Genes, Chromosomes and Cancer, 1045-2257

Tidskrift

Fler filtreringsmöjligheter
  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, I : Genes Chromosomes and Cancer. 58, 9, s. 607-611 5 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  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, I : Genes Chromosomes and Cancer. 58, 7, s. 452-461

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  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, I : Genes, Chromosomes and Cancer. 57, 11, s. 564-572 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  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, I : Genes Chromosomes and Cancer. 57, 3, s. 123-139 17 s.

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  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 okt 1, I : Genes Chromosomes and Cancer. 56, 10, s. 750-757 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Pediatric T-cell acute lymphoblastic leukemia

    Karrman, K. & Bertil Johansson, 2017 feb 1, I : Genes Chromosomes and Cancer. 56, 2, s. 89-116 28 s.

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  11. 2016
  12. Improved minimal residual disease detection by targeted quantitative polymerase chain reaction in Nucleophosmin 1 type a mutated acute myeloid leukemia

    Louise Pettersson, Levéen, P., Axler, O., Dvorakova, D., Gunnar Juliusson & Mats Ehinger, 2016 okt 1, I : Genes, Chromosomes and Cancer. 55, 10, s. 750-766 17 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. 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, I : Genes Chromosomes and Cancer. 55, 9, s. 719-726 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  15. Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.

    Charles Walther, Mayrhofer, M., Nilsson, J., Jakob Hofvander, Tord Jonson, Nils Mandahl, Ingrid Øra, David Gisselsson Nord & Fredrik Mertens, 2016, I : Genes, Chromosomes and Cancer. 55, 1, s. 3-15

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. 2015
  17. 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, I : Genes, Chromosomes and Cancer. 54, 5, s. 326-333

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.

    Linda Olsson, Albitar, F., Anders Castor, Behrendtz, M., Biloglav, A., Kajsa Paulsson & Bertil Johansson, 2015, I : Genes, Chromosomes and Cancer. 54, 5, s. 315-325

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. 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, I : Genes, Chromosomes and Cancer. 54, 4, s. 260-266

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 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, I : Genes, Chromosomes and Cancer. 54, 3, s. 156-167

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  21. 2014
  22. 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, I : Genes Chromosomes and Cancer. 53, 9, s. 750-768 19 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.

    Jenny Karlsson, Linda Holmquist Mengelbier, Ciornei, C., Naranjo, A., O'Sullivan, M. J. & David Gisselsson Nord, 2014, I : Genes, Chromosomes and Cancer. 53, 5, s. 381-391

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer.

    Anders Valind, Pal, N., Asmundsson, J., David Gisselsson Nord & Linda Holmquist Mengelbier, 2014, I : Genes, Chromosomes and Cancer. 53, 7, s. 634-638

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. 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, I : Genes, Chromosomes and Cancer. 53, 1, s. 15-24

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. 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, I : Genes, Chromosomes and Cancer. 53, 8, s. 667-675

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. 2013
  28. 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, I : Genes, Chromosomes and Cancer. 52, 10, s. 873-886

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. Histological specificity of alterations and expression of KIT and KITLG in non-small cell lung carcinoma.

    Annette Salomonsson, Mats Jönsson, Sofi Isaksson, Karlsson, A., Jönsson, P., Gaber, A., Pär-Ola Bendahl, Johansson, L., Hans Brunnström, Karin Jirström, Åke Borg, Johan Staaf & Maria Planck, 2013, I : Genes, Chromosomes and Cancer. 52, 11, s. 1088-1096

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. 2012
  31. 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, I : Genes, Chromosomes and Cancer. 51, 9, s. 832-840

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. 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, I : Genes, Chromosomes and Cancer. 51, 1, s. 10-19

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  33. 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, I : Genes, Chromosomes and Cancer. 51, 5, s. 510-520

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  34. 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, I : Genes, Chromosomes and Cancer. 51, s. 196-206

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. 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, I : Genes, Chromosomes and Cancer. 51, 2, s. 127-139

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. 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, I : Genes, Chromosomes and Cancer.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  37. 2011
  38. 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, I : Genes, Chromosomes and Cancer. 50, 4, s. 250-262

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. 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, I : Genes, Chromosomes and Cancer. 50, 5, s. 348-357

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  40. 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, I : Genes, Chromosomes and Cancer. 50, s. 619-632

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  41. 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, I : Genes, Chromosomes and Cancer. 50, 2, s. 113-121

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  42. Prognostic Value of SOX2 Expression in Neuroblastoma

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

    Forskningsoutput: TidskriftsbidragLetter

  43. 2010
  44. Genomic alterations in histopathologically normal breast tissue from BRCA1 mutation carriers may be caused by BRCA1 haploinsufficiency.

    Rennstam, K., Anita Ringberg, Cunliffe, H. E., Håkan Olsson, Landberg, G. & Ingrid Hedenfalk, 2010, I : Genes, Chromosomes and Cancer. 49, s. 78-90

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  45. 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, I : Genes, Chromosomes and Cancer. 49, 3, s. 270-281

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  46. 2009
  47. 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, I : Genes, Chromosomes and Cancer. 48, 11, s. 993-1001

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  48. 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, I : Genes, Chromosomes and Cancer. 48, 9, s. 795-805

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  49. 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, I : Genes, Chromosomes and Cancer. 48, 7, s. 583-602

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  50. High hyperdiploid childhood acute lymphoblastic leukemia.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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