Division of Clinical Genetics

Organisational unit: Division

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  1. HIF1 alpha isoforms in benign and malignant prostate tissue and their correlation to neuroendocrine differentiation

    Monsef, N., Soller, M., Panagopoulos, I. & Abrahamsson, P-A., 2010, In : BMC Cancer. 10

    Research output: Contribution to journalArticle

  2. The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia.

    Monsef, N., Soller, M., Isaksson, M., Abrahamsson, P-A. & Panagopoulos, I., 2009, In : The Prostate. 69, p. 909-916

    Research output: Contribution to journalArticle

  3. Lentiviral gene transfer of TCIRG1 into peripheral blood CD34(+) cells restores osteoclast function in infantile malignant osteopetrosis.

    Ilana Moscatelli, Thudium, C., Flores Bjurström, C., Schulz, A., Askmyr, M., Gudmann, N. S., Andersen, N. M., Porras, O., Karsdal, M. A., Villa, A., Fasth, A., Henriksen, K. & Johan Richter, 2013, In : Bone. 57, 1, p. 1-9

    Research output: Contribution to journalArticle

  4. Analysis of giant cell tumour of bone cells for Noonan syndrome/Cherubism-related mutations.

    Moskovszky, L., Idowu, B., Taylor, R., Fredrik Mertens, Athanasou, N. & Flanagan, A., 2012, In : Journal of Oral Pathology & Medicine.

    Research output: Contribution to journalArticle

  5. External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years

    Mueller, CR., Ulf Kristoffersson & Stoppa-Lyonnet, D., 2004, In : Annals of Oncology. 15, Suppl. 1, p. I14-I17

    Research output: Contribution to journalArticle

  6. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

    Mulligan, A. M., Couch, F. J., Barrowdale, D., Domchek, S. M., Eccles, D., Nevanlinna, H., Ramus, S. J., Robson, M., Sherman, M., Spurdle, A. B., Wappenschmidt, B., Lee, A., McGuffog, L., Healey, S., Sinilnikova, O. M., Janavicius, R., Hansen, T. V. O., Nielsen, F. C., Ejlertsen, B., Osorio, A. & 162 others, Munoz-Repeto, I., Duran, M., Godino, J., Pertesi, M., Benitez, J., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Cattaneo, E., Bonanni, B., Viel, A., Pasini, B., Papi, L., Ottini, L., Savarese, A., Bernard, L., Radice, P., Hamann, U., Verheus, M., Meijers-Heijboer, H. E. J., Wijnen, J., Garcia, E. B. G., Nelen, M. R., Kets, C. M., Seynaeve, C., Tilanus-Linthorst, M. M. A., van der Luijt, R. B., van Os, T., Rookus, M., Frost, D., Jones, J. L., Evans, D. G., Lalloo, F., Eeles, R., Izatt, L., Adlard, J., Davidson, R., Cook, J., Donaldson, A., Dorkins, H., Gregory, H., Eason, J., Houghton, C., Barwell, J., Side, L. E., McCann, E., Murray, A., Peock, S., Godwin, A. K., Schmutzler, R. K., Rhiem, K., Engel, C., Meindl, A., Ruehl, I., Arnold, N., Niederacher, D., Sutter, C., Deissler, H., Gadzicki, D., Kast, K., Preisler-Adams, S., Varon-Mateeva, R., Schoenbuchner, I., Fiebig, B., Heinritz, W., Schaefer, D., Gevensleben, H., Caux-Moncoutier, V., Fassy-Colcombet, M., Cornelis, F., Mazoyer, S., Leone, M., Boutry-Kryza, N., Hardouin, A., Berthet, P., Muller, D., Fricker, J-P., Mortemousque, I., Pujol, P., Coupier, I., Lebrun, M., Kientz, C., Longy, M., Sevenet, N., Stoppa-Lyonnet, D., Isaacs, C., Caldes, T., de la Hoya, M., Heikkinen, T., Aittomaki, K., Blanco, I., Lazaro, C., Barkardottir, R. B., Soucy, P., Dumont, M., Simard, J., Montagna, M., Tognazzo, S., D'Andrea, E., Fox, S., Yan, M., Rebbeck, T., Olopade, O. I., Weitzel, J. N., Lynch, H. T., Ganz, P. A., Tomlinson, G. E., Wang, X., Fredericksen, Z., Pankratz, V. S., Lindor, N. M., Szabo, C., Offit, K., Sakr, R., Gaudet, M., Bhatia, J., Kauff, N., Singer, C. F., Tea, M-K., Gschwantler-Kaulich, D., Fink-Retter, A., Mai, P. L., Greene, M. H., Imyanitov, E., O'Malley, F. P., Ozcelik, H., Glendon, G., Toland, A. E., Gerdes, A-M., Thomassen, M., Kruse, T. A., Jensen, U. B., Skytte, A-B., Caligo, M. A., Soller, M., Henriksson, K., Wachenfeldt, V. A., Arver, B., Stenmark-Askmalm, M., Karlsson, P., Ding, Y. C., Neuhausen, S. L., Beattie, M., Pharoah, P. D. P., Moysich, K. B., Nathanson, K. L., Karlan, B. Y., Gross, J., John, E. M., Daly, M. B., Buys, S. M., Southey, M. C., Hopper, J. L., Terry, M. B., Chung, W., Miron, A. F., Goldgar, D., Chenevix-Trench, G., Easton, D. F., Andrulis, I. L. & Antoniou, A. C., 2011, In : Breast Cancer Research. 13, 6

