Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. Artikel i vetenskaplig tidskrift
  2. Heterogeneous genetic profiles in soft tissue myoepitheliomas

    Karolin Hansén Nord, Teixeira, M. R., Fletcher, C. D. M., Bizarro, S., Johan Staaf, Domanski, H., Fredrik Vult von Steyern, Panagopoulos, I., Nils Mandahl & Fredrik Mertens, 2008, I : Modern Pathology. 21, 11, s. 1311-1319

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.

    Josef Davidsson, Collin, A., Olsson, M. E., Lundgren, J. & Soller, M., 2008, I : Epilepsy Research. Jun 6, s. 69-79

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.

    Stewénius, Y., Jin, Y., Ingrid Øra, Panagopoulos, I., Möller, E., Fredrik Mertens, Sandstedt, B., Alumets, J., Åkerman, M., Merks, J. H., de Kraker, J. & David Gisselsson Nord, 2008, I : Genes, Chromosomes and Cancer. 47, 10, s. 845-852

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 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

  6. Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.

    Karolin Hansén Nord, Johan Staaf, Göran B Jönsson, Heidenblad, M., Fredrik Vult von Steyern, Bauer, H. C. F., Ijszenga, M., Hogendoorn, P. C. W., Nils Mandahl, Szuhai, K. & Fredrik Mertens, 2008, I : British Journal of Cancer. 98, 2, s. 434-442

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Promoter analysis of epigenetically controlled genes in bladder cancer.

    Srinivas Veerla, Panagopoulos, I., Jin, Y., David Lindgren & Mattias Höglund, 2008, I : Genes, Chromosomes and Cancer. 47, s. 368-378

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.

    Möller, E., Stenman, G., Nils Mandahl, Hamberg, H., Mölne, L., van den Oord, J., Brosjö, O., Fredrik Mertens & Panagopoulos, I., 2008, I : Journal of Pathology. 215, s. 78-86

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.

    Anna Andersson, Kajsa Paulsson, Henrik Lilljebjörn, Lassen, C., Strömbeck, B., Heldrup, J., Behrendtz, M., Bertil Johansson & Thoas Fioretos, 2008, I : Genes, Chromosomes and Cancer. 47, s. 64-70

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients.

    Jin, C., Jin, Y., Johan Wennerberg, Rosenquist, B. & Fredrik Mertens, 2008, I : Mutation Research. 652, s. 30-37

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. When the genome plays dice: circumvention of the spindle assembly checkpoint and near-random chromosome segregation in multipolar cancer cell mitoses.

    David Gisselsson Nord, Håkanson, U., Stoller, P., Marti, D., Jin, Y., Anders Rosengren, Stewénius, Y., Kahl, F. & Panagopoulos, I., 2008, I : PLoS ONE. 3, 4, e1871.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. Cytogenetic and molecular cytogenetic findings in lipoblastoma.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Regulatory Issues for Genetic Testing in Clinical Practice.

    Ulf Kristoffersson, 2008, I : Molecular Biotechnology. 40, s. 113-117

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. 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

  16. Recurrent and multiple bladder tumors show conserved expression profiles.

    David Lindgren, Gudjonsson, S., Jee, K. J., Fredrik Liedberg, Sonja Aits, Anna Andersson, Chebil, G., Åke Borg, Knuutila, S., Thoas Fioretos, Wiking Månsson & Mattias Höglund, 2008, I : BMC Cancer. 8, June 30, 183.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. Classification of chromosome segregation errors in cancer.

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. Exit of pediatric pre-B acute lymphoblastic leukaemia cells from the bone marrow to the peripheral blood is not associated with cell maturation or alterations in gene expression.

    Hansson, F., Toporski, J., Månsson, R., Bertil Johansson, Norén-Nyström, U., Jacobsen, S. E. W., Thomas Wiebe, Larsson, M., Mikael Sigvardsson & Anders Castor, 2008, I : Molecular Cancer. 7, 67.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 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

  21. Fusion genes in angiomatoid fibrous histiocytoma

    Karolin Hansén Nord, Micci, F., Meis-Kindblom, J. M., Kindblom, L-G., Bacchini, P., Nils Mandahl, Fredrik Mertens & Panagopoulos, I., 2007 jun 18, I : Cancer Letters. 251, 1, s. 158-163 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. 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

  23. 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

  24. Cytogenetic findings in pediatric renal cell carcinoma

    Soller, M. J., Kullendorff, C-M., Békássy, A. N., Alumets, J. & Fredrik Mertens, 2007 feb, I : Cancer Genetics and Cytogenetics. 173, 1, s. 75-80 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. Report of an international survey of molecular genetic testing laboratories

    McGovern, M. M., Elles, R., Beretta, I., Somerville, M. J., Hoefler, G., Keinanen, M., Barton, D., Carson, N., Dequeker, E., Brdicka, R., Blazkova, A., Ayme, S., Schnieders, B., Mueller, C. R., Dalen, V., Martinez, A. A., Kristoffersson, U., Ozguc, M., Mueller, H., Boone, J. & 7 andra, Lubin, I. M., Sequeiros, J., Taruscios, D., Williamson, B., Mainland, L., Yoshikura, H. & Ronchi, E., 2007, I : Community Genetics. 10, 3, s. 123-131

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes

    Haferlach, C., Rieder, H., Lillington, D. M., Dastugue, N., Hagemeijer, A., Harbott, J., Stilgenbauer, S., Knuutila, S., Bertil Johansson & Fonatsch, C., 2007, I : Genes, Chromosomes and Cancer. 46, 5, s. 494-499

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. Cytogenetic evolution patterns in CML post-SCT.

    Karrman, K., Sallerfors, B., Lenhoff, S., Thoas Fioretos & Bertil Johansson, 2007, I : Bone Marrow Transplantation. 39, 3, s. 165-171

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. Distinct mitotic segregation errors mediate chromosomal instability in aggressive urothelial cancers.

    Jin, Y., Stewénius, Y., David Lindgren, Attila Frigyesi, Olga Calcagnile, Tord Jonson, Edqvist, A., Larsson, N., Lundberg, L-M., Chebil, G., Fredrik Liedberg, Gudjonsson, S., Wiking Månsson, Mattias Höglund & David Gisselsson Nord, 2007, I : Clinical Cancer Research. 13, 6, s. 1703-1712

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. 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

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors

    Stewénius, Y., Jin, Y., Ingrid Øra, de Kraker, J., Bras, J., Attila Frigyesi, Alumets, J., Sandstedt, B., Meeker, A. K. & David Gisselsson Nord, 2007, I : Clinical Cancer Research. 13, 22, s. 6593-6602

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. 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

  37. Reduced high-frequency QRS components in electrocardiogram leads facing an area of the heart with intraventricular conduction delay due to bundle branch block.

    Elin Trägårdh, Pettersson, J., Wagner, G. S. & Pahlm, O., 2007, I : Journal of Electrocardiology. 40, 2, s. 127-132

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  38. Successful treatment of a child with t(15;19)-positive tumor.

    Fredrik Mertens, Thomas Wiebe, Adlercreutz, C., Nils Mandahl & French, C. A., 2007, I : Pediatric Blood & Cancer. 49, s. 1015-1017

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations

    Hastings, R. J., Cavani, S., Bricarelli, F. D., Patsalis, P. C. & Ulf Kristoffersson, 2007, I : European Journal of Human Genetics. 15, 5, s. 525-527

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift