51. Dencic-Fekete M, Dordevic V, Storlazzi CT, Jankovic G, Bogdanovic A, Jovanovic J, Rocchi M, Todoric-Zivanovic B, Strnad M, Gotic M: t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia. Int J Hematol. 2009 Mar 26. [Epub ahead of print]

50. Monticone M, Biollo E, Maffei M, Donadini A, Romeo F, Storlazzi CT, Giaretti W, Castagnola P: Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context. Mol Cancer. 2008 Dec 16;7:92.

49. Guastadisegni MC, Lonoce A, Impera L, Albano F, D'Addabbo P, Caruso S, Vasta I, Panagopoulos I, Leszl A, Basso G, Rocchi M, Storlazzi CT: Bone marrow ectopic expression of a non-coding RNA in childhood T-cell acute lymphoblastic leukemia with a novel t(2;11)(q11.2;p15.1) translocation. Mol Cancer 7:80 (2008) DOI 10.1186/1476-4598-7-80 I.F. 3.690

48. Impera L, Albano F, Lo Cunsolo C, Funes S, Iuzzolino P, Laveder F, Panagopoulos I, Rocchi M, Storlazzi CT: A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma. Oncogene 27:6187-6190 (2008) I.F. 6.440

47. Impera L, Albano F, Mancini M, Aventin A, Rocchi M, Storlazzi CT: Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia. Cancer Genet Cytogenet 181:131-137 (2008) I.F. 1.559

46. Silva FP, Morolli B, Storlazzi CT, Zagaria A, Impera L, Klein B, Vrieling H, Kluin-Nelemans HC, Giphart-Gassler M: ETV6 mutations and loss in AML-M0. Leukemia 22:1639-1643 (2008) I.F. 6.924

45. Storlazzi CT, Albano F, Guastadisegni MC, Impera L, Muhlematter D, Meyer-Monard S, Wuillemin W, Rocchi M, Jotterand M: Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia. Blood Cells Mol Dis 40:452-455 (2008) I.F. 2.555

44. Surace C, Pedeutour F, Trombetta D, Burel-Vandenbos F, Rocchi M, Storlazzi CT: Episomal amplification of MYCN in a case of medulloblastoma. Virchows Arch 452:491-497 (2008) I.F. 2.029

43. Storlazzi CT, Albano F, Dencic-Fekete M, Djordjevic V, Rocchi M: Late-appearing pseudocentric fission event during chronic myeloid leukemia progression. Cancer Genet Cytogenet 174:61-67 (2007) I.F. 1.559

42. Storlazzi CT, Albano F, Lo Cunsolo C, Doglioni C, Guastadisegni MC, Impera L, Lonoce A, Funes S, Macri E, Iuzzolino P, Panagopoulos I, Specchia G, Rocchi M: Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma. Leukemia 17:2221-2225 (2007) I.F. 6.924

41. Storlazzi C, Brekke H, Mandahl N, Brosjo O, Smeland S, Lothe R, Mertens F: Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours. J Pathol 209:492-500 (2006) I.F. 5.759

40. Storlazzi CT, Albano F, Locunsolo C, Lonoce A, Funes S, Guastadisegni MC, Cimarosto L, Impera L, D'Addabbo P, Panagopoulos I, Specchia G, Rocchi M: t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene. Leukemia 20:2190-2192 (2006) I.F. 6.146

39. Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strombeck B, D'Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Muhlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Sole F, Van Roy N, Johansson B, Rocchi M: MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Hum Mol Genet 15:933-942 (2006) I.F. 8.099

38. Storlazzi CT, Von Steyern FV, Domanski HA, Mandahl N, Mertens F: Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma. Int J Cancer 117:1055-1057 (2005) I.F. 4.700

37. Storlazzi CT, Wozniak A, Panagopoulos I, Sciot R, Mandahl N, Mertens F, Debiec-Rychter M: Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocationt(X;6)(q13-14;q22). Int J Cancer 18:1972-1976 (2005) I.F. 4.693

36. Surace C, Storlazzi CT, Engellau J, Domanski HA, Gustafson P, Panagopoulos I, D'Addabbo P, Rocchi M, Mandahl N, Mertens F: Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma. Virchows Arch 447:869-874 (2005) I.F. 2.224

35. Wieser R, Fritz B, Ullmann R, Muller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H: Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney. Hum Mutat 26:78-83 (2005) I.F. 7.923

34. Intini D, Fabris S, Storlazzi T, Otsuki T, Ciceri G, Verdelli D, Lombardi L, Rocchi M, Neri A: Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation. Br J Haematol 126:437-439 (2004 3