    Research output: Contribution to journalArticle

  7. The Proportion of Ph+CD34(+)CD38(neg) Leukemic Stem Cells In the Bone Marrow of Newly Diagnosed Patients with Chronic Myeloid Leukemia (CML) In Chronic Phase (CP) Is Variable and Correlates with High Sokal Risk, High Leukocyte Count, Low Hemoglobin Concentration, Splenomegaly and Increased Hematological Toxicity During Initial TKI Therapy Data From a Randomized Phase II NordCML006 Study

    Mustjoki, S., Richter, J., Barbany, G., Dybedal, I., Fioretos, T., Dahl, T. G., Gjertsen, B. T., Hovland, R., Jalkanen, S., Josefsen, D., Koskenvesa, P., Lassen, C., Latvala, K., Majeed, W., Malm, C., Markevarn, B., Moshfegh, A., Ohm, L., Olofsson, T., Stromberg, U. O. & 10 others, Rapakko, K., Remes, K., Stentoft, J., Stenke, L., Suominen, M., Thunberg, S., Bjerrum, O. W., Simonsson, B., Porkka, K. & Hansen, H. H., 2010, In : Blood. 116, 21, p. 291-292

    Research output: Contribution to journalPublished meeting abstract

  8. Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients

    Mustjoki, S., Richter, J., Barbany, G., Ehrencrona, H., Fioretos, T., Gedde-Dahl, T., Gjertsen, B. T., Hovland, R., Hernesniemi, S., Josefsen, D., Koskenvesa, P., Dybedal, I., Markevarn, B., Olofsson, T., Olsson-Stromberg, U., Rapakko, K., Thunberg, S., Stenke, L., Simonsson, B., Porkka, K. & 1 others, Hjorth-Hansen, H., 2013, In : Leukemia. 27, 7, p. 1520-1526

    Research output: Contribution to journalArticle

  9. Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma

    Muth, A., Crona, J., Gimm, O., Elmgren, A., K. Filipsson, Stenmark Askmalm, M., Sandstedt, J., Tengvar, M. & Tham, E., 2019, In : Journal of Internal Medicine. 285, 2, p. 187-204

    Research output: Contribution to journalReview article

  10. Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study

    Niini, T., Scheinin, I., Lahti, L., Savola, S., Fredrik Mertens, Hollmen, J., Bohling, T., Kivioja, A., Karolin Hansén Nord & Knuutila, S., 2012, In : Cancer genetics. 205, 11, p. 588-593

