Curriculum Vitae

Date and place of birth: 1/9/1971, Martina Franca (TA)
Nationality: Italian
Family status: Married
Present Address: Department of Biology, Via Amendola 165/A, 70126 Bari

Education

• 1995 Degree in Biology with mark 110/110 cum laude, University of Bari.
• 2001 Specialization Course in Applied Genetics with mark 70/70 cum laude, University of Rome.
• 2004 PhD in Genetics and Molecular Evolution, University of Bari

Career

1996
Fellowship at the University of Bari, Genetics Institute.

1997/98
Fellowship sponsored by AULL (Association from Umbria on Leukemia and Lymphoma) at "Policlinico Monteluce", Perugia-Istitute of Internal Medicine and Oncological Sciences.

1999/2001
Fellowship sponsored by FIRC (Federazione Italiana Ricerca sul Cancro), Genetics Department of the University of Bari

2001/03
PhD course in Genetics and Molecular Evolution, University of Bari

2001
Member of the COST (European Co-operation in the field of Scientific and Technical Research) Action B19 WorkGroup 4.

2002/03
Visiting Scientist at the Department of Clinical Genetics, University Hospital, Lund (Sweden), directed by Prof. F. Mitelman.

2002
EMBO (European Molecular Biology Organisation) Short Term Fellowship to support a practical stage abroad (Sweden).

2003
Cost Action STSM (Short Term Scientific Mission) fellowship to support a practical stage abroad (Sweden)

2004
Permanent position as a researcher at the University of Bari, Department of Genetics and Microbiology (now Department of Biology).

2004
Member of the International European Workgroup "LeukemiaNet", WorkPackage 11-Cytogenetics.

2005
Tutor of PhD Student Course in Genetics and Molecular Evolution

Since November 2008
Management Committee member of Cost Action EuGESMA, and Vice-Chair of Working Group 2: Whole genome mutations and abnormalities.

Reviewer for: Leukemia, Genes Chromosomes & Cancer, BMC Genomics, Cancer Letters.

Seminars

11/10/1996
XI National FISME Congress (Spoleto). Oral presentation: Chromosome Y evolution in primates.

11/10/2000
Invited Speaker: FISH applications in onco-haematology. XVII National Meeting of Cytometry, GIC (Urbino)

November 2001
IV SIGU Congress (Orvieto) Oral presentation: Deletions on chromosome der(9) in CML.

23/3/2004
Invited speaker: Identification of structural karyotypic abnormalities in onco-haematology by FISH.

7/5/2004
Invited speaker: Study of the mechanisms of proto-oncogenes activation. University of Foggia.

9/9/2004
XV International Chromosome Conference - London Oral presentation: Identification of two genomic hot-spot regions in 8q24-dmin in hematologicalmalignancies

18/2/2005
Fragilome meeting-Heidelberg Oral presentation:Identification of two genomic hot-spot regions in 8q24-dmin in hematological malignancies.

22/10/2005
Array-CGH meeting-Marie Curie Actions, Porto Giardino (BA), Claus Lundsten best oral presentation award: Detailed characterization of MYC-containing double minutes in hematological malignancies.

15-16/10/2007
Invited speaker: FISH in hematological malignancies. 9th Course in Molecular Cytogenetics and DNA Microarrays (Bertinoro di Romagna)

8/11/2007
Seminar: Chromosomal rearrangements in hematological tumors. Casa Sollievo della Sofferenza, S. Giovanni Rotondo (FG)

6/2/2008
Seminar: Chromosomal rearrangements in hematological tumors. Istituto di Ematologia e Oncologia Medica "Seragnoli", Bologna.

21/2/2008
Seminar: Molecular characterization of two cases of follicular lymphoma. IRCCS Ospedale Oncologico, Bari

6/9/2008
Oral presentation: Molecular characterization of dmin/hsr in tumors, 11th EWCMGST, Bilbao, Spain.

25/9/2008
Oral presentation: A novel fusion 5'AFF3/3'BCL2 in follicular lymphoma. X SIES (Società Italiana Ematologia Sperimentale) Conference, Bari, Italy.

