Division of Clinical Genetics

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  1. Generation of trisomies in cancer cells by multipolar mitosis and incomplete cytokinesis.

    David Gisselsson Nord, Jin, Y., David Lindgren, Persson, J., Gisselsson, L., Hanks, S., Sehic, D., Linda Holmquist Mengelbier, Ingrid Øra, Rahman, N., Fredrik Mertens, Felix Mitelman & Nils Mandahl, 2010, In : Proceedings of the National Academy of Sciences. 107, 47, p. 20489-20493

    Research output: Contribution to journalArticle

  2. When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses.

    David Gisselsson Nord, Håkanson, U., Stoller, P., Marti, D., Jin, Y., Anders Rosengren, Stewénius, Y., Kahl, F. & Panagopoulos, I., 2008, In : PLoS ONE. 3, 4, e1871.

    Research output: Contribution to journalArticle

  3. Classification of chromosome segregation errors in cancer.

    David Gisselsson Nord, 2008, In : Chromosoma. Jun 6, p. 511-519

    Research output: Contribution to journalArticle

  4. Chromosomal Instability and Genomic Amplification in Bone and Soft Tissue Tumours

    David Gisselsson Nord, 2000, Department of Clinical Genetics, Lund University. 140 p.

    Research output: ThesisDoctoral Thesis (compilation)

  5. Provision of genetic services in Europe: current practices and issues

    Godard, B., Kaariainen, H., Ulf Kristoffersson, Tranebjaerg, L., Coviello, D. & Ayme, S., 2003, In : European Journal of Human Genetics. 11, p. S13-S48

    Research output: Contribution to journalArticle

  6. 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

  7. Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma

    Gorunova, L., Dawiskiba, S., Andren-Sandberg, Å., Mattias Höglund & Bertil Johansson, 2001, In : Cancer Genetics and Cytogenetics. 127, 2, p. 148-154

    Research output: Contribution to journalArticle

  8. Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas

    Gorunova, L., Parada, L. A., Limon, J., Jin, Y., Hallén, M., Hagerstrand, I., Iliszko, M., Wajda, Z. & Bertil Johansson, 1999, In : Genes, Chromosomes and Cancer. 26, 4, p. 312-21

    Research output: Contribution to journalArticle

  9. Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation

    Guastadisegni, M. C., Lonoce, A., Impera, L., Albano, F., D'Addabbo, P., Caruso, S., Vasta, I., Panagopoulos, I., Leszl, A., Basso, G., Rocchi, M. & Storlazzi, C. T., 2008, In : Molecular Cancer. 7

    Research output: Contribution to journalArticle

  10. Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma

    Guenat, D., Quentin, S., Rizzari, C., Lundin, C., Coliva, T., Edery, P., Fryssira, H., Bermont, L., Ferrand, C., Soulier, J., Borg, C. & Rohrlich, P-S., 2014, In : Journal of Hematology & Oncology. 7, 82.

    Research output: Contribution to journalLetter

  11. Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia

    Rebeqa Gunnarsson, Dilorenzo, S., Kristina B. Lundin-Ström, Linda Olsson, Biloglav, A., Henrik Lilljebjörn, Rissler, M., Wahlberg, P., Lundmark, A., Anders Castor, Behrendtz, M., Thoas Fioretos, Kajsa Paulsson, Isaksson, A. & Bertil Johansson, 2018, In : Leukemia. 32, 10, p. 2117-2125

    Research output: Contribution to journalArticle

  12. Solide Kindertumoren: Ein Streifzug durch das Raritätenkabinett

    Gürtl-Lackner, B., D. Gisselsson-Nord & Vujanic, G., 2017 Jul 1, In : Pathologe. 38, 4, p. 278-285 8 p.