    Research output: Contribution to journalArticle

  11. 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

  12. High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer.

    Martin Nilsson, Linda Werner Hartman, Ulf Kristoffersson, Johannsson, O. T., Åke Borg, Henriksson, K., Lanke, E., Håkan Olsson & Niklas Loman, 2014, In : Breast Cancer Research and Treatment. 147, 3, p. 571-578

    Research output: Contribution to journalArticle

  13. Involvement and intrinsic deficiencies of hematopoietic stem cells in MDS patients with trisomy 8

    Nilsson, L., Åstrand-Grundström, I., Anderson, K., Arvidsson, I., Hokland, P., Kjeldsen, L., Turesson, I., Bertil Johansson, Hellstrom-Lindberg, E., Hast, R. & Jacobsen, S. E. W., 2001, In : Blood. 98, 11, p. 354A-354A

    Research output: Contribution to journalArticle

  14. The molecular signature of MDS stem cells supports a stem-cell origin of 5q - myelodysplastic syndromes

    Nilsson, L., Patrik Edén, Olsson, E., Månsson, R., Åstrand-Grundström, I., Strömbeck, B., Theilgaard-Moench, K., Anderson, K., Hast, R., Hellström, E., Samuelsson, J., Bergh, G., Nerlov, C., Bertil Johansson, Mikael Sigvardsson, Åke Borg & Jacobsen, S. E. W., 2007, In : Blood. 110, 8, p. 3005-3014

    Research output: Contribution to journalArticle

  15. Approximate geodesic distances reveal biologically relevant structures in microarray data

    Nilsson, J., Thoas Fioretos, Mattias Höglund & Fontes, M., 2004, In : Bioinformatics. 20, 6, p. 874-880

    Research output: Contribution to journalArticle

  16. Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas

    Nilsson, M. A., Meza-Zepeda, L. A., Fredrik Mertens, Forus, A., Myklebost, O. & Nils Mandahl, 2004 Apr 10, In : International Journal of Cancer. 109, 3, p. 363-369 7 p.

    Research output: Contribution to journalArticle

  17. Threshold-free high-power methods for the ontological analysis of genome-wide gene expression studies

    Björn Nilsson, Johnels, P., Johansson, M., Nelander, S. & Thoas Fioretos, 2007, In : Genome Biology. 8, 5

    Research output: Contribution to journalArticle

  18. Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8.

    Nilsson, L., Åstrand-Grundström, I., Anderson, K., Arvidsson, I., Hokland, P., David Bryder, Kjeldsen, L., Bertil Johansson, Hellström-Lindberg, E., Hast, R. & Jacobsen, S. E. W., 2002, In : Blood. 100, 1, p. 259-267

    Research output: Contribution to journalArticle

  19. Cross-platform classification in microarray-based leukemia diagnostics

    Björn Nilsson, Anna Andersson, Johansson, M. & Thoas Fioretos, 2006, In : Haematologica. 91, 6, p. 821-824 4 p.

    Research output: Contribution to journalArticle

  20. Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.

    Nilsson, M. A., Fredrik Mertens, Mattias Höglund, Nils Mandahl & Panagopoulos, I., 2006, In : Cytogenetic and Genome Research. 112, 1-2, p. 60-66

    Research output: Contribution to journalArticle

  21. An improved method for detecting and delineating genomic regions with altered gene expression in cancer

    Björn Nilsson, Johansson, M., Anders Heyden, Nelander, S. & Thoas Fioretos, 2008, In : Genome Biology. 9, 1, R13.

    Research output: Contribution to journalArticle

  22. Sudanesiska cytogenetiker - vision om en ny form av bistånd

    Nilsson, T., Ellaithy, M., Ibrahim, M. E., Elmula, I. & David Gisselsson Nord, 2004, In : Läkartidningen. 101, 8, p. 702-5

    Research output: Contribution to journalArticle

  23. Fusion of the HMGA2 and NFIB genes in lipoma

    Martin Nilsson, Panagopoulos, I., F Mertens & N Mandahl, 2005 Nov, In : Virchows Archiv: an international journal of pathology. 447, 5, p. 855-858 4 p.

    Research output: Contribution to journalArticle

  24. Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.

