Genes, Chromosomes and Cancer, 1045-2257

Journal

More filtering options
  1. 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

  2. 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

  3. A model for karyotypic evolution in testicular germ cell tumors.

    Attila Frigyesi, David Gisselsson Nord, Hansen, G. B., Soller, M., Felix Mitelman & Mattias Höglund, 2004, In : Genes, Chromosomes and Cancer. 40, 3, p. 172-178

    Research output: Contribution to journalArticle

  4. 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

  5. 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

  6. A novel fusion gene, SS18L1/SSX1, in synovial sarcoma

    Storlazzi, T., Fredrik Mertens, Nils Mandahl, David Gisselsson, Isaksson, M., Pelle Gustafson, Domanski, H. A. & Panagopoulos, I., 2003 Jun, In : Genes, Chromosomes and Cancer. 37, 2, p. 195-200 6 p.

    Research output: Contribution to journalArticle

  7. A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.

    Panagopoulos, I., Möller, E., Isaksson, M. & Fredrik Mertens, 2008, In : Genes, Chromosomes and Cancer. 47, p. 521-529

    Research output: Contribution to journalArticle

  8. 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

  9. Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype

    Bartuma, H., Karolin Hansén Nord, Panagopoulos, I., Collin, A., Anders Rydholm, Pelle Gustafson, Bauer, H. C. F., Brosjö, O., Domanski, H. A., Nils Mandahl & Fredrik Mertens, 2007 Jun, In : Genes, Chromosomes and Cancer. 46, 6, p. 594-606 13 p.

    Research output: Contribution to journalArticle

  10. Balanced chromosome abnormalities inv(16) and t(15;17) in therapy-related myelodysplastic syndromes and acute leukemia: Report from an international workshop

    Andersen, MK., Larson, RA., Mauritzson, N., Schnittger, S., Jhanwar, SC. & Pedersen-Bjergaard, J., 2002, In : Genes, Chromosomes and Cancer. 33, 4, p. 395-400

    Research output: Contribution to journalArticle

  11. BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusion

    Andreasson, P., Bertil Johansson, Carlsson, M., Jarlsfelt, I., Thoas Fioretos, Felix Mitelman & Mattias Höglund, 1997, In : Genes, Chromosomes and Cancer. 20, 3, p. 299-304

    Research output: Contribution to journalArticle

  12. Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors

    Lothe, R. A., Smith-Sorensen, B., Hektoen, M., Stenwig, A. E., Nils Mandahl, Saeter, G. & Fredrik Mertens, 2001, In : Genes, Chromosomes and Cancer. 30, 2, p. 202-206

    Research output: Contribution to journalArticle

  13. BRCA2 mutation in a family with hereditary prostate cancer

    Grönberg, H., Åhman, A-K., Emanuelsson, M., Bergh, A., Damber, J-E. & Åke Borg, 2001, In : Genes, Chromosomes and Cancer. 30, 3, p. 299-301

    Research output: Contribution to journalArticle

  14. 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

  15. Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma

    Nils Mandahl, Heim, S., Willén, H., Anders Rydholm, Magnus Eneroth, Mef Nilbert, Kreicbergs, A. & Felix Mitelman, 1989, In : Genes, Chromosomes and Cancer. 1, 1, p. 9-14 6 p.

    Research output: Contribution to journalArticle

  16. 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

  17. Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH

    Jin, C., Martins, C., Jin, Y., Wiegant, J., Johan Wennerberg, Michael Dictor, David Gisselsson Nord, Strömbeck, B., Fonseca, I., Felix Mitelman, Tanke, H. J., Mattias Höglund & Fredrik Mertens, 2001, In : Genes, Chromosomes and Cancer. 30, 2, p. 161-167

    Research output: Contribution to journalArticle

  18. Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera

    Panagopoulos, I., Möller, E., Dahlén, A., Isaksson, M., Nils Mandahl, Vlamis-Gardikas, A. & Fredrik Mertens, 2007 Feb, In : Genes, Chromosomes and Cancer. 46, 2, p. 181-191 11 p.

    Research output: Contribution to journalArticle

  19. Chromosome aberrations in 35 primary ovarian carcinomas

    Pejovic, T., Heim, S., Mandahl, N., Bo Baldetorp, Elmfors, B., Floderus, U-M., Furgyik, S., Helm, G., Himmelmann, A., Willen, H. & Felix Mitelman, 1992, In : Genes, Chromosomes and Cancer. 4, 1, p. 58-68

    Research output: Contribution to journalArticle

  20. Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families

    Petersson, C., Pandis, N., F Mertens, Adeyinka, A., C Ingvar, A Ringberg, Idvall, I., Bondeson, L., A Borg, Håkan Olsson, U Kristoffersson & F Mitelman, 1996 Jul, In : Genes, Chromosomes and Cancer. 16, 3, p. 185-188 4 p.