    Research output: Contribution to journalArticle

  13. Diagnostisk korionbiopsi vid Lasarettet i Lund

    Gustavii, B., Chester, A., Edvall, H., Iosif, S., Ulf Kristoffersson, Löfberg, L., Mineur, A. & Felix Mitelman, 1983, In : Läkartidningen. 80, 36, p. 3179-3181

    Research output: Contribution to journalArticle

  14. First-trimester diagnosis on chorionic villi obtained by direct vision technique

    Gustavii, B., Chester, A., Edvall, H., Iosif, S., Ulf Kristoffersson, Löfberg, L., Mineur, A. & Felix Mitelman, 1984, In : Human Genetics. 65, 4, p. 373-376

    Research output: Contribution to journalArticle

  15. Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes

    Haferlach, C., Rieder, H., Lillington, D. M., Dastugue, N., Hagemeijer, A., Harbott, J., Stilgenbauer, S., Knuutila, S., Bertil Johansson & Fonatsch, C., 2007, In : Genes, Chromosomes and Cancer. 46, 5, p. 494-499

    Research output: Contribution to journalArticle

  16. Immune effector monocyte–neutrophil cooperation induced by the primary tumor prevents metastatic progression of breast cancer

    Catharina Hagerling, Gonzalez, H., Salari, K., Wang, C. Y., Lin, C., Robles, I., van Gogh, M., Dejmek, A., Karin Jirström & Werb, Z., 2019, In : Proceedings of the National Academy of Sciences of the United States of America. 116, 43, p. 21704-21714 11 p.

    Research output: Contribution to journalArticle

  17. Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer

    Hakansson, S., Johannsson, O., Johansson, U., Sellberg, G., N Loman, Gerdes, A. M., Holmberg, E., Dahl, N., Pandis, N., U Kristoffersson, Håkan Olsson & Åke Borg, 1997 May, In : American Journal of Human Genetics. 60, 5, p. 1068-1078 11 p.

    Research output: Contribution to journalArticle

  18. Mantle cell lymphoma displays a homogenous methylation profile: A comparative analysis with chronic lymphocytic leukemia

    Halldorsdottir, A. M., Kanduri, M., Marincevic, M., Mansouri, L., Isaksson, A., Goransson, H., Axelsson, T., Agarwal, P., Jernberg-Wiklund, H., Stamatopoulos, K., Sander, B., Hans Ehrencrona & Rosenquist, R., 2012, In : American Journal of Hematology. 87, 4, p. 361-367

    Research output: Contribution to journalArticle

  19. Genome Wide Array Based Methylation Profiling Reveals Preferential Methylation of Homeobox Transcription Factor Genes In Mantle Cell Lymphoma and Pro Apoptotic Genes In Chronic Lymphocytic Leukemia

    Halldorsdottir, A. M., Kanduri, M., Marincevic, M., Goransson, H., Isaksson, A., Mansouri, M., Stamatopoulos, K., Sander, B., Hans Ehrencrona & Rosenquist, R., 2010, In : Blood. 116, 21, p. 239-239

    Research output: Contribution to journalPublished meeting abstract

  20. Impact of TP53 mutation and 17p deletion in mantle cell lymphoma

    Halldorsdottir, A. M., Lundin, A., Murray, F., Mansouri, L., Knuutila, S., Sundstrom, C., Laurell, A., Hans Ehrencrona, Sander, B. & Rosenquist, R., 2011, In : Leukemia. 25, 12, p. 1904-1908

    Research output: Contribution to journalLetter

  21. Cytogenetic abnormalities in a hemangiopericytoma of the spleen.

    Hallén, M., Parada, L. A., Gorunova, L., Birger Pålsson, Michael Dictor & Bertil Johansson, 2002, In : Cancer Genetics and Cytogenetics. 136, 1, p. 62-65

    Research output: Contribution to journalArticle

  22. Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma

    Karolin Hansén Hallor, Fredrik Mertens, Jin, Y., Meis-Kindblom, J. M., Kindblom, L-G., Behrendtz, M., Kalén, A., Nils Mandahl & Panagopoulos, I., 2005 Sep, In : Genes, Chromosomes and Cancer. 44, 1, p. 97-102 6 p.

    Research output: Contribution to journalArticle

  23. Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.

    Hallor, K. H., Sciot, R., Johan Staaf, Heidenblad, M., Anders Rydholm, Bauer, H. C., Aström, K., Domanski, H., Meis, J. M., Kindblom, L-G., Panagopoulos, I., Nils Mandahl & Fredrik Mertens, 2009, In : Journal of Pathology. 217, p. 716-727

    Research output: Contribution to journalArticle

  24. Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.