    Nilsson, M. A., Mattias Höglund, Panagopoulos, I., Sciot, R., Dal Cin, P., Debiec-Rychter, M., Fredrik Mertens & Nils Mandahl, 2002, In : Virchows Archiv: an international journal of pathology. 441, 5, p. 475-480

    Research output: Contribution to journalArticle

  25. Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12

    Nilsson, M. A., Domanski, H., Fredrik Mertens & Nils Mandahl, 2005 Apr, In : Oncology Reports. 13, 4, p. 649-652 4 p.

    Research output: Contribution to journalArticle

  26. ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders

    Nilsson, T., Andreasson, P., Mattias Höglund, Thoas Fioretos, Billstrom, R., Garwicz, S., Felix Mitelman & Bertil Johansson, 1998, In : Leukemia. 12, 7, p. 1167-1168

    Research output: Contribution to journalArticle

  27. Molecular cytogenetic characterization of chromosome aberrations in soft tissue and bone tumors

    Nilsson, M. A., 2005, Divison of Clinical Genetics, Lund University. 110 p.

    Research output: ThesisDoctoral Thesis (compilation)

  28. Genetic analyses of multiple myeloma and related plasma cell dyscrasias

    Nilsson, T., 2004, Therese Nilsson, Department of Clinical Genetics, University Hospital, SE-221 85 Lund, Sweden,. 137 p.

    Research output: ThesisDoctoral Thesis (compilation)

  29. Nollutsläpp i basindustrin - förutsättningar för en ny industripolitik

    Lars J Nilsson (ed.), Bengt Johansson (ed.), Karin Ericsson, Roger Hildingsson, Jamil Khan, Kronsell, A., Fredrik N G Andersson, Oscar Svensson, Teis Hansen, Coenen, L. & Max Åhman, 2017 May 17, 101 ed. Lund: Miljö- och energisystem, LTH, Lunds universitet. 128 p. (IMES/EESS report )

    Research output: Book/ReportReport

  30. Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping

    Nordgren, A., Farnebo, F., Bertil Johansson, Holmgren, G., Forestier, E., Larsson, C., Söderhäll, S., Nordenskjöld, M. & Blennow, E., 2001, In : European Journal of Haematology. 66, 5, p. 297-304

    Research output: Contribution to journalArticle

  31. PAX5 is part of a functional transcription factor network targeted in lymphoid leukemia

    Okuyama, K., Tobias Strid, Kuruvilla, J., Somasundaram, R., Cristobal, S., Emma Smith, Prasad, M., Thoas Fioretos, Henrik Lilljebjörn, Shamit Soneji, Stefan Lang, Jonas Ungerbäck & Mikael Sigvardsson, 2019 Aug 1, In : PLoS Genetics. 15, 8, e1008280.

    Research output: Contribution to journalArticle

  32. Identification of human candidate genes for male infertility by digital differential display

    Olesen, C., Hansen, C., Bendsen, E., Byskov, A. G., Schwinger, E., Lopez-Pajares, I., Jensen, P. K. A., Ulf Kristoffersson, Schubert, R., Van Assche, E., Wahlstroem, J., Lespinasse, J. & Tommerup, N., 2001, In : Molecular Human Reproduction. 7, 1, p. 41598

    Research output: Contribution to journalArticle

  33. Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

    Olkinuora, A., Nieminen, T. T., Mårtensson, E., Rohlin, A., Ristimäki, A., Koskenvuo, L., Lepistö, A., Samuel Gebre-Medhin, Nordling, M., Peltomäki, P. & Swedish Extended Genetic Analysis of Colorectal Neoplasia (SWEN) Study Group, 2019, In : Genetics in Medicine. 21, 8, p. 1868-1873

    Research output: Contribution to journalArticle

  34. Ikaros and leukaemia.

    Linda Olsson & Bertil Johansson, 2015, In : British Journal of Haematology. 169, 4, p. 479-491

    Research output: Contribution to journalReview article

  35. The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013.

    Linda Olsson, Ivanov Öfverholm, I., Norén-Nyström, U., Zachariadis, V., Nordlund, J., Sjögren, H., Golovleva, I., Nordgren, A., Kajsa Paulsson, Heyman, M., Barbany, G. & Bertil Johansson, 2015, In : British Journal of Haematology. 170, 6, p. 847-858

    Research output: Contribution to journalArticle

  36. IKAROS and LEUKEMIA

    Linda Olsson, 2014, Division of Clinical Genetics, Lund University. 96 p.

