Genes, Chromosomes and Cancer, 1045-2257

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

    Anna Lena Volckmar, Holger Sültmann, Anja Riediger, Thoas Fioretos, Peter Schirmacher, Volker Endris, Albrecht Stenzinger & Steffen Dietz, 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.

    Gisela Lundberg, Daniel Sehic, John-Kalle Länsberg, Ingrid Øra, Attila Frigyesi, Victoria Castel, Samuel Navarro, Marta Piqueras, Tommy Martinsson, Rosa Noguera & 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, Gunnar B Hansen, Maria Soller, 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

    Laura Partanen, Johan Staaf, Minna Tanner, Vilppu J. Tuominen, Åke Borg & Jorma Isola, 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, Koichi Ichimura, Mattias Berglund, Andrii Dinets, Luqman Sulaiman, V. Peter Collins, Catharina Larsson, Anna Porwit & Svetlana Bajalica Lagercrantz, 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

    Tiziana Storlazzi, Fredrik Mertens, Nils Mandahl, David Gisselsson, Margareth Isaksson, Pelle Gustafson, Henryk A Domanski & Ioannis Panagopoulos, 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.

    Ioannis Panagopoulos, Emely Möller, Margareth Isaksson & 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

    Vaidas Dirse, Agne Bertasiute, Egle Gineikiene, Tadas Zvirblis, Ruta Dambrauskiene, Rolandas Gerbutavicius, Elona Juozaityte, Ligita Malciute, Kajsa Paulsson & Laimonas Griskevicius, 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

    Hammurabi Bartuma, Karolin Hansén Nord, Ioannis Panagopoulos, Anna Collin, Anders Rydholm, Pelle Gustafson, Henrik C F Bauer, Otte Brosjö, Henryk A Domanski, 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

    MK Andersen, RA Larson, Nils Mauritzson, S Schnittger, SC Jhanwar & J Pedersen-Bjergaard, 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

    Patrik Andreasson, Bertil Johansson, Magnus Carlsson, Ingvar Jarlsfelt, 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

    Ragnhild A. Lothe, Birgitte Smith-Sorensen, Merete Hektoen, Anna Elisabeth Stenwig, Nils Mandahl, Gunnar Saeter & 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

    Henrik Grönberg, Anna-Karin Åhman, Monica Emanuelsson, Anders Bergh, Jan-Erik Damber & 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, Tommy Schyman & 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, Sverre Heim, Helena Willén, Anders Rydholm, Magnus Eneroth, Mef Nilbert, Andris Kreicbergs & 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

    Domenico Trombetta, Fredrik Mertens, Angelo Lonoce, Pietro D'Addabbo, Karin Rennstam, Nils Mandahl & Clelia Tiziana Storlazzi, 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

    Charlotte Jin, Carmo Martins, Yuesheng Jin, Joop Wiegant, Johan Wennerberg, Michael Dictor, David Gisselsson Nord, Bodil Strömbeck, Isabel Fonseca, Felix Mitelman, Hans J Tanke, 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

    Ioannis Panagopoulos, Emely Möller, Anna Dahlén, Margareth Isaksson, Nils Mandahl, Alexios Vlamis-Gardikas & Fredrik Mertens, 2007 Feb, In: Genes, Chromosomes and Cancer. 46, 2, p. 181-191 11 p.

    Research output: Contribution to journalArticle

  19. Chromosomal aberrations in breast cancer: a comparison between cytogenetics and comparative genomic hybridization

    Karin Persson, Nikos Pandis, Fredrik Mertens, Åke Borg, Bo Baldetorp, Dick Killander & Jorma Isola, 1999, In: Genes, Chromosomes and Cancer. 25, 2, p. 115-122

    Research output: Contribution to journalArticle

  20. Chromosome aberrations in 35 primary ovarian carcinomas

    Tanja Pejovic, Sverre Heim, Nils Mandahl, Bo Baldetorp, Bengt Elmfors, Ulla-Maria Floderus, Stefan Furgyik, Göran Helm, Anna Himmelmann, Helena Willen & Felix Mitelman, 1992, In: Genes, Chromosomes and Cancer. 4, 1, p. 58-68