    Hallor, K. H., Johan Staaf, Bovée, J. V. M. G., Hogendoorn, P. C. W., Cleton-Jansen, A-M., Knuutila, S., Savola, S., Niini, T., Brosjö, O., Bauer, H. C. F., Fredrik Vult von Steyern, Jonsson, K., Skorpil, M., Nils Mandahl & Fredrik Mertens, 2009, In : Clinical Cancer Research. 15, 8, p. 2685-2694

    Research output: Contribution to journalArticle

  25. Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro

    Hamaguchi, I., N B Woods, Panagopoulos, I., Andersson, E., Mikkola, H., Fahlman, C., Zufferey, R., Carlsson, L., Trono, D. & S Karlsson, 2000 Nov, In : Journal of Virology. 74, 22, p. 10778-84

    Research output: Contribution to journalArticle

  26. SOCS2 is dispensable for BCR/ABL1-induced chronic myeloid leukemia-like disease and for normal hematopoietic stem cell function.

    Hansen, N., Helena Ågerstam, Martin Wahlestedt, Niklas Landberg, Askmyr, M., Mats Ehinger, Rissler, M., Henrik Lilljebjörn, Johnels, P., Ishiko, J., Melo, J. V., Whalen, A., David Bryder, Marcus Järås & Thoas Fioretos, 2013, In : Leukemia. 27, p. 130-135

    Research output: Contribution to journalArticle

  27. Functional Modeling of Genes Upregulated in Chronic Myeloid Leukemia

    Hansen, N., 2013, Division of Clinical Genetics, Lund University. 70 p.

    Research output: ThesisDoctoral Thesis (compilation)

  28. GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma.

    Karolin Hansén Nord, Henrik Lilljebjörn, Vezzi, F., Nilsson, J., Magnusson, L., Tayebwa, J., de Jong, D., Bovée, J. V. M. G., Hogendoorn, P. C. W. & Szuhai, K., 2014, In : Nature Genetics. 46, 5, p. 474-477

    Research output: Contribution to journalArticle

  29. Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.

    Karolin Hansén Nord, Macchia, G., Tayebwa, J., Nilsson, J., Fredrik Vult von Steyern, Brosjö, O., Nils Mandahl & Fredrik Mertens, 2014, In : Human Molecular Genetics. 23, 4, p. 878-888

    Research output: Contribution to journalArticle

  30. Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the wnt/beta-catenin signaling pathway.

    Karolin Hansén Nord, Nilsson, J., Elsa Arbajian, Fredrik Vult von Steyern, Brosjö, O., Cleton-Jansen, A-M., Szuhai, K. & Hogendoorn, P. C. W., 2013, In : PLoS ONE. 8, 11, e80725.

    Research output: Contribution to journalArticle

  31. Heterogeneous genetic profiles in soft tissue myoepitheliomas

    Karolin Hansén Nord, Teixeira, M. R., Fletcher, C. D. M., Bizarro, S., Johan Staaf, Domanski, H., Fredrik Vult von Steyern, Panagopoulos, I., Nils Mandahl & Fredrik Mertens, 2008, In : Modern Pathology. 21, 11, p. 1311-1319

    Research output: Contribution to journalArticle

  32. Array based genetic profiling of bone and soft tissue tumors

    Karolin Hansén Nord, 2008, Department of Clinical Genetics, Lund University. 95 p.

    Research output: ThesisDoctoral Thesis (compilation)

  33. Fusion genes in angiomatoid fibrous histiocytoma

    Karolin Hansén Nord, Micci, F., Meis-Kindblom, J. M., Kindblom, L-G., Bacchini, P., Nils Mandahl, Fredrik Mertens & Panagopoulos, I., 2007 Jun 18, In : Cancer Letters. 251, 1, p. 158-163 6 p.

    Research output: Contribution to journalArticle

  34. Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.

