Division of Clinical Genetics

Organisational unit: Division

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  1. ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization

    Adem, C., David Gisselsson Nord, Cin, P. D. & Nascimento, A. G., 2001, In : Modern Pathology. 14, 12, p. 1246-1251

    Research output: Contribution to journalArticle

  2. Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas

    Adeyinka, A., Bo Baldetorp, Fredrik Mertens, Håkan Olsson, Johannsson, O., Heim, S. & Pandis, N., 2003 Nov, In : Cancer Genetics and Cytogenetics. 147, 1, p. 62-67 6 p.

    Research output: Contribution to journalArticle

  3. Cytogenetic studies of primary and metastatic breast cancer

    Adeyinka, A., 1999, Department of Clinical Genetics, Lund University. 166 p.

    Research output: ThesisDoctoral Thesis (compilation)

  4. Modeling the human 8p11-myeloproliferative syndrome in immunodeficient mice

    Helena Ågerstam, Marcus Järås, Anna Andersson, Johnels, P., Hansen, N., Lassen, C., Rissler, M., David Gisselsson Nord, Olofsson, T., Johan Richter, Xiaolong Fan, Mats Ehinger & Thoas Fioretos, 2010, In : Blood. 116, 12, p. 2103-2111

    Research output: Contribution to journalArticle

  5. Antibodies targeting human IL1RAP (IL1R3) show therapeutic effects in xenograft models of acute myeloid leukemia.

    Helena Ågerstam, Christine Karlsson, Hansen, N., Carl Sandén, Askmyr, M., Sofia von Palffy, Högberg, C., Rissler, M., Wunderlich, M., Gunnar Juliusson, Johan Richter, Sjöström, K., Bhatia, R., Mulloy, J. C., Marcus Järås & Thoas Fioretos, 2015, In : Proceedings of the National Academy of Sciences. 112, 34, p. 10786-10791

    Research output: Contribution to journalArticle

  6. Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms

    Helena Ågerstam, 2010, Section of clinical genetics. 64 p.

    Research output: ThesisDoctoral Thesis (compilation)

  7. IL1RAP antibodies block IL-1-induced expansion of candidate CML stem cells and mediate cell killing in xenograft models

    Helena Ågerstam, Hansen, N., Sofia von Palffy, Carl Sandén, Reckzeh, K., Christine Karlsson, Henrik Lilljebjörn, Niklas Landberg, Askmyr, M., Högberg, C., Rissler, M., Porkka, K., Wadenvik, H., Mustjoki, S., Johan Richter, Marcus Järås & Thoas Fioretos, 2016 Dec 8, In : Blood. 128, 23, p. 2683-2693

    Research output: Contribution to journalArticle

  8. Complex karyotypes in flow cytometrically DNA-diploid squamous cell carcinomas of the head and neck

    Åkervall, J., Jin, Y., Bo Baldetorp, Fredrik Mertens & Johan Wennerberg, 1998, In : British Journal of Cancer. 77, 7, p. 1082-1088

    Research output: Contribution to journalArticle

  9. Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck

    Åkervall, J., Åke Borg, Michael Dictor, Jin, C., Jin, Y., Tanner, M., Isola, J., Fredrik Mertens & Johan Wennerberg, 2002 Jan, In : International Journal of Oncology. 20, 1, p. 45-52 8 p.

    Research output: Contribution to journalArticle

  10. Naturvetare och kulturforskare kan överbrygga ämnesgränser

    Lynn Åkesson, Susanne Lundin, Ulf Kristoffersson, Tibell, A., Frykman, I. & Cecilia Fredriksson, 2000, In : Läkartidningen. 97, 4, p. 350-351

    Research output: Contribution to journalArticle

  11. Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.

    Maria Albin, Jonas Björk, Welinder, H., Håkan Tinnerberg, Mauritzson, N., Billström, R., Ulf Strömberg, Mikoczy, Z., Johansson, B., Ahlgren, T., Nilsson, P-G., Felix Mitelman & Hagmar, L., 2003, In : Scandinavian Journal of Work, Environment and Health. 29, 5, p. 378-387

    Research output: Contribution to journalArticle

  12. Vitamin d receptor is expressed in pancreatic cancer cells and a vitamin d(3) analogue decreases cell number.

    Albrechtsson, E., Jonsson, T., Möller, S., Mattias Höglund, Bodil Ohlsson & Axelson, J., 2003, In : Pancreatology. 3, 1, p. 41-46

    Research output: Contribution to journalArticle

  13. Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases

    Al-Ibraheemi, A., Folpe, A. L., Perez-Atayde, A. R., Perry, K., Jakob Hofvander, Elsa Arbajian, Magnusson, L., Nilsson, J. & Fredrik Mertens, 2019, In : Modern Pathology. 32, 3, p. 423-434

    Research output: Contribution to journalArticle

  14. Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)

    Åman, P., Ron, D., Nils Mandahl, Thoas Fioretos, Heim, S., Arheden, K., Willen, H., Anders Rydholm & Felix Mitelman, 1992, In : Genes, Chromosomes and Cancer. 5, 4, p. 278-285

    Research output: Contribution to journalArticle

  15. Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS

    Åman, P., Panagopoulos, I., Lassen, C., Thoas Fioretos, Mencinger, M., Håkan Toresson, Mattias Höglund, Forster, A., Rabbitts, T. H., Ron, D., Nils Mandahl & Felix Mitelman, 1996, In : Genomics. 37, 1, p. 1-8

    Research output: Contribution to journalArticle

  16. An EcoRI polymorphism at the insulin receptor locus on a fragment comprising exons 4 to 8

    Åman, P., Pejovic, T. & Thoas Fioretos, 1991, In : Nucleic Acids Research. 19, 19, p. 5452-5452

    Research output: Contribution to journalArticle

  17. NTRK fusions in osteosarcoma are rare and non-functional events

    Ameline, B., Karim H. Saba, Kovac, M., Magnusson, L., Witt, O., Bielack, S., Nathrath, M., Karolin H. Nord & Baumhoer, D., 2020, In : Journal of Pathology: Clinical Research.

    Research output: Contribution to journalArticle

  18. Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.

    Andersen, M. K., Autio, K., Barbany, G., Borgström, G., Cavelier, L., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Bertil Johansson, Kjeldsen, E., Nordgren, A., Palmqvist, L. & Forestier, E., 2011, In : British Journal of Haematology. 155, p. 235-243

    Research output: Contribution to journalArticle

  19. The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.

    Andersson, A., Ma, J., Wang, J., Chen, X., Gedman, A. L., Dang, J., Nakitandwe, J., Holmfeldt, L., Parker, M., Easton, J., Huether, R., Kriwacki, R., Rusch, M., Wu, G., Li, Y., Mulder, H., Raimondi, S., Pounds, S., Kang, G., Shi, L. & 30 others, Becksfort, J., Gupta, P., Payne-Turner, D., Vadodaria, B., Boggs, K., Yergeau, D., Manne, J., Song, G., Edmonson, M., Nagahawatte, P., Wei, L., Cheng, C., Pei, D., Sutton, R., Venn, N. C., Chetcuti, A., Rush, A., Catchpoole, D., Heldrup, J., Thoas Fioretos, Lu, C., Ding, L., Pui, C-H., Shurtleff, S., Mullighan, C. G., Mardis, E. R., Wilson, R. K., Gruber, T. A., Zhang, J. & Downing, J. R., 2015, In : Nature Genetics. 47, 4, p. 330-U192

    Research output: Contribution to journalArticle

  20. Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status.

    Anna Andersson, Ritz, C., David Lindgren, Patrik Edén, Lassen, C., Heldrup, J., Olofsson, T., Råde, J., Fontes, M., Porwit-Macdonald, A., Behrendtz, M., Mattias Höglund, Bertil Johansson & Thoas Fioretos, 2007, In : Leukemia. 21, 6, p. 1198-1203

    Research output: Contribution to journalArticle

  21. Rapid identification of frequent MLL rearrangements in hematologic malignancies by multiplex RT-PCR in a single assay - Reply

    Anna Andersson & Fioretos, T., 2002, In : Leukemia. 16, 8, p. 1576-1576

    Research output: Contribution to journalLetter

  22. Rapid identification of frequent MLL rearrangements in hematologic malignancies by multiplex RT-PCR in a single assay - Reply

    Anna Andersson & Fioretos, F., 2002, In : Leukemia. 16, 8, p. 1575-1575

    Research output: Contribution to journalLetter

  23. Gene Expression Studies of Hematologic Malignacies

    Anna Andersson, 2005, Divison of Clinical Genetics. 125 p.

    Research output: ThesisDoctoral Thesis (compilation)

  24. Extensive clonal branching shapes the evolutionary history of high-risk pediatric cancers

    Andersson, N., Bakker, B., Karlsson, J., Anders Valind, Linda Holmquist Mengelbier, Spierings, D. C. J., Foijer, F. & David Gisselsson, 2020 Feb 10, In : Cancer Research.

    Research output: Contribution to journalArticle

  25. Analysis of Mice Lacking the Heparin-Binding Splice Isoform of Platelet-Derived Growth Factor A

    Andrae, J., Hans Ehrencrona, Gallini, R., Lal, M., Ding, H. & Betsholtz, C., 2013, In : Molecular and Cellular Biology. 33, 20, p. 4030-4040

    Research output: Contribution to journalArticle

  26. Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias

    Andreasson, P., Mattias Höglund, Békássy, A., Garwicz, S., Heldrup, J., Felix Mitelman & Bertil Johansson, 2000, In : European Journal of Haematology. 65, 1, p. 40-51

    Research output: Contribution to journalArticle

  27. 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

  28. Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia

    Andreasson, P., Johansson, E., Arheden, K., U Tedgård, R Ljung, Heim, S. & Mitelmann, F., 1996 Feb, In : Leukemia. 10, 2, p. 378-83

    Research output: Contribution to journalArticle

  29. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

    Antoniou, A. C., Beesley, J., McGuffog, L., Sinilnikova, O. M., Healey, S., Neuhausen, S. L., Ding, Y. C., Rebbeck, T. R., Weitzel, J. N., Lynch, H. T., Isaacs, C., Ganz, P. A., Tomlinson, G., Olopade, O. I., Couch, F. J., Wang, X., Lindor, N. M., Pankratz, V. S., Radice, P., Manoukian, S. & 31 others, Peissel, B., Zaffaroni, D., Barile, M., Viel, A., Allavena, A., Dall'Olio, V., Peterlongo, P., Szabo, C. I., Zikan, M., Claes, K., Poppe, B., Foretova, L., Mai, P. L., Greene, M. H., Rennert, G., Lejbkowicz, F., Glendon, G., Ozcelik, H., Andrulis, I. L., Thomassen, M., Gerdes, A-M., Sunde, L., Cruger, D., Birk Jensen, U., Caligo, M., Friedman, E., Kaufman, B., Laitman, Y., Helena Jernström, Stenmark-Askmalm, M. & Ontario Cancer Genetics Network, 2010 Dec 1, In : Cancer Research. 70, 23, p. 9742-54 13 p.

    Research output: Contribution to journalArticle

  30. Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma.

    Elsa Arbajian, Puls, F., Magnusson, L., Thway, K., Fisher, C., Sumathi, V. P., Tayebwa, J., Karolin Hansén Nord, Kindblom, L-G. & Fredrik Mertens, 2014, In : American Journal of Surgical Pathology. 38, 6, p. 801-808

    Research output: Contribution to journalArticle

  31. A Benign Vascular Tumor With a New Fusion Gene: EWSR1-NFATC1 in Hemangioma of the Bone.

    Elsa Arbajian, Magnusson, L., Brosjö, O., Wejde, J., Folpe, A. L., Karolin Hansén Nord & Fredrik Mertens, 2013, In : American Journal of Surgical Pathology. 37, 4, p. 613-616

    Research output: Contribution to journalArticle

  32. Pathogenetic Mechanisms in Soft Tissue Tumors

    Elsa Arbajian, 2017, Lund: Lund University: Faculty of Medicine. 58 p.

