Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. 13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking

    Minjun Yang, Safavi, S., Eleanor L Woodward, Duployez, N., Olsson-arvidsson, L., Jonas Ungerbäck, Mikael Sigvardsson, Zaliova, M., Zuna, J., Thoas Fioretos, Bertil Johansson, Karolin H Nord & Kajsa Paulsson, 2020 maj 8, I : Blood.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha

    Johansson, B., Thoas Fioretos, Billstrom, R. & Felix Mitelman, 1996, I : Leukemia. 10, 7, s. 1134-1138

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. ABCB1 single-nucleotide variants and survival in patients with glioblastoma treated with radiotherapy concomitant with temozolomide

    Malmström, A., Łysiak, M., Åkesson, L., Jakobsen, I., Mudaisi, M., Milos, P., Hallbeck, M., Fomichov, V., Broholm, H., Grunnet, K., Poulsen, H. S., Bratthäll, C., Strandeus, M., Papagiannopoulou, A., Stenmark-Askmalm, M., Green, H. & Söderkvist, P., 2019 okt 17, I : Pharmacogenomics Journal.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. 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, I : American Journal of Surgical Pathology. 37, 4, s. 613-616

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Aberrant epigenetic regulation in clear cell sarcoma of the kidney featuring distinct DNA hypermethylation and EZH2 overexpression.

    Jenny Karlsson, Anders Valind, Jansson, C., O'Sullivan, M. J., Linda Holmquist Mengelbier & David Gisselsson Nord, 2016 mar, I : Oncotarget. 7, 10, s. 11127-36

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. 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, I : Modern Pathology. 32, 3, s. 423-434

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Abnormal nuclear shape in solid tumors reflects mitotic instability

    D Gisselsson, J Björk, M Höglund, F Mertens, Dal Cin, P., Akerman, M. & N Mandahl, 2001 jan, I : American Journal of Pathology. 158, 1, s. 199-206 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

    Felix Mitelman, Fredrik Mertens & Bertil Johansson, 1997 apr 1, I : Nature Genetics. 15, 4, s. 417-474 58 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Absence of Epstein-Barr and Cytomegalovirus Infection in Neuroblastoma Cells by Standard Detection Methodologies.

    Sehic, D., Ola Forslund, Emma Sandén, Linda Holmquist Mengelbier, Jenny Karlsson, Bzhalava, D., Ekström, J., Warenholt, J., Anna Darabi, Dillner, J., Ingrid Øra & David Gisselsson Nord, 2013, I : Pediatric Blood & Cancer. 60, 9, s. E91-E93

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. 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 andra, Chagin, A. S., Nishimura, G., Aschenbrenner, D., Alkuraya, F. S., Laurence, A., Cormier-Daire, V. & Uhlig, H. H., 2020, I : The Journal of experimental medicine. 217, 3, e20191306.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. 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, I : Cancer Genetics and Cytogenetics. 156, 1, s. 74-76 3 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology

    Leif Salford, Peter Siesjö, Gunnar Skagerberg, Edward Visse, Anna Darabi, Åsa Lilja, Blennow, C., Strömblad, S., Ask, E., Anna Rydelius, Bertil R Persson, Baureus Koch, C., Elisabet Englund, Larsson, E-M., Nils Mandahl & Widegren, B., 2004, I : Neuro-Oncology. 6, 4, s. 307-400

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. A case of Cornelia de Lange syndrome from Sudan

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences

    D Gisselsson, M Höglund, O'Brien, K. P., Dumanski, J. P., F Mertens & N Mandahl, 1998 nov 27, I : Cancer Letters. 133, 2, s. 129-34 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. A certified plasmid reference material for the standardisation of BCR-ABL1 mRNA quantification by real time quantitative PCR.

    White, H., Deprez, L., Corbisier, P., Hall, V., Lin, F., Mazoua, S., Trapmann, S., Aggerholm, A., Andrikovics, H., Akiki, S., Barbany, G., Boeckx, N., Bench, A., Catherwood, M., Cayuela, J-M., Chudleigh, S., Clench, T., Colomer, D., Daraio, F., Dulucq, S. & 51 andra, Farrugia, J., Fletcher, L., Foroni, L., Ganderton, R., Gerrard, G., Gineikienė, E., Hayette, S., El Housni, H., Izzo, B., Jansson, M., Johnels, P., Jurcek, T., Kairisto, V., Kizilors, A., Kim, D-W., Lange, T., Lion, T., Polakova, K. M., Martinelli, G., McCarron, S., Merle, P. A., Milner, B., Mitterbauer-Hohendanner, G., Nagar, M., Nickless, G., Nomdedéu, J., Nymoen, D. A., Leibundgut, E. O., Ozbek, U., Pajič, T., Pfeifer, H., Preudhomme, C., Raudsepp, K., Romeo, G., Sacha, T., Talmaci, R., Touloumenidou, T., Van der Velden, V. H. J., Waits, P., Wang, L., Wilkinson, E., Wilson, G., Wren, D., Zadro, R., Ziermann, J., Zoi, K., Müller, M. C., Hochhaus, A., Schimmel, H., Cross, N. C. P. & Emons, H., 2015, I : Leukemia. 29, 2, s. 369-376

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. 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, I : American Journal of Pathology. 164, 5, s. 1645-1653

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. Acute lymphoblastic leukemia

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

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  19. Acute myeloid leukemia

    Bertil Johansson & Harrison, C. J., 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (red.). 4th uppl. Wiley-Blackwell, s. 62-125 64 s.

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  20. 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, I : American Journal of Hematology. 71, 1, s. 15-19

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. Acute Traumatic Brain Injury Mortality in the elderly.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. 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, I : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 36, 7, s. 936-938

    Forskningsoutput: TidskriftsbidragLetter

  24. 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, I : BMC Pediatrics. 6, 11

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Volckmar, A. L., Sültmann, H., Riediger, A., Thoas Fioretos, Schirmacher, P., Endris, V., Stenzinger, A. & Dietz, S., 2018 mar 1, I : Genes Chromosomes and Cancer. 57, 3, s. 123-139 17 s.

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  26. 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 andra, 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, I : Human Molecular Genetics. 11, 25, s. 3221-3229

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. A gene fusion network in human neoplasia.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. A glioma classification scheme based on coexpression modules of EGFR and PDGFRA

    Sun, Y., Zhang, W., Chen, D., Lv, Y., Zheng, J., Henrik Lilljebjörn, Ran, L., Bao, Z., Soneson, C., Hans Olov Sjögren, Leif G. Salford, Jianguang Ji, Frenc, P. J., Thoas Fioretos, Jiang, T. & Xiaolong Fan, 2014 mar 4, I : Proceedings of the National Academy of Sciences of the United States of America. 111, 9, s. 3538-3543 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. 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 okt 24, I : Blood Advances. 1, 23, s. 2046-2057 12 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families

    von Wachenfeldt, A., Lindblom, A., Gronberg, H., Einbeigi, Z., Rosenquist, R., Gardman, C., Iselius, L., Henriksson, K., Niklas Loman, Ulf Kristoffersson, Håkan Olsson & Johansson, O., 2007, I : Hereditary Cancer in Clinical Practice. 5, 1, s. 17-24

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  31. A large deletion identified in a Swedish family with type 1 VWD

    Johansson, A. M., Lanke, E., Torbjörn Säll, Lethagen, S. & Halldén, C., 2011, I : Thrombosis and Haemostasis. 105, 4, s. 733-734

    Forskningsoutput: TidskriftsbidragLetter

  32. Alterations of the fragile histidine triad gene, FHIT, and its encoded products contribute to testicular germ cell tumorigenesis

    Kraggerud, SM., Åman, P., Holm, R., Stenwig, AE., Fossa, SD., Nesland, JM. & Lothe, RA., 2002, I : Cancer Research. 62, 2, s. 512-517

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  33. Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas

    Tord Jonson, Albrechtsson, E., Axelson, J., Heidenblad, M., Gorunova, L., Bertil Johansson & Mattias Höglund, 2001, I : International Journal of Oncology. 19, 1, s. 71-81

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  34. Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.