    Research output: ThesisDoctoral Thesis (compilation)

  37. Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma.

    Linda Olsson, Kajsa Paulsson, Bovée, J. V. M. G. & Karolin Hansén Nord, 2011, In : PLoS ONE. 6, 9, e24977.

    Research output: Contribution to journalArticle

  38. Food intake and meal pattern in IAPP knockout mice with and without infusion of exogenous IAPP

    Olsson, M., Herrington, M. K., Reidelberger, R. D., Permert, J., Samuel Gebre-Medhin & Arnelo, U., 2012, In : Scandinavian Journal of Gastroenterology. 47, 2, p. 191-196

    Research output: Contribution to journalArticle

  39. Frequent false-negative FIP1L1-PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis

    Olsson-Arvidsson, L., Norberg, A., Sjögren, H. & Bertil Johansson, 2019 Dec 18, In : British Journal of Haematology.

    Research output: Contribution to journalLetter

  40. Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney

    O'Meara, E., Stack, D., Lee, C-H., Garvin, A. J., Morris, T., Argani, P., Han, J. S., Jenny Karlsson, David Gisselsson Nord, Leuschner, I., Gessler, M., Graf, N., Fletcher, J. A. & O'Sullivan, M. J., 2012, In : Journal of Pathology. 227, 1, p. 72-80

    Research output: Contribution to journalArticle

  41. A Comparison of Rectal Suction and Full Wall Biopsy in Hirschsprung’s Disease

    Örnö Ax, S., Einar Arnbjörnsson & David Gisselsson Nord, 2014, In : Surgical Science. 5, p. 15-19

    Research output: Contribution to journalArticle

  42. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

    Osorio, A., Milne, R. L., Kuchenbaecker, K., Vaclová, T., Pita, G., Alonso, R., Peterlongo, P., Blanco, I., de la Hoya, M., Duran, M., Díez, O., Ramón Y Cajal, T., Konstantopoulou, I., Martínez-Bouzas, C., Andrés Conejero, R., Soucy, P., McGuffog, L., Barrowdale, D., Lee, A., Swe-Brca, S-B. & 180 others, Arver, B., Rantala, J., Niklas Loman, Hans Ehrencrona, Olopade, O. I., Beattie, M. S., Domchek, S. M., Nathanson, K., Rebbeck, T. R., Arun, B. K., Karlan, B. Y., Walsh, C., Lester, J., John, E. M., Whittemore, A. S., Daly, M. B., Southey, M., Hopper, J., Terry, M. B., Buys, S. S., Janavicius, R., Dorfling, C. M., van Rensburg, E. J., Steele, L., Neuhausen, S. L., Ding, Y. C., Hansen, T. V. O., Jønson, L., Ejlertsen, B., Gerdes, A-M., Infante, M., Herráez, B., Moreno, L. T., Weitzel, J. N., Herzog, J., Weeman, K., Manoukian, S., Peissel, B., Zaffaroni, D., Scuvera, G., Bonanni, B., Mariette, F., Volorio, S., Viel, A., Varesco, L., Papi, L., Ottini, L., Tibiletti, M. G., Radice, P., Yannoukakos, D., Garber, J., Ellis, S., Frost, D., Platte, R., Fineberg, E., Evans, G., Lalloo, F., Izatt, L., Eeles, R., Adlard, J., Davidson, R., Cole, T., Eccles, D., Cook, J., Hodgson, S., Brewer, C., Tischkowitz, M., Douglas, F., Porteous, M., Side, L., Walker, L., Morrison, P., Donaldson, A., Kennedy, J., Foo, C., Godwin, A. K., Schmutzler, R. K., Wappenschmidt, B., Rhiem, K., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Plendl, H. J., Niederacher, D., Sutter, C., Wang-Gohrke, S., Steinemann, D., Preisler-Adams, S., Kast, K., Varon-Mateeva, R., Gehrig, A., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Damiola, F., Poppe, B., Claes, K., Piedmonte, M., Tucker, K., Backes, F., Rodríguez, G., Brewster, W., Wakeley, K., Rutherford, T., Caldés, T., Nevanlinna, H., Aittomäki, K., Rookus, M. A., van Os, T. A. M., van der Kolk, L., de Lange, J. L., Meijers-Heijboer, H. E. J., van der Hout, A. H., van Asperen, C. J., Gómez Garcia, E. B., Hoogerbrugge, N., Collée, J. M., van Deurzen, C. H. M., van der Luijt, R. B., Devilee, P., Hebon, H., Olah, E., Lázaro, C., Teulé, A., Menéndez, M., Jakubowska, A., Cybulski, C., Gronwald, J., Lubinski, J., Durda, K., Jaworska-Bieniek, K., Johannsson, O. T., Maugard, C., Montagna, M., Tognazzo, S., Teixeira, M. R., Healey, S., Investigators, K., Olswold, C., Guidugli, L., Lindor, N., Slager, S., Szabo, C. I., Vijai, J., Robson, M., Kauff, N., Zhang, L., Rau-Murthy, R., Fink-Retter, A., Singer, C. F., Rappaport, C., Geschwantler Kaulich, D., Pfeiler, G., Tea, M-K., Berger, A., Phelan, C. M., Greene, M. H., Mai, P. L., Lejbkowicz, F., Andrulis, I., Mulligan, A. M., Glendon, G., Toland, A. E., Bojesen, A., Pedersen, I. S., Sunde, L., Thomassen, M., Kruse, T. A., Jensen, U. B., Friedman, E., Laitman, Y., Shimon, S. P., Simard, J., Easton, D. F., Offit, K., Couch, F. J., Chenevix-Trench, G., Antoniou, A. C. & Benitez, J., 2014, In : PLoS Genetics. 10, 4, e1004256.