    Karolin Hansén Nord, Magnusson, L., Isaksson, M., Nilsson, J., Henrik Lilljebjörn, Domanski, H., Kindblom, L-G., Nils Mandahl & Fredrik Mertens, 2010, In : Proceedings of the National Academy of Sciences. Dec, p. 21122-21127

    Research output: Contribution to journalArticle

  35. Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

    Karolin Hansén Nord, Kajsa Paulsson, Veerla, S., Wejde, J., Brosjö, O., Nils Mandahl & Fredrik Mertens, 2012, In : Neoplasia. 14, 9, p. 807-812

    Research output: Contribution to journalArticle

  36. Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.

    Karolin Hansén Nord, Johan Staaf, Göran B Jönsson, Heidenblad, M., Fredrik Vult von Steyern, Bauer, H. C. F., Ijszenga, M., Hogendoorn, P. C. W., Nils Mandahl, Szuhai, K. & Fredrik Mertens, 2008, In : British Journal of Cancer. 98, 2, p. 434-442

    Research output: Contribution to journalArticle

  37. Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression.

    Hansson, F., Toporski, J., Månsson, R., Bertil Johansson, Norén-Nyström, U., Jacobsen, S. E. W., Thomas Wiebe, Larsson, M., Mikael Sigvardsson & Anders Castor, 2008, In : Molecular Cancer. 7, 67.

    Research output: Contribution to journalArticle

  38. Intact glucose uptake despite deteriorating signaling in adipocytes with high-fat feeding

    Hansson, B., Sebastian Wasserstrom, Björn Morén, Periwal, V., Petter Vikman, Cushman, S. W., Olga Göransson, Petter Storm & Karin G. Stenkula, 2018 Apr 1, In : Journal of Molecular Endocrinology. 60, 3, p. 199-211 13 p.

    Research output: Contribution to journalArticle

  39. Essential genetics education for non-genetics health professionals (EC Project GenEd)

    Harris, R., Harris, H. J., Challen, K., Ten Kate, L., Schmidtke, J., Nippert, I., Reynier, C. J. & Ulf Kristoffersson, 2001, In : American Journal of Human Genetics. 69, 4, Suppl., p. 433-433

    Research output: Contribution to journalArticle

  40. Genetic education for non-geneticist health professionals

    Harris, R., Challen, K., Benjamin, C., Harris, H. & Ulf Kristoffersson, 2006, In : Community Genetics. 9, 4, p. 224-226

    Research output: Contribution to journalArticle

  41. Acute lymphoblastic leukemia

    Harrison, C. J. & Bertil Johansson, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (eds.). 4th ed. Wiley-Blackwell, p. 198-251 54 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  42. Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations

    Hastings, R. J., Cavani, S., Bricarelli, F. D., Patsalis, P. C. & Ulf Kristoffersson, 2007, In : European Journal of Human Genetics. 15, 5, p. 525-527

    Research output: Contribution to journalArticle

  43. Sequencing IDH1/2 glioma mutation hotspots in gliomas and malignant peripheral nerve sheath tumors.

    Håvik, A. B., Lind, G. E., Honne, H., Meling, T. R., Scheie, D., Hall, K. S., van den Berg, E., Fredrik Mertens, Picci, P., Lothe, R. A., Heim, S. & Brandal, P., 2014, In : Neuro-Oncology. 16, 2, p. 320-322

    Research output: Contribution to journalLetter

  44. Editorial: Genetics and Democracy

    Maria Hedlund, Hagen, N. & Ulf Kristoffersson, 2012, In : Journal of Community Genetics. 3, 2, p. 57-59

    Research output: Contribution to journalLetter

  45. 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

  46. Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.

    Heidenblad, M., David Lindgren, Veltman, J. A., Tord Jonson, Mahlamäki, E. H., Gorunova, L., van Kessel, A. G., Schoenmakers, E. F. P. M. & Mattias Höglund, 2005, In : Oncogene. 24, 10, p. 1794-1801

    Research output: Contribution to journalArticle

  47. Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.

    Heidenblad, M., Schoenmakers, E. F. P. M., Tord Jonson, Gorunova, L., Veltman, J. A., van Kessel, A. G. & Mattias Höglund, 2004, In : Cancer Research. 64, 9, p. 3052-3059

    Research output: Contribution to journalArticle

  48. Molecular Characterization of Genomic Amplifications in Pancreatic Cancer

    Heidenblad, M., 2004, Markus Heidenblad, Department of Clinical Genetics, Lund University Hospital, SE-221 85 LUND, Sweden,. 90 p.