    Lundberg, G., Sehic, D., Länsberg, J-K., Ingrid Øra, Attila Frigyesi, Castel, V., Navarro, S., Piqueras, M., Martinsson, T., Noguera, R. & David Gisselsson Nord, 2011, I : Genes, Chromosomes and Cancer. 50, 4, s. 250-262

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. A model for karyotypic evolution in testicular germ cell tumors.

    Attila Frigyesi, David Gisselsson Nord, Hansen, G. B., Soller, M., Felix Mitelman & Mattias Höglund, 2004, I : Genes, Chromosomes and Cancer. 40, 3, s. 172-178

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. 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, I : Molecular Carcinogenesis. 43, 3, s. 165-174

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  37. Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma

    D Gisselsson, Andreasson, P., Meis-Kindblom, J. M., Kindblom, L. G., F Mertens & N Mandahl, 1998 dec, I : Cancer Genetics and Cytogenetics. 107, 2, s. 102-106 5 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  38. 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, I : International Journal of Cancer. 109, 3, s. 363-369 7 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?

    Micale, L., Augello, B., Daniele, G., Macchia, G., L'Abbate, A., Muehlematter, D., Vandenberghe, P., Bertil Johansson, Cabrol, C., Sole, F., Dastugue, N., Slovak, M. L., Lillington, D., Raynaud, S., Lafage, M., Nacheva, E. D., Merla, G. & Storlazzi, C. T., 2011, I : Blood Cells, Molecules & Diseases. 47, 4, s. 259-261

    Forskningsoutput: TidskriftsbidragLetter

  40. 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, I : Journal of Cell Biology. 164, 4, s. 509-514

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  41. 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, I : Journal of Oral Pathology & Medicine.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  42. 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, I : Molecular and Cellular Biology. 33, 20, s. 4030-4040

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  43. 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, I : Cancer Genetics and Cytogenetics. 131, 1, s. 19-24 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  46. Aneuploidy in cancer: Sudden or sequential?

    David Gisselsson Nord, 2011, I : Cell Cycle. 10, 3, s. 359-361

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  47. A New Method for Endoscopic Sampling of Submucosal Tissue in the Gastrointestinal Tract: A Comparison of the Biopsy Forceps and a New Drill Instrument

    Charles Walther, Martin Jeremiasen, Rissler, P., Jan L M Johansson, Larsson, M. S. & Walther, B. S. C. S., 2016 dec 1, I : Surgical Innovation. 23, 6, s. 572-580 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  48. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.

    Langbehn, D., Brinkman, R., Falush, D., Paulsen, J., Hayden, M., Landberg, I., Ulf Kristoffersson & International Huntington's Disease, C. G., 2004, I : Clinical Genetics. 65, 4, s. 267-277

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  50. 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 andra, 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, I : European Journal of Human Genetics. 12, 12, s. 993-1000

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  51. 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, I : Genome Biology. 9, 1, R13.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  52. 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 andra, 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, I : Cancer Epidemiology Biomarkers & Prevention. 21, 8, s. 1362-1370

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  53. A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42

    Kajsa Paulsson, Békássy, A., Olofsson, T., Felix Mitelman, Bertil Johansson & Panagopoulos, I., 2006, I : Leukemia. 20, 2, s. 224-229

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  54. A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1

    Storlazzi, C., Anelli, L., Albano, F., Zagaria, A., Ventura, M., Rocchi, M., Panagopoulos, I., Pannunzio, A., Ottaviani, E., Liso, V. & Specchia, G., 2003, I : American Journal of Human Genetics. 73, 5, s. 223

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  55. A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1

    Storlazzi, CT., Anelli, L., Albano, F., Zagaria, A., Ventura, M., Rocchi, M., Panagopoulos, I., Pannunzio, A., Ottaviani, E., Liso, V. & Specchia, G., 2004, I : Annals of Hematology. 83, 2, s. 78-83

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  56. A novel FISH assay for SS18-SSX fusion type in synovial sarcoma

    Surace, C., Panagopoulos, I., Pålsson, E., Rocchi, M., Nils Mandahl & Fredrik Mertens, 2004 sep, I : Laboratory Investigation. 84, 9, s. 1185-1192 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  57. A novel fusion 5 ' AFF3/3 ' BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma

    Impera, L., Albano, F., Lo Cunsolo, C., Funes, S., Iuzzolino, P., Laveder, F., Panagopoulos, I., Rocchi, M. & Storlazzi, C. T., 2008, I : Oncogene. 27, 47, s. 6187-6190

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  58. A Novel Fusion 5'Aff3/3'Bcl2 Originated From A T(2;18)(Q11.2-Q21.33) Translocation In Follicular Lymphoma

    Impera, L., Albano, F., Lo Cunsolo, C., Funes, S., Iuzzolino, P., Laveder, F., Panagopoulos, I., Rocchi, M. & Storlazzi, C. T., 2008, I : Haematologica-The Hematology Journal. 93, s. S27-S27

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  59. A novel fusion gene, SS18L1/SSX1, in synovial sarcoma

    Storlazzi, T., Fredrik Mertens, Nils Mandahl, David Gisselsson, Isaksson, M., Pelle Gustafson, Domanski, H. A. & Panagopoulos, I., 2003 jun, I : Genes, Chromosomes and Cancer. 37, 2, s. 195-200 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  60. A novel human in vitro papillomavirus type 16 positive tonsil cancer cell line with high sensitivity to radiation and cisplatin

    Ola Forslund, Sugiyama, N., Chengjun Wu, Naveen Ravi, Jin, Y., Swoboda, S., Andersson, F., Bzhalava, D., Hultin, E., Kajsa Paulsson, Dillner, J., Stefan Schwartz, Johan Wennerberg & Lars Ekblad, 2019 mar 25, I : BMC Cancer. 19, 1, 265.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  61. A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.

    Charles Walther, Tayebwa, J., Henrik Lilljebjörn, Magnusson, L., Nilsson, J., Fredrik Vult von Steyern, Ingrid Øra, Domanski, H., Thoas Fioretos, Karolin Hansén Nord, Fletcher, C. D. & Fredrik Mertens, 2014, I : Journal of Pathology. 232, 5, s. 534-540

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  62. 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, I : Proceedings of the National Academy of Sciences. 112, 34, s. 10786-10791

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  63. 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, I : Haematologica. 91, 5, s. 667-670

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  64. An update of a classical textbook.

