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Emanuela Maserati

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Elisa Tassano; Elisa Tavella; Roberto Valli; Francesco Pasquali; Cristina Cuoco; Emanuela Maserati; Concetta Micalizzi; Cristina Morerio
New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6.
Alessandra Pangrazio; Waleed Al-Herz; Annalisa Frattini; Emanuela Maserati; Lucia Susani; Roberto Valli; Paolo Vezzoni; Anna Villa; Cristina Sobacchi
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.
Patrizia Noris; Alessandro Pecci; Roberto Valli; Carlo L Balduini; Rosangela Invernizzi; Lydia Mare; Cristina Marletta; Emanuela Maserati
Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type.

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2012: Elisa Tassano; Elisa Tavella; Roberto Valli; Francesco Pasquali; Cristina Cuoco; Emanuela Maserati; Concetta Micalizzi; Cristina Morerio
New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6.
Leukemia & lymphoma 2012;53(12):2434-8.
2012: Alessandra Pangrazio; Waleed Al-Herz; Annalisa Frattini; Emanuela Maserati; Lucia Susani; Roberto Valli; Paolo Vezzoni; Anna Villa; Cristina Sobacchi
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.
Calcified tissue international 2012;91(4):250-4.
2012: Patrizia Noris; Alessandro Pecci; Roberto Valli; Carlo L Balduini; Rosangela Invernizzi; Lydia Mare; Cristina Marletta; Emanuela Maserati
Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris-Trousseau type.
European journal of haematology 2012;89(4):345-9.
2012: Paola De Filippi; Daniela Lisini; Claudia Cagioni; Carmelo Carlo-Stella; Cesare Danesino; Emanuela Maserati; Francesca Novara; Daria Pagliara; Francesco Pasquali; Vittorio Rosti; Niki Zavras; Marco Zecca; Orsetta Zuffardi; Franco Locatelli
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia.
Pediatric blood & cancer 2012;59(3):580-2.
2012: Barbara Pressato; Roberto Valli; Francesco Lo Curto; Lydia Mare; Cristina Marletta; Giuseppe Montalbano; Francesco Pasquali; Emanuela Maserati
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
British journal of haematology 2012;157(4):503-5.
2012: V André; Andrea Biondi; S Bresolin; Cristina Bugarin; C Cappuzzello; Giovanni Cazzaniga; M Cipolli; Erica Dander; A Di Meglio; M Galbiati; Daniela Longoni; Emanuela Maserati; ELENA NICOLIS; L Sainati; M Serafini; Geertruy Te Kronnie; A J Warren; Giovanna D'Amico
Mesenchymal stem cells from Shwachman-Diamond syndrome patients display normal functions and do not contribute to hematological defects.
Blood cancer journal 2012;2():e94.
2012: Cristina Marletta; Maria Ester Bernardo; Alessandra Di Cesare Merlone; Simona Ferrari; Francesco Lo Curto; Franco Locatelli; Giuseppe Loffredo; Lydia Mare; Giuseppe Menna; Giuseppe Montalbano; Francesco Pasquali; Barbara Pressato; Roberto Valli; Luciana Vinti; Marco Zecca; Emanuela Maserati
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes.
Molecular cytogenetics 2012;5(1):39.
2011: Roberto Valli; Emanuela Maserati; Cristina Marletta; Barbara Pressato; Francesco Lo Curto; Francesco Pasquali
Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula.
Cancer genetics 2011;204(4):216-8.
2011: Roberto Valli; Cristina Marletta; Barbara Pressato; Giuseppe Montalbano; Francesco Lo Curto; Francesco Pasquali; Emanuela Maserati
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.
Molecular cytogenetics 2011;4():13.
2010: Barbara Pressato; Cristina Marletta; Giuseppe Montalbano; Roberto Valli; Emanuela Maserati
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome.
British journal of haematology 2010;150(5):632-3.
2009: Emanuela Maserati; Barbara Pressato; Roberto Valli; Antonella Minelli; Laura Sainati; Francesco Patitucci; Cristina Marletta; Angela Mastronuzzi; Furio Poli; Francesco Lo Curto; Franco Locatelli; Cesare Danesino; Francesco Pasquali
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
British journal of haematology 2009;145(2):190-7.