    Research output: Contribution to journalArticle

  43. Fast isolation of proteins from bioreactors using affinity chromatography techniques

    Pålsson, E., 2000, Eva Pålsson, Tillämpad biokemi, Lunds universitet. 130 p.

    Research output: ThesisDoctoral Thesis (compilation)

  44. MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).

    Panagopoulos, I., Kitagawa, A., Isaksson, M., Helena Mörse, Felix Mitelman & Bertil Johansson, 2004, In : Genes, Chromosomes and Cancer. 41, 4, p. 400-404

    Research output: Contribution to journalArticle

  45. 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

  46. Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)

    Panagopoulos, I., Åman, P., Thoas Fioretos, Mattias Höglund, Bertil Johansson, Nils Mandahl, Heim, S., Behrendtz, M. & Felix Mitelman, 1994, In : Genes, Chromosomes and Cancer. 11, 4, p. 256-262

    Research output: Contribution to journalArticle

  47. No EWS/FLI1 fusion transcripts in giant-cell tumors of bone

    Panagopoulos, I., Fredrik Mertens, Domanski, H., Isaksson, M., Brosjö, O., Pelle Gustafson & Nils Mandahl, 2001, In : International Journal of Cancer. 93, 6, p. 769-772

    Research output: Contribution to journalArticle

  48. Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.

    Panagopoulos, I., Nilsson, T., Domanski, H., Isaksson, M., Lindblom, P., Fredrik Mertens & Nils Mandahl, 2006, In : International Journal of Cancer. 118, 5, p. 1181-1186

    Research output: Contribution to journalArticle

  49. RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13)

    Panagopoulos, I., Isaksson, M., Lindvall, C., Bjorkholm, M., Ahlgren, T., Thoas Fioretos, Heim, S., Felix Mitelman & Bertil Johansson, 2000, In : Genes, Chromosomes and Cancer. 28, 4, p. 415-424

    Research output: Contribution to journalArticle

  50. Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)

    Panagopoulos, I., Thoas Fioretos, Isaksson, M., Samuelsson, U., Billström, R., Strömbeck, B., Felix Mitelman & Bertil Johansson, 2001, In : Human Molecular Genetics. 10, 4, p. 395-404

    Research output: Contribution to journalArticle

  51. 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

  52. Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).