    Ulf Kristoffersson, 2016, I : European Journal of Human Genetics. 24, 3, s. 467

    Forskningsoutput: TidskriftsbidragRecension av bok/film/utställning etc.

  65. 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, I : Genes, Chromosomes and Cancer. 47, s. 521-529

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  66. 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, I : Genes, Chromosomes and Cancer. 54, 5, s. 326-333

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  68. Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?

    Håkan Lövkvist, Marketa Sjögren, Höglund, P., Gunnar Engström, Jern, C., Olsson, S., Smith, J. G., Bo Hedblad, Gunnar Andsberg, Hossein Delavaran, Jood, K., Ulf Kristoffersson, Bo Norrving, Olle Melander & Arne Lindgren, 2013, I : European Journal of Neurology. 20, 9, s. 1284-1291

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  69. 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, I : Occupational and Environmental Medicine. 58, 11, s. 722-727

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  70. A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families 11 Medical and Health Sciences 1112 Oncology and Carcinogenesis 11 Medical and Health Sciences 1117 Public Health and Health Services

    Karimi, M., Von Salomé, J., Aravidis, C., Silander, G., Askmalm, M. S., Henriksson, I., Samuel Gebre-Medhin, Frödin, J. E., Björck, E., Lagerstedt-Robinson, K., Lindblom, A. & Tham, E., 2018, I : Hereditary Cancer in Clinical Practice. 16, 1, 16.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  73. A short history of chromosome rearrangements and gene fusions in cancer

    Felix Mitelman, 2015, Chromosomal Translocations and Genome Rearrangements in Cancer. Rowley, J. D., Le Beau, M. M. & Rabbitts, T. H. (red.). Springer International Publishing, s. 3-11 9 s.

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  74. A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender

    Mauritzson, N., Johansson, B., Maria Albin, Billstrom, R., Ahlgren, T., Mikoczy, Z., Nilsson, P-G., Hagmar, L. & Felix Mitelman, 1999, I : European Journal of Haematology. 62, 2, s. 95-102

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  75. 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, I : Genetics in Medicine. 10, 2, s. 99-106

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  76. Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray

    Lovf, M., Thomassen, G. O. S., Fredrik Mertens, Cerveira, N., Teixeira, M. R., Lothe, R. A. & Skotheim, R. I., 2013, I : PLoS ONE. 8, 8, e70649.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  77. 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, I : Genes, Chromosomes and Cancer. 46, 6, s. 594-606 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  78. 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 andra, 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, I : JAMA: The Journal of the American Medical Association. 307, 4, s. 382-390

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  79. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

    Patel, V. L., Åke Borg, Hans Ehrencrona, Rebbeck, T. R., EMBRACE Collaborators & GEMO Study Collaborators, 2020, I : Cancer Research. 80, 3, s. 624-638 15 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  80. 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 andra, 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, I : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 19, s. 2859-2868

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  81. Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

    Rebbeck, T. R., Mitra, N., Wan, F., Sinilnikova, O. M., Healey, S., McGuffog, L., Mazoyer, S., Chenevix-Trench, G., Easton, D. F., Antoniou, A. C., Nathanson, K. L., Laitman, Y., Kushnir, A., Paluch-Shimon, S., Berger, R., Zidan, J., Friedman, E., Ehrencrona, H., Stenmark-Askmalm, M., Einbeigi, Z. & 238 andra, Loman, N., Harbst, K., Rantala, J., Melin, B., Huo, D., Olopade, O. I., Seldon, J., Ganz, P. A., Nussbaum, R. L., Chan, S. B., Odunsi, K., Gayther, S. A., Domchek, S. M., Arun, B. K., Lu, K. H., Mitchell, G., Karlan, B. Y., Walsh, C., Lester, J., Godwin, A. K., Pathak, H., Ross, E., Daly, M. B., Whittemore, A. S., John, E. M., Miron, A., Terry, M. B., Chung, W. K., Goldgar, D. E., Buys, S. S., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, C. M., van Rensburg, E. J., Steele, L., Neuhausen, S. L., Ding, Y. C., Ejlertsen, B., Gerdes, A-M., Hansen, T. V. O., Ramón y Cajal, T., Osorio, A., Benitez, J., Godino, J., Tejada, M-I., Duran, M., Weitzel, J. N., Bobolis, K. A., Sand, S. R., Fontaine, A., Savarese, A., Pasini, B., Peissel, B., Bonanni, B., Zaffaroni, D., Vignolo-Lutati, F., Scuvera, G., Giannini, G., Bernard, L., Genuardi, M., Radice, P., Dolcetti, R., Manoukian, S., Pensotti, V., Gismondi, V., Yannoukakos, D., Fostira, F., Garber, J., Torres, D., Rashid, M. U., Hamann, U., Peock, S., Frost, D., Platte, R., Evans, D. G., Eeles, R., Davidson, R., Eccles, D., Cole, T., Cook, J., Brewer, C., Hodgson, S., Morrison, P. J., Walker, L., Porteous, M. E., Kennedy, M. J., Izatt, L., Adlard, J., Donaldson, A., Ellis, S., Sharma, P., Schmutzler, R. K., Wappenschmidt, B., Becker, A., Rhiem, K., Hahnen, E., Engel, C., Meindl, A., Engert, S., Ditsch, N., Arnold, N., Plendl, H. J., Mundhenke, C., Niederacher, D., Fleisch, M., Sutter, C., Bartram, C. R., Dikow, N., Wang-Gohrke, S., Gadzicki, D., Steinemann, D., Kast, K., Beer, M., Varon-Mateeva, R., Gehrig, A., Weber, B. H., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Houdayer, C., Belotti, M., Gauthier-Villars, M., Damiola, F., Boutry-Kryza, N., Lasset, C., Sobol, H., Peyrat, J-P., Muller, D., Fricker, J-P., Collonge-Rame, M-A., Mortemousque, I., Nogues, C., Rouleau, E., Isaacs, C., De Paepe, A., Poppe, B., Claes, K., De Leeneer, K., Piedmonte, M., Rodriguez, G., Wakely, K., Boggess, J., Blank, S. V., Basil, J., Azodi, M., Phillips, K-A., Caldes, T., de la Hoya, M., Romero, A., Nevanlinna, H., Aittomäki, K., van der Hout, A. H., Hogervorst, F. B. L., Verhoef, S., Collée, J. M., Seynaeve, C., Oosterwijk, J. C., Gille, J. J. P., Wijnen, J. T., Garcia, E. B. G., Kets, C. M., Ausems, M. G. E. M., Aalfs, C. M., Devilee, P., Mensenkamp, A. R., Kwong, A., Olah, E., Papp, J., Diez, O., Lazaro, C., Darder, E., Blanco, I., Salinas, M., Jakubowska, A., Lubinski, J., Gronwald, J., Jaworska-Bieniek, K., Durda, K., Sukiennicki, G., Huzarski, T., Byrski, T., Cybulski, C., Toloczko-Grabarek, A., Złowocka-Perłowska, E., Menkiszak, J., Arason, A., Barkardottir, R. B., Simard, J., Laframboise, R., Montagna, M., Agata, S., Alducci, E., Peixoto, A., Teixeira, M. R., Spurdle, A. B., Lee, M. H., Park, S. K., Kim, S-W., Friebel, T. M., Couch, F. J., Lindor, N. M., Pankratz, V. S., Guidugli, L., Wang, X., Tischkowitz, M., Foretova, L., Vijai, J., Offit, K., Robson, M., Rau-Murthy, R., Kauff, N., Fink-Retter, A., Singer, C. F., Rappaport, C., Gschwantler-Kaulich, D., Pfeiler, G., Tea, M-K., Berger, A., Greene, M. H., Mai, P. L., Imyanitov, E. N., Toland, A. E., Senter, L., Bojesen, A., Pedersen, I. S., Skytte, A-B., Sunde, L., Thomassen, M., Moeller, S. T., Kruse, T. A., Jensen, U. B., Caligo, M. A., Aretini, P., Teo, S-H., Selkirk, C. G., Hulick, P. J. & Andrulis, I., 2015, I : JAMA: The Journal of the American Medical Association. 313, 13, s. 1347-1361