    Research output: ThesisDoctoral Thesis (compilation)

  33. In-depth genetic analysis of sclerosing epithelioid fibrosarcoma reveals recurrent genomic alterations and potential treatment targets

    Elsa Arbajian, Puls, F., Antonescu, C. R., Amary, F. M., Sciot, R., Debiec-Rychter, M., Sumathi, V., Marcus Järås, Magnusson, L., Nilsson, J., Jakob Hofvander & Fredrik Mertens, 2017 Dec, In : Clinical Cancer Research. 23, 23, p. 7426-7434

    Research output: Contribution to journalArticle

  34. Deep sequencing of myxoinflammatory fibroblastic sarcoma

    Elsa Arbajian, Jakob Hofvander, Magnusson, L. & Fredrik Mertens, 2020 Jan 3, In : Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  35. Bilateral Prophylactic Mastectomy in Swedish Women at High Risk of Breast Cancer: A National Survey.

    Arver, B., Isaksson, K., Atterhem, H., Baan, A., Bergkvist, L., Brandberg, Y., Hans Ehrencrona, Emanuelsson, M., Hellborg, H., Henriksson, K., Karlsson, P., Niklas Loman, Lundberg, J., Anita Ringberg, Askmalm, M. S., Wickman, M. & Sandelin, K., 2011, In : Annals of Surgery. 253, 6, p. 1147-1154

    Research output: Contribution to journalArticle

  36. Selective killing of candidate AML stem cells by antibody targeting of IL1RAP.

    Askmyr, M., Helena Ågerstam, Hansen, N., Gordon, S., Alexandros Arvanitakis, Rissler, M., Gunnar Juliusson, Johan Richter, Marcus Järås & Thoas Fioretos, 2013, In : Blood. 121, 18, p. 3709-3713

    Research output: Contribution to journalArticle

  37. Ciliary neurotrophic factor has intrinsic and extrinsic roles in regulating B cell differentiation and bone structure.

    Askmyr, M., White, K. E., Jovic, T., King, H. A., Quach, J. M., Maluenda, A. C., Baker, E. K., Smeets, M. F., Walkley, C. R. & Purton, L. E., 2015, In : Scientific Reports. 5, 15529.

    Research output: Contribution to journalArticle

  38. Transgenic expression of human cytokines in immunodeficient mice does not facilitate myeloid expansion of BCR-ABL1 transduced human cord blood cells

    Askmyr, M., Sofia Von Palffy, Hansen, N., Niklas Landberg, Högberg, C., Rissler, M., Helena Ågerstam & Thoas Fioretos, 2017 Oct 1, In : PLoS ONE. 12, 10, e0186035.

    Research output: Contribution to journalArticle

  39. Provision of genetic service in Europe: current practices and issues.

    Aymé, S., Cassiman, J-J., Coviello, D., Evers-Kiebooms, G., Kääriäinen, H., Ulf Kristoffersson, Pembrey, M., Schmidtke, J., ten Kate, L. & Tranebjaerg, L., 2003, In : European Journal of Human Genetics. 11, p. 900-902

    Research output: Contribution to journalArticle

  40. An excess of chromosome 1 breakpoints in male infertility.

    Bache, I., Van Assche, E., Cingoz, S., Bugge, M., Tümer, Z., Hjorth, M., Lundsteen, C., Lespinasse, J., Winther, K., Niebuhr, A., Kalscheuer, V., Liebaers, I., Bonduelle, M., Tournaye, H., Ayuso, C., Barbi, G., Blennow, E., Bourrouillou, G., Brondum-Nielsen, K., Bruun-Petersen, G. & 39 others, Croquette, M-F., Dahoun, S., Dallapiccola, B., Davison, V., Delobel, B., Duba, H-C., Duprez, L., Ferguson-Smith, M., FitzPatrick, D. R., Grace, E., Hansmann, I., Hultén, M., Jensen, P. KA., Jonveaux, P., Ulf Kristoffersson, Lopez-Pajares, I., McGowan-Jordan, J., Murken, J., Orera, M., Parkin, T., Passarge, E., Ramos, C., Rasmussen, K., Schempp, W., Schubert, R., Schwinger, E., Shabtai, F., Smith, K., Stallings, R., Stefanova, M., Tranebjerg, L., Turleau, C., van der Hagen, C. B., Vekemans, M., Kokalj Vokac, N., Wagner, K., Wahlstroem, J., Zelante, L. & Tommerup, N., 2004, In : European Journal of Human Genetics. 12, 12, p. 993-1000

    Research output: Contribution to journalArticle

  41. Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol

    Barbany, G., Andersen, M. K., Autio, K., Borgstrom, G., Franco, L. C., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Bertil Johansson, Johannsson, J. H., Kjeldsen, E., Nordgren, A., Palmqvist, L. & Forestier, E., 2012, In : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 36, 7, p. 936-938

    Research output: Contribution to journalLetter

  42. Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.

    Barbouti, A., Bertil Johansson, Mattias Höglund, Mauritzson, N., Strömbeck, B., Nilsson, P-G., Tanke, H. J., Hagemeijer, A., Felix Mitelman & Thoas Fioretos, 2002, In : Genes, Chromosomes and Cancer. 35, 2, p. 127-137

    Research output: Contribution to journalArticle

  43. The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.

    Barbouti, A., Stankiewicz, P., Nusbaum, C., Cuomo, C., Cook, A., Mattias Höglund, Bertil Johansson, Hagemeijer, A., Park, S-S., Felix Mitelman, Lupski, J. R. & Thoas Fioretos, 2004, In : American Journal of Human Genetics. 74, 1, p. 1-10

    Research output: Contribution to journalArticle

  44. Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia

    Barbouti, A., 2004, Anette Welin, Academic Secretary, Department of Clinical Genetics, Lund University Hospital, SE-221 85 Lund, Sweden,. 100 p.

    Research output: ThesisDoctoral Thesis (compilation)

  45. Tumor karyotype predicts clinical outcome in colorectal cancer patients

    Bardi, G., Fenger, C., Bertil Johansson, Felix Mitelman & Heim, S., 2004, In : Journal of Clinical Oncology. 22, 13, p. 2623-2634

    Research output: Contribution to journalArticle

  46. Delay between fusion pore opening and peptide release from large dense-core vesicles in neuroendocrine cells.

    Barg, S., Olofsson, C., Schriever-Abeln, J., Anna Wendt, Samuel Gebre-Medhin, Erik Renström & Rorsman, P., 2002, In : Neuron. 33, 2, p. 287-299

    Research output: Contribution to journalArticle

  47. 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

  48. Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer

    Bartuma, K., Mef Nilbert, Soller, M., Silfverberg, B. & Christina Carlsson, 2007, In : Genetic Testing. 11, 2, p. 183-186

    Research output: Contribution to journalArticle

  49. CYTOGENETIC AND MOLECULAR GENETIC CHARACTERIZATION OF LIPOMAS

    Bartuma, H., 2011, Department of Clinical Genetics, Lund University. 166 p.

    Research output: ThesisDoctoral Thesis (compilation)

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

    Bartuma, H., Karolin Hansén Nord, Macchia, G., Isaksson, M., Nilsson, J., Domanski, H., Nils Mandahl & Fredrik Mertens, 2011, In : Genes, Chromosomes and Cancer. 50, p. 619-632

    Research output: Contribution to journalArticle

  51. Cytogenetic and molecular cytogenetic findings in lipoblastoma.

    Bartuma, H., Domanski, H., Fredrik Vult von Steyern, Kullendorff, C-M., Nils Mandahl & Fredrik Mertens, 2008, In : Cancer Genetics and Cytogenetics. 183, 1, p. 60-63

    Research output: Contribution to journalArticle

  52. Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.

    Bartuma, H., Panagopoulos, I., Collin, A., Trombetta, D., Domanski, H., Nils Mandahl & Fredrik Mertens, 2009, In : Molecular Cancer. 8, Jun 9, 36.

    Research output: Contribution to journalArticle

  53. Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.

    Bartuma, H., Möller, E., Collin, A., Domanski, H., Fredrik Vult von Steyern, Nils Mandahl & Fredrik Mertens, 2010, In : Cancer Genetics and Cytogenetics. 199, 2, p. 143-146

    Research output: Contribution to journalArticle

  54. Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities Background Document to the ESHG recommendations on genetic testing and common disorders

    Becker, F., van El, C. G., Ibarreta, D., Zika, E., Hogarth, S., Borry, P., Cambon-Thomsen, A., Cassiman, J. J., Evers-Kiebooms, G., Hodgson, S., Janssens, A. C. J. W., Kaariainen, H., Krawczak, M., Kristoffersson, U., Lubinski, J., Patch, C., Penchaszadeh, V. B., Read, A., Rogowski, W., Sequeiros, J. & 6 others, Tranebjaerg, L., van Langen, I. M., Wallace, H., Zimmern, R., Schmidtke, J. & Cornel, M. C., 2011, In : European Journal of Human Genetics. 19, S.1, p. S6-S44

    Research output: Contribution to journalArticle

  55. 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

  56. Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases

    Bekers, E. M., Groenen, P. J. T. A., Verdijk, M. A. J., Raaijmakers-van Geloof, W. L., Roepman, P., Vink, R., Gilhuijs, N. D. B., van Gorp, J. M., Bovée, J. V. M. G., Creytens, D. H., Flanagan, A. M., Suurmeijer, A. J. H., Mentzel, T., Elsa Arbajian & Flucke, U., 2017 Oct 1, In : Genes Chromosomes and Cancer. 56, 10, p. 750-757 8 p.

    Research output: Contribution to journalArticle

  57. Montelukast, a CysLT1 receptor antagonist, reduces colon cancer stemness and tumor burden in a mouse xenograft model of human colon cancer

    Bellamkonda, K., Shakti Ranjan Satapathy, Douglas, D., Chandrashekar, N., Selvanesan, B. C., Liu, M., Savari, S., Jonsson, G. & Anita Sjölander, 2018 Nov 28, In : Cancer Letters. 437, p. 13-24 12 p.

    Research output: Contribution to journalArticle

  58. Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort

    Bengtsson, D., Joost, P., Aravidis, C., Askmalm Stenmark, M., Backman, A. S., Melin, B., von Salomé, J., Zagoras, T., Samuel Gebre-Medhin & Pia Burman, 2017 Nov 1, In : The Journal of clinical endocrinology and metabolism. 102, 11, p. 3928-3932 5 p.

    Research output: Contribution to journalArticle

  59. Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden

    Benjamin, C. M., Anionwu, E. N., Ulf Kristoffersson, ten Kate, L. P., Plass, A. M. C., Nippert, I., Julian-Reynier, C., Harris, H. J., Schmidtke, J., Challen, K., Calefato, J. M., Waterman, C., Powell, E. & Harris, R., 2009, In : Midwifery. 25, 5, p. 483-499

    Research output: Contribution to journalArticle

  60. C-band heteromorphism in breast cancer patients

    Berger, R., Bernheim, A., Ulf Kristoffersson, Felix Mitelman & Håkan Olsson, 1985 Jan 1, In : Cancer Genetics and Cytogenetics. 18, 1, p. 37-42 6 p.