    Research output: Contribution to journalArticle

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

    C Petersson, N Pandis, F Mertens, A Adeyinka, C Ingvar, A Ringberg, I Idvall, L Bondeson, 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

  22. Chromosome I alterations in breast cancer: Allelic loss on Ip and Iq Is related to lymphogenic metastases and poor prognosis

    Åke Borg, Qiu‐Xia Zhang, Håkan Olsson & Eva Wenngren, 1992 Jan 1, In: Genes, Chromosomes and Cancer. 5, 4, p. 311-320

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalArticle

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

    Jenny Karlsson, Linda Holmquist Mengelbier, Cristina Ciornei, Arlene Naranjo, Maureen J O'Sullivan & David Gisselsson Nord, 2014, In: Genes, Chromosomes and Cancer. 53, 5, p. 381-391

    Research output: Contribution to journalArticle

  25. 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.

    Kristina Karrman, Erik Forestier, Mats Heyman, Mette K Andersen, Kirsi Autio, Elisabeth Blennow, Georg Borgström, Hans Ehrencrona, Irina Golovleva, Sverre Heim, Kristiina Heinonen, Randi Hovland, Johann H Johannsson, Gitte Kerndrup, Ann Nordgren, Lars Palmqvist & Bertil Johansson, 2009, In: Genes, Chromosomes and Cancer. 48, 9, p. 795-805

    Research output: Contribution to journalArticle

  26. 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

    Erik Forestier, Fredrika Gauffin, Mette K. Andersen, Kirsi Autio, Georg Borgstrom, Irina Golovleva, Britt Gustafsson, Sverre Heim, Kristina Heinonen, Mats Heyman, Randi Hovland, Johann H. Johannsson, Gitte Kerndrup, Richard Rosenquist, Jacqueline Schoumans, Birgitta Swolin, Bertil Johansson & Ann Nordgren, 2008, In: Genes, Chromosomes and Cancer. 47, 2, p. 149-158

    Research output: Contribution to journalReview article

  27. Clinical and genomic characterization of patients diagnosed with the provisional entity Acute myeloid leukemia with BCR-ABL1, a Swedish population-based study

    Christina Orsmark-Pietras, Niklas Landberg, Fryderyk Lorenz, Bertil Uggla, Martin Höglund, Sören Lehmann, Åsa Derolf, Stefan Deneberg, Petar Antunovic, Jörg Cammenga, Lars Möllgård, Lovisa Wennström, Henrik Lilljebjörn, Marianne Rissler, Thoas Fioretos & Vladimir Lj Lazarevic, 2021 Jan 12, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalArticle

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

    David Gisselsson, Daniel Lichtenzstejn, Polina Kachko, Jenny Karlsson, Esther Manor & Sabine Mai, 2019, In: Genes Chromosomes and Cancer. 58, 7, p. 452-461

    Research output: Contribution to journalReview article

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

    Mef Nilbert, Sverre Heim, Nils Mandahl, Ulla-Maria Flodérus, Helena Willén, Bo Baldetorp & Felix Mitelman, 1989, In: Genes, Chromosomes and Cancer. 1, 2, p. 131-134

    Research output: Contribution to journalArticle

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

    Arezoo Mohajeri, Johnbosco Tayebwa, Anna Collin, Jenny Nilsson, Linda Magnusson, Fredrik Vult von Steyern, Otte Brosjö, Henryk Domanski, Olle Larsson, Raf Sciot, Maria Debiec-Rychter, Jason L Hornick, Nils Mandahl, Karolin Hansén Nord & Fredrik Mertens GCC Klinisk genetik, 2013, In: Genes, Chromosomes and Cancer. 52, 10, p. 873-886

    Research output: Contribution to journalArticle

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

    Maria Soller, Margareth Isaksson, Peter Elfving, Wolfgang Soller, Rolf Lundgren & Ioannis Panagopoulos, 2006, In: Genes, Chromosomes and Cancer. 45, 7, p. 717-719