    Research output: ThesisDoctoral Thesis (compilation)

  49. Bone marrow karyotypes in 94 children with acute leukemia

    Heim, S., Békássy, A., Garwicz, S., Heldrup, J., Ulf Kristoffersson, Nils Mandahl, Thomas Wiebe & Felix Mitelman, 1990, In : European Journal of Haematology. 44, 4, p. 227-233

    Research output: Contribution to journalArticle

  50. A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia

    Heim, S., Avanzi, G-C., Billström, R., Ulf Kristoffersson, Nils Mandahl, Békássy, A., Garwicz, S., Thomas Wiebe, Pegoraro, L., Falda, M., Resegotti, L. & Felix Mitelman, 1987, In : British Journal of Haematology. 66, 3, p. 323-326

    Research output: Contribution to journalArticle

  51. Molecular screening for new fusion genes in cancer

    Heim, S. & Felix Mitelman, 2008, In : Nature Genetics. 40, 6, p. 685-686

    Research output: Contribution to journalDebate/Note/Editorial

  52. New structural chromosomal rearrangements in congenital leukemia

    Heim, S., Békássy, A., Garwicz, S., Heldrup, J., Thomas Wiebe, Ulf Kristoffersson, Nils Mandahl & Felix Mitelman, 1987, In : Leukemia. 1, 1, p. 16-23

    Research output: Contribution to journalArticle

  53. Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia

    Heim, S., Egelund Christensen, B., Thoas Fioretos, Sorensen, A-G. & Tinggaard Pedersen, N., 1992, In : Cancer Genetics and Cytogenetics. 59, 1, p. 35-38

    Research output: Contribution to journalArticle

  54. Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia

    Heim, S., Ulf Kristoffersson, Nils Mandahl, Felix Mitelman, Békássy, A., Garwicz, S., Heldrup, J. & Thomas Wiebe, 1986, In : Cancer Genetics and Cytogenetics. 23, 3, p. 239-244

    Research output: Contribution to journalArticle

  55. Preface to the Fourth Edition

    Heim, S. & Felix Mitelman, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (eds.). 4th ed. Wiley-Blackwell, p. ix

    Research output: Chapter in Book/Report/Conference proceedingForeword/postscript

  56. Cancer cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells

    Heim, S. (ed.) & Felix Mitelman (ed.), 2015, 4th ed. Wiley-Blackwell. 632 p.

    Research output: Book/ReportAnthology (editor)

  57. Cytogenetic nomenclature

    Heim, S. & Felix Mitelman, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells,. Heim, S. & Mitelman, F. (eds.). 4th ed. Wiley-Blackwell, p. 19-25 7 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  58. Nonrandom chromosome abnormalities in cancer: An overview

    Heim, S. & Felix Mitelman, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (eds.). 4th ed. Wiley-Blackwell, p. 26-41 16 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  59. Smooth muscle actin expression in primary bone tumours

    Hemingway, F., Kashima, T. G., Mahendra, G., Dhongre, A., Hogendoorn, P. C. W., Fredrik Mertens & Athanasou, N. A., 2012, In : Virchows Archiv: an international journal of pathology. 460, 5, p. 525-534

    Research output: Contribution to journalArticle

  60. Education in medical genetics for non-genetic health care providers in sweden.

    Henriksson, K. & Ulf Kristoffersson, 2006, In : Community Genetics. 9, 4, p. 240-245

    Research output: Contribution to journalArticle

  61. The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic

    Henriksson, K., Håkan Olsson & Ulf Kristoffersson, 2004, In : Acta Oncologica. 43, 7, p. 637-649

    Research output: Contribution to journalArticle

  62. Acute Traumatic Brain Injury Mortality in the elderly.

    Erik Herou, Romner, B. & Tomasevic, G., 2015, In : Surgical Neurology. 83, 6, p. 996-1001