    Research output: Contribution to journalArticle

  61. Establishment of a cell line from a chemotherapy resistant diffuse large B-cell lymphoma

    Berglund, M., Thunberg, U., Fridberg, M., Gjörloff Wingren, A., Gullbo, J., Leuchowius, K-J., Amini, R-M., Lagercrantz, S., Biloglav, A., Enblad, G. & Soderberg, O., 2007, In : Leukemia & Lymphoma. 48, 5, p. 1038-1041

    Research output: Contribution to journalLetter

  62. Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)

    Beverloo, H. B., Panagopoulos, I., Isaksson, M., van Wering, E., van Drunen, E., de Klein, A., Bertil Johansson & Slater, R., 2001, In : Cancer Research. 61, 14, p. 5374-5377

    Research output: Contribution to journalArticle

  63. Tumor Specific Migration Of Bone-Marrow Derived Rat Mesenchymal Stem Cells In The Invasive N29 Rat Brain Tumor Model

    Daniel Bexell, Gunnarsson, S., Tormin, A., David Gisselsson Nord, Stefan Scheding & Johan Bengzon, 2008, In : Neuro-Oncology. 10, 6, p. 1066-1066

    Research output: Contribution to journalPublished meeting abstract

  64. Poor survival in t(8;21) (q22;q22)-associated acute myeloid leukaemia with leukocytosis

    Billstrom, R., Bertil Johansson, Thoas Fioretos, Garwicz, S., Malm, C., Zettervall, O. & Felix Mitelman, 1997, In : European Journal of Haematology. 59, 1, p. 47-52

    Research output: Contribution to journalArticle

  65. Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.

    Billström, R., Ahlgren, T., Békássy, A., Malm, C., Olofsson, T., Mattias Höglund, Felix Mitelman & Bertil Johansson, 2002, In : American Journal of Hematology. 71, 1, p. 15-19

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  66. Smoking and myelodysplastic syndromes

    Jonas Björk, Maria Albin, Mauritzson, N., Ulf Strömberg, Bertil Johansson & Hagmar, L., 2000, In : Epidemiology. 11, 3, p. 285-291

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  67. Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?

    Jonas Björk, Maria Albin, Welinder, H., Håkan Tinnerberg, Mauritzson, N., Kauppinen, T., Ulf Strömberg, Bertil Johansson, Billström, R., Mikoczy, Z., Ahlgren, T., Nilsson, P. G., Felix Mitelman & Hagmar, L., 2001, In : Occupational and Environmental Medicine. 58, 11, p. 722-727

    Research output: Contribution to journalArticle

  68. Reduced proliferative capacity of hematopoietic stem cells deficient in hoxb3 and hoxb4.

    Björnsson, J. M., Larsson, N., Brun, A., Mattias Magnusson, Andersson, E., Lundström, P., Jonas Larsson, Repetowska, E., Mats Ehinger, Humphries, R. K. & Stefan Karlsson, 2003, In : Molecular and Cellular Biology. 23, 11, p. 3872-3883

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  69. Proliferation of primitive myeloid progenitors can be reversibly induced by HOXA10

    Björnsson, J. M., Andersson, E., Lundström, P., Larsson, N., Xu, X., Repetowska, E., Humphries, R. K. & Stefan Karlsson, 2001, In : Blood. 98, 12, p. 3301-3308

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  70. Myeloid Leukemia of Down Syndrome The Results of An International Retrospective Study

    Blink, M., Eibrink, M. M. V. D. H., de Haas, V., Hasle, H., Brien, M. O., Stark, B., Tandonnet, J., Pession, A., Tousovska, K., Cheuk, D. K. L., Kudo, K., Taga, T., Rubnitz, J., Haltrich, I., Balwierz, W., Johansson, B., Zimmermann, M., Reinhardt, D., Pieters, R., Forestier, E. & 1 others, Zwaan, C. M., 2010, In : Blood. 116, 21, p. 1120-1120

    Research output: Contribution to journalPublished meeting abstract

  71. Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study

    Blink, M., Zimmermann, M., von Neuhoff, C., Reinhardt, D., de Haas, V., Hasle, H., O'Brien, M. M., Stark, B., Tandonnet, J., Pession, A., Tousovska, K., Cheuk, D. K. L., Kudo, K., Taga, T., Rubnitz, J. E., Haltrich, I., Balwierz, W., Pieters, R., Forestier, E., Johansson, B. & 2 others, van den Heuvel-Eibrink, M. M. & Zwaan, C. M., 2014, In : Haematologica. 99, 2, p. 299-307

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  72. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

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E., Caldes, T., Imyanitov, E. N., Tihomirova, L., Arun, B. K., Campbell, I., Mensenkamp, A. R., van Asperen, C. J., van Roozendaa, K. E. P., Meijers-Heijboer, H., Collee, J. M., Oosterwijk, J. C., Hooning, M. J., Rookus, M. A., van der Luijt, R. B., Os, T. A. M., Evans, D. G., Frost, D., Fineberg, E., Barwell, J., Walker, L., Kennedy, M. J., Platte, R., Davidson, R., Ellis, S. D., Cole, T., Bressac-de Paillerets, B., Buecher, B., Damiola, F., Faivre, L., Frenay, M., Sinilnikova, O. M., Caron, O., Giraud, S., Mazoyer, S., Bonadona, V., Caux-Moncoutier, V., Toloczko-Grabarek, A., Gronwald, J., Byrski, T., Spurdle, A. B., Bonanni, B., Zaffaroni, D., Giannini, G., Bernard, L., Dolcetti, R., Manoukian, S., Arnold, N., Engel, C., Deissler, H., Rhiem, K., Niederacher, D., Pendl, H., Sutter, C., Wappenschmidt, B., Åke Borg, Mein, B., Rantala, J., Soller, M., Nathanson, K. L., Domchek, S. M., Rodriguez, G. C., Salani, R., Kaulich, D. G., Tea, M-K., Paluch, S. S., Laitman, Y., Skytte, A-B., Kruse, T. A., Jensen, U. B., Robson, M., Gerdes, A-M., Ejlertsen, B., Foretova, L., Savage, S. A., Lesterm, J., Soucy, P., Kuchenbaecker, K. B., Olswold, C., Cunningham, J. M., Slager, S., Pankratz, V. S., Dicks, E., Lakhani, S. R., Couch, F. J., Hall, P., Monteiro, A. N. A., Gayther, S. A., Pharoah, P. D. P., Reddel, R. R., Goode, E. L., Greene, M. H., Easton, D. F., Berchuck, A., Antoniou, A. C., Chenevix-Trench, G. & Dunning, A. M., 2013, In : Nature Genetics. 45, 4, p. 371-384

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  73. Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

    Bolton, K. L., Chenevix-Trench, G., Goh, C., Sadetzki, S., Ramus, S. J., Karlan, B. Y., Lambrechts, D., Despierre, E., Barrowdale, D., McGuffog, L., Healey, S., Easton, D. F., Sinilnikova, O., Benitez, J., Garcia, M. J., Neuhausen, S., Gail, M. H., Hartge, P., Peock, S., Frost, D. & 55 others, Evans, G., Eeles, R., Godwin, A. K., Daly, M. B., Kwong, A., Ma, E. S. K., Lazaro, C., Blanco, I., Montagna, M., D'Andrea, E., Nicoletto, M. O., Johnatty, S. E., Krueger, S., Jensen, A., Hogdall, E., Goode, E. L., Fridley, B. L., Loud, J. T., Greene, M. H., Mai, P. L., Chetrit, A., Lubin, F., Hirsh-Yechezkel, G., Glendon, G., Andrulis, I. L., Toland, A. E., Senter, L., Gore, M. E., Gourley, C., Michie, C. O., Song, H., Tyrer, J., Whittemore, A. S., McGuire, V., Sieh, W., Ulf Kristoffersson, Håkan Olsson, Åke Borg, Levine, D. A., Steele, L., Beattie, M. S., Chan, S., Nussbaum, R. L., Moysich, K. B., Gross, J., Cass, I., Walsh, C., Li, A. J., Leuchter, R., Gordon, O., Garcia-Closas, M., Gayther, S. A., Chanock, S. J., Antoniou, A. C. & Pharoah, P. D. P., 2012, In : JAMA: The Journal of the American Medical Association. 307, 4, p. 382-390

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  74. Diagnosis of acute promyelocytic leukaemia by RT-PCR: detection of PML-RARA and RARA-PML fusion transcripts

    Borrow, J., Goddard, A. D., Gibbons, B., Katz, F., Swirsky, D., Thoas Fioretos, Dube, I., Winfield, D. A., Kingston, J., Hagemeijer, A., Rees, J. K. H., Lister, T. A. & Solomon, E., 1992, In : British Journal of Haematology. 82, 3, p. 529-540

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  75. Molecular analysis of simple variant translocations in acute promyelocytic leukemia

    Borrow, J., Shipley, J., Howe, K., Kiely, F., Goddard, A., Sheer, D., Srivastava, A., Antony, A. C., Thoas Fioretos & Mitelman, F., 1994, In : Genes, Chromosomes and Cancer. 9, 4, p. 234-243

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  76. Promoter DNA Methylation Pattern Identifies Prognostic Subgroups in Childhood T-Cell Acute Lymphoblastic Leukemia

    Borssen, M., Palmqvist, L., Karrman, K., Abrahamsson, J., Behrendtz, M., Heldrup, J., Forestier, E., Roos, G. & Degerman, S., 2013, In : PLoS ONE. 8, 6, e65373.

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  77. Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours

    Bottillo, I., Ahiquist, T., Brekke, H., Danielsen, S. A., van den Berg, E., Fredrik Mertens, Lothe, R. A. & Dallapiccola, B., 2009, In : Journal of Pathology. 217, 5, p. 693-701

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  78. Neuroblastoma Patient-Derived Orthotopic Xenografts Retain Metastatic Patterns and Geno- and Phenotypes of Patient Tumours.

    Braekeveldt, N., Wigerup, C., David Gisselsson Nord, Sofie Mohlin, Merselius, M., Beckman, S., Tord Jonson, Anna Börjesson, Backman, T., Tadeo, I., Berbegall, A. P., Ingrid Øra, Navarro, S., Noguera, R., Sven Påhlman & Daniel Bexell, 2015, In : International Journal of Cancer. 136, 5, p. E252-E261

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  79. Neuroblastoma patient-derived orthotopic xenografts reflect the microenvironmental hallmarks of aggressive patient tumours

    Braekeveldt, N., Wigerup, C., Tadeo, I., Beckman, S., Caroline Sandén, Jönsson, J., Jonas S Erjefält, Berbegall, A. P., Anna Börjesson, Backman, T., Ingrid Øra, Navarro, S., Noguera, R., David Gisselsson, Sven Påhlman & Daniel Bexell, 2016, In : Cancer Letters. 375, 2, p. 384-389

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  80. Patient-derived xenograft models reveal intratumor heterogeneity and temporal stability in neuroblastoma

    Braekeveldt, N., Von Stedingk, K., Fransson, S., Martinez-Monleon, A., Lindgren, D., Axelson, H., Levander, F., Willforss, J., Hansson, K., Øra, I., Backman, T., Börjesson, A., Beckman, S., Esfandyari, J., Berbegall, A. P., Noguera, R., Karlsson, J., Koster, J., Martinsson, T., Gisselsson, D. & 2 others, Sven Påhlman & Daniel Bexell, 2018, In : Cancer Research. 78, 20, p. 5958-5969 12 p.