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  82. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    Kuchenbaecker, K. B., Niklas Loman, Åke Borg, Hans Ehrencrona, Antoniou, A. C., Håkan Olsson, Helena Jernström, Henriksson, K., Katja Harbst, Soller, M., Ulf Kristoffersson & EMBRACE Study, 2014 dec 31, I : Breast Cancer Research. 16, 6, s. 1-27 3416.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  83. A stroke gene panel for whole-exome sequencing

    Andreea Ilinca, Sofie Samuelsson, Paul Piccinelli, Soller, M., Ulf Kristoffersson & Arne G. Lindgren, 2019, I : European Journal of Human Genetics. 27, 2, s. 317-324

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  84. 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.

    Forskningsoutput: Bidrag till övrig tidskrift/dags- eller nyhetstidningDagstidnings-/nyhetsartikel

  85. Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.

    EMIL YGLAND, Taroni, F., Gellera, C., Caldarazzo, S., Duno, M., Soller, M. & Andreas Puschmann, 2014, I : Parkinsonism & Related Disorders. 20, 8, s. 919-923

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Nilsson, M. A., Domanski, H., Fredrik Mertens & Nils Mandahl, 2005 apr, I : Oncology Reports. 13, 4, s. 649-652 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  87. Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.

    Dykes, J., Lindmark, A., Lenhoff, S., Winqvist, I., Bertil Johansson, Olofsson, T. & Martin L Olsson, 2004, I : Bone Marrow Transplantation. 33, 5, s. 559-563

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  88. Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?

    Wictorin, K., Brådvik, B., Nilsson, K., Soller, M., Danielle van Westen, Bynke, G., Bauer, P., Schöls, L. & Andreas Puschmann, 2014, I : Parkinsonism & Related Disorders. 20, 7, s. 748-754

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  89. Balanced and Unbalanced Rearrangement of Chromosome Arm 6q in Chondromyxoid Fibroma (CMF): Delineation of Breakpoints and Analysis of Candidate Target Genes

    Romeo, S., Duim, R. A. J., Fredrik Mertens, De Jong, D., Dal Cin, P., Debiec-Rychter, M., Sciot, R., Rosenberg, A., Szuhai, K. & Hogendoorn, P. C. W., 2009, I : Laboratory Investigation. 89, S1, s. 21A-21A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  90. B-cell precursor t(8;14)(q11;q32)-positive acute lymphoblastic leukemia in children is strongly associated with Down syndrome or with a concomitant Philadelphia chromosome.

    Lundin, C., Heldrup, J., Ahlgren, T., Olofsson, T. & Bertil Johansson, 2009, I : European Journal of Haematology. 82, 1, s. 46-53

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  91. 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, I : Genes, Chromosomes and Cancer. 20, 3, s. 299-304

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  92. 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 andra, Stuhrman, M. & Cuppens, H., 2010, I : Journal of Cystic Fibrosis. 9, 3, s. 165-178

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  93. 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, I : PLoS ONE. 8, 4, e61556.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  94. 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, I : Genetics in Medicine. 21, 8, s. 1868-1873

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  95. Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors

    Lothe, R. A., Smith-Sorensen, B., Hektoen, M., Stenwig, A. E., Nils Mandahl, Saeter, G. & Fredrik Mertens, 2001, I : Genes, Chromosomes and Cancer. 30, 2, s. 202-206

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  96. Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma

    Storlazzi, CT., Fredrik Vult von Steyern, Domanski, H., Nils Mandahl & Fredrik Mertens, 2005, I : International Journal of Cancer. 117, 6, s. 1055-1057

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  97. Bidirectionality and transcriptional activity of the EWSR1 promoter region

    Möller, E., Nils Mandahl, Iliszko, M., Fredrik Mertens & Panagopoulos, I., 2009 mar, I : Oncology Reports. 21, 3, s. 641-648 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  98. 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, I : Annals of Surgery. 253, 6, s. 1147-1154

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  99. Binomial mitotic segregation of MYCN-carrying double minutes in neuroblastoma illustrates the role of randomness in oncogene amplification.

    Lundberg, G., Anders Rosengren, Håkanson, U., Stewenius, H., Jin, Y., Stewénius, Y., Sven Påhlman & David Gisselsson Nord, 2008, I : PLoS ONE. 3, 8, e3099.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  100. Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation

    Gilling, M., Lind-Thomsen, A., Mang, Y., Bak, M., Moller, M., Ullmann, R., Ulf Kristoffersson, Kalscheuer, V. M., Henriksen, K. F., Bugge, M., Tumer, Z. & Tommerup, N., 2011, I : European Journal of Medical Genetics. 54, 4, s. E383-E388

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  101. Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?

    Charles Walther, David Gisselsson Nord, Magnusson, L., Nilsson, J., Grabau, D., Kullendorff, C-M., Karolin Hansén Nord & Fredrik Mertens, 2012, I : Journal of Pediatric Hematology/Oncology.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  102. Bladder cancer, a two phased disease?

    Mattias Höglund, 2007, I : Seminars in Cancer Biology. 17, 3, s. 225-232

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  104. Bone marrow karyotypes in 94 children with acute leukemia

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  105. Bone Marrow Multipotent Mesenchymal Stroma Cells Act as Pericyte-like Migratory Vehicles in Experimental Gliomas.

    Daniel Bexell, Gunnarsson, S., Tormin, A., Anna Darabi, David Gisselsson Nord, Laurent Roybon, Stefan Scheding & Johan Bengzon, 2009, I : Molecular Therapy. 2008, Nov 4., s. 183-190

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  106. Book review: Genetic predisposition of cancer, 2nd ed.

    Ulf Kristoffersson, 2005, I : Human Genetics. 117, 4, s. 406-407

    Forskningsoutput: TidskriftsbidragRecension av bok/film/utställning etc.