21/03/2009
Oral presentation: “ Deep sequencing and SNP Array technologies in AML/MDS”. III EuGESMA Management Committee meeting, Antwerp

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Attivita' Didattica:

Anno Accademico 2004/2005:
Esercitazioni e seminari relativi all’insegnamento di Ricerca Diagnostica in Genetica Molecolare (Scienze Biosanitarie, Laurea Specialistica);

Anno Accademico 2005/2006:
Corso di Genetica Vegetale (in affidamento), Corso di Laurea Specialistica in Biologia Cellulare e Molecolare (I semestre): 3 CFU
Corso di Terapia Genica e Laboratorio di Citogenetica Umana (in affidamento), Corso di Laurea Specialistica in Biotecnologie Mediche e Medicina Molecolare (II semestre): 5 (3+2) CFU;

Anno Accademico 2006/2007:
Corso di Terapia Genica e Laboratorio di Citogenetica Umana (in affidamento), Corso di Laurea Specialistica in Biotecnologie Mediche e Medicina Molecolare (II semestre): 5 (3+2) CFU;

Anno Accademico 2007/2008:
Corso di Genetica Vegetale (in affidamento), Corso di Laurea Specialistica in Biologia Cellulare e Molecolare (I semestre): 3 CFU;

Anno Accademico 2008/2009:
Corso di Genetica (in affidamento), Corso di Laurea Triennale in Scienze Naturali (I semestre): 6 CFU.

Anno Accademico 2009/2010:
Corso di Genetica (in affidamento), Corso di Laurea Triennale in Scienze Naturali (II semestre): 6 CFU;

Anno Accademico 2010/2011:
Corso di Laboratorio di Citogenetica Umana (in affidamento), Corso di Laurea Specialistica Biotecnologie Mediche e Medicina Molecolare (II semestre): 3 (2+1) CFU

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Finanziamenti

Progetto di ricerca “Giovani Ricercatori” (1 Agosto 2002)
PRIN 2005 (biennale, come componente unita’ operativa)
AIRC 2004 (annuale, come componente del progetto)
AIRC 2005 (annuale, come componente del progetto)
AIRC 2006 (annuale, come componente del progetto)
AIRC 2007 (triennale, come componente del progetto)
PRIN 2007 (biennale, come coordinatore scientifico)
AIRC 2010 (annuale, come componente del progetto)

Top Collaborazioni:

-       Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo (FG), (Dr. Massimo Carella, Dr. Giuseppe Merla, Dr.ssa Paola Parrella, Dr.ssa Muscarella Lucia Anna);

-       Molecular Biology Unit, Department of Hematology/Oncology Seràgnoli, University of Bologna (Prof. Giovanni Martinelli);
-       Department of Biomedical Sciences, University of Modena and Reggio Emilia (Prof. Sergio Ferrari);
-       Division of Hematology, Department of Critical Care, University of Florence (Prof. Alessandro Vannucchi);
-       Centro Ricerca Tettamanti, Clinica Pediatrica Univ. Milano-Bicocca, Ospedale San Gerardo, Monza (Dr. Gianni Cazzaniga)
-       Dipartimento di Biologia e Patologia Molecolare e Cellulare, Università Federico II, Naples (Prof. Antonio Feliciello)
-       Dipartimento di Anatomia Patologica, Ospedale S. Martino, Belluno (Dr.ssa Crocifissa Locunsolo)
-       Laboratory of Cytogenetics, Department of Internal Medicine, University of Genova (Dr.ssa Giuseppina Fugazza)
-       Laboratoire d'Oncohématologie, Hôpital Pasteur, Pavillon J niveau 0, Nice cedex, France (Prof. Sophie Raynaud)
-       Unité de cytogénétique du cancer, Service de génétique médicale, Centre Hospitalier Universitaire Vaudois, Lausanne,  Switzerland (Dr. Dominique Mühlematter)
-       Department of Clinical Genetics, Lund University Hospital, Lund, Sweden (Prof. Fredrik Mertens, Prof. Bertil Johansson)

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Pubblicazioni:

1.     Barbano R, Copetti M, Perrone G, Pazienza V, Anna Muscarella L, Balsamo T, Tiziana Storlazzi C, Ripoli M, Rinaldi M, Maria Valori V, Pia Latiano T, Maiello E, Stanziale P, Carella M, Mangia A, Pellegrini F, Bisceglia M, Onetti Muda A, Altomare V, Murgo R, Michele Fazio V, Parrella P. High RAD51 mRNA expression characterize estrogen receptor-positive/progesteron receptor-negative breast cancer and is associated with patient's outcome. INTERNATIONAL JOURNAL OF CANCER 2010 Nov 9. [Epub ahead of print]

