Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. 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 andraJarosz, 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

  3. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. 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

  11. 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

  12. 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 andraMichel, 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. 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

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

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  16. Study of ATP-release from acoustically levitated eryhrocytes

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

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  17. Study of ATP-release from acoustically levitated eryhrocytes

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

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

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

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

    Forskningsoutput: TidskriftsbidragLetter

  19. 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

  20. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations

    Thoas Fioretos, Strömbeck, B., Therese Törngren, Bertil Johansson, Billstrom, R., Åke Borg, Nilsson, P-G., Van Den Berghe, H., Hagemeijer, A., Felix Mitelman & Mattias Höglund, 1999, I : Blood. 94, 1, s. 225-232

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  28. Standpoint on imprinting of BCR and ABL

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. Molekylär medicin: Molekylärgenetisk metodik avslöjar mekanismerna bakom tumörutveckling

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  34. Mechanisms underlying neoplasia-associated genomic rearrangements

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

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  35. 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

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

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

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

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

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

    Forskningsoutput: Bok/rapportAntologi (redaktör)

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

    Forestier, E., Andersen, M. K., Autio, K., Blennow, E., Borgstrom, G., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kerndrup, G., Nordgren, A., Rosenquist, R., Swolin, B. & Bertil Johansson, 2007, I : Genes, Chromosomes and Cancer. 46, 5, s. 440-450

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  40. 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

  41. Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.

    Forestier, E., Heim, S., Blennow, E., Borgström, G., Holmgren, G., Heinonen, K., Johannsson, J., Kerndrup, G., Andersen, M. K., Lundin, C., Nordgren, A., Rosenquist, R., Swolin, B. & Bertil Johansson, 2003, I : British Journal of Haematology. 121, 4, s. 566-577

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  42. Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival

    Forestier, E., Heyman, M., Andersen, M. K., Autio, K., Blennow, E., Borgstrom, G., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Kerndrup, G., Nordgren, A., Rosenquist, R., Swolin, B. & Bertil Johansson, 2008, I : British Journal of Haematology. 140, 6, s. 665-672

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  43. Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study

    Forestier, E., Izraeli, S., Beverloo, B., Haas, O., Pession, A., Michalova, K., Stark, B., Harrison, C. J., Teigler-Schlegel, A. & Bertil Johansson, 2008, I : Blood. 111, 3, s. 1575-1583

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  44. Mosaicism in health and disease — clones picking up speed

    Forsberg, L. A., David Gisselsson & Dumanski, J. P., 2017, I : Nature Reviews. Genetics. 18, s. 128-142

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Ola Forslund, Natsuki Sugiyama, 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

  46. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia

    Foster, N., Kajsa Paulsson, Sales, M., Cunningham, J., Groves, M., O'Connor, N., Begum, S., Stubbs, T., McMullan, D. J., Griffiths, M., Pratt, N. & Tauro, S., 2010, I : British Journal of Haematology. 148, 6, s. 938-943

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  47. 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 andraHardemark, 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 & Sons, Vol. 58. s. 350-353

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