 2, p. 89-116 28 p.

    Research output: Contribution to journalReview article

  11. 2016
  12. 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

  13. Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.

    Fredrik Mertens, Antonescu, C. R. & Felix Mitelman, 2016, In : Genes, Chromosomes and Cancer. 55, 4, p. 291-310

    Research output: Contribution to journalReview article

  14. 2015
  15. 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

  16. 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

  17. 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

  18. 2014
  19. 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

  20. 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

  21. 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

  22. 2013
  23. 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

  24. 2012
  25. 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

  26. 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

  27. 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

  28. 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

  29. 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

  30. 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

  31. 2011
  32. 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

  33. 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

  34. 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

  35. 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

  36. Prognostic Value of SOX2 Expression in Neuroblastoma

    del Carmen Gomez-Mateo, M., Piqueras, M., Castel, V., Sven Påhlman, Noguera, R. & Navarro, S., 2011, In : Genes, Chromosomes and Cancer. 50, 5, p. 374-377

    Research output: Contribution to journalLetter

  37. 2010
  38. 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

  39. 2009
  40. 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

  41. 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

  42. 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

  43. 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

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