Genes, Chromosomes and Cancer, 1045-2257

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  1. 2021
  2. Genomic and transcriptomic characterization of desmoplastic small round cell tumors

    Saskia Sydow, Yvonne M.H. Versleijen-Jonkers, Magnus Hansson, Anke E.M. van Erp, Melissa H.S. Hillebrandt-Roeffen, Winette T.A. van der Graaf, Paul Piccinelli, Pehr Rissler, Uta E. Flucke & Fredrik Mertens, 2021 Apr 30, In: Genes Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  3. Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs

    Ulrich Pfisterer, Julia Bräunig, Per Brattås, Markus Heidenblad, Göran Karlsson & Thoas Fioretos, 2021 Feb 21, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalReview article

  4. 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

  5. 2020
  6. 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

  7. SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemias

    Andrea Biloglav, LINDA OLSSON, Johan Theander, Mikael Behrendtz, Anders Castor & Bertil Johansson, 2020 Apr 19, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalLetter

  8. Farewell message from the Editor-in-Chief of Genes, Chromosomes & Cancer

    Felix Mitelman, 2020, In: Genes Chromosomes and Cancer. 59, 1, p. 3-4 2 p.

    Research output: Contribution to journalDebate/Note/Editorial

  9. 2019
  10. Most gene fusions in cancer are stochastic events

    Bertil Johansson, Fredrik Mertens, Tommy Schyman, 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

  11. 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

  12. 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

  13. Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion

    Karim H Saba, Louise Cornmark, Marianne Rissler, Thoas Fioretos, Kristina Åström, Felix Haglund, Andrew E Rosenberg, Otte Brosjö & Karolin H Nord, 2019, In: Genes, Chromosomes and Cancer. 58, 10, p. 731-736

    Research output: Contribution to journalArticle

  14. 2018
  15. Telomere length, telomerase reverse transcriptase promoter mutations, and melanoma risk

    Sivaramakrishna Rachakonda, Haiying Kong, Nalini Srinivas, Zaida Garcia-Casado, Celia Requena, Mahdi Fallah, Barbara Heidenreich, Dolores Planelles, Victor Traves, Dirk Schadendorf, Eduardo Nagore & Rajiv Kumar, 2018 Nov, In: Genes, Chromosomes and Cancer. 57, 11, p. 564-572 9 p.

    Research output: Contribution to journalArticle

  16. 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

  17. 2017
  18. Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases

    Elise M. Bekers, Patricia J.T.A. Groenen, Marian A.J. Verdijk, Winny L. Raaijmakers-van Geloof, Paul Roepman, Robert Vink, Nathalie D.B. Gilhuijs, Joost M. van Gorp, Judith V M G Bovée, David H. Creytens, Adrienne M. Flanagan, Albert J. H. Suurmeijer, Thomas Mentzel, Elsa Arbajian & Uta Flucke, 2017 Oct 1, In: Genes Chromosomes and Cancer. 56, 10, p. 750-757 8 p.

    Research output: Contribution to journalArticle

  19. Pediatric T-cell acute lymphoblastic leukemia

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

    Research output: Contribution to journalReview article

  20. 2016
  21. Trisomy 8 in pediatric acute myeloid leukemia: A NOPHO-AML study

    Anne Cathrine Lund Laursen, Julie Damgaard Sandahl, Eigil Kjeldsen, Jonas Abrahamsson, Peter Asdahl, Shau Yin Ha, Jesper Heldrup, Kirsi Jahnukainen, Ólafur G. Jónsson, Birgitte Lausen, Josefine Palle, Bernward Zeller, Erik Forestier & Henrik Hasle, 2016 Sep 1, In: Genes Chromosomes and Cancer. 55, 9, p. 719-726 8 p.