  107. BRCA1 and BRCA2 mutations in ovarian cancer: Covariation with specific cytogenetic features

    Koul, A., Malander, S., N. Loman, Pejovic, T., Heim, S., Willen, R., Johannsson, O., H. Olsson, Ridderheim, M. & Å. Borg Å, 2000, I : International Journal of Gynecological Cancer. 10, 4, s. 289-295 7 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  108. 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 andra, 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, I : Nature Genetics.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  109. Brister i genetisk kunskap i vården?

    Ulf Kristoffersson, 2007, Att forma vår framtid. Bioteknikens möjligheter och problem. Görman, U., Hermerén, G. & Andrén, CG. (red.). Nordic Academic Press, s. 109

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  110. C2028T polymorphism in exon 12 and dinucleotide repeat polymorphism in intron 13 of the HIF-1 alpha gene define HIF-1 alpha protein expression in non-small cell lung cancer

    Koukourakis, M. I., Papazoglou, D., Giatromanolaki, A., Panagopoulos, I., Maltezos, E., Harris, A. L., Gatter, K. C. & Sivridis, E., 2006, I : Lung Cancer. 53, 3, s. 257-262

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  111. CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk

    Bratt, O., Åke Borg, U Kristoffersson, Lundgren, R., Zhang, Q. X. & Håkan Olsson, 1999 okt, I : British Journal of Cancer. 81, 4, s. 672-6 5 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  112. Cancer - An Insurgency of Clones

    David Gisselsson & Egnell, R., 2017, I : Trends in Cancer. 3, 2, s. 73-75

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  113. Cancer chromosome breakpoints cluster in gene-rich genomic regions

    Felix Mitelman, Bertil Johansson, Fredrik Mertens, Schyman, T. & Nils Mandahl, 2019, I : Genes Chromosomes and Cancer. 58, 3, s. 149-154

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  114. Cancer Chromosomes: From Meaningless Noise to Proof of Principle.

    Felix Mitelman, 2009, I : Chromosome Research. 17, s. 9-9

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

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

    Heim, S. (red.) & Felix Mitelman (red.), 2015, 4th uppl. Wiley-Blackwell. 632 s.

    Forskningsoutput: Bok/rapportAntologi (redaktör)

  116. CANCER-RELATED GENE REGULATION MECHANISMS

    Srinivas Veerla, 2008, Department of Clinical Genetics, Lund University. 104 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  117. Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.

    Peterlongo, P., Chang-Claude, J., Moysich, K. B., Rudolph, A., Schmutzler, R. K., Simard, J., Soucy, P., Eeles, R. A., Easton, D. F., Hamann, U., Wilkening, S., Chen, B., Rookus, M. A., Schmidt, M. K., van der Baan, F. H., Spurdle, A. B., Walker, L. C., Lose, F., Maia, A-T., Montagna, M. & 181 andra, Matricardi, L., Lubinski, J., Jakubowska, A., Gomez-Garcia, E. B., Olopade, O. I., Nussbaum, R. L., Nathanson, K. L., Domchek, S. M., Rebbeck, T. R., Arun, B. K., Karlan, B. Y., Orsulic, S., Lester, J., Chung, W. K., Miron, A., Southey, M. C., Goldgar, D. E., Buys, S. S., Janavicius, R., Dorfling, C. M., van Rensburg, E. J., Ding, Y. C., Neuhausen, S. L., Hansen, T. V. O., Gerdes, A-M., Ejlertsen, B., Jønson, L., Osorio, A., Martinez-Bouzas, C., Benitez, J., Conway, E. E., Blazer, K. R., Weitzel, J. N., Manoukian, S., Peissel, B., Zaffaroni, D., Scuvera, G., Barile, M., Ficarazzi, F., Mariette, F., Fortuzzi, S., Viel, A., Giannini, G., Papi, L., Martayan, A., Tibiletti, M. G., Radice, P., Vratimos, A., Fostira, F., Garber, J. E., Donaldson, A., Brewer, C., Foo, C., Evans, D. G. R., Frost, D., Eccles, D., Brady, A., Cook, J., Tischkowitz, M., Adlard, J., Barwell, J., Walker, L., Izatt, L., Side, L. E., Kennedy, M. J., Rogers, M. T., Porteous, M. E., Morrison, P. J., Platte, R., Davidson, R., Hodgson, S. V., Ellis, S., Cole, T., Godwin, A. K., Claes, K., Van Maerken, T., Meindl, A., Gehrig, A., Sutter, C., Engel, C., Niederacher, D., Steinemann, D., Plendl, H., Kast, K., Rhiem, K., Ditsch, N., Arnold, N., Varon-Mateeva, R., Wappenschmidt, B., Wang-Gohrke, S., Bressac-de Paillerets, B., Buecher, B., Delnatte, C., Houdayer, C., Stoppa-Lyonnet, D., Damiola, F., Coupier, I., Barjhoux, L., Venat-Bouvet, L., Golmard, L., Boutry-Kryza, N., Sinilnikova, O. M., Caron, O., Pujol, P., Mazoyer, S., Belotti, M., Piedmonte, M., Friedlander, M. L., Rodriguez, G. C., Copeland, L. J., de la Hoya, M., Perez Segura, P., Nevanlinna, H., Aittomäki, K., van Os, T. A. M., Meijers-Heijboer, H. E. J., Van der Hout, A. H., Vreeswijk, M. P. G., Hoogerbrugge, N., Ausems, M. G. E. M., Van Doorn, H. C., Collée, J. M., Olah, E., Díez, O., Blanco, I., Lazaro, C., Brunet, J., Feliubadaló, L., Cybulski, C., Gronwald, J., Durda, K., Jaworska-Bieniek, K., Sukiennicki, G., Arason, A., Chiquette, J., Teixeira, M. R., Olswold, C., Couch, F. J., Lindor, N. M., Wang, X., Szabo, C. I., Offit, K., Corines, M., Jacobs, L., Robson, M., Zhang, L., Joseph, V., Berger, A., Singer, C. F., Rappaport, C., Geschwantler Kaulich, D., Pfeiler, G., Tea, M-K. M., Phelan, C. M., Greene, M. H., Mai, P. L., Rennert, G., Mulligan, A. M., Glendon, G., Tchatchou, S., Andrulis, I. L., Toland, A. E., Bojesen, A., Pedersen, I. S., Thomassen, M., Jensen, U. B., Laitman, Y., Rantala, J., von Wachenfeldt, A., Hans Ehrencrona, Stenmark Askmalm, M., Åke Borg, Kuchenbaecker, K. B., McGuffog, L., Barrowdale, D., Healey, S., Lee, A., Pharoah, P. D. P., Chenevix-Trench, G., Antoniou, A. C. & Friedman, E., 2015, I : Cancer Epidemiology Biomarkers & Prevention. 24, 1, s. 308-316

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  118. C-band heteromorphism in breast cancer patients

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  119. C‐band polymorphism in non‐Hodgkin lymphoma

    ULF KRISTOFFERSSON, BERGER, ROLAND., BERNHEIM, ALAIN., ÅKERMAN, MÅNS., HÅKAN OLSSON & FELIX MITELMAN, 1985 jan 1, I : Hereditas. 103, 1, s. 85-87 3 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  120. CCL2 secreted from cancer-associated mesothelial cells promotes peritoneal metastasis of ovarian cancer cells through the P38-MAPK pathway

    Hiroaki Yasui, Kajiyama, H., Tamauchi, S., Suzuki, S., Peng, Y., Yoshikawa, N., Sugiyama, M., Nakamura, K. & Kikkawa, F., 2019 sep 21, I : Clinical and Experimental Metastasis.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  121. CD36 defines primitive chronic myeloid leukemia cells less responsive to imatinib but vulnerable to antibody-based therapeutic targeting

    Niklas Landberg, Sofia von Palffy, Askmyr, M., Henrik Lilljebjörn, Carl Sandén, Rissler, M., Mustjoki, S., Hjorth-Hansen, H., Johan Richter, Helena Ågerstam, Marcus Järås & Thoas Fioretos, 2018 feb 28, I : Haematologica. 103, 3, s. 447-455

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  122. Cell Surface Markers as Therapeutic Targets in Myeloid Leukemia

    Niklas Landberg, 2020, Lund: Lund University, Faculty of Medicine. 79 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  123. Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.

