IRIS - Res&Arch Institutional Research Information System - Research & Archive

LA STARZA, Roberta
 Distribuzione geografica
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Continente #
NA - Nord America 3.301
EU - Europa 2.593
AS - Asia 