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  81. 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

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  82. t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma

    Brandal, P., Panagopoulos, I., Bjerkehagen, B. & Heim, S., 2009, In : Genes, Chromosomes and Cancer. 48, 12, p. 1051-1056

    Research output: Contribution to journalArticle

  83. Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer

    Bratt, O., Damber, J. E., Emanuelsson, M., U Kristoffersson, Lundgren, R., Håkan Olsson & Grönberg, H., 2000 Jan, In : European Journal of Cancer. 36, 2, p. 235-241

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  84. Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study

    Bratt, O., U Kristoffersson, Lundgren, R. & Håkan Olsson, 1999 Feb, In : European Journal of Cancer. 35, 2, p. 272-7 6 p.

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  85. Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor

    Bratt, O., U Kristoffersson, Håkan Olsson & Lundgren, R., 1998, In : European Urology. 34, 1, p. 19-24 6 p.

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  86. Forskningsframsteg om hereditär prostatacancer. Riskfamiljer bör kartläggas och erbjudas screening

    Bratt, O., Abrahamsson, P. A., Lundgren, R., Håkan Olsson & U Kristoffersson, 1998 Apr 1, In : Läkartidningen. 95, 14, p. 1494-6 3 p.

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  87. Sons of men with prostate cancer: their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing

    Bratt, O., U Kristoffersson, Lundgren, R. & Håkan Olsson, 1997 Sep, In : Urology. 50, 3, p. 360-5 6 p.

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  88. Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

    Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., de Pauw, A., Tischkowitz, M., Hans Ehrencrona, Dolbeault, S., Robieux, L., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D. & Schmutlzer, R., 2018, In : Familial Cancer. 17, 1, p. 31-41

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  89. Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey

    Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., de Pauw, A., Tischkowitz, M., Hans Ehrencrona, Schmidt, M. K., Dolbeault, S., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D. & Schmutlzer, R., 2019 Jan, In : Journal of Community Genetics. 10, 1, p. 61-71

    Research output: Contribution to journalArticle

  90. Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors

    Brekke, H. R., Kolberg, M., Skotheim, R. I., Hall, K. S., Bjerkehagen, B., Risberg, B., Domanski, H., Nils Mandahl, Liestol, K., Smeland, S., Danielsen, H. E., Fredrik Mertens & Lothe, R. A., 2009, In : Neuro-Oncology. 11, 5, p. 514-528

    Research output: Contribution to journalArticle

  91. Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.

    Brekke, H. R., Ribeiro, F. R., Kolberg, M., Agesen, T. H., Lind, G. E., Eknæs, M., Hall, K. S., Bjerkehagen, B., van den Berg, E., Teixeira, M. R., Nils Mandahl, Smeland, S., Fredrik Mertens, Skotheim, R. I. & Lothe, R. A., 2010, In : Journal of Clinical Oncology. 28, p. 1573-1582

    Research output: Contribution to journalArticle

  92. Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia

    Broberg, K., Sören Toksvig-Larsen, Lindstrand, A. & Fredrik Mertens, 2001, In : Genes, Chromosomes and Cancer. 30, 3, p. 310-315

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  93. Characterization of somatic mutations in nonneoplastic cells

    Broberg, K., 2001, Department of Clinical Genetics, Lund University. 110 p.

    Research output: ThesisDoctoral Thesis (compilation)

  94. Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis

    K Broberg, M Höglund, Limon, J., Lindstrand, A., S Toksvig-Larsen, N Mandahl & F Mertens, 1999 Mar, In : Genes, Chromosomes and Cancer. 24, 3, p. 278-82

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  95. Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis

    Broberg, K., Limon, J., Pålsson, E., Lindstrand, A., S Toksvig-Larsen, N Mandahl & F Mertens, 1997 Dec, In : Human Genetics. 101, 3, p. 295-8 4 p.

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  96. Vi måste ta ställning till den nya gentekniken

    Karin Broberg, Ingrid Dunér, Kristofer Hansson, Mats Hansson, Johan Jakobsson, Marcus Järås, Ulf Kristoffersson, Hindrik Mulder, Ana Nordberg, Anna Tunlid, Niklas Vareman & Karin E Wahlberg, 2019 Nov 24, Svenska Dagbladet, Stockholm 1 p.

    Research output: Contribution to specialist publication or newspaperNewspaper article

  97. Att inte debattera är inte ett alternativ

    Karin Broberg, Ingrid Dunér, Kristofer Hansson, Mats Hansson, Johan Jakobsson, Marcus Järås, Ulf Kristoffersson, Hindrik Mulder, Ana Nordberg, Anna Tunlid, Niklas Vareman & Karin E Wahlberg, 2019 Dec 8, Svenska Dagbladet, Stockholm.

    Research output: Contribution to specialist publication or newspaperNewspaper article

  98. Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.

    Karin Broberg Palmgren, Zhang, M., Strömbeck, B., Isaksson, M., Nilsson, M. A., Fredrik Mertens, Nils Mandahl & Panagopoulos, I., 2002, In : International Journal of Oncology. 21, 2, p. 321-326

    Research output: Contribution to journalArticle

  99. Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes

    Broliden, PA., Dahl, IM., Hast, R., Bertil Johansson, Juvonen, E., Kjeldsen, L., Porwit-MacDonald, A., Sjoo, M., Tangen, JM., Uggla, B., Oberg, G. & Hellstrom-Lindberg, E., 2006, In : Haematologica. 91, 5, p. 667-670

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  100. Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells

    Brun, A., Björnsson, J. M., Mattias Magnusson, Larsson, N., Levéen, P., Mats Ehinger, Nilsson, E. C. & Stefan Karlsson, 2004, In : Blood. 103, 11, p. 4126-4133

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  101. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.

    Buckley, P. G., Mantripragada, K. K., Benetkiewicz, M., Tapia-Páez, I., Diaz De Ståhl, T., Rosenquist, M., Ali, H., Jarbo, C., De Bustos, C., Hirvelä, C., Sinder Wilén, B., Fransson, I., Thyr, C., Johnsson, B-I., Bruder, C. E. G., Menzel, U., Hergersberg, M., Mandahl, N., Blennow, E., Wedell, A. & 11 others, Beare, D. M., Collins, J. E., Dunham, I., Albertson, D., Pinkel, D., Bastian, B. C., Faruqi, A. F., Lasken, R. S., Ichimura, K., Collins, V. P. & Dumanski, J. P., 2002, In : Human Molecular Genetics. 11, 25, p. 3221-3229

    Research output: Contribution to journalArticle

  102. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R. A. J., Buerger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoom, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, In : Clinical Cancer Research. 17, 8, p. 2110-2119

    Research output: Contribution to journalArticle

  103. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage-Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R., Burger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoorn, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, In : Laboratory Investigation. 91, Feb 26 - Mar 4, 2011, p. 10A

    Research output: Contribution to journalPublished meeting abstract

  104. Tumors of endocrine glands

    Bullerdiek, J. & David Gisselsson, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (eds.). 4th ed. Wiley-Blackwell, p. 497-514 18 p.

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

  105. Generation of human cortical neurons from a new immortal fetal neural stem cell line.

    Cacci, E., Villa, A., Malin Parmar, Cavallaro, M., Nils Mandahl, Olle Lindvall, Martinez-Serrano, A. & Zaal Kokaia, 2007, In : Experimental Cell Research. 313, 3, p. 588-601

    Research output: Contribution to journalArticle

  106. Telomere dysfunction and telomerase activation in cancer - a pathological paradox?

    Calcagnile, O. & David Gisselsson Nord, 2007, In : Cytogenetic and Genome Research. 118, 2-4, p. 270-276

    Research output: Contribution to journalArticle

  107. Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

    Calefato, J-M., Nippert, I., Harris, H. J., Ulf Kristoffersson, Schmidtke, J., Ten Kate, L. P., Anionwu, E., Benjamin, C., Challen, K., Plass, A-M., Harris, R. & Julian-Reynier, C., 2008, In : Genetics in Medicine. 10, 2, p. 99-106

    Research output: Contribution to journalArticle

  108. New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia

    Callen, D. F., Hull, Y. J., Toogood, I. R., Thoas Fioretos, Heim, S., Nils Mandahl & Felix Mitelman, 1991, In : Cancer Genetics and Cytogenetics. 51, 2, p. 255-258

    Research output: Contribution to journalArticle

  109. Unaltered pancreatic islet blood perfusion in islet amyloid polypeptide-deficient mice

    Carlsson, PO., Karlsson, E., Hindrik Mulder & Samuel Gebre-Medhin, 2002, In : European Journal of Endocrinology. 146, 1, p. 107-112

    Research output: Contribution to journalArticle

  110. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

    Carpten, JD., Robbins, CM., Villablanca, A., Forsberg, L., Presciuttini, S., Bailey-Wilson, J., Simonds, WF., Gillanders, EM., Kennedy, AM., Chen, JD., Agarwal, SK., Sood, R., Jones, MP., Moses, TY., Haven, C., Petillo, D., Leotlela, PD., Harding, B., Cameron, D., Pannett, AA. & 21 others, Hoog, A., Heath, H., James-Newton, LA., Robinson, B., Zarbo, RJ., Cavaco, BM., Wassif, W., Perrier, ND., Rosen, IB., Ulf Kristoffersson, Turnpenny, PD., Farnebo, LO., Besser, GM., Jackson, CE., Morreau, H., Trent, JM., Thakker, RV., Marx, SJ., Teh, BT., Larsson, C. & Hobbs, MR., 2002, In : Nature Genetics. 32, 4, p. 676-680

    Research output: Contribution to journalArticle

  111. Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

    Castellani, C., Macek, M. J., Cassiman, J-J., Duff, A., Massie, J., ten Kate, L. P., Barton, D., Cutting, G., Dallapiccola, B., Dequeker, E., Girodon, E., Grody, W., Highsmith, E. W., Kaariainen, H., Kruip, S., Morris, M., Pignatti, P. F., Pypops, U., Schwarz, M., Soller, M. & 2 others, Stuhrman, M. & Cuppens, H., 2010, In : Journal of Cystic Fibrosis. 9, 3, p. 165-178

    Research output: Contribution to journalReview article

  112. Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.

    Anders Castor, Nilsson, L., Åstrand-Grundström, I., Buitenhuis, M., Ramirez, C., Anderson, K., Strömbeck, B., Garwicz, S., Békássy, A., Schmiegelow, K., Lausen, B., Hokland, P., Lehmann, S., Gunnar Juliusson, Bertil Johansson & Jacobsen, S. E. W., 2005, In : Nature Medicine. 11, 6, p. 630-637

    Research output: Contribution to journalArticle

  113. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

    Catucci, I., Osorio, A., Arver, B., Neidhardt, G., Bogliolo, M., Zanardi, F., Riboni, M., Minardi, S., Pujol, R., Azzollini, J., Peissel, B., Manoukian, S., De Vecchi, G., Casola, S., Hauke, J., Richters, L., Rhiem, K., Schmutzler, R. K., Wallander, K., Törngren, T. & 8 others, Åke Borg, Radice, P., Surrallés, J., Hahnen, E., Hans Ehrencrona, Anders Kvist, Benitez, J. & Peterlongo, P., 2018, In : Genetics in Medicine. 20, p. 452–457 6 p.

    Research output: Contribution to journalArticle

  114. Gain of 1q as a prognostic biomarker in Wilms Tumors (WTs) treated with preoperative chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 trial: A SIOP renal tumours biology consortium study

    Chagtai, T., Zill, C., Dainese, L., Wegert, J., Savola, S., Popov, S., Mifsud, W., Vujanić, G., Sebire, N., Le Bouc, Y., Ambros, P. F., Kager, L., O'Sullivan, M. J., Blaise, A., Bergeron, C., Mengelbier, L. H., Gisselsson, D., Kool, M., Tytgat, G. A. M., Van Den Heuvel-Eibrink, M. M. & 6 others, Graf, N., Van Tinteren, H., Coulomb, A., Gessler, M., Williams, R. D. & Pritchard-Jones, K., 2016 Sep 10, In : Journal of Clinical Oncology. 34, 26, p. 3195-3203 9 p.