2.     ASCHERO S, VALLERO S, MORRA I, IMPERA L, FORNI M, SANDRI A, BASSO ME, STORLAZZI C., GIORDANO F, FIDANI P, DE IORIS MA, DI MONTEZEMOLO LC (2010). A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature. JOURNAL OF NEURO-ONCOLOGY, vol. 99; p. 141-146, ISSN: 0167-594X

3.     CARELLA M, SPREAFICO F, PALUMBO O, STORLAZZI C., TABANO S, MIOZZO M, MIGLIONICO L, CALVANO S, SINDICI G, GAMBA B, IMPERA L, COLLINI P, ZELANTE L, RADICE P, PEROTTI D (2010). Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico-pathological studies. AMERICAN JOURNAL OF MEDICAL GENETICS. PART A, vol. 152A; p. 1756-1763, ISSN: 1552-4825

4.     D'ALESSANDRO V, MUSCARELLA LA, LA TORRE A, BISCEGLIA M, PARRELLA P, SCARAMUZZI G, STORLAZZI C., TROMBETTA D, KOK K, DE CATA A, SPERANDEO M, ZELANTE L, CARELLA M, VENDEMIALE G (2010). Molecular analysis of the HuD gene in neuroendocrine lung cancers. LUNG CANCER, vol. 67(1); p. 69-75, ISSN: 0169-5002

5.     GUASTADISEGNI MC, LONOCE A, IMPERA L, DI TERLIZZI F, FUGAZZA G, ALIANO S, GRASSO R, CLUZEAU T, RAYNAUD S, ROCCHI M, STORLAZZI C. (2010). CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia. LEUKEMIA, vol. 24; p. 1516-1519, ISSN: 0887-6924

6.     IACOBUCCI I, PAPAYANNIDIS C, PAOLONI F, STORLAZZI C., LONETTI A, VIGNETTI M, FERRARI A, CILLONI D, MESSA F, PAOLINI S, CHIARETTI S, GUADAGNUOLO V, VITALE A, MELONI G, SOVERINI S, FAZI P, PANE F, BACCARANI M, FO√Ä R, MARTINELLI G (2010). The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. On behalf of the GIMEMA Acute Leukemia Working Party. HAEMATOLOGICA, ISSN: 0390-6078

7.     STORLAZZI C., LONOCE A, GUASTADISEGNI MC, TROMBETTA D, D'ADDABBO P, DANIELE G, L'ABBATE A, MACCHIA G, SURACE C, KOK K, ULLMANN R, PURGATO S, PALUMBO O, CARELLA M, AMBROS PF, ROCCHI M (2010). Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure. GENOME RESEARCH, vol. 20; p. 1198-1206, ISSN: 1088-9051

8.     DENCIC FEKETE M, DORDJEVIC V, STORLAZZI C., JANKOVIC G, BOGDANOVIC A, JOVANOVIC J, ROCCHI M, TODORIC-ZIVANOVIC B, STRNAD M, GOTIC M (2009). t(5;6;12) associated with resistance to imatinib mesylate in chronic myeloid leukemia. INTERNATIONAL JOURNAL OF HEMATOLOGY, vol. 89; p. 508-512, ISSN: 0925-5710

9.     GORUNOVA L, VULT VON STEYERN F, STORLAZZI C., BJERKEHAGEN B, FOLLER√ÖS G, HEIM S, MANDAHL N, MERTENS F (2009). Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations. GENES, CHROMOSOMES & CANCER, vol. 48; p. 583-602, ISSN: 1045-2257

10.  IACOBUCCI I, STORLAZZI C., CILLONI D, LONETTI A, OTTAVIANI E, SOVERINI S, ASTOLFI A, CHIARETTI S, VITALE A, MESSA F, IMPERA L, BALDAZZI C, D'ADDABBO P, PAPAYANNIDIS C, LONOCE A, COLAROSSI S, VIGNETTI M, PICCALUGA PP, PAOLINI S, RUSSO D, PANE F, SAGLIO G, BACCARANI M, FO√Ä R, MARTINELLI G (2009). Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute Leukemia Working Party (GIMEMA AL WP). BLOOD, vol. 114; p. 1739-1753, ISSN: 0006-4971