    D Gisselsson, T Jonson, Yu, C., Martins, C., N Mandahl, Wiegant, J., Jin, Y., F Mertens & Jin, C., 2002 jul 15, I : British Journal of Cancer. 87, 2, s. 202-207 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  124. Changes in high-frequency QRS components are more sensitive than ST segment deviation for detecting acute coronary artery occlusion

    Pettersson, J., Carro, E., Edenbrandt, L., Ringborn, M., Leif Sörnmo, Warren, S. G. & Wagner, G. S., 2000, I : Journal of the American College of Cardiology. 36, 6, s. 1827-1834

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  125. Changes in the Prevalence of Embryologic Remnants in Umbilical Cord With Gestational Age

    Emma Grottling & David Gisselsson, 2019, I : Pediatric and Developmental Pathology. 22, 4, s. 288-291

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  126. Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2

    Schoumans, J., Bertil Johansson, Corcoran, M., Kuchinskaya, E., Golovleva, I., Grander, D., Forestier, E., Johan Staaf, Åke Borg, Gustafsson, B., Blennow, E. & Nordgren, A., 2006, I : British Journal of Haematology. 135, 4, s. 492-499

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  127. Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors

    Trombetta, D., Fredrik Mertens, Lonoce, A., D'Addabbo, P., Rennstam, K., Nils Mandahl & Storlazzi, C. T., 2009, I : Genes, Chromosomes and Cancer. 48, 11, s. 993-1001

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  129. Characterization of a novel breast carcinoma xenograft and cell line derived from a BRCA1 germ-line mutation carrier

    Johannsson, O. T., Staff, S., Johan Vallon-Christersson, Kytöla, S., Gudjonsson, T., Rennstam, K., Ingrid A Hedenfalk, Adeyinka, A., Kjellén, E., Wennerberg, J., Bo Baldetorp, Petersen, O. W., Håkan Olsson, Stina Oredsson, Isola, J. & Borg, A., 2003 mar, I : Laboratory Investigation. 83, 3, s. 387-96 10 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  130. 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, I : International Journal of Cancer. 92, 6, s. 824-831

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  131. Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH

    Jin, C., Martins, C., Jin, Y., Wiegant, J., Johan Wennerberg, Michael Dictor, David Gisselsson Nord, Strömbeck, B., Fonseca, I., Felix Mitelman, Tanke, H. J., Mattias Höglund & Fredrik Mertens, 2001, I : Genes, Chromosomes and Cancer. 30, 2, s. 161-167

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  132. 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 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  133. Characterization of genomically amplified segments using PCR: optimizing relative-PCR for reliable and simple gene expression and gene copy analyses

    Tord Jonson, Mahlamaki, E. H., Karhu, R., Gorunova, L., Bertil Johansson & Mattias Höglund, 2000, I : Genes, Chromosomes and Cancer. 29, 2, s. 192-199

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  134. Characterization Of Non-Small Cell Lung Cancer Using Tiling Resolution Bacterial Artificial Chromosome Microarrays

    Isaksson, S., Solomonsson, A., Pär-Ola Bendahl, Jansson, L. I., Johansson, L., Jönsson, P., Anna F Karlsson, Soller, M., Göran B Jönsson & Maria Planck, 2008, I : Anticancer research. 28, 5C, s. 538

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  135. Characterization of somatic mutations in nonneoplastic cells

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  136. 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, I : Journal of Pathology. 227, 1, s. 72-80

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  137. Characterization of the human CREB3L2 gene promoter

    Panagopoulos, I. & Fredrik Mertens, 2009 mar, I : Oncology Reports. 21, 3, s. 615-624 10 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  138. 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, I : Genes, Chromosomes and Cancer. 46, 2, s. 181-191 11 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  139. CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome

    Wincent, J., Holmberg, E., Stromland, K., Soller, M., Mirzaei, L., Djureinovic, T., Robinson, K. L., Anderlid, B. M. & Schoumans, J., 2008, I : Clinical Genetics. 74, 1, s. 31-38

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  140. Chordoma

    Mirra, JM., Nelson, SD., Della Rocca, C. & Fredrik Mertens, 2002, World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Fletcher, CDM., Unni, KK. & Mertens, F. (red.). IARC Press, s. 316

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  141. 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, I : BMC Cancer. 2:5

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Persson, K., Pandis, N., Fredrik Mertens, Åke Borg, Bo Baldetorp, Dick Killander & Isola, J., 1999, I : Genes, Chromosomes and Cancer. 25, 2, s. 115-122

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  143. Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  144. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity

    David Gisselsson Nord, Pettersson, L., Mattias Höglund, Heidenblad, M., Gorunova, L., Wiegant, J., Fredrik Mertens, Dal Cin, P., Felix Mitelman & Nils Mandahl, 2000, I : Proceedings of the National Academy of Sciences. 97, 10, s. 5357-5362

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  146. 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, I : International Journal of Oncology. 20, 1, s. 45-52 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  147. Chromosome aberrations in 35 primary ovarian carcinomas

    Pejovic, T., Heim, S., Mandahl, N., Bo Baldetorp, Elmfors, B., Floderus, U-M., Furgyik, S., Helm, G., Himmelmann, A., Willen, H. & Felix Mitelman, 1992, I : Genes, Chromosomes and Cancer. 4, 1, s. 58-68

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Petersson, C., Pandis, N., F Mertens, Adeyinka, A., C Ingvar, A Ringberg, Idvall, I., Bondeson, L., A Borg, Håkan Olsson, U Kristoffersson & F Mitelman, 1996 jul, I : Genes, Chromosomes and Cancer. 16, 3, s. 185-188 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  149. Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes.

    Lundberg, G., 2012, Faculty of Medicine, Lund University. 132 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  150. Chromosome gains drive childhood ALL.

    Kajsa Paulsson, 2015, I : Oncotarget. 6, 23, s. 19360-19361

    Forskningsoutput: TidskriftsbidragDebate/Note/Editorial

  151. Chromosome instability in cancer: how, when, and why?

    David Gisselsson Nord, 2003, I : Advances in Cancer Research. 87, s. 1-29

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  152. Chronic myeloid leukemia

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

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  153. 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, I : Scientific Reports. 5, 15529.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  154. Classification of chromosome segregation errors in cancer.