33. Panagopoulos I, Storlazzi CT, Fletcher CD, Fletcher JA, Nascimento A, Domanski HA, Wejde J, Brosjo O, Rydholm A, Isaksson M, Mandahl N, Mertens F: The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma. Genes Chromosomes Cancer 40:218-228 (2004) I.F. 4.276

32. Specchia G, Albano F, Anelli L, Storlazzi CT, Zagaria A, Liso A, Pannunzio A, Pastore D, Mestice A, Greco G, Liso V, Rocchi M: Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes. Leuk Lymphoma 45:689-694 (2004) I.F. 1.147

31. Storlazzi CT, Anelli L, Albano F, Zagaria A, Ventura M, Rocchi M, Panagopoulos I, Pannunzio A, Ottaviani E, Liso V, Specchia G: A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1. Ann Hematol 83:78-83 (2004) I.F. 1.291

30. Storlazzi CT, Fioretos T, Paulsson K, Strombeck B, Lassen C, Ahlgren T, Juliusson G, Mitelman F, Rocchi M, Johansson B: Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies. Hum Mol Genet 13:1479-1485 (2004) I.F. 7.801

29. Zagaria A, Anelli L, Albano F, Tiziana Storlazzi C, Liso A, Grazia Roberti M, Buquicchio C, Liso V, Rocchi M, Specchia G: A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome. Cancer Genet Cytogenet 150:81-85 (2004) I.F. 1.577

28. Albano F, Specchia G, Anelli L, Zagaria A, Storlazzi CT, Buquicchio C, Roberti MG, Liso V, Rocchi M: Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases. Genes Chromosomes Cancer 36:353-360 (2003) I.F. 4.192

27. Fabris S, Storlazzi CT, Baldini L, Nobili L, Lombardi L, Maiolo AT, Rocchi M, Neri A: Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma. Genes Chromosomes Cancer 37:261-269 (2003) I.F. 4.192

26. Silva FP, Morolli B, Storlazzi CT, Anelli L, Wessels H, Bezrookove V, Kluin-Nelemans HC, Giphart-Gassler M: Identification of RUNX1/AML1 as a classical tumor suppressor gene. Oncogene 22:538-547 (2003) I.F. 6.495

25. Specchia G, Albano F, Anelli L, Storlazzi CT, Zagaria A, Mancini M, Cuneo A, Pane F, Foa R, Manolelli F, Liso V, Rocchi M: Deletions on der(9) chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia. Leukemia 17:528-531 (2003) I.F. 5.116

24. Storlazzi CT, Mertens F, Domanski H, Fletcher CD, Wiegant J, Mandahl N: Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia. Int J Oncol 23:67-71 (2003) I.F. 2.536

23. Storlazzi CT, Mertens F, Mandahl N, Gisselsson D, Isaksson M, Gustafson P, Domanski HA, Panagopoulos I: A novel fusion gene, SS18L1/SSX1, in synovial sarcoma. Genes Chromosomes Cancer 37:195-200 (2003) I.F. 2.536

22. Storlazzi CT, Mertens F, Nascimento A, Isaksson M, Wejde J, Brosjo O, Mandahl N, Panagopoulos I: Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma. Hum Mol Genet 12:2349-2358 (2003) I.F. 8.597

21. Specchia G, Albano F, Anelli L, Storlazzi CT, Cimino G, Liso A, Zagaria A, Liso V, Rocchi M: Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukaemia. Br J Haematol 119:488-491 (2002) I.F. 3.052

20. Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G, Zagaria A, Jimenez Velasco A, Heiniger A, Scaravaglio P, Torres Gomez A, Roman Gomez J, Archidiacono N, Banfi S, Rocchi M: A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation. Proc Natl Acad Sci U S A 99:9882-9887 (2002) I.F. 10.700

19. Specchia G, Albano F, Anelli L, Storlazzi CT, Monaco M, Capalbo S, Rocchi M, Liso V: Concomitant tetrasomy 3q and trisomy 18 in CD5(-), CD13(+) chronic lymphocytic leukemia. Cancer Genet Cytogenet 133:160-163 (2002) I.F. 1.713

18. Specchia G, Albano F, Storlazzi CT, Anelli L, Zagaria A, Liso V, Rocchi M: t(15;17) in acute promyelocytic leukemia is not associated with submicroscopic deletions on der(17). Haematologica 87:775-777 (2002) I.F. 3.226