11.  KRSTIC AD, IMPERA L, GUC-SCEKIC M, LAKIC N, DJOKIC D, SLAVKOVIC B, STORLAZZI C. (2009). A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia. CANCER GENETICS AND CYTOGENETICS, vol. 195(2); p. 125-131, ISSN: 0165-4608

12.  MARTINELLI G, IACOBUCCI I, STORLAZZI C., VIGNETTI M, PAOLONI F, CILLONI D, SOVERINI S, VITALE A, CHIARETTI S, CIMINO G, PAPAYANNIDIS C, PAOLINI S, ELIA L, FAZI P, MELONI G, AMADORI S, SAGLIO G, PANE F, BACCARANI M, FO√Ä R (2009). IKZF1 (Ikaros) deletions in BCR-ABL1-positive acute lymphoblastic leukemia are associated with short disease-free survival and high rate of cumulative incidence of relapse: a GIMEMA AL WP report. JOURNAL OF CLINICAL ONCOLOGY, vol. 27(31; p. 5202-5207, ISSN: 0732-183X

13.  TRAGESER D, IACOBUCCI I, NAHAR R, DUY C, VON LEVETZOW G, KLEMM L, PARK E, SCHUH W, GRUBER T, HERZOG S, KIM YM, HOFMANN WK, LI A, STORLAZZI C., J√ÑCK HM, GROFFEN J, MARTINELLI G, HEISTERKAMP N, JUMAA H, M√úSCHEN M (2009). Pre-B cell receptor-mediated cell cycle arrest in Philadelphia chromosome-positive acute lymphoblastic leukemia requires IKAROS function. JOURNAL OF EXPERIMENTAL MEDICINE, vol. 206; p. 1739-1753, ISSN: 0022-1007

14.  TROMBETTA D, MERTENS F, LONOCE A, D'ADDABBO P, RENNSTAM K, MANDAHL N, STORLAZZI C. (2009). Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors. GENES, CHROMOSOMES & CANCER, vol. 48; p. 993-1001, ISSN: 1045-2257

15.  GUASTADISEGNI MC, LONOCE A, IMPERA L, ALBANO F, D'ADDABBO P, CARUSO S, VASTA I, PANAGOPOULOS I, LESZL A, BASSO G, ROCCHI M, STORLAZZI C. (2008). 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. MOLECULAR CANCER, vol. 7(1); p. 80, ISSN: 1476-4598

16.  IMPERA L, ALBANO F, LO CUNSOLO C, FUNES S, IUZZOLINO P, LAVEDER F, PANAGOPOULOS I, ROCCHI M, STORLAZZI C. (2008). A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma. ONCOGENE, vol. 27; p. 6187-6190, ISSN: 0950-9232

17.  IMPERA L, ALBANO F, MANCINI M, AVENTIN A, ROCCHI M, STORLAZZI C. (2008). Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia. CANCER GENETICS AND CYTOGENETICS, vol. 181(2); p. 131-137, ISSN: 0165-4608

18.  MONTICONE M, BIOLLO E, MAFFEI M, DONADINI A, ROMEO F, STORLAZZI C., GIARETTI W, CASTAGNOLA P (2008). Gene expression deregulation by KRAS G12D and G12V in a BRAF V600E context. MOLECULAR CANCER, vol. 7:92, ISSN: 1476-4598

19.  SILVA FP, MOROLLI B, STORLAZZI C., ZAGARIA A, IMPERA L, KLEIN B, VRIELING H, KLUIN-NELEMANS HC, GIPHART-GASSLER M (2008). ETV6 mutations and loss in AML-M0. LEUKEMIA, vol. 22(8); p. 1639-1643, ISSN: 0887-6924

20.  STORLAZZI C., ALBANO F, GUASTADISEGNI MC, IMPERA L, M√úHLEMATTER D, MEYER-MONARD S, WUILLEMIN W, ROCCHI M, JOTTERAND M (2008). 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, MOLECULES, & DISEASES, vol. 40(3); p. 452-455, ISSN: 1079-9796

