Skip to main content

6 Result(s)

within J Staaf Remove this filter

and

  1. No Access

    Article

    Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients

    R Gunnarsson, A Isaksson, M Mansouri, H Göransson, M Jansson, N Cahill… in Leukemia (2010)

  2. Article

    Open Access

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

    The initiating somatic genetic events in chordoma development have not yet been identified. Most cytogenetically investigated chordomas have displayed near-diploid or moderately hypodiploid karyotypes, with se...

    K H Hallor, J Staaf, G Jönsson, M Heidenblad… in British Journal of Cancer (2008)

    Download PDF (2281 KB) View Article

  3. No Access

    Article

    Genomic profiling of malignant melanoma using tiling-resolution arrayCGH

    Malignant melanoma is an aggressive, heterogeneous disease where new biomarkers for diagnosis and clinical outcome are needed. We searched for chromosomal aberrations that characterize its pathogenesis using 4...

    G Jönsson, C Dahl, J Staaf, T Sandberg, P-O Bendahl, M Ringnér, P Guldberg… in Oncogene (2007)

  4. No Access

    Article

    Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage/fusion/breakage cycles?

    E Kuchinskaya, A Nordgren, M Heyman, J Schoumans, M Corcoran, J Staaf, Å Borg… in Leukemia (2007)

  5. No Access

    Article

    Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays

    Ring chromosomes and/or giant marker chromosomes have been observed in a variety of human tumor types, but they are particularly common in a subgroup of mesenchymal tumors of low-grade or borderline malignancy...

    M Heidenblad, K H Hallor, J Staaf, G Jönsson, Å Borg, M Höglund, F Mertens… in Oncogene (2006)

  6. No Access

    Article

    High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

    Although trisomy 8 as the sole chromosome aberration is the most common numerical abnormality in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), little is known about its pathogenetic effects...

    K Paulsson, M Heidenblad, B Strömbeck, J Staaf, G Jönsson, Å Borg, T Fioretos… in Leukemia (2006)