    Research output: Contribution to journalArticle

  63. New Probabilistic network models and algorithms for oncogenesis

    Hjelm, M., Mattias Höglund & Lagergren, J., 2006, In : Journal of Computational Biology. 13, 4, p. 853-865

    Research output: Contribution to journalArticle

  64. Dasatinib induces fast and deep responses in newly diagnosed chronic myeloid leukaemia patients in chronic phase: clinical results from a randomised phase-2 study (NordCML006)

    Hjorth-Hansen, H., Stenke, L., Soderlund, S., Dreimane, A., Hans Ehrencrona, Gedde-Dahl, T., Gjertsen, B. T., Hoglund, M., Koskenvesa, P., Lotfi, K., Majeed, W., Markevarn, B., Ohm, L., Olsson-Stromberg, U., Remes, K., Suominen, M., Simonsson, B., Porkka, K., Mustjoki, S. & Johan Richter, 2015, In : European Journal of Haematology. 94, 3, p. 243-250

    Research output: Contribution to journalArticle

  65. Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.

    Jakob Hofvander, Tayebwa, J., Nilsson, J., Magnusson, L., Brosjö, O., Larsson, O. L., Fredrik Vult von Steyern, Mandahl, N., Fletcher, C. & Fredrik Mertens, 2015, In : Clinical Cancer Research. 21, 4, p. 864-869

    Research output: Contribution to journalArticle

  66. RNA sequencing of sarcomas with simple karyotypes: identification and enrichment of fusion transcripts.

    Jakob Hofvander, Tayebwa, J., Nilsson, J., Magnusson, L., Brosjö, O., Larsson, O., Fredrik Vult von Steyern, Domanski, H., Nils Mandahl & Fredrik Mertens, 2015, In : Laboratory Investigation. 95, 6, p. 603-609

    Research output: Contribution to journalArticle

  67. Frequent low-level mutations of Protein Kinase D2 in angiolipoma

    Jakob Hofvander, Elsa Arbajian, Karin G Stenkula, Karin Lindkvist-Petersson, Larsson, M., Nilsson, J., Magnusson, L., Fredrik Vult von Steyern, Rissler, P., L Hornick, J. & Fredrik Mertens, 2017, In : Journal of Pathology. 241, 5, p. 578-582

    Research output: Contribution to journalArticle

  68. Different patterns of clonal evolution among different sarcoma subtypes followed for up to 25 years

    Jakob Hofvander, Viklund, B., Isaksson, A., Brosjö, O., Fredrik Vult von Steyern, Rissler, P., Nils Mandahl & Fredrik Mertens, 2018 Dec 1, In : Nature Communications. 9, 1, 3662.

    Research output: Contribution to journalArticle

  69. Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas

    Jakob Hofvander, 2019, Lund: Lund University: Faculty of Medicine. 49 p.

    Research output: ThesisDoctoral Thesis (compilation)

  70. Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile

    Jakob Hofvander, Puls, F., Pillay, N., Steele, C. D., Flanagan, A. M., Magnusson, L., Nilsson, J. & Fredrik Mertens, 2019, In : Journal of Pathology. 249, 4, p. 425-434

    Research output: Contribution to journalArticle

  71. PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells

    Jakob Hofvander, Jo, V. Y., Fletcher, C. D. M., Puls, F., Flucke, U., Nilsson, J., Magnusson, L. & Fredrik Mertens, 2020, In : Modern Pathology.

    Research output: Contribution to journalArticle

  72. A gene fusion network in human neoplasia.

    Mattias Höglund, Attila Frigyesi & Felix Mitelman, 2006, In : Oncogene. 25, 18, p. 2674-2678

    Research output: Contribution to journalArticle

  73. Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.

    Mattias Höglund, Sehn, L., Connors, J. M., Gascoyne, R. D., Siebert, R., Torbjörn Säll, Felix Mitelman & Horsman, D. E., 2004, In : Genes, Chromosomes and Cancer. 39, 3, p. 195-204

    Research output: Contribution to journalArticle

  74. Bladder cancer, a two phased disease?

    Mattias Höglund, 2007, In : Seminars in Cancer Biology. 17, 3, p. 225-232

    Research output: Contribution to journalReview article

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