Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

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

    Leif Salford, Peter Siesjö, Gunnar Skagerberg, Visse, E., 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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

  21. 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

  22. 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

  23. 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

  24. 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

  25. 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

  26. 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

  27. 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

  28. 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

  29. 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

  30. 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

  31. 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

  32. 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

  33. 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

  34. 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

  35. 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

  36. 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

  37. 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

  38. 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

  39. 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

  40. 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

  41. 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

  42. 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

  43. 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

  44. Aneuploidy in cancer: Sudden or sequential?

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  45. 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

  46. 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

  47. 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

  48. 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

  49. 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

  50. 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

  51. 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

  52. 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

  53. 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

  54. 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

  55. 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

  56. 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

  57. 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

  58. 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

  59. 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

  60. 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

  61. 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

  62. 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.

  63. 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

  64. 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

  65. 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

  66. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  68. 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

  69. 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)

  70. 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

  71. 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

  72. 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

  73. 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

  74. 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

  75. 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

  76. 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

  77. 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

  78. 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

  79. 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

  80. 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

  81. 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

  82. 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

  83. 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

  84. 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

  85. 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

  86. 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

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