2009: Antonella Minelli; Emanuela Maserati; ELENA NICOLIS; Marco Zecca; Laura Sainati; Daniela Longoni; Francesco Lo Curto; G Menna; F Poli; E De Paoli; M Cipolli; Franco Locatelli; Francesco Pasquali; Cesare Danesino
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Leukemia 2009;23(4):708-11.
2008: Giuseppina Fogu; Emanuela Maserati; Francesca Cambosu; Maria Antonietta Moro; Fausto Poddie; Giovanna Soro; Pasquale Bandiera; Gigliola Serra; Gianni Tusacciu; Giuseppina Sanna; Vittorio Mazzarello; Andrea Montella
Patau syndrome with long survival in a case of unusual mosaic trisomy 13.
European journal of medical genetics 2008;51(4):303-14.
2007: Emanuela Maserati; Barbara Pressato; Roberto Valli; Francesco Patitucci; Francesco Lo Curto; Francesco Pasquali; Antonella Minelli; Cesare Danesino; Monia Marchetti; Giovanni Barosi
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.
Cancer genetics and cytogenetics 2007;179(1):79-81.
2007: Giovanni Porta; Emanuela Maserati; Elia Mattarucchi; Antonella Minelli; Barbara Pressato; Roberto Valli; Marco Zecca; Maria Ester Bernardo; Francesco Lo Curto; Franco Locatelli; Cesare Danesino; Francesco Pasquali
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.
Leukemia 2007;21(8):1833-5.
2007: Giovanni Porta; Elia Mattarucchi; Emanuela Maserati; Barbara Pressato; Roberto Valli; Cristina Morerio; Marco Zecca; Claudio Panarello; Franco Locatelli; Francesco Lo Curto; Francesco Pasquali
Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.
Journal of pediatric hematology/oncology 2007;29(3):163-5.
2006: Emanuela Maserati; Antonella Minelli; Barbara Pressato; Roberto Valli; Barbara Crescenzi; Maurizio Stefanelli; Giuseppe Menna; Laura Sainati; Furio Poli; Claudio Panarello; Marco Zecca; Francesco Lo Curto; Cristina Mecucci; Cesare Danesino; Francesco Pasquali
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Genes, chromosomes & cancer 2006;45(4):375-82.
2004: Cristina Morerio; Annamaria Rapella; Cristina Rosanda; Edoardo Lanino; Luca Lo Nigro; Andrea Di Cataldo; Emanuela Maserati; Francesco Pasquali; Claudio Panarello
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity.
Cancer genetics and cytogenetics 2004;152(2):108-12.
2004: Antonella Minelli; Emanuela Maserati; Gabriele Rossi; Maria Ester Bernardo; Piero De Stefano; Maria Paola Cecchini; Roberto Valli; Veronica Albano; Paolo Pierani; Anna Leszl; Laura Sainati; Francesco Lo Curto; Cesare Danesino; Franco Locatelli; Francesco Pasquali
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
Genes, chromosomes & cancer 2004;40(3):165-71.
2004: Cristina Morerio; Maura Acquila; Cristina Rosanda; Annamaria Rapella; Carlo Dufour; Franco Locatelli; Emanuela Maserati; Francesco Pasquali; Claudio Panarello
HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2).
Cancer research 2004;64(8):2649-51.
2004: Emanuela Maserati; Antonella Minelli; Giuseppe Menna; Maria Paola Cecchini; Maria Ester Bernardo; Gabriele Rossi; Paola De Filippi; Francesco Lo Curto; Cesare Danesino; Franco Locatelli; Francesco Pasquali
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects.
Cancer genetics and cytogenetics 2004;148(2):155-8.
2003: Carla Olivieri; Paola Maraschio; Desiree Caselli; Carla Martini; Giampiero Beluffi; Emanuela Maserati; Cesare Danesino
Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.
European journal of pediatrics 2003;162(2):100-3.
2003: Francesco Pasquali; Emanuela Maserati
Minimal residual disease and trisomy 8.
Cancer genetics and cytogenetics 2003;140(2):176.
2002: Emanuela Maserati; Fiorenza Aprili; Fabrizio Vinante; Franco Locatelli; Giovanni Amendola; Adriana Zatterale; Giuseppe Milone; Antonella Minelli; Franca Bernardi; Francesco Lo Curto; Francesco Pasquali
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases.
Genes, chromosomes & cancer 2002;33(1):93-7.
2001: Antonella Minelli; Cristina Morerio; Emanuela Maserati; Carla Olivieri; Claudio Panarello; L Bonvini; Anna Leszl; Cristina Rosanda; Edoardo Lanino; Cesare Danesino; Francesco Pasquali
Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia.