    Panagopoulos, I., Isaksson, M., Billström, R., Strömbeck, B., Felix Mitelman & Bertil Johansson, 2003, In : Genes, Chromosomes and Cancer. 36, 1, p. 107-112

    Research output: Contribution to journalArticle

  53. Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.

    Panagopoulos, I., Strömbeck, B., Isaksson, M., Heldrup, J., Olofsson, T. & Bertil Johansson, 2006, In : British Journal of Haematology. 133, 3, p. 270-275

    Research output: Contribution to journalArticle

  54. Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.

    Panagopoulos, I., Fredrik Mertens, Dêbiec-Rychter, M., Isaksson, M., Limon, J., Kardas, I., Domanski, H., Sciot, R., Perek, D., Crnalic, S., Larsson, O. & Nils Mandahl, 2002, In : International Journal of Cancer. 99, 4, p. 560-567

    Research output: Contribution to journalArticle

  55. 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

  56. Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.

    Panagopoulos, I., Fredrik Mertens, Isaksson, M., Domanski, H., Brosjö, O., Heim, S., Bjerkehagen, B., Sciot, R., Dal Cin, P., Fletcher, J. A., Fletcher, C. D. M. & Nils Mandahl, 2002, In : Genes, Chromosomes and Cancer. 35, 4, p. 340-352

    Research output: Contribution to journalArticle

  57. The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.

    Panagopoulos, I., Tiziana Storlazzi, C., Fletcher, C. D. M., Fletcher, J. A., Nascimento, A., Domanski, H. A., Wejde, J., Brosjö, O., Anders Rydholm, Isaksson, M., Mandahl, N. & Mertens, F., 2004, In : Genes, Chromosomes and Cancer. 40, 3, p. 218-228

    Research output: Contribution to journalArticle

  58. Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).

    Panagopoulos, I., Kerndrup, G., Carlsen, N., Strömbeck, B., Isaksson, M. & Bertil Johansson, 2007, In : British Journal of Haematology. 136, 2, p. 294-296

    Research output: Contribution to journalArticle

  59. Fusion of the COL1A1 and USP6 genes in a benign bone tumor.

    Panagopoulos, I., Fredrik Mertens, Löfvenberg, R. & Nils Mandahl, 2008, In : Cancer Genetics and Cytogenetics. 180, 1, p. 70-73

    Research output: Contribution to journalArticle

  60. Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)

    Panagopoulos, I., Fredrik Mertens, Isaksson, M. & Nils Mandahl, 2005 Jan 1, In : Cancer Genetics and Cytogenetics. 156, 1, p. 74-76 3 p.

    Research output: Contribution to journalArticle

  61. Response of sugar beet plants to ultraviolet-B (280-320 nm) radiation and Cercospora leaf spot disease

    Panagopoulos, I., Bornman, J. & Lars Olof Björn, 1992, In : Physiologia Plantarum. 84, 1, p. 140-145

    Research output: Contribution to journalArticle

  62. MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia

    Panagopoulos, I., Henrik Lilljebjörn, Strömbeck, B., Lars Hjorth, Olofsson, T. & Bertil Johansson, 2006, In : Haematologica. 91, 9, p. 1287-1288

    Research output: Contribution to journalLetter

  63. The effect of UV-B and UV-C radiation on hibiscus leaves determined by ultraweak luminescence and fluorecence induction

    Panagopoulos, I., Bornman, J. & Lars Olof Björn, 1989, In : Physiologia Plantarum. 76, 4, p. 461-465

    Research output: Contribution to journalArticle

  64. 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

  65. Characterization of the human CREB3L2 gene promoter

    Panagopoulos, I. & Fredrik Mertens, 2009 Mar, In : Oncology Reports. 21, 3, p. 615-624 10 p.