    Research output: Contribution to journalArticle

  21. Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion

    Behboudi, A., Winnes, M., Gorunova, L., van den Oord, J. J., Fredrik Mertens, Enlund, F. & Stenman, G., 2005, In : Genes, Chromosomes and Cancer. 43, 2, p. 202-205

    Research output: Contribution to journalArticle

  22. 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

  23. Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature

    Forestier, E., Gauffin, F., Andersen, M. K., Autio, K., Borgstrom, G., Golovleva, I., Gustafsson, B., Heim, S., Heinonen, K., Heyman, M., Hovland, R., Johannsson, J. H., Kerndrup, G., Rosenquist, R., Schoumans, J., Swolin, B., Bertil Johansson & Nordgren, A., 2008, In : Genes, Chromosomes and Cancer. 47, 2, p. 149-158

    Research output: Contribution to journalReview article

  24. Clinical impact of molecular and cytogenetic findings in synovial sarcoma

    Panagopoulos, I., F Mertens, Isaksson, M., Limon, J., Pelle Gustafson, Skytting, B., Åkerman, M., Sciot, R., Dal Cin, P., Samson, I., Iliszko, M., Ryoe, J., Dêbiec-Rychter, M., Szadowska, A., Brosjö, O., Larsson, O., A Rydholm & N Mandahl, 2001 Aug, In : Genes, Chromosomes and Cancer. 31, 4, p. 362-72 11 p.

    Research output: Contribution to journalArticle

  25. 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

  26. Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.

    Mef Nilbert, Heim, S., Nils Mandahl, Flodérus, U-M., Willén, H., Bo Baldetorp & Felix Mitelman, 1989, In : Genes, Chromosomes and Cancer. 1, 2, p. 131-134

    Research output: Contribution to journalArticle

  27. 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

  28. Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.

    Soller, M., Isaksson, M., Peter Elfving, Soller, W., Lundgren, R. & Panagopoulos, I., 2006, In : Genes, Chromosomes and Cancer. 45, 7, p. 717-719

    Research output: Contribution to journalLetter

  29. 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

  30. Cytogenetic aberrations and their prognostic impact in chondrosarcoma

    Nils Mandahl, Pelle Gustafson, Fredrik Mertens, Åkerman, M., Bo Baldetorp, David Gisselsson, Knuutila, S., Bauer, H. C. F. & Larsson, O., 2002 Feb, In : Genes, Chromosomes and Cancer. 33, 2, p. 188-200 13 p.

    Research output: Contribution to journalArticle

  31. 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

  32. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

    Forestier, E., Andersen, M. K., Autio, K., Blennow, E., Borgstrom, G., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kerndrup, G., Nordgren, A., Rosenquist, R., Swolin, B. & Bertil Johansson, 2007, In : Genes, Chromosomes and Cancer. 46, 5, p. 440-450

    Research output: Contribution to journalReview article

  33. Cytogenetic polyclonality in hematologic malignancies

    Bertil Johansson, Billström, R., Karin Broberg Palmgren, Thoas Fioretos, Nilsson, P-G., Ahlgren, T., Malm, C., Samuelsson, B. O. & Felix Mitelman, 1999, In : Genes, Chromosomes and Cancer. 24, 3, p. 222-229

    Research output: Contribution to journalArticle

  34. Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.

    Heidenblad, M., Tord Jonson, Mahlamäki, E. H., Gorunova, L., Karhu, R., Bertil Johansson & Mattias Höglund, 2002, In : Genes, Chromosomes and Cancer. 34, 2, p. 211-223

    Research output: Contribution to journalArticle

  35. 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

  36. Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.

    David Gisselsson Nord, Pålsson, E., Mattias Höglund, Domanski, H., Fredrik Mertens, Pandis, N., Sciot, R., Dal Cin, P., Bridge, J. A. & Nils Mandahl, 2002, In : Genes, Chromosomes and Cancer. 33, 2, p. 133-140

    Research output: Contribution to journalArticle

  37. 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

  38. Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).

    Panagopoulos, I., Thoas Fioretos, Isaksson, M., Larsson, G., Billström, R., Felix Mitelman & Bertil Johansson, 2002, In : Genes, Chromosomes and Cancer. 34, 2, p. 249-254

    Research output: Contribution to journalArticle

Previous 1 2 3 Next