21.  SURACE C, PEDEUTOUR F, TROMBETTA D, BUREL-VANDENBOS F, ROCCHI M, STORLAZZI C. (2008). Episomal amplification of MYCN in a case of medulloblastoma. VIRCHOWS ARCHIV, vol. 452(5); p. 491-497, ISSN: 0945-6317

22.  STORLAZZI C., ALBANO F, DENCIC-FEKETE M, DJORDJEVIC V, ROCCHI M (2007). Late-appearing pseudocentric fission event during chronic myeloid leukemia progression. CANCER GENETICS AND CYTOGENETICS, vol. 174; p. 61-67, ISSN: 0165-4608

23.  STORLAZZI C., 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 (2007). Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma. LEUKEMIA, vol. 21(10); p. 2221-2225, ISSN: 0887-6924

24.  STORLAZZI C., ALBANO F, LOCUNSOLO C, LONOCE A, FUNES S, GUASTADISEGNI MC, CIMAROSTO L, IMPERA L, D'ADDABBO P, PANAGOPOULOS I, SPECCHIA G, ROCCHI M (2006). t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene. LEUKEMIA, vol. 20(12); p. 2190-2192, ISSN: 0887-6924

25.  STORLAZZI C., BREKKE HR, MANDAHL N, BROSJO O, SMELAND S, LOTHE RA, MERTENS F (2006). Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours. JOURNAL OF PATHOLOGY, vol. 209(4); p. 492-500, ISSN: 0022-3417

26.  STORLAZZI C., FIORETOS T, SURACE C, LONOCE A, MASTRORILLI A, STRMBECK B, DADDABBO P, IACOVELLI F, MINERVINI C, AVENTIN A, DASTUGUE N, FONATSCH C, HAGEMEIJER A, JOTTERAND M, MHLEMATTER D, LAFAGE-POCHITALOFF M, NGUYEN-KHAC F, SCHOCH C, SLOVAK ML, SMITH A, SOL F, VAN ROY N, JOHANSSON B, ROCCHI M. (2006). MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. HUMAN MOLECULAR GENETICS, vol. 15 (6); p. 933-942, ISSN: 0964-6906

27.  STORLAZZI C., WOZNIAK A, PANAGOPOULOS I, SCIOT R, MANDAHL N, MERTENS F, DEBIEC-RYCHTER M (2006). Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocationt(X;6)(q13-14;q22). INTERNATIONAL JOURNAL OF CANCER, vol. 118(8); p. 1972-1976, ISSN: 0020-7136

28.  STORLAZZI C., VON STEYERN FV, DOMANSKI HA, MANDAHL N, MERTENS F. (2005). Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma. INTERNATIONAL JOURNAL OF CANCER, vol. 117(6); p. 1055-1057, ISSN: 0020-7136

29.  SURACE C, STORLAZZI C., ENGELLAU J, DOMANSKI HA, GUSTAFSON P, PANAGOPOULOS I, D'ADDABBO P, ROCCHI M, MANDAHL N, MERTENS F. (2005). Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma. VIRCHOWS ARCHIV, vol. 447(5); p. 869-874, ISSN: 0945-6317

30.  WIESER R, FRITZ B, ULLMANN R, MULLER I, GALHUBER M, STORLAZZI C., RAMASWAMY A, CHRISTIANSEN H, SHIMIZU N, REHDER H (2005). Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney. HUMAN MUTATION, vol. Aug;26(2); p. 78-83, ISSN: 1059-7794

31.  INTINI D, FABRIS S, STORLAZZI C., OTSUKI T, CICERI G, VERDELLI D, LOMBARDI L, ROCCHI M, NERI A. (2004). Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation. BRITISH JOURNAL OF HAEMATOLOGY, vol. 126(3); p. 437-439, ISSN: 0007-1048

32.  PANAGOPOULOS I, STORLAZZI C., FLETCHER CD, FLETCHER JA, NASCIMENTO A, DOMANSKI HA, WEJDE J, BROSJO O, RYDHOLM A, ISAKSSON M, MANDAHL N, MERTENS F. (2004). The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma. GENES, CHROMOSOMES & CANCER, vol. 40; p. 218-228, ISSN: 1045-2257