    David Gisselsson Nord, 2008, I : Chromosoma. Jun 6, s. 511-519

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  155. 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, I : Genes, Chromosomes and Cancer. 43, 2, s. 202-205

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Jenny Karlsson, Linda Holmquist Mengelbier, Ciornei, C., Naranjo, A., O'Sullivan, M. J. & David Gisselsson Nord, 2014, I : Genes, Chromosomes and Cancer. 53, 5, s. 381-391

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  157. Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.

    Karrman, K., Forestier, E., Heyman, M., K Andersen, M., Autio, K., Blennow, E., Borgström, G., Hans Ehrencrona, Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kerndrup, G., Nordgren, A., Palmqvist, L. & Bertil Johansson, 2009, I : Genes, Chromosomes and Cancer. 48, 9, s. 795-805

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  158. 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, I : Genes, Chromosomes and Cancer. 47, 2, s. 149-158

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  159. Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries

    Lundin, C., Forestier, E., Andersen, M. K., Autio, K., Barbany, G., Cavelier, L., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kjeldsen, E., Nordgren, A., Palmqvist, L. & Bertil Johansson, 2014, I : Journal of Hematology & Oncology. 7, 32.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  160. 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, I : European Urology. 34, 1, s. 19-24 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  161. 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, I : Leukemia. 7, 8, s. 1225-1231

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  162. 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, I : Genes, Chromosomes and Cancer. 31, 4, s. 362-72 11 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  163. Clinical Variability of Waardenburg-Shah Syndrome in Patients With Proximal 13q Deletion Syndrome Including the Endothelin-B Receptor Locus

    Tuysuz, B., Collin, A., Arapoglu, M. & Suyugul, N., 2009, I : American Journal of Medical Genetics. Part A. 149A, 10, s. 2290-2295

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  164. 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, I : Journal of Community Genetics. 10, 1, s. 61-71

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  165. Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene

    Fredrik Mertens, Fletcher, C. D. M., Antonescu, C. R., Coindre, J-M., Colecchia, M., Domanski, H. A., Downs-Kelly, E., Fisher, C., Goldblum, J. R., Guillou, L., Reid, R., Rosai, J., Sciot, R., Nils Mandahl & Panagopoulos, I., 2005 mar, I : Laboratory Investigation. 85, 3, s. 408-415 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  166. 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, I : Human Genetics. 101, 3, s. 295-8 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  167. Clonal chromosome aberrations in a sialoblastoma

    Fredrik Mertens, Wahlberg, P. & Domanski, H., 2009, I : Cancer Genetics and Cytogenetics. 189, 1, s. 68-69

    Forskningsoutput: TidskriftsbidragLetter

  168. Clonal chromosome abnormalities in premalignant lesions of the skin.

    Jin, Y., Jin, C., Salemark, L., Johan Wennerberg, Persson, B. & Jonsson, N., 2002, I : Cancer Genetics and Cytogenetics. 136, 1, s. 48-52

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  169. Clonal conversion of B lymphoid leukemia reveals cross-lineage transfer of malignant states

    Somasundaram, R., Åhsberg, J., Okuyama, K., Ungerbäck, J., Henrik Lilljebjörn, Thoas Fioretos, Tobias Strid & Mikael Sigvardsson, 2016 nov 15, I : Genes and Development. 30, 22, s. 2486-2499 14 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    David Gisselsson, Lichtenzstejn, D., Kachko, P., Jenny Karlsson, Manor, E. & Mai, S., 2019, I : Genes Chromosomes and Cancer. 58, 7, s. 452-461

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  172. Cloning of the der(17)t(X;17)(p11;q25) alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker

    Ladanyi, M., Lui, M. Y., Antonescu, C. R., Krause-Boehm, A., Meloni-Ehrig, A., Argani, P., Sorensen, P. H. B., Fredrik Mertens, Nils Mandahl, van den Berghe, H., Sciot, R., Dal Cin, P. & Bridge, J. A., 2001, I : Laboratory Investigation. 81, 1, s. 14A-14A

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  173. Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker

    Ladanyi, M., Lui, M. Y., Antonescu, C. R., Krause-Boehm, A., Meloni-Ehrig, A., Argani, P., Sorensen, P. H. B., Mertens, F., Nils Mandahl, van den Berghe, H., Sciot, R., Dal Cin, P. & Bridge, J. A., 2001, I : Modern Pathology. 14, 1, s. 14A-14A

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  174. 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, I : International Journal of Cancer. 103, 5, s. 616-623 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  175. Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas

    Yang, K., Lui, WO., Xie, YT., Zhang, AJ., Skytting, B., Nils Mandahl, Larsson, C. & Larsson, O., 2002, I : Oncogene. 21, 26, s. 4181-4190

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  176. Combination of pegylated IFN-alpha 2b with imatinib increases molecular response rates in patients with low- or intermediate-risk chronic myeloid leukemia

    Simonsson, B., Gedde-Dahl, T., Markevarn, B., Remes, K., Stentoft, J., Almqvist, A., Bjoreman, M., Flogegard, M., Koskenvesa, P., Lindblom, A., Malm, C., Mustjoki, S., Myhr-Eriksson, K., Ohm, L., Rasanen, A., Sinisalo, M., Sjalander, A., Stromberg, U., Bjerrum, O. W., Ehrencrona, H. & 8 andra, Gruber, F., Kairisto, V., Olsson, K., Sandin, F., Nagler, A., Nielsen, J. L., Hjorth-Hansen, H. & Porkka, K., 2011, I : Blood. 118, 12, s. 3228-3235

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  177. Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma

    Kuźniacka, A., Fredrik Mertens, Strömbeck, B., Wiegant, J. & Nils Mandahl, 2004 jun, I : Cancer Genetics and Cytogenetics. 151, 2, s. 178-181 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  178. 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 andra, 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, I : Cancer Research. 70, 23, s. 9742-54 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  179. 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 andra, 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, I : Breast Cancer Research. 13, 6

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  180. 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 andra, 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, I : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 21, 4, s. 645-657

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  181. Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors

    Nils Mandahl, Bo Baldetorp, Mårten Fernö, Åkerman, M., Anders Rydholm, Heim, S., Willén, H., Dick Killander & Felix Mitelman, 1993, I : International Journal of Cancer. 53, 3, s. 358-364

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  182. 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, I : Cancer Genetics and Cytogenetics. 147, 1, s. 62-67 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  183. Comparative genomic hybridization of postirradiation sarcomas

    Tarkkanen, M., Wiklund, T. A., Virolainen, M. J., Larramendy, M. L., Nils Mandahl, Fredrik Mertens, Blomqvist, C. P., Tukiainen, E. J., Miettinen, M. M. A., Elomaa, A. I. & Knuutila, Y. S., 2001, I : Cancer. 92, 7, s. 1992-1998

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  184. Comparison of EASI-derived 12-lead electrocardiograms versus paramedic-acquired 12-lead electrocardiograms using Mason-Likar limb lead configuration in patients with chest pain

    Sejersten, M., Pahlm, O., Pettersson, J., Zhou, S., Maynard, C., Feldman, CL. & Wagner, GS., 2006, I : Journal of Electrocardiology. 39, 1, s. 13-21

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  185. Comparison of high-frequency QRS components and ST-segment elevation to detect and quantify acute myocardial ischemia.

