References
- Döhner H, Stilgenbauer S, Benner A, et al Genomic aberration and survival in chronic lymphocytic leukemia. N Engl J Med 2000;343:1910–1916.
- Juliusson G, Oscier DG, Fitchett M, et al Prognostic subgroups in B-cell chronic lymphocytic leukemia defined by specific chromosomal abnormalities. N Engl J Med 1990;323:720–724.
- Mayr CH, Speicher MR, Kofler DM, et al Chromosomal translocations are associated with poor prognosis in chronic lymphocytic leukemia. Blood 2006;107:742–751.
- Schwaenen C, Nessling M, Wessendorf S, et al Automated array-based gemonic profiling in chronic lymphocytic leukemia: develop of a clinical tool and discovery of recurrent genomic alteration. Proc Natl Acad Sci USA 2004;101:1039–1044.
- Pfeifer D, Pantic M, Skatulla I, et al Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays. Blood 2007;109:1202–1210.
- Gunn SR, Mohammed MS, Gorre ME, et al Whole-genome screening by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia. J Mol Diagn 2008;10:442–451.
- Patel A, Kang SH, Lennon PA, et al Validation of targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia. Am J Hematol 2007;83:540–546.
- Ferreira BI, García JF, Suela J, et al Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasia. Haematologica 2008;93:670–679.
- Dicker F, Schnittger S, Haferlach T, Kern W, Schoch C. Immunostimulatory oligonucleotide-induced metaphase cytogenetic detect chromosomal aberrations in 80% of CLL patients: a study of 132 CLL cases with correlation to FISH, IgVH status, and CD138 expression. Blood 2006;108:3152–3160.
- ISCN 2005. An international system for human cytogenetic nomenclature. In: Shaffer LG, Tommerup N, editors. Basel: S. Karger; 2005.
- Jarosova M, Jedlickova K, Holzerova M, et al Contribution of comparative genomic hybridization and fluorescence in situ hybridization to the detection of chromosomal abnormalities in B-cell chronic lymphocytic leukemia. Onkologie 2001;24:60–65.
- Fiegler H, Carr P, Douglas EJ, et al DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones. Genes Chromosomes Cancer 2003;36:361–374.
- Bea S, Lopez-Guillermo A, Ribas M, et al Genetic imbalances in progressed B-cell chronic lymphocytic leukemia and transformed large-cell lymphoma (Richter's syndrome). Am J Pathol 2002;161:957–968.
- Forconi F, Rinald A, Kwee I, et al Genome-wide DNA analysis identifies recurrent imbalances predicting outcome in chronic lymphocytic leukaemia with 17p deletion. Br J Haematol 2008;143:532–536.
- Tyybakinoja A, Vilpo J, Knuutila S. High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia. Cytogenet Genome Res 2007;118:8–12.
- Joos S, Menz CHK, Wrobel G, et al Classical Hodgkin lymphoma is characterized by recurrent copy number gains of the short arm of chromosome 2. Blood 2002;99:1381–1387.
- Martinez-Climent JA, Ash AA, Segraves R, et al Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations. Blood 2003;101:3109–3117.
- Fukuhara N, Tagawa H, Kameoka Y, et al Characterization of target genes at the 2p15–16 amplicon in diffuse large B-cell lymphoma. Cancer Sci 2006;97:499–504.
- Hatzi E, Murphy C, Zoephel A, et al N-myc oncogene overexpression down-regulates leukemia inhibitory factor in neuroblastoma. Eur J Biochem 2002;269:3732–3741.
- Berger R, Busson-Le Coniat M. Centric and pericentric chromosome rearrangements in hematopoietic malignancies. Leukemia 1999;13:671–678.
- Callet-Bauchu E, Salles G, Gazzo S, et al Translocations involving the short arm of chromosome 17 in chronic B-lymphoid disorders: frequent occurrence of dicentric rearrangements and possible association with adverse outcome. Leukemia 1999;13:460–468.
- Higgins RA, Gunn SR, Robetorye RS. Clinical application of array-based comparative genomic hybridization for the identification of prognostically important genetic alterations in chronic lymphocytic leukemia. Mol Diagn Ther 2008;12:271–280.
- Andersen MK, Pedersen-Bjergaard J. Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere. Leukemia 2000;14:105–111.
- Wiestner A, Rosenwald A, Barry TS, et al ZAP-70 expression identifies a chronic lymphocytic leukemia subtype with unmutated immunoglobulin genes, inferior clinical outcome and distinct gene expression profile. Blood 2003;101:4944–4951.