33.  SPECCHIA G, ALBANO F, ANELLI L, STORLAZZI C., ZAGARIA A, LISO A, PANNUNZIO A, PASTORE D, MESTICE A, GRECO G, LISO V, ROCCHI M. (2004). Derivative chromosome 9 deletions in chronic myeloid leukemia are associated with loss of tumor suppressor genes. LEUKEMIA & LYMPHOMA, vol. 45; p. 689-694, ISSN: 1042-8194

34.  STORLAZZI C., ANELLI L, ALBANO F, ZAGARIA A, VENTURA M, ROCCHI M, PANAGOPOULOS I, PANNUNZIO A, OTTAVIANI E, LISO V, SPECCHIA G (2004). A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1. ANNALS OF HEMATOLOGY, vol. 83; p. 78-83, ISSN: 0939-5555

35.  STORLAZZI C., FIORETOS T, PAULSSON K, STROMBECK B, LASSEN C, AHLGREN T, JULIUSSON G, MITELMAN F, ROCCHI M, JOHANSSON B. (2004). Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies. HUMAN MOLECULAR GENETICS, vol. 13; p. 1479-1485, ISSN: 0964-6906

36.  STORLAZZI C., MERTENS F, NASCIMENTO A, ISAKSSON M, WEJDE J, BROSJ O, MANDAHL N, PANAGOPOULOS I (2004). Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma. HUMAN MOLECULAR GENETICS, vol. 12; p. 2349-2358, ISSN: 0964-6906

37.  ZAGARIA A, ANELLI L, ALBANO F, STORLAZZI C., LISO A, ROBERTI MG, BUQUICCHIO C, LISO V, ROCCHI M, SPECCHIA G. (2004). A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome. CANCER GENETICS AND CYTOGENETICS, vol. 150; p. 81-85, ISSN: 0165-4608

38.  ALBANO F, SPECCHIA G, ANELLI L, STORLAZZI C., BUQUICCHIO, ROBERTI MG, LISO V, ROCCHI M. (2003). Genomic deletions on the third chromosome involved in variant t(9;22) chronic myeloid leukemia cases. GENES, CHROMOSOMES & CANCER, vol. 36; p. 353-360, ISSN: 1045-2257

39.  SILVA FP, MOROLLI B, STORLAZZI C., ANELLI L, WESSELS H, BEZROOKOVE V, KLUIN-NELEMANS HC, GIPHART-GASSLER M. (2003). Identification of RUNX1/AML1 as a classical tumor suppressor gene. ONCOGENE, vol. 22; p. 538-547, ISSN: 0950-9232

40.  SONIA FABRIS, STORLAZZI C., LUCA BALDINI, LUCIA NOBILI, LUIGIA LOMBARDI, ANNA TERESA MAIOLO, MARIANO ROCCHI, AND ANTONINO NERI. (2003). Heterogeneous pattern of chromosomal breakpoint involving the c-MYC locus in multiple myeloma. GENES, CHROMOSOMES & CANCER, vol. 37; p. 261-269, ISSN: 1045-2257

41.  SPECCHIA G, ALBANO F, ANELLI L, STORLAZZI C., ZAGARIA A, MANCINI M, CUNEO A, PANE F, FOA' R, LISO V, ROCCHI M. (2003). Deletions on der(9) chromosomes chromosome in adult Ph-positive acute lymphoblastic leukemia occur with a frequency similar to that observed in chronic myeloid leukemia. LEUKEMIA, vol. 17; p. 528-531, ISSN: 0887-6924

42.  STORLAZZI C., FREDRIK MERTENS, HENRYK DOMANSKI, CHRISTOPHER D.M. FLETCHER, JOOP WIEGANT AND NILS MANDAHL. (2003). Ring Chromosomes and Low-grade Gene Amplification in an Atypical Lipomatous Tumor with Minimal Nuclear Atypia. INTERNATIONAL JOURNAL OF ONCOLOGY, vol. 23; p. 67-71, ISSN: 1019-6439

43.  STORLAZZI C., FREDRIK MERTENS, NILS MANDAHL, DAVID GISSELSSON, MARGARETH ISAKSSON, PELLE GUSTAFSON, HENRYK A. DOMANSKI, AND IOANNIS PANAGOPOULOS (2003). A Novel Fusion Gene, SS18L1/SSX1, in Synovial Sarcoma. GENES, CHROMOSOMES & CANCER, vol. 37; p. 195-200, ISSN: 1045-2257