    Ringborn, M., Pettersson, J., Persson, E., Warren, S. G., Pyotr Platonov, Pahlm, O. & Wagner, G. S., 2010, I : Journal of Electrocardiology. 43, s. 113-120

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  186. Comparison of signal quality between EASI and Mason-Likar 12-lead electrocardiograms during physical activity.

    Welinder, A., Leif Sörnmo, Feild, D. Q., Feldman, C. L., Pettersson, J., Wagner, G. S. & Pahlm, O., 2004, I : American Journal of Critical Care. 13, 3, s. 228-234

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  187. Comparison of ST-Segment Deviation to Scintigraphically Quantified Myocardial Ischemia During Acute Coronary Occlusion Induced by Percutaneous Transluminal Coronary Angioplasty.

    Persson, E., Pettersson, J., Ringborn, M., Leif Sörnmo, Warren, S. G., Wagner, G. S., Maynard, C. & Pahlm, O., 2006, I : American Journal of Cardiology. 97, 3, s. 295-300

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  188. Comparison of the proximal promoter regions of the PAX3 and PAX7 genes

    Möller, E., Isaksson, M., Nils Mandahl, Fredrik Mertens & Panagopoulos, I., 2007 okt 15, I : Cancer Genetics and Cytogenetics. 178, 2, s. 114-119 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  189. 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, I : British Journal of Cancer. 77, 7, s. 1082-1088

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  190. 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, I : Genes, Chromosomes and Cancer. 1, 2, s. 131-134

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  191. Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas

    Mef Nilbert, Nils Mandahl, Heim, S., Anders Rydholm, Helm, G., Willén, H., Bo Baldetorp & Felix Mitelman, 1990, I : Cancer Genetics and Cytogenetics. 48, 2, s. 217-223

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Mohajeri, A., Tayebwa, J., Collin, A., Nilsson, J., Magnusson, L., Fredrik Vult von Steyern, Brosjö, O., Domanski, H., Larsson, O., Sciot, R., Debiec-Rychter, M., Hornick, J. L., Nils Mandahl, Karolin Hansén Nord & GCC Klinisk genetik, F. M., 2013, I : Genes, Chromosomes and Cancer. 52, 10, s. 873-886

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  193. Comprehensive genetic analysis of a pediatric pleomorphic myxoid liposarcoma reveals near-haploidization and loss of the RB1 gene.

    Jakob Hofvander, Jo, V. Y., Iman Ghanei, David Gisselsson Nord, Mårtensson, E. & Fredrik Mertens, 2016, I : Histopathology. 69, 1, s. 141–147

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  194. Comprehensive genetic characterization of pediatric T-cell acute lymphoblastic leukemia

    Karrman, K., Anders Castor, Behrendtz, M., Forestier, E., Linda Olsson, Mats Ehinger, Biloglav, A., Thoas Fioretos, Kajsa Paulsson & Bertil Johansson, 2014 dec 6, I : Blood. 124, 21, s. 1084

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  196. Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma

    Lindberg, E., Persson, A., Ingrid Øra, Fredrik Mertens, Elisabet Englund & David Gisselsson Nord, 2007, I : Neuropathology. 27, 6, s. 556-560

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  197. Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer.

    Anders Valind, Pal, N., Asmundsson, J., David Gisselsson Nord & Linda Holmquist Mengelbier, 2014, I : Genes, Chromosomes and Cancer. 53, 7, s. 634-638

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Soller, M., Isaksson, M., Peter Elfving, Soller, W., Lundgren, R. & Panagopoulos, I., 2006, I : Genes, Chromosomes and Cancer. 45, 7, s. 717-719

    Forskningsoutput: TidskriftsbidragLetter

  199. Congenital and inherited syndromes associated with bone and soft tissue tumours

    Fredrik Mertens, 2002, World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. Fletcher, CDM., Unni, KK. & Mertens, F. (red.). IARC Press, s. 349

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  200. Consequences of eliminating adenosine A(1) receptors in mice

    Fredholm, BB., Halldner, L., Johansson, C., Schulte, G., Lovdahl, C., Thoren, P., Dunwiddie, TV., Masino, SA., Poelchen, W., Diao, LH., Illes, P., Zahniser, NR., Valen, G., Tokuno, S., Sommerschild, H., Gimenez-Llort, L., Fernandez-Teruel, A., Escorihuela, RM., Wiesenfeld-Hallin, Z., Xu, XJ. & 9 andra, Hardemark, A., Herlenius, E., Pekny, S., Samuel Gebre-Medhin, Brown, R., Ollerstam, A., Persson, AEG., Skott, O. & Johansson, B., 2003, Drug Development Research (Proceedings of the Seventh International Symposium on Adenosine and Adenine Nucleotides - Part 1). John Wiley and Sons Inc., Vol. 58. s. 350-353

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKonferenspaper i proceeding

  201. Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma

    Micci, F., Panagopoulos, I., Bjerkehagen, B. & Heim, S., 2006, I : Cancer Research. 66, 1, s. 107-112

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragLetter

  203. Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.

    Karin Broberg Palmgren, Jonas Björk, Paulsson, K., Mattias Höglund & Maria Albin, 2005, I : Carcinogenesis. 26, 7, s. 1263-1271

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  204. Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

    Anders Valind, Wessman, S., Pal, N., Jenny Karlsson, Tord Jonson, Sandstedt, B. & David Gisselsson, 2018 nov 1, I : Pediatric Blood & Cancer. 65, 11, e27301.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Linda Olsson, Albitar, F., Anders Castor, Behrendtz, M., Biloglav, A., Kajsa Paulsson & Bertil Johansson, 2015, I : Genes, Chromosomes and Cancer. 54, 5, s. 315-325

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  206. Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis

    Molenaar, J. J., Koster, J., Ebus, M. E., van Sluis, P., Westerhout, E. M., de Preter, K., David Gisselsson Nord, Ingrid Øra, Speleman, F., Caron, H. N. & Versteeg, R., 2012, I : Genes, Chromosomes and Cancer. 51, 1, s. 10-19

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  207. Core Circadian Clock Genes Regulate Leukemia Stem Cells in AML

    Puram, R. V., Kowalczyk, M. S., de Boer, C. G., Schneider, R. K., Miller, P. G., McConkey, M., Tothova, Z., Tejero, H., Heckl, D., Marcus Järås, Chen, M. C., Li, H., Tamayo, A., Cowley, G. S., Rozenblatt-Rosen, O., Al-Shahrour, F., Regev, A. & Ebert, B. L., 2016, I : Cell. 165, 2, s. 303-16 14 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  208. 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, I : Cancer. 105, 4, s. 229-239 11 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  209. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group

    Tallini, G., Dorfman, H., Brys, P., Dal Cin, P., De Wever, I., Fletcher, CDM., Jonsson, K., Nils Mandahl, Fredrik Mertens, Felix Mitelman, Rosai, J., Anders Rydholm, Samson, I., Sciot, R., Van den Berghe, H., Vanni, R. & Willen, H., 2002, I : Journal of Pathology. 196, 2, s. 194-203

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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