    Research output: Contribution to journalArticle

  115. Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.

    Challen, K., Harris, H., Julian-Reynier, C., Ten Kate, L., Ulf Kristoffersson, Nippert, I., Schmidtke, J., Benjamin, C. & Harris, R., 2005, In : Genetics in Medicine. 7, 5, p. 302-310

    Research output: Contribution to journalArticle

  116. Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort

    U. Chaudhry, P. G. Platonov, Rubulis, A., Bergfeldt, L., Jensen, S. M., Lundin, C. & R. Borgquist, 2019, In : Journal of Electrocardiology. 56, p. 46-51 6 p.

    Research output: Contribution to journalArticle

  117. Better Prognosis of Patients with Glioma Expressing FGF2-Dependent PDGFRA Irrespective of Morphological Diagnosis.

    Chen, D., Persson, A., Sun, Y., Leif Salford, David Gisselsson Nord, Elisabet Englund, Jiang, T. & Xiaolong Fan, 2013, In : PLoS ONE. 8, 4, e61556.

    Research output: Contribution to journalArticle

  118. Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome

    Chen, Y. H., Grigelioniene, G., Newton, P. T., Gullander, J., Elfving, M., Hammarsjö, A., Batkovskyte, D., Alsaif, H. S., Kurdi, W. I. Y., Abdulwahab, F., Shanmugasundaram, V., Devey, L., Bacrot, S., Brodszki, J., Huber, C., Hamel, B., Gisselsson, D., Papadogiannakis, N., Jedrycha, K., Gürtl-Lackner, B. & 7 others, Chagin, A. S., Nishimura, G., Aschenbrenner, D., Alkuraya, F. S., Laurence, A., Cormier-Daire, V. & Uhlig, H. H., 2020, In : The Journal of experimental medicine. 217, 3, e20191306.

    Research output: Contribution to journalArticle

  119. L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.

    Christaller, W. A. A., Vos, Y., Samuel Gebre-Medhin, Hofstra, R. M. W. & Schäfer, M. K. E., 2016, In : Clinical Genetics.

    Research output: Contribution to journalArticle

  120. Amplification and overexpression of Aurora kinase A (AURKA) in immortalized human ovarian epithelial (HOSE) cells

    Chung, C. M., Man, C., Jin, Y., Jin, C., Guan, X. Y., Wang, Q., Wan, T. S. K., Cheung, A. L. M. & Tsao, S. W., 2005, In : Molecular Carcinogenesis. 43, 3, p. 165-174

    Research output: Contribution to journalArticle

  121. Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

    Couch, F. J., Gaudet, M. M., Antoniou, A. C., Ramus, S. J., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., Wang, X., Kirchhoff, T., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Sinilnikova, O. M., Andrulis, I. L., Ozcelik, H., Mulligan, A. M., Thomassen, M., Gerdes, A-M. & 170 others, Jensen, U. B., Skytte, A-B., Kruse, T. A., Caligo, M. A., von Wachenfeldt, A., Barbany-Bustinza, G., Niklas Loman, Soller, M., Hans Ehrencrona, Karlsson, P., Nathanson, K. L., Rebbeck, T. R., Domchek, S. M., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Zlowocka, E., Huzarski, T., Byrski, T., Gronwald, J., Cybulski, C., Górski, B., Osorio, A., Durán, M., Tejada, M. I., Benitez, J., Hamann, U., Hogervorst, F. B. L., van Os, T. A., van Leeuwen, F. E., Meijers-Heijboer, H. E. J., Wijnen, J., Blok, M. J., Kets, M., Hooning, M. J., Oldenburg, R. A., Ausems, M. G. E. M., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Jacobs, C., Eeles, R. A., Adlard, J., Davidson, R., Eccles, D. M., Cole, T., Cook, J., Paterson, J., Brewer, C., Douglas, F., Hodgson, S. V., Morrison, P. J., Walker, L., Porteous, M. E., Kennedy, M. J., Side, L. E., Bove, B., Godwin, A. K., Stoppa-Lyonnet, D., Fassy-Colcombet, M., Castera, L., Cornelis, F., Mazoyer, S., Léoné, M., Boutry-Kryza, N., Bressac-de Paillerets, B., Caron, O., Pujol, P., Coupier, I., Delnatte, C., Akloul, L., Lynch, H. T., Snyder, C. L., Buys, S. S., Daly, M. B., Terry, M., Chung, W. K., John, E. M., Miron, A., Southey, M. C., Hopper, J. L., Goldgar, D. E., Singer, C. F., Rappaport, C., Tea, M-K. M., Fink-Retter, A., Hansen, T. V. O., Nielsen, F. C., Arason, A., Vijai, J., Shah, S., Sarrel, K., Robson, M. E., Piedmonte, M., Phillips, K., Basil, J., Rubinstein, W. S., Boggess, J., Wakeley, K., Ewart-Toland, A., Montagna, M., Agata, S., Imyanitov, E. N., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Feliubadalo, L., Brunet, J., Gayther, S. A., Pharoah, P. P. D., Odunsi, K. O., Karlan, B. Y., Walsh, C. S., Olah, E., Teo, S. H., Ganz, P. A., Beattie, M. S., van Rensburg, E. J., Dorfling, C. M., Diez, O., Kwong, A., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Heidemann, S., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Fiebig, B., Heinritz, W., Caldes, T., de la Hoya, M., Muranen, T. A., Nevanlinna, H., Tischkowitz, M. D., Spurdle, A. B., Neuhausen, S. L., Ding, Y. C., Lindor, N. M., Fredericksen, Z., Pankratz, V. S., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Barile, M., Bernard, L., Viel, A., Giannini, G., Varesco, L., Radice, P., Greene, M. H., Mai, P. L., Easton, D. F., Chenevix-Trench, G., Offit, K. & Simard, J., 2012, In : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 21, 4, p. 645-657

    Research output: Contribution to journalArticle

  122. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

    Couch, F. J., Kuchenbaecker, K. B., Michailidou, K., Mendoza-Fandino, G. A., Nord, S., Lilyquist, J., Olswold, C., Hallberg, E., Agata, S., Ahsan, H., Aittomäki, K., Ambrosone, C., Andrulis, I. L., Anton-Culver, H., Arndt, V., Arun, B. K., Arver, B., Barile, M., Barkardottir, R. B., Barrowdale, D. & 229 others, Beckmann, L., Beckmann, M. W., Benitez, J., Blank, S. V., Blomqvist, C., Bogdanova, N. V., Bojesen, S. E., Bolla, M. K., Bonanni, B., Brauch, H., Brenner, H., Burwinkel, B., Buys, S., Caldes, T., Caligo, M. A., Canzian, F., Carpenter, J., Chang-Claude, J., Chanock, S. J., Chung, W. K., Claes, K. B. M., Cox, A., Cross, S. S., Cunningham, J. M., Czene, K., Daly, M. B., Damiola, F., Darabi, H., de la Hoya, M., Devilee, P., Diez, O., Ding, Y. C., Dolcetti, R., Domchek, S. M., Dorfling, C. M., Dos Santos Silva, I., Dumont, M., Dunning, A. M., Eccles, D. M., Hans Ehrencrona, Ekici, A. B., Eliassen, A. H., Ellis, S., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Asta Försti, Fostira, F., Foulkes, W. D., Friebel, T., Friedman, E., Frost, D., Gabrielson, M., Gammon, M. D., Ganz, P. A., Gapstur, S. M., Garber, J., Gaudet, M., Gayther, S. A., Gerdes, A-M., Ghoussaini, M., Giles, G. G., Glendon, G., Godwin, A. K., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Greene, M. H., Gronwald, J., Guénel, P., Gunter, M., Haeberle, L., Haiman, C. A., Hamann, U., Hansen, T. V. O., Hart, S., Healey, S., Heikkinen, T., Henderson, B. E., Herzog, J., Hogervorst, F. B. L., Hollestelle, A., Hooning, M. J., Hoover, R. N., Hopper, J. L., Humphreys, K., Hunter, D. J., Huzarski, T., Imyanitov, E. N., Isaacs, C., Jakubowska, A., James, P., Janavicius, R., Jensen, U. B., John, E. M., Jones, M., Kabisch, M., Kar, S., Karlan, B. Y., Khan, S., Khaw, K. T., Kibriya, M. G., Knight, J. A., Ko, Y-D., Konstantopoulou, I., Kosma, V-M., Kristensen, V., Kwong, A., Laitman, Y., Lambrechts, D., Lazaro, C., Lee, E., Le Marchand, L., Lester, J., Lindblom, A., Lindor, N., Lindstrom, S., Liu, J., Long, J., Lubinski, J., Mai, P. L., Makalic, E., Malone, K. E., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., Martens, J. W. M., McGuffog, L., Meindl, A., Miller, A., Milne, R. L., Miron, P., Montagna, M., Mazoyer, S., Mulligan, A. M., Muranen, T. A., Nathanson, K. L., Neuhausen, S. L., Nevanlinna, H., Nordestgaard, B. G., Nussbaum, R. L., Offit, K., Olah, E., Olopade, O. I., Olson, J. E., Osorio, A., Park, S. K., Peeters, P. H., Peissel, B., Peterlongo, P., Peto, J., Phelan, C. M., Pilarski, R., Poppe, B., Pylkäs, K., Radice, P., Rahman, N., Rantala, J., Rappaport, C., Rennert, G., Richardson, A. L., Robson, M., Romieu, I., Rudolph, A., Rutgers, E. J., Sanchez, M-J., Santella, R. M., Sawyer, E. J., Schmidt, D. F., Schmidt, M. K., Schmutzler, R. K., Schumacher, F., Scott, R., Senter, L., Sharma, P., Simard, J., Singer, C. F., Sinilnikova, O. M., Soucy, P., Southey, M., Steinemann, D., Stenmark-Askmalm, M., Stoppa-Lyonnet, D., Swerdlow, A., Szabo, C. I., Tamimi, R., Tapper, W., Teixeira, M. R., Teo, S-H., Terry, M. B., Thomassen, M., Thompson, D., Tihomirova, L., Toland, A. E., Tollenaar, R. A. E. M., Tomlinson, I., Truong, T., Tsimiklis, H., Teulé, A., Tumino, R., Tung, N., Turnbull, C., Ursin, G., van Deurzen, C. H. M., van Rensburg, E. J., Varon-Mateeva, R., Wang, Z., Wang-Gohrke, S., Weiderpass, E., Weitzel, J. N., Whittemore, A. S., Wildiers, H., Winqvist, R., Yang, X. R., Yannoukakos, D., Yao, S., Zamora, M. P., Zheng, W., Hall, P., Kraft, P., Vachon, C., Slager, S., Chenevix-Trench, G., Pharoah, P. P. D., Monteiro, A. N., García-Closas, M., Easton, D. F. & Antoniou, A. C., 2016 Apr 27, In : Nature Communications. 7, 11375.