Leukemia 2001;15(6):971-5.
2001: A De Simone; A Cantù-Rajnoldi; Laura Sainati; Michele D'Avanzo; M Allen; Emanuela Maserati; Francesco Pasquali; Maurizio Aricò
Spontaneous remission from RAEB in a child.
Leukemia 2001;15(5):856-7.
2001: Antonella Minelli; Emanuela Maserati; Giovanni Giudici; Sabrina Tosi; Carla Olivieri; L Bonvini; Paola De Filippi; Andrea Biondi; Francesco Lo Curto; Francesco Pasquali; Cesare Danesino
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.
Cancer genetics and cytogenetics 2001;124(2):147-51.
2001: Cristina Morerio; I Russo; Cristina Rosanda; Annamaria Rapella; Anna Leszl; Giuseppe Basso; Emanuela Maserati; Francesco Pasquali; Claudio Panarello
17q21-qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia.
Cancer genetics and cytogenetics 2001;124(1):12-5.
2000: Emanuela Maserati; Antonella Minelli; Carla Olivieri; L Bonvini; A Marchi; Mauro Bozzola; Cesare Danesino; Susi Scappaticci; Francesco Pasquali
Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Cancer genetics and cytogenetics 2000;121(2):167-71.
1999: L Seghezzi; Paola Maraschio; Mauro Bozzola; Emanuela Maserati; Rossella Tupler; A Marchi; Luciano Tiepolo
Ring chromosome 9 with a 9p22.3-p24.3 duplication.
European journal of pediatrics 1999;158(10):791-3.
1999: Emanuela Maserati; Annalisa Verri; L Seghezzi; Rossella Tupler; A Federico; Luciano Tiepolo; Paola Maraschio
Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.
Annales de génétique 1999;42(4):210-4.
1998: Cesare Danesino; Francesco Pasquali; C Dellavecchia; Emanuela Maserati; Antonella Minelli; L Seghezzi
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.
American journal of medical genetics 1998;80(5):540.
1998: Emanuela Maserati; L Seghezzi; Francesco Pasquali; Franco Locatelli; P Viero; L Cavanna
Parental origin of chromosomes 9 and 22 involved in the Ph chromosome translocation in chronic myelocytic leukemia.
Cancer genetics and cytogenetics 1998;107(2):151-2.
1998: Paola Maraschio; Emanuela Maserati; L Seghezzi; Rossella Tupler; M P Verri; Luciano Tiepolo
Involvement of 9q22.1-31.3 region in pyloric stenosis.
Clinical genetics 1998;54(2):159-60.
1997: Laura Sainati; Anna Leszl; Maria Caterina Putti; Francesco Pasquali; Emanuela Maserati; Emilio Donti; Giovanna Venti; P Simi; C Giuliani; A Angioni; M Stella; Anna Montaldi; M Sessarego; Luigi Zanesco; Andrea Biondi; Giuseppe Basso
Centralized cytogenetic analysis of pediatric acute leukemia: results of an Italian collaborative experience.
Haematologica 1997;82(6):654-9.
1997: L Seghezzi; C Dellavecchia; Emanuela Maserati; Antonella Minelli; AM Carrà; Franco Locatelli; A Argusti; Francesco Lo Curto; Cesare Danesino; Francesco Pasquali
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.
Cancer genetics and cytogenetics 1997;99(1):77-80.
1996: L Seghezzi; Emanuela Maserati; Antonella Minelli; C Dellavecchia; P Addis; Franco Locatelli; A Angioni; P Balloni; C Miano; P Cavalli; Cesare Danesino; Francesco Pasquali
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.
Genes, chromosomes & cancer 1996;17(2):94-101.
1995: Franco Locatelli; Marco Zecca; Andrea Pession; Emanuela Maserati; Piero De Stefano; Francesca Severi
Myelodysplastic syndromes: the pediatric point of view.
Haematologica 1995;80(3):268-79.
1995: L Seghezzi; P Addis; S Giglio; R Invernizzi; Emanuela Maserati
Jumping translocations in acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1995;80(1):80-1.
1994: Franco Locatelli; Andrea Pession; Federico Bonetti; Emanuela Maserati; L Prete; Paolo Pedrazzoli; Marco Zecca; Arcangelo Prete; P Paolucci; Mario Cazzola
Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromes.