44.  G.SAGLIO, STORLAZZI C., E.GIUGLIANO, C.SURACE, L.ANELLI, G.REGE-CAMBRIN, A.ZAGARIA, A.JIMENEZ VELASCO, A.HEINIGER, P.SCARAVAGLIO, A.TORRES GOMEZ, J.ROMAN GOMEZ, N.ARCHIDIACONO, S.BANFI, M.ROCCHI (2002). A 76kb interchromosomal duplicon maps close to BCR gene on chromosome 22 and to ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia-chromosome translocation. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol. 99; p. 9882-9887, ISSN: 0027-8424

45.  G.SPECCHIA, F.ALBANO, STORLAZZI C., L.ANELLI, A.ZAGARIA, V.LISO, M. ROCCHI (2002). t(15;17) in acute promyelocytic leukemia is not associated with  submicroscopic deletions on der(17). HAEMATOLOGICA, vol. 87; p. 775-777, ISSN: 0390-6078

46.  SPECCHIA G, ALBANO F, ANELLI L, STORLAZZI C., CIMINO G, LISO A, ZAGARIA A, LISO V, ROCCHI M. (2002). Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia. BRITISH JOURNAL OF HAEMATOLOGY, vol. 119; p. 488-491, ISSN: 0007-1048

47.  STORLAZZI C., ANELLI L, SURACE C, ROCCHI M, ALBANO F, PASTORE D, LISO V, SPECCHIA G (2002). Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a PH-positive chronic myeloid leukemia. CANCER GENETICS AND CYTOGENETICS, vol. 134; p. 109-113, ISSN: 0165-4608

48.  STORLAZZI C., G.SPECCHIA, L.ANELLI, F.ALBANO, D.PASTORE, M.ROCCHI, AND V.LISO (2002). Characterization of der(9) deletions in CML patients. CANCER GENETICS AND CYTOGENETICS, vol. 35; p. 271-276, ISSN: 0165-4608

49.  STORLAZZI C., L.ANELLI, C.SURACE, A. LONOCE, A.ZAGARIA, M.NANNI, P.CURZI, M.ROCCHI (2002). Molecular Cytogenetic Characterization of a Complex Rearrangement Involving Chromosomes 9 and 22 in a Case of Ph Negative Chronic Myeloid Leukemia. CANCER GENETICS AND CYTOGENETICS, vol. 136; p. 141-145, ISSN: 0165-4608

50.  G.SPECCHIA, A.MESTICE, STORLAZZI C., L.ANELLI, A.PANNUNZIO, M.G. ROBERTI, M.ROCCHI, V.LISO (2001). A novel translocation t(2;9)(q14;p12) in AML-M2 with an uncommon phenotype: myeloperoxidase-positive and myeloid antigen-negative. LEUKEMIA RESEARCH, vol. 25; p. 501-507, ISSN: 0145-2126

51.  G.SPECCHIA, F.ALBANO, L.ANELLI, STORLAZZI C., M.MONACO, S.CAPALBO, M.ROCCHI, V.LISO (2001). Concomitant tetrasomy 3q and trisomy 18 in CD5- CD13+ chronic lymphocytic leukemia. CANCER GENETICS AND CYTOGENETICS, vol. 94; p. 127-130, ISSN: 0165-4608

52.  G.SPECCHIA, STORLAZZI C., A.CUNEO, C.SURACE, A.MESTICE, A.PANNUNZIO, M.ROCCHI, V.LISO (2001). Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case. ANNALS OF HEMATOLOGY, vol. 80; p. 246-250, ISSN: 0939-5555

53.  L.DE BENEDICTIS, A.POLIZZI, G.CANGIANO, M.BUTTIGLIONE, S.ARBIA, STORLAZZI C., M.ROCCHI, G.GENNARINI. (2001). Alternative Promoters Drive The Expression Of The Gene Encoding The Mouse Axonal Glycoprotein F3/Contactin. MOLECULAR BRAIN RESEARCH, vol. 95; p. 55-74, ISSN: 0169-328X