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalReview article

  23. 2015
  24. 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

  25. 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

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

    Kari Hemminki, Christoph Frank, Asta Försti, Ludovit Musak, Alena Kazimirova, Magdalena Barancokova, Alexandra Horska, Veronika Vymetalkova, Zdenek Smerhovsky, Alessio Naccarati, Pavel Soucek, Ludmila Vodickova, Janka Buchancova, Bozena Smolkova, Maria Dusinska & Pavel Vodicka, 2015, In: Genes, Chromosomes and Cancer. 54, 4, p. 260-266

    Research output: Contribution to journalArticle

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

    Gemma Macchia, Karolin Hansén Nord, Monica Zoli, Stefania Purgato, Pietro D'Addabbo, Christopher W Whelan, Lucia Carbone, Giovanni Perini, Fredrik Mertens, Mariano Rocchi & Clelia Tiziana Storlazzi, 2015, In: Genes, Chromosomes and Cancer. 54, 3, p. 156-167

    Research output: Contribution to journalArticle

  28. 2014
  29. 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

  30. 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

  31. 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

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

    Julie Damgaard Sandahl, Eigil Kjeldsen, Jonas Abrahamsson, Shau-Yin Ha, Jesper Heldrup, Kirsi Jahnukainen, Olafur G. Jonsson, Birgitte Lausen, Josefine Palle, Bernward Zeller, Erik Forestier & Henrik Hasle, 2014, In: Genes, Chromosomes and Cancer. 53, 8, p. 667-675

    Research output: Contribution to journalArticle

  33. 2013
  34. 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

  35. 2012
  36. 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

  37. 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

  38. 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.

    Yuesheng Jin, Emely Möller, Karolin Hansén Nord, Nils Mandahl, Fredrik Vult von Steyern, Henryk Domanski, Adrian Mariño-Enríquez, Linda Magnusson, Jenny Nilsson, Raf Sciot, Christopher D M Fletcher, Maria Debiec-Rychter & Fredrik Mertens, 2012, In: Genes, Chromosomes and Cancer. 51, 5, p. 510-520

    Research output: Contribution to journalArticle

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

    Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Ann Nordgren, Lars Palmqvist, Mette Klarskov Andersen, Andrea Biloglav, Erik Forestier, Kajsa Paulsson & Bertil Johansson, 2012, In: Genes, Chromosomes and Cancer. 51, p. 196-206

    Research output: Contribution to journalArticle

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

    Lu Wang, Toru Motoi, Raya Khanin, Adam Olshen, Fredrik Mertens, Julia Bridge, Paola Dal Cin, Cristina R. Antonescu, Samuel Singer, Meera Hameed, Judith V. M. G. Bovee, Pancras C. W. Hogendoorn, Nicholas Socci & Marc Ladanyi, 2012, In: Genes, Chromosomes and Cancer. 51, 2, p. 127-139

    Research output: Contribution to journalArticle

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

    Huiqi Li, Hilde Tveitan Hilmarsen, Mohammad Bakhtiar Hossain, Jonas Björk, Inger-Lise Hansteen, Maria Albin, Camilla Furu Skjelbred & Karin Broberg Palmgren, 2012, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  42. 2011
  43. 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

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

    Marthe Lovf, Gard O. S. Thomassen, Anne Cathrine Bakken, Ricardo Celestino, Thoas Fioretos, Guro E. Lind, Ragnhild A. Lothe & Rolf I. Skotheim, 2011, In: Genes, Chromosomes and Cancer. 50, 5, p. 348-357

    Research output: Contribution to journalArticle

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

    Hammurabi Bartuma, Karolin Hansén Nord, Gemma Macchia, Margareth Isaksson, Jenny Nilsson, Henryk Domanski, Nils Mandahl & Fredrik Mertens, 2011, In: Genes, Chromosomes and Cancer. 50, p. 619-632

    Research output: Contribution to journalArticle

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

    Anna M. Halldórsdóttir, Birgitta Sander, Hanna Göransson, Anders Isaksson, Eva Kimby, Mahmoud Mansouri, Richard Rosenquist & Hans Ehrencrona, 2011, In: Genes, Chromosomes and Cancer. 50, 2, p. 113-121

    Research output: Contribution to journalArticle

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