Leukemia 1994;8(5):844-9.
1994: Andrea Casasco; Emanuela Maserati; M Giordano; Marco Casasco; M Ciuffreda; S Sander; Marco Danova; Susi Scappaticci; Alberto Calligaro; D R Springall
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp.
Archives of oral biology 1994;39(3):245-9.
1992: Emanuela Maserati; M Casali; Rosangela Invernizzi; S Brugnatelli
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.
Cancer genetics and cytogenetics 1992;61(2):218-9.
1992: Emanuela Maserati; M Casali; G Fogu; R Sanna; Rosangela Invernizzi; G Latte; Paolo Simi; A Gabbas; Edoardo Ascari; Francesco Pasquali
Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosome.
Cancer genetics and cytogenetics 1992;61(2):152-7.
1992: M Casali; F Truglio; G Milone; Francesco Di Raimondo; G Parrinello; Emanuela Maserati; Francesco Pasquali
Trisomy 8 in Philadelphia chromosome (Ph1)-negative cells in the course of Ph1-positive chronic myelocytic leukemia.
Genes, chromosomes & cancer 1992;4(3):269-70.
1992: Emanuela Maserati; M Casali; Francesco Pasquali; Franco Locatelli; S Giani; L Prete; Marco Zecca; Rosangela Invernizzi; R Bassan
Translocation (8;21) in two cases of refractory anemia with excess of blasts in transformation.
Cancer genetics and cytogenetics 1992;58(1):76-8.
1992: Giovanni Lanzi; Umberto Balottin; Diego Franciotta; Emanuela Maserati; A Ottolini; Francesco Pasquali; Pierangelo Veggiotti
Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia.
European neurology 1992;32(3):121-5.
1991: Gaetano Bergamaschi; C C Stella; G Cattoretti; Rosangela Invernizzi; Emanuela Maserati; G Nalli; Paolo Pedrazzoli; F A Peverali; G Della Valle; Edoardo Ascari
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers.
British journal of haematology 1991;78(2):167-72.
1991: Emanuela Maserati; Francesco Pasquali; Orsetta Zuffardi; P Buttitta; C Cuoco; G Defant; Giorgio Gimelli; M Fraccaro
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection.
Annales de génétique 1991;34(3-4):239-46.
1990: Emanuela Maserati; E Campagnoli; F Truglio; F Porta; L Nespoli; G R Burgio; Francesco Pasquali
Cytogenetics in autologous bone marrow transplantation.
Cancer genetics and cytogenetics 1990;45(1):137-8.
1990: Antonella Minelli; M Piantanida; Emanuela Maserati; E Campagnoli; Francesco Pasquali; Cesare Danesino
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase.
Genes, chromosomes & cancer 1990;1(3):216-20.
1989: Emanuela Maserati; E Campagnoli; F Truglio; R Casalone; A Geniram; R Invernizzi; F Pasquali
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia.
Hereditas 1989;111(3):305-8.
1988: Barbara Bardoni; S Guioli; Emanuela Maserati; Paola Maraschio; G Camerino
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.
Human genetics 1988;81(1):23-5.
1988: Emanuela Maserati; A Ottolini; Pierangelo Veggiotti; Giovanni Lanzi; Francesco Pasquali
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14.
Clinical genetics 1988;34(5):283-7.
1988: R Casalone; Emanuela Maserati
A case of chronic myelocytic leukemia with five Philadelphia chromosomes.
Cancer genetics and cytogenetics 1988;34(2):257-9.
1988: Emanuela Maserati; P Cavalli; R Casalone; S Morandi; Francesco Pasquali
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase.
Human genetics 1988;78(3):248-50.
1987: M Aricò; A Colombo; Emanuela Maserati; Francesco Pasquali; G R Burgio
The 47,XXY karyotype and unrelated malformative patterns: an unusual association.
Helvetica paediatrica acta 1987;42(5-6):457-61.
1986: Emanuela Maserati; F Waibel; B Weber; M Fraccaro; A Gal; Francesco Pasquali; W Schempp; G Scherer; R Vaccaro; J Weissenbach
A 45,X male with a Yp/18 translocation.
Human genetics 1986;74(2):126-32.
1986: Emanuela Maserati; Francesco Pasquali; D Peretti
Different break-points in Philadelphia chromosome variant translocations and in constitutional and sporadic translocations.
Annals of human genetics 1986;50(Pt 2):153-62.