54.  M.ROSATI, M.ROCCHI, STORLAZZI C., G.GRIMALDI (2001). Gene organization, splicing and mapping to chromosome 12q24.33 of the human ZNF84 KRAB/FPB containing zinc finger gene. CYTOGENETICS AND CELL GENETICS, vol. 2001; p. 127-130, ISSN: 0301-0171

55.  F. VITELLI, I. MELONI, S. FINESCHI, F. FAVARA, STORLAZZI C., M. ROCCHI, A. RENIERI (2000). Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3. CYTOGENETICS AND CELL GENETICS, vol. 88; p. 259-263, ISSN: 0301-0171

56.  R. MARZELLA, L. VIGGIANO, V. MIOLLA, STORLAZZI C., A.RICCO, E. GENTILE, R. ROBERTO, A.FRATELLO, M. MANCINI, N. ARCHIDIACONO, M. ROCCHI (2000). Molecular Cytogenetic Resources for Chromosome 4 and Comparative Analysis of Phylogenetic Chromosome IV in Great Apes. GENOMICS, vol. 63; p. 307-313, ISSN: 0888-7543

57.  STORLAZZI C., V.LISO, F.ALBANO, G.CASTOLDI, M.ROCCHI, G.SPECCHIA. (2000). Acute myeloblastic leukemia with minimal myeloid differentiation featuring a three-way translocation t(8;13;14). HAEMATOLOGICA, vol. 85; p. 1099-1100, ISSN: 0390-6078

58.  L VIGGIANO, V MIOLLA, A RICCO, STORLAZZI C., M PENNACCHIA, A FRATELLO, M MANCINI, R MARZELLA, N ARCHIDIACONO, M ROCCHI (1999). Molecular Cytogenetic Resources Specific For Chromosome 12. AMERICAN JOURNAL OF MEDICAL GENETICS, vol. 87; p. 40-44, ISSN: 0148-7299

59.  ARCHIDIACONO A, STORLAZZI C., SPALLUTO C, RICCO AS, MARZELLA R, ROCCHI M (1998). Evolution of Chromosome Y in primates. CHROMOSOMA, vol. 107; p. 241-246, ISSN: 0009-5915

60.  PANARELLO C, ROSANDA C, MORERIO C, RUSSO I, DALLORSO S, GAMBINI C, RICCO AS, STORLAZZI C., ARCHIDIACONO N, MARIANO ROCCHI (1998). Lipoblastoma: a case with t(7;8)(q31)(q13). CANCER GENETICS AND CYTOGENETICS, vol. 102; p. 12-14, ISSN: 0165-4608

61.  VIGGIANO L, MARZELLA R, RICCO AS, STORLAZZI C., FRATELLO A, VARELLA-GARCIA M, ARCHIDIACONO N, ROCCHI M (1998). Panel  of  Partial Chromosome Paints and YAC probes Specific  for Human Chromosome 2. SOMATIC CELL AND MOLECULAR GENETICS, vol. 24; p. 13-21, ISSN: 0740-7750

62.  ZINGONI A, SOTO H, HEDRICK J, STOPPACCIARO A, STORLAZZI C., SINIGAGLIA F, D'AMBROSIO D, O'GARRA A, ROBINSON D, ROCCHI M, SANTONI A, ZLOTNIK A, AND NAPOLITANO M (1998). The Chemokine Receptor CCR8 is Preferentially Expressed in Th2 cells but not Th1 cells. JOURNAL OF IMMUNOLOGY, vol. 161; p. 547-551, ISSN: 0022-1767

63.  ZINGONI A, ROCCHI M, STORLAZZI C., BERNARDINI G, SANTONI A, NAPOLITANO M (1997). Isolation and chromosomal localization of GPR31, a human gene encoding a novel G-protein coupled receptor. GENOMICS, vol. 42; p. 519-523, ISSN: 0888-7543

64.  NAPOLITANO M, ZINGONI A, BERNARDINI G, SPINETTI G, NISTA A, STORLAZZI C., ROCCHI M, SANTONI A (1996). Molecular cloning of TER1 a chemokine receptor-like gene expressed by lymphoid tissues. JOURNAL OF IMMUNOLOGY, vol. 157; p. 2759-2763, ISSN: 0022-1767

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