    Research output: Contribution to journalArticle

  66. Characterization of an alternative transcript of the human CREB3L2 gene.

    Panagopoulos, I., Monsef, N., Collin, A. & Fredrik Mertens, 2010, In : Oncology Reports. 24, 5, p. 1133-1139

    Research output: Contribution to journalArticle

  67. The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.

    Panagopoulos, I., Möller, E., Collin, A. & Fredrik Mertens, 2008, In : Oncology Reports. 20, 5, p. 1029-1033

    Research output: Contribution to journalArticle

  68. An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera

    Panagopoulos, I., Fredrik Mertens & Griffin, C. A., 2008 Sep, In : Cancer Genetics and Cytogenetics. 185, 2, p. 74-77 4 p.

    Research output: Contribution to journalArticle

  69. Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1

    Panagopoulos, I., Fredrik Mertens, Isaksson, M. & Nils Mandahl, 2004, In : Oncology Reports. 12, 1, p. 107-110

    Research output: Contribution to journalArticle

  70. Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases

    Pandis, N., Idvall, I., Bardi, G., Jin, Y., Gorunova, L., F Mertens, Håkan Olsson, C Ingvar, Beroukas, K., F Mitelman & Heim, S., 1996 Apr 10, In : International Journal of Cancer. 66, 2, p. 191-6 6 p.

    Research output: Contribution to journalArticle

  71. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

    Pansuriya, T. C., van Eijk, R., d'Adamo, P., van Ruler, M. A. J. H., Kuijjer, M. L., Oosting, J., Cleton-Jansen, A-M., van Oosterwijk, J. G., Verbeke, S. L. J., Meijer, D., van Wezel, T., Hansén Nord, K., Sangiorgi, L., Toker, B., Liegl-Atzwanger, B., San-Julian, M., Sciot, R., Limaye, N., Kindblom, L-G., Daugaard, S. & 7 others, Godfraind, C., Boon, L. M., Vikkula, M., Kurek, K. C., Szuhai, K., French, P. J. & Bovee, J. V. M. G., 2011, In : Nature Genetics. 43, 12, p. 1256-1261

    Research output: Contribution to journalArticle

  72. Vascular endothelial growth factor gene polymorphisms and pre-eclampsia

    Papazoglou, D., Galazios, G., Koukourakis, MI., Panagopoulos, I., Kontomanolis, EN., Papatheodorou, K. & Maltezos, E., 2004, In : Molecular Human Reproduction. 10, 5, p. 321-324

    Research output: Contribution to journalArticle

  73. Prevalence of hemochromatosis gene (HFE) mutations in Greece

    Papazoglou, D., Exiara, T., Speletas, M., Panagopoulos, I. & Maltezos, E., 2003, In : Acta Haematologica. 109, 3, p. 137-140

    Research output: Contribution to journalArticle

  74. The Fatty Acid Amide Hydrolase (FAAH) Pro129Thr Polymorphism is not Associated with Severe Obesity in Greek Subjects

    Papazoglou, D., Panagopoulos, I., Papanas, N., Gioka, T., Papadopoulos, T., Papathanasiou, P., Kaitozis, O., Papatheodorou, K. & Maltezos, E., 2008, In : Hormone and Metabolic Research. 40, 12, p. 907-910

    Research output: Contribution to journalArticle

  75. Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer

    Parada, L. A., Hallén, M., Karl-Göran Tranberg, Hagerstrand, I., Bondeson, L., Felix Mitelman & Bertil Johansson, 1998, In : Genes, Chromosomes and Cancer. 23, 1, p. 26-35

    Research output: Contribution to journalArticle

  76. Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma

    Parada, L. A., Bardi, G., Hallén, M., Hagerstrand, I., Karl-Göran Tranberg, Felix Mitelman & Bertil Johansson, 1997, In : American Journal of Surgical Pathology. 21, 11, p. 1381-6

    Research output: Contribution to journalArticle

  77. Monosomy 22 in a case of biliary adenofibroma

    Parada, L. A., Bardi, G., Hallén, M., Hagerstrand, I., Karl-Göran Tranberg, Felix Mitelman & Bertil Johansson, 1997, In : Cancer Genetics and Cytogenetics. 93, 2, p. 183-4

    Research output: Contribution to journalArticle