    Research output: Contribution to journalLetter

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

    Linda Olsson, Ferras Albitar, Anders Castor, Mikael Behrendtz, Andrea Biloglav, Kajsa Paulsson & Bertil Johansson, 2015, In: Genes, Chromosomes and Cancer. 54, 5, p. 315-325

    Research output: Contribution to journalArticle

  34. 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

    Jan J. Molenaar, Jan Koster, Marli E. Ebus, Peter van Sluis, Ellen M. Westerhout, Katleen de Preter, David Gisselsson Nord, Ingrid Øra, Frank Speleman, Huib N. Caron & Rogier Versteeg, 2012, In: Genes, Chromosomes and Cancer. 51, 1, p. 10-19

    Research output: Contribution to journalArticle

  35. Cytogenetic aberrations and their prognostic impact in chondrosarcoma

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

    Research output: Contribution to journalArticle

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

    Ludmila Gorunova, Fredrik Vult von Steyern, Tiziana Storlazzi, Bodil Bjerkehagen, Gunnar Folleras, Sverre Heim, Nils Mandahl & Fredrik Mertens, 2009, In: Genes, Chromosomes and Cancer. 48, 7, p. 583-602

    Research output: Contribution to journalArticle

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

    Erik Forestier, Mette K. Andersen, Kirsi Autio, Elisabeth Blennow, Georg Borgstrom, Irina Golovleva, Sverre Heim, Kristina Heinonen, Randi Hovland, Johann H. Johannsson, Gitte Kerndrup, Ann Nordgren, Richard Rosenquist, Birgitta Swolin & Bertil Johansson, 2007, In: Genes, Chromosomes and Cancer. 46, 5, p. 440-450

    Research output: Contribution to journalReview article

  38. Cytogenetic polyclonality in hematologic malignancies

    Bertil Johansson, Rolf Billström, Karin Broberg Palmgren, Thoas Fioretos, Per-Gunnar Nilsson, Tomas Ahlgren, Claes Malm, Bengt O Samuelsson & Felix Mitelman, 1999, In: Genes, Chromosomes and Cancer. 24, 3, p. 222-229

    Research output: Contribution to journalArticle

  39. Deep sequencing of myxoinflammatory fibroblastic sarcoma

    Elsa Arbajian, Jakob Hofvander, Linda Magnusson & Fredrik Mertens, 2020 May, In: Genes, Chromosomes and Cancer. 59, 5, p. 309-317 9 p.

    Research output: Contribution to journalArticle

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

    Markus Heidenblad, Tord Jonson, Eija H Mahlamäki, Ludmila Gorunova, Ritva Karhu, Bertil Johansson & Mattias Höglund, 2002, In: Genes, Chromosomes and Cancer. 34, 2, p. 211-223

    Research output: Contribution to journalArticle

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

    Petter Brandal, Ioannis Panagopoulos, Bodil Bjerkehagen, Ludmilla Gorunova, Sigmund Skjeldal, Francesca Micci & Sverre Heim, 2008, In: Genes, Chromosomes and Cancer. 47, 7, p. 558-564

    Research output: Contribution to journalArticle

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

    David Gisselsson Nord, Eva Pålsson, Mattias Höglund, Henryk Domanski, Fredrik Mertens, Nikos Pandis, Raf Sciot, Paola Dal Cin, Julia A Bridge & Nils Mandahl, 2002, In: Genes, Chromosomes and Cancer. 33, 2, p. 133-140

    Research output: Contribution to journalArticle

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

    Christine G. Joseph, Heejung Hwang, Yuchen Jiao, Laura D. Wood, Isaac Kinde, Jian Wu, Nils Mandahl, Jinyong Luo, Ralph H. Hruban, Luis A. Diaz Jr, Tong-Chuan He, Bert Vogelstein, Kenneth W. Kinzler, Fredrik Mertens & Nickolas Papadopoulos, 2014, In: Genes, Chromosomes and Cancer. 53, 1, p. 15-24

    Research output: Contribution to journalArticle

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