    Research output: Contribution to journalArticle

  123. Establishment and characterisation of a human clear cell sarcoma model in nude mice

    Crnalic, S., Panagopoulos, I., Boquist, L., Nils Mandahl, Stenling, R. & Lofvenberg, R., 2002, In : International Journal of Cancer. 101, 6, p. 505-511

    Research output: Contribution to journalArticle

  124. Laboratory recommendations for scoring deep molecular responses following treatment for chronic myeloid leukemia.

    Cross, N. C. P., White, H. E., Colomer, D., Ehrencrona, H., Foroni, L., Gottardi, E., Lange, T., Lion, T., Machova Polakova, K., Dulucq, S., Martinelli, G., Oppliger Leibundgut, E., Pallisgaard, N., Barbany, G., Sacha, T., Talmaci, R., Izzo, B., Saglio, G., Pane, F., Müller, M. C. & 1 others, Hochhaus, A., 2015, In : Leukemia. 29, 5, p. 999-1003

    Research output: Contribution to journalReview article

  125. No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies

    da Costa, C. E. T., Szuhai, K., van Eijk, R., Hoogeboom, M., Sciot, R., Fredrik Mertens, Bjorgvinsdottir, H., Debiec-Rychter, M., de Krijger, R. R., Hogendoorn, P. C. W., Egeler, R. M. & Annels, N. E., 2009, In : Genes, Chromosomes and Cancer. 48, 3, p. 239-249

    Research output: Contribution to journalArticle

  126. Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo

    Dacquin, R., Davey, RA., Laplace, C., Levasseur, G., Morris, HA., Goldring, SR., Samuel Gebre-Medhin, Galson, DL., Zajac, JD. & Karsenty, G., 2004, In : Journal of Cell Biology. 164, 4, p. 509-514

    Research output: Contribution to journalArticle

  127. Genetic Characterization of Bone and Soft Tissue Tumors

    Dahlen, A., 2005, Department of Clinical Genetics, Lund University. 117 p.

    Research output: ThesisDoctoral Thesis (compilation)

  128. Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors

    Dahlén, A., Debiec-Rychter, M., Pedeutour, F., Domanski, H. A., Mattias Höglund, Bauer, H. C. F., Anders Rydholm, Sciot, R., Nils Mandahl & Fredrik Mertens, 2003 Feb 20, In : International Journal of Cancer. 103, 5, p. 616-623 8 p.

    Research output: Contribution to journalArticle

  129. Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).

    Dahlén, A., Fletcher, C. D. M., Fredrik Mertens, Fletcher, J. A., Perez-Atayde, A. R., Hicks, M. J., Debiec-Rychter, M., Sciot, R., Wejde, J., Wedin, R., Nils Mandahl & Panagopoulos, I., 2004, In : American Journal of Pathology. 164, 5, p. 1645-1653

    Research output: Contribution to journalArticle

  130. Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis

    Dahlén, A., Broberg, K., Domanski, H. A., S Toksvig-Larsen, Lindstrand, A., N Mandahl & F Mertens, 2001 Nov, In : Cancer Genetics and Cytogenetics. 131, 1, p. 19-24 6 p.

    Research output: Contribution to journalArticle

  131. Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas

    Dahlén, A., Fredrik Mertens, Anders Rydholm, Brosjö, O., Wejde, J., Nils Mandahl & Panagopoulos, I., 2003 Nov, In : Modern Pathology. 16, 11, p. 1132-1140 9 p.

    Research output: Contribution to journalArticle

  132. Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).

    Dahlén, A., Fredrik Mertens, Nils Mandahl & Panagopoulos, I., 2004, In : Biochemical and Biophysical Research Communications. 325, 4, p. 1318-1323

    Research output: Contribution to journalArticle

  133. Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.

    Danielsen, S. A., Lind, G. E., Kolberg, M., Høland, M., Bjerkehagen, B., Sundby Hall, K., van den Berg, E., Fredrik Mertens, Smeland, S., Picci, P. & Lothe, R. A., 2015, In : Neuro-Oncology. 17, 1, p. 63-69

    Research output: Contribution to journalArticle

  134. Epigenetic target genes in malignant peripheral nerve sheath tumours identified as surrogate prognostic biomarkers

    Danielsen, S. A., Lind, G. E., Hall, K. S., Smeland, S., van den Berg, E., Fredrik Mertens, Kolberg, M. & Lothe, R. A., 2010, In : EJC Supplements. 8, 5, p. 163

    Research output: Contribution to journalPublished meeting abstract

  135. Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia

    Daskalakis, M., Mauritzson, N., Bertil Johansson, Bouabdallah, K., Onida, F., Kunzmann, R., Mueller-Berndorff, H., Schmitt-Graeff, A. & Luebbert, M., 2006, In : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 30, 8, p. 1043-1047

    Research output: Contribution to journalArticle

  136. Relapsed Childhood High Hyperdiploid Acute Lymphoblastic Leukemia: Genome-Wide Screening Reveals the Presence of Preleukemic Ancestral Clones and the Secondary Nature of Microdeletions and RTK-RAS Mutations

    Josef Davidsson, Kajsa Paulsson, David Lindgren, Henrik Lilljebjörn, Chaplin, T., Forestier, E., Andersen, M. K., Nordgren, A., Rosenquist, R., Thoas Fioretos, Young, B. D. & Bertil Johansson, 2009, In : Blood. 114, 22, p. 1017-1017

    Research output: Contribution to journalPublished meeting abstract

  137. Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12

    Josef Davidsson, Collin, A., Oereberg, M. & David Gisselsson Nord, 2008, In : Clinical Genetics. 73, 1, p. 44-49

    Research output: Contribution to journalArticle

  138. The hypermethylome of pediatric acute lymphoblastic leukemia

    Josef Davidsson, Henrik Lilljebjörn, Anna Andersson, Srinivas Veerla, Heldrup, J., Behrendtz, M., Thoas Fioretos & Bertil Johansson, 2008, In : Cellular Oncology. 30, 3, p. 252-252

    Research output: Contribution to journalPublished meeting abstract

  139. Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia

    Josef Davidsson, 2009, Lund University: Faculty of Medicine. 193 p.

    Research output: ThesisDoctoral Thesis (compilation)

  140. dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome.

    Josef Davidsson, Jahnke, K., Forsgren, M., Collin, A. & Soller, M., 2010, In : Obesity. 18, p. 580-587

    Research output: Contribution to journalArticle

  141. The DNA methylome of pediatric acute lymphoblastic leukemia.

    Josef Davidsson, Henrik Lilljebjörn, Anna Andersson, Srinivas Veerla, Heldrup, J., Behrendtz, M., Thoas Fioretos & Bertil Johansson, 2009, In : Human Molecular Genetics. Aug 13, p. 4054-4065

    Research output: Contribution to journalArticle

  142. Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area

    Josef Davidsson, Collin, A., Engman Olsson, M., Lundgren, J. & Soller, M., 2008, In : Epilepsy Res. 81, 1, p. 69-79

    Research output: Contribution to journalArticle

  143. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

    Depienne, C., Nava, C., Keren, B., Heide, S., Rastetter, A., Passemard, S., Chantot-Bastaraud, S., Moutard, M. L., Agrawal, P. B., VanNoy, G., Stoler, J. M., Amor, D. J., Billette de Villemeur, T., Doummar, D., Alby, C., Cormier-Daire, V., Garel, C., Marzin, P., Scheidecker, S., de Saint-Martin, A. & 31 others, Hirsch, E., Korff, C., Bottani, A., Faivre, L., Verloes, A., Orzechowski, C., Burglen, L., Leheup, B., Roume, J., Andrieux, J., Sheth, F., Datar, C., Parker, M. J., Pasquier, L., Odent, S., Naudion, S., Delrue, M. A., Le Caignec, C., Vincent, M., Isidor, B., Renaldo, F., Stewart, F., Toutain, A., Koehler, U., Häckl, B., von Stülpnagel, C., Kluger, G., Møller, R. S., Tord Jonson, Soller, M. & DDD Study, 2017, In : Human Genetics. 136, 4, p. 463-479 17 p.

    Research output: Contribution to journalArticle

  144. Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis

    Diep, CB., Parada, LA., Teixeira, MR., Eknaes, M., Nesland, JM., Bertil Johansson & Lothe, RA., 2003, In : Genes, Chromosomes and Cancer. 36, 2, p. 189-197

    Research output: Contribution to journalArticle

  145. Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients

    Diep, C. B., Teixeira, M. R., Thorstensen, L., Wiig, J. N., Eknaes, M., Nesland, J. M., Giercksky, K-E., Bertil Johansson & Lothe, R. A., 2004, In : Molecular Cancer. 3, 6.

    Research output: Contribution to journalArticle

  146. A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

    Ding, Y. C., McGuffog, L., Healey, S., Friedman, E., Laitman, Y., Paluch-Shimon, S., Kaufman, B., Liljegren, A., Lindblom, A., Olsson, H., Kristoffersson, U., Stenmark-Askmalm, M., Melin, B., Domchek, S. M., Nathanson, K. L., Rebbeck, T. R., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K. & 141 others, Gronwald, J., Huzarski, T., Cybulski, C., Byrski, T., Osorio, A., Ramony Cajal, T., Stavropoulou, A. V., Benitez, J., Hamann, U., Rookus, M., Aalfs, C. M., de Lange, J. L., Meijers-Heijboer, H. E. J., Oosterwijk, J. C., van Asperen, C. J., Garcia, E. B. G., Hoogerbrugge, N., Jager, A., van der Luijt, R. B., Easton, D. F., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Lalloo, F., Izatt, L., Eeles, R., Adlard, J., Davidson, R., Eccles, D., Cole, T., Cook, J., Brewer, C., Tischkowitz, M., Godwin, A. K., Pathak, H., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Barjhoux, L., Leone, M., Gauthier-Villars, M., Caux-Moncoutier, V., de Pauw, A., Hardouin, A., Berthet, P., Dreyfus, H., Ferrer, S. F., Collonge-Rame, M-A., Sokolowska, J., Buys, S., Daly, M., Miron, A., Terry, M. B., Chung, W., John, E. M., Southey, M., Goldgar, D., Singer, C. F., Tea, M-K. M., Gschwantler-Kaulich, D., Fink-Retter, A., Hansen, T. V. O., Ejlertsen, B., Johannsson, O. T., Offit, K., Sarrel, K., Gaudet, M. M., Vijai, J., Robson, M., Piedmonte, M. R., Andrews, L., Cohn, D., DeMars, L. R., DiSilvestro, P., Rodriguez, G., Toland, A. E., Montagna, M., Agata, S., Imyanitov, E., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Ramus, S. J., Sucheston, L., Karlan, B. Y., Gross, J., Ganz, P. A., Beattie, M. S., Schmutzler, R. K., Wappenschmidt, B., Meindl, A., Arnold, N., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Nevanlinna, H., Aittomaki, K., Simard, J., Spurdle, A. B., Beesley, J., Chen, X., Tomlinson, G. E., Weitzel, J., Garber, J. E., Olopade, O. I., Rubinstein, W. S., Tung, N., Blum, J. L., Narod, S. A., Brummel, S., Gillen, D. L., Lindor, N., Fredericksen, Z., Pankratz, V. S., Couch, F. J., Radice, P., Peterlongo, P., Greene, M. H., Loud, J. T., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Gerdes, A-M., Thomassen, M., Jensen, U. B., Skytte, A-B., Caligo, M. A., Lee, A., Chenevix-Trench, G., Antoniou, A. C. & Neuhausen, S. L., 2012, In : Cancer Epidemiology Biomarkers & Prevention. 21, 8, p. 1362-1370

    Research output: Contribution to journalArticle

  147. 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

  148. Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia

    Dirse, V., Gineikiene, E., Zvirblis, T., Bertasiute, R., Kajsa Paulsson & Griskevicius, L., 2016, In : Leukemia & Lymphoma. 57, 11, p. 2716-2719 4 p.

    Research output: Contribution to journalArticle

  149. Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients

    Domanski, H. A., Åkerman, M., Jacob Engellau, Pelle Gustafson, Fredrik Mertens & Anders Rydholm, 2006 Jun, In : Diagnostic Cytopathology. 34, 6, p. 403-412 10 p.

    Research output: Contribution to journalArticle

  150. Core-needle biopsy performed by the cytopathologist: a technique to complement fine-needle aspiration of soft tissue and bone lesions

    Domanski, H. A., Åkerman, M., Carlén, B., Jacob Engellau, Pelle Gustafson, Jonsson, K., Fredrik Mertens & Anders Rydholm, 2005 Aug 25, In : Cancer. 105, 4, p. 229-239 11 p.

    Research output: Contribution to journalArticle

  151. Distinct cytologic features of spindle cell lipoma - A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations

    Domanski, H., Carlén, B., Jonsson, K., Fredrik Mertens & Åkerman, M., 2001, In : Cancer. 93, 6, p. 381-389

    Research output: Contribution to journalArticle

  152. Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.

    Domanski, H., Fredrik Mertens, Panagopoulos, I. & Åkerman, M., 2009, In : Cytopathology. 20, p. 304-314

    Research output: Contribution to journalArticle

  153. FNA Cytology of Soft Tissue and Bone Tumors

    Domanski, H. A. & Charles S. Walther, 2017, Karger. (Monographs in Clinical Cytology; vol. 22)

    Research output: Book/ReportBook

  154. Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein.

    Dominguez, M., Drost, M., Therkildsen, C., Rambech, E., Hans Ehrencrona, Angleys, M., Lau Hansen, T., de Wind, N., Mef Nilbert & Juel Rasmussen, L., 2014, In : Molecular Genetics & Genomic Medicine. 2, 4, p. 352-355

    Research output: Contribution to journalArticle

  155. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

    Dondorp, W., de Wert, G., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., Chitty, L. S., Fellmann, F., Forzano, F., Hall, A., Henneman, L., Howard, H. C., Lucassen, A., Ormond, K., Peterlin, B., Radojkovic, D., Rogowski, W., Soller, M., Tibben, A., Tranebjærg, L. & 2 others, van El, C. G. & Cornel, M. C., 2015, In : European Journal of Human Genetics. 23, 11, p. 1438-1450

    Research output: Contribution to journalArticle

  156. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.

    Dondorp, W., de Wert, G., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., Chitty, L. S., Fellmann, F., Forzano, F., Hall, A., Henneman, L., Howard, H. C., Lucassen, A., Ormond, K., Peterlin, B., Radojkovic, D., Rogowski, W., Soller, M., Tibben, A., Tranebjærg, L. & 2 others, van El, C. G. & Cornel, M. C., 2015, In : European Journal of Human Genetics.

    Research output: Contribution to journalArticle

  157. The utility of fluorescence in situ hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms

    Downs-Kelly, E., Goldblum, J. R., Patel, R. M., Weiss, S. W., Folpe, A. L., Fredrik Mertens, Hartke, M., Tubbs, R. R. & Skacel, M., 2008, In : American Journal of Surgical Pathology. 32, 1, p. 8-13

    Research output: Contribution to journalArticle

  158. MUC4 Is a Sensitive and Extremely Useful Marker for Sclerosing Epithelioid Fibrosarcoma: Association With FUS Gene Rearrangement.

    Doyle, L. A., Wang, W-L., Dal Cin, P., Lopez-Terrada, D., Fredrik Mertens, Lazar, A. J. F., Fletcher, C. D. M. & Hornick, J. L., 2012, In : American Journal of Surgical Pathology. 36, 10, p. 1444-1451

    Research output: Contribution to journalArticle

  159. MUC4 Is a Highly Sensitive and Specific Marker for Low-Grade Fibromyxoid Sarcoma

    Doyle, L. A., Möller, E., Fredrik Mertens & Hornick, J. L., 2011, In : Laboratory Investigation. 91, p. 12A

    Research output: Contribution to journalPublished meeting abstract

  160. Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics

    Doyle, L. A., Vivero, M., Fletcher, C. D. M., Fredrik Mertens & Hornick, J. L., 2014, In : Modern Pathology. 27, 3, p. 390-395

    Research output: Contribution to journalArticle

  161. MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma.

    Doyle, L. A., Möller, E., Cin, P. D., Fletcher, C. D. M., Fredrik Mertens & Hornick, J. L., 2011, In : American Journal of Surgical Pathology. 35, p. 733-741

    Research output: Contribution to journalArticle

  162. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

    Dunning, A. M., Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., Healey, C. S., Kar, S., Pooley, K. A., Lopez-Knowles, E., Dicks, E., Barrowdale, D., Sinnott-Armstrong, N. A., Sallari, R. C., Hillman, K. M., Kaufmann, S., Sivakumaran, H., Marjaneh, M. M., Lee, J. S., Hills, M. & 228 others, Jarosz, M., Drury, S., Canisius, S., Bolla, M. K., Dennis, J., Wang, Q., Hopper, J. L., Southey, M. C., Broeks, A., Schmidt, M. K., Lophatananon, A., Muir, K., Beckmann, M. W., Fasching, P. A., Dos Santos Silva, G., Peto, J., Sawyer, E. J., Tomlinson, I., Burwinkel, B., Marme, F., Guénel, P., Truong, T., Bojesen, S. E., Flyger, H., González-Neira, A., Perez, J. I. A., Anton-Culver, H., Eunjung, L., Arndt, V., Brenner, H., Meindl, A., Schmutzler, R. K., Brauch, H., Hamann, U., Aittomäki, K., Blomqvist, C., Ito, H., Matsuo, K., Bogdanova, N., Dörk, T., Lindblom, A., Margolin, S., Kosma, V-M., Mannermaa, A., Tseng, C-C., Wu, A. H., Lambrechts, D., Wildiers, H., Chang-Claude, J., Rudolph, A., Peterlongo, P., Radice, P., Olson, J. E., Giles, G. G., Milne, R. L., Haiman, C. A., Henderson, B. E., Goldberg, M. S., Teo, S. H., Yip, C. H., Nord, S., Borresen-Dale, A-L., Kristensen, V., Long, J., Zheng, W., Pylkäs, K., Winqvist, R., Andrulis, I. L., Knight, J. A., Devilee, P., Seynaeve, C., Figueroa, J., Sherman, M. E., Czene, K., Darabi, H., Hollestelle, A., van den Ouweland, A. M. W., Humphreys, K., Gao, Y-T., Shu, X-O., Cox, A., Cross, S. S., Blot, W., Cai, Q., Ghoussaini, M., Perkins, B. J., Shah, M., Choi, J-Y., Kang, D., Lee, S. C., Hartman, M., Kabisch, M., Torres, D., Jakubowska, A., Lubinski, J., Brennan, P., Sangrajrang, S., Ambrosone, C. B., Toland, A. E., Shen, C-Y., Wu, P-E., Orr, N., Swerdlow, A., McGuffog, L., Healey, S., Lee, A., Kapuscinski, M., John, E. M., Terry, M. B., Daly, M. B., Goldgar, D. E., Buys, S. S., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, C. M., van Rensburg, E. J., Neuhausen, S. L., Ejlertsen, B., Hansen, T. V. O., Osorio, A., Benitez, J., Rando, R., Weitzel, J. N., Bonanni, B., Peissel, B., Manoukian, S., Papi, L., Ottini, L., Konstantopoulou, I., Apostolou, P., Garber, J., Rashid, M. U., Frost, D., Izatt, L., Ellis, S., Godwin, A. K., Arnold, N., Niederacher, D., Rhiem, K., Bogdanova-Markov, N., Sagne, C., Stoppa-Lyonnet, D., Damiola, F., Sinilnikova, O. M., Mazoyer, S., Isaacs, C., Claes, K. B. M., De Leeneer, K., de la Hoya, M., Caldes, T., Nevanlinna, H., Khan, S., Mensenkamp, A. R., Hooning, M. J., Rookus, M. A., Kwong, A., Olah, E., Diez, O., Brunet, J., Pujana, M. A., Gronwald, J., Huzarski, T., Barkardottir, R. B., Laframboise, R., Soucy, P., Montagna, M., Agata, S., Teixeira, M. R., Park, S. K., Lindor, N., Couch, F. J., Tischkowitz, M., Foretova, L., Vijai, J., Offit, K., Singer, C. F., Rappaport, C., Phelan, C. M., Greene, M. H., Mai, P. L., Rennert, G., Imyanitov, E. N., Hulick, P. J., Phillips, K-A., Piedmonte, M., Mulligan, A. M., Glendon, G., Bojesen, A., Thomassen, M., Caligo, M. A., Yoon, S-Y., Friedman, E., Laitman, Y., Borg, A., von Wachenfeldt, A., Hans Ehrencrona, Rantala, J., Olopade, O. I., Ganz, P. A., Nussbaum, R. L., Gayther, S. A., Nathanson, K. L., Domchek, S. M., Arun, B. K., Mitchell, G., Karlan, B. Y., Lester, J., Maskarinec, G., Woolcott, C., Scott, C., Stone, J., Apicella, C., Tamimi, R., Luben, R., Khaw, K-T., Helland, Å., Haakensen, V., Dowsett, M., Pharoah, P. D. P., Simard, J., Hall, P., García-Closas, M., Vachon, C., Chenevix-Trench, G., Antoniou, A. C., Easton, D. F. & Edwards, S. L., 2016, In : Nature Genetics.

    Research output: Contribution to journalArticle

  163. Etisk argumentation och klinisk verklighet kan med fördel förenas.

    Eckerdal, G., Engström, I., Ulf Kristoffersson, Löfmark, R., Sallin, K., Thulesius, H. & Johnsson, L-Å., 2007, In : Läkartidningen. 104, 28, p. 2097-2098

    Research output: Contribution to journalArticle

  164. Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8

    Arne Egesten, Hagerstrand, I., Ulf Kristoffersson & Garwicz, S., 1997, In : British Journal of Haematology. 96, 2, p. 369-73

    Research output: Contribution to journalArticle

  165. Increased expression of cyclin A1 protein is associated with all-trans retinoic acid-induced apoptosis.

    Ekberg, J., Brunhoff, C., Marcus Järås, Xiaolong Fan, Landberg, G. & Persson, J. L., 2006, In : International Journal of Biochemistry & Cell Biology. 38, 8, p. 1330-1339

    Research output: Contribution to journalArticle

  166. Proteoglycan production in disomic and trisomy 7-carrying human synovial cells.

    Eklund, E., Broberg, K., Gunilla Westergren-Thorsson, Bjärdahlen, A., Hedlund, M. & Anders Malmström, 2002, In : Matrix Biology. 21, 4, p. 325-335

    Research output: Contribution to journalArticle

  167. A del(X)(p11) carrying SRY sequences in an infant with ambiguous genitalia

    Ellaithi, M., David Gisselsson Nord, Nilsson, T., Abd El-Fatah, S., Ali, T., Elagib, A., Ibrahim, M. E. & Fadl-Elmula, I., 2006, In : BMC Pediatrics. 6, 11

    Research output: Contribution to journalArticle

  168. Female genital mutilation of a karyotypic male presenting as a female with delayed puberty

    Ellaithi, M., Nilsson, T., David Gisselsson Nord, Elagib, A., Eltigani, H. & Fadl-Elmula, I., 2006, In : BMC Women's Health. 6, 6

    Research output: Contribution to journalArticle

  169. A case of Cornelia de Lange syndrome from Sudan

    Ellaithi, M., David Gisselsson Nord, Nilsson, T., Elagib, A., Fadl-Elmula, I. & Abdelgadir, M., 2007, In : BMC Pediatrics. 7, 6.

    Research output: Contribution to journalArticle

  170. Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.

    Elmula, I., Kytola, S., Leithy, M., Abdel-Hameed, M., Nils Mandahl, Elagib, A., Ibrahim, M., Larsson, C. & Heim, S., 2002, In : BMC Cancer. 2:5

    Research output: Contribution to journalArticle

  171. Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

    Engel, C., Versmold, B., Wappenschmidt, B., Simard, J., Easton, D. F., Peock, S., Cook, M., Oliver, C., Frost, D., Mayes, R., Evans, D. G., Eeles, R., Paterson, J., Brewer, C., McGuffog, L., Antoniou, A. C., Stoppa-Lyonnet, D., Sinilnikova, O. M., Barjhoux, L., Frenay, M. & 48 others, Michel, C., Leroux, D., Dreyfus, H., Toulas, C., Gladieff, L., Uhrhammer, N., Bignon, Y-J., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Preisler-Adams, S., Kast, K., Deissler, H., Sutter, C., Gadzicki, D., Chenevix-Trench, G., Spurdle, A. B., Chen, X., Beesley, J., Håkan Olsson, Ulf Kristoffersson, Hans Ehrencrona, Liljegren, A., van der Luijt, R. B., van Os, T. A., van Leeuwen, F. E., Domchek, S. M., Rebbeck, T. R., Nathanson, K. L., Osorio, A., Ramón Y Cajal, T., Konstantopoulou, I., Benítez, J., Friedman, E., Kaufman, B., Laitman, Y., Mai, P. L., Greene, M. H., Nevanlinna, H., Aittomäki, K., Szabo, C. I., Caldes, T., Couch, F. J., Andrulis, I. L., Godwin, A. K., Hamann, U. & Schmutzler, R. K., 2010, In : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 19, p. 2859-2868

    Research output: Contribution to journalArticle

  172. Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy

    Engleson, J., Soller, M., Panagopoulos, I., Dahlen, A., Michael Dictor & Mats Jerkeman, 2006, In : BMC Cancer. 6

    Research output: Contribution to journalArticle

  173. Agonistic targeting of TLR1/TLR2 induces p38 MAPK-dependent apoptosis and NFκB-dependent differentiation of AML cells

    Eriksson, M., Pablo Peña-Martínez, Ramprasad Ramakrishnan, Chapellier, M., Högberg, C., Glowacki, G., Christina Orsmark-Pietras, Velasco-Hernández, T., Lazarević, V. L., Gunnar Juliusson, Cammenga, J., Mulloy, J. C., Johan Richter, Thoas Fioretos, Ebert, B. L. & Marcus Järås, 2017 Oct 24, In : Blood Advances. 1, 23, p. 2046-2057 12 p.

    Research output: Contribution to journalArticle

  174. Identification and characterization of candidate therapeutic targets in acute myeloid leukemia

    Eriksson, M., 2018, Lund: Lund University: Faculty of Medicine. 69 p.

    Research output: ThesisDoctoral Thesis (compilation)

  175. Study of ATP-release from acoustically levitated eryhrocytes

    Mikael Evander, Mileros, K., Högberg, C., David Erlinge, Monica Almqvist, Thomas Laurell & Johan Nilsson, 2007, In : Nano2Life Autumn Meeting. 1, p. 24-24

    Research output: Contribution to journalPublished meeting abstract

  176. Study of ATP-release from acoustically levitated eryhrocytes

    Mikael Evander, Mileros, K., Högberg, C., David Erlinge, Monica Almqvist, Thomas Laurell & Johan Nilsson, 2007, The proceedings of micro total analysis systems 2007. Viovy, J-L., Tabeling, P., Descroix, S. & Malaquin, L. (eds.). Chemical and Biological Microsystems Society, Vol. 2. p. 1372-1374 3 p.

    Research output: Chapter in Book/Report/Conference proceedingPaper in conference proceeding

  177. The genomic landscape of core-binding factor acute myeloid leukemias

    Faber, Z. J., Chen, X., Gedman, A. L., Boggs, K., Cheng, J., Ma, J., Radtke, I., Chao, J-R., Walsh, M. P., Song, G., Andersson, A. K., Dang, J., Dong, L., Liu, Y., Huether, R., Cai, Z., Mulder, H., Wu, G., Edmonson, M., Rusch, M. & 29 others, Qu, C., Li, Y., Vadodaria, B., Wang, J., Hedlund, E., Cao, X., Yergeau, D., Nakitandwe, J., Pounds, S. B., Shurtleff, S., Fulton, R. S., Fulton, L. L., Easton, J., Parganas, E., Pui, C-H., Rubnitz, J. E., Ding, L., Mardis, E. R., Wilson, R. K., Gruber, T. A., Mullighan, C. G., Schlenk, R. F., Paschka, P., Döhner, K., Döhner, H., Bullinger, L., Zhang, J., Klco, J. M. & Downing, J. R., 2016 Oct 31, In : Nature Genetics. 48, p. 1551–1556 6 p.

    Research output: Contribution to journalLetter

  178. Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and fish analysis

    Fadl-Elmula, I., Kytola, S., Pan, Y., Lui, W-O., Derienzo, G., Forsberg, L., Nils Mandahl, Gorunova, L., Bergerheim, U. S. R., Heim, S. & Larsson, C., 2001, In : International Journal of Cancer. 92, 6, p. 824-831

    Research output: Contribution to journalArticle

  179. Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder

    Fadl-Elmula, I., Gorunova, L., Nils Mandahl & Heim, S., 2003, In : Cancer Genetics and Cytogenetics. 143, 2, p. 169-171

    Research output: Contribution to journalArticle

  180. Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations

    Fergelot, P., Van Belzen, M., Van Gils, J., Afenjar, A., Armour, C. M., Arveiler, B., Beets, L., Burglen, L., Busa, T., Collet, M., Deforges, J., de Vries, B. B. A., Dominguez Garrido, E., Dorison, N., Dupont, J., Francannet, C., Garciá-Minaúr, S., Gabau Vila, E., Gebre-Medhin, S., Gener Querol, B. & 33 others, Geneviève, D., Gérard, M., Gervasini, C. G., Goldenberg, A., Josifova, D., Lachlan, K., Maas, S., Maranda, B., Moilanen, J. S., Nordgren, A., Parent, P., Rankin, J., Reardon, W., Rio, M., Roume, J., Shaw, A., Smigiel, R., Sojo, A., Solomon, B., Stembalska, A., Stumpel, C., Suarez, F., Terhal, P., Thomas, S., Touraine, R., Verloes, A., Vincent-Delorme, C., Wincent, J., Peters, D. J. M., Bartsch, O., Larizza, L., Lacombe, D. & Hennekam, R. C., 2016 Dec 1, In : American Journal of Medical Genetics, Part A. 170, 12, p. 3069-3082 14 p.

    Research output: Contribution to journalArticle

  181. Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma

    Fernebro, J., Francis, P., Patrik Edén, Åke Borg, Panagopoulos, I., Fredrik Mertens, Johan Vallon-Christersson, Åkerman, M., Anders Rydholm, Bauer, H., Nils Mandahl & Mef Nilbert, 2006, In : International Journal of Cancer. 118, 5, p. 1165-1172

    Research output: Contribution to journalArticle

  182. Novel Mutation in the KCNJ2 Gene Is Associated with a Malignant Arrhythmic Phenotype of Andersen-Tawil Syndrome.

    Eva Fernlund, Lundin, C., Hertervig, E., Kongstad Rasmussen, O., Alders, M. & Pyotr Platonov, 2013, In : Annals of Noninvasive Electrocardiology. 18, 5, p. 471-478

    Research output: Contribution to journalArticle

  183. Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL

    Thoas Fioretos, Panagopoulos, I., Lassen, C., Swedin, A., Billström, R., Isaksson, M., Strömbeck, B., Olofsson, T., Felix Mitelman & Bertil Johansson, 2001, In : Genes, Chromosomes and Cancer. 32, 4, p. 302-310

    Research output: Contribution to journalArticle

  184. No evidence for genomic imprinting of the human BCR gene

    Thoas Fioretos, Heisterkamp, N. & Groffen, J., 1994, In : Blood. 83, 12, p. 3441-3444

    Research output: Contribution to journalArticle

  185. Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder

    Thoas Fioretos, Panagopoulos, I., Lassen, C., Swedin, A., Billstrom, R., Isaksson, M., Strombeck, B., Olofsson, T., Mitelman, F. & Johansson, B., 2001, In : Blood. 98, 11, p. 558A

    Research output: Contribution to journalPublished meeting abstract

  186. Standpoint on imprinting of BCR and ABL

    Thoas Fioretos, Heisterkamp, N. & Groffen, J., 1995, In : Leukemia. 9, 4, p. 743-744

    Research output: Contribution to journalArticle

  187. Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia

    Thoas Fioretos, Nilsson, P-G., Åman, P., Heim, S., Ulf Kristoffersson, Malm, C., Simonsson, B., Ingemar Turesson & Felix Mitelman, 1993, In : Leukemia. 7, 8, p. 1225-1231

    Research output: Contribution to journalArticle

  188. Regional localization and developmental expression of the BCR gene in rodent brain

    Thoas Fioretos, Voncken, J. W., Baram, T. Z., Kamme, F., Groffen, J. & Heisterkamp, N., 1995, In : Cellular & molecular biology research. 41, 2, p. 97-102

    Research output: Contribution to journalArticle

  189. Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia.

    Thoas Fioretos, Heim, S., Garwicz, S., Ludvigsson, J. & Felix Mitelman, 1992, In : Leukemia. 6, 7, p. 723-725

    Research output: Contribution to journalArticle

  190. Molekylär medicin: Molekylärgenetisk metodik avslöjar mekanismerna bakom tumörutveckling

    Thoas Fioretos & Åman, P., 1991, In : Läkartidningen. 88, 32-33, p. 2597-2602

    Research output: Contribution to journalArticle

  191. Molecular Genetic Studies of Ph-positive Leukemias and the BCR and ABL Genes

    Thoas Fioretos, 1996, Department of Clinical Genetics, Lund University. 60 p.

    Research output: ThesisDoctoral Thesis (compilation)

  192. Mechanisms underlying neoplasia-associated genomic rearrangements

    Thoas Fioretos, 2006, Genomic disorders: The Genomic basis of disease. Lupski, J. R. & Stankiewicz, P. (eds.). Humana Press, p. 327-337

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

  193. Chronic myeloid leukemia

    Thoas Fioretos, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (eds.). 4 ed. Wiley-Blackwell, p. 153-174 22 p.

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

  194. Unrelated clones in AML/MDS - characterisation and prognostic relevance

    Fischer, S., Haase, D., Haferlach, C., Bardi, G., Slovak, M., Bertil Johansson, Ohyashiki, K., Sole, F., Ecclache, V., Greenberg, P., LeBeau, M. M., Bennett, J., Prescher, G., Germing, U. & Schanz, J., 2010, In : Onkologie. 33, p. 37-37

    Research output: Contribution to journalPublished meeting abstract

  195. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone

    Fletcher, C. D. M. (ed.), Unni, K. (ed.) & Fredrik Mertens (ed.), 2002, IARC Press. 432 p.

    Research output: Book/ReportAnthology (editor)

  196. Prognostic Implications of Mutations in NOTCH1 and FBXW7 in Childhood T-ALL Treated According to the NOPHO ALL-1992 and ALL-2000 Protocols

    Fogelstrand, L., Staffas, A., Wasslavik, C., Sjogren, H., Soderhall, S., Frost, B-M., Forestier, E., Degerman, S., Behrendtz, M., Heldrup, J., Karrman, K., Bertil Johansson, Heyman, M., Abrahamsson, J. & Palmqvist, L., 2014, In : Pediatric Blood & Cancer. 61, 3, p. 424-430

    Research output: Contribution to journalArticle

  197. 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

  198. 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

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