17. Storlazzi CT, Anelli L, Surace C, Lonoce A, Zagaria A, Nanni M, Curzi P, Rocchi M: Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia. Cancer Genet Cytogenet 136:141-145 (2002) I.F. 1.544

16. Storlazzi CT, Anelli L, Surace C, Rocchi M, Albano F, Pastore D, Liso V, Specchia G: Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia. Cancer Genet Cytogenet 134:109-113 (2002) I.F. 1.713

15. Storlazzi CT, Specchia G, Anelli L, Albano F, Pastore D, Zagaria A, Rocchi M, Liso V: Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients. Genes Chromosomes Cancer 35:271-276 (2002) I.F. 4.199

14. De Benedictis L, Polizzi A, Cangiano G, Buttiglione M, Arbia S, Tiziana Storlazzi C, Rocchi M, Gennarini G: Alternative promoters drive the expression of the gene encoding the mouse axonal glycoprotein F3/contactin. Brain Res Mol Brain Res 95:55-74 (2001) I.F. 2.341

13. Rosati M, Rocchi M, Storlazzi CT, Grimaldi G: Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84. Cytogenet Cell Genet 94:127-130 (2001) I.F. 1.993

12. Specchia G, Mestice A, Clelia Storlazzi T, Anelli L, Pannunzio A, Grazia Roberti M, Rocchi M, Liso V: A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative. Leuk Res 25:501-507 (2001) I.F. 2.483

11. Specchia G, Storlazzi CT, Cuneo A, Surace C, Mestice A, Pannunzio A, Rocchi M, Liso V: Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case. Ann Hematol 80:246-250 (2001 4

10. Marzella R, Viggiano L, Miolla V, Storlazzi CT, Ricco A, Gentile E, Roberto R, Surace C, Fratello A, Mancini M, Archidiacono N, Rocchi M: Molecular cytogenetic resources for chromosome 4 and comparative analysis of phylogenetic chromosome IV in great apes. Genomics 63:307-313 (2000) I.F. 3.483

9. Storlazzi TC, Liso V, Albano F, Castoldi G, Rocchi M, Specchia G: Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14). Haematologica 85:1099-1100 (2000) I.F. 5.032

08. Vitelli F, Meloni I, Fineschi S, Favara F, Tiziana Storlazzi C, Rocchi M, Renieri A: Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3. Cytogenet Cell Genet 88:259-263 (2000) I.F. 1.993

07. Viggiano L, Miolla V, Ricco A, Storlazzi CT, Pennacchia M, Fratello A, Mancini M, Marzella R, Archidiacono N, Rocchi M: Molecular cytogenetic resources specific for chromosome 12. Am J Med Genet 87:40-44 (1999) I.F. 2.063

06. Archidiacono N, Storlazzi CT, Spalluto C, Ricco AS, Marzella R, Rocchi M: Evolution of chromosome Y in primates. Chromosoma 107:241-246 (1998) I.F. 4.065

05. Panarello C, Rosanda C, Morerio C, Russo I, Dallorso S, Gambini C, Ricco AS, Storlazzi T, Archidiacono N, Rocchi M: Lipoblastoma: a case with t(7;8)(q31;q13). Cancer Genet Cytogenet 102:12-14 (1998) I.F. 1.544

04. Viggiano L, Marzella R, Ricco AS, Storlazzi TC, Fratello A, Varella-Garcia M, Archidiacono N, Rocchi M: A panel of partial chromosome paints and YAC probes specific for human chromosome 2. Somat Cell Mol Genet 24:13-21 (1998 1

03. Zingoni A, Soto H, Hedrick JA, Stoppacciaro A, Storlazzi CT, Sinigaglia F, D'Ambrosio D, O'Garra A, Robinson D, Rocchi M, Santoni A, Zlotnik A, Napolitano M: The chemokine receptor CCR8 is preferentially expressed in Th2 but not Th1 cells. J Immunol 161:547-551 (1998) I.F. 6.293

02. Zingoni A, Rocchi M, Storlazzi CT, Bernardini G, Santoni A, Napolitano M: Isolation and chromosomal localization of GPR31, a human gene encoding a putative G protein-coupled receptor. Genomics 42:519-523 (1997) I.F. 3.558

01. Napolitano M, Zingoni A, Bernardini G, Spinetti G, Nista A, Storlazzi CT, Rocchi M, Santoni A: Molecular cloning of CHR2, a cytokine receptor-like gene expressed by lymphoid cells. J Immunol 157:2759-2763 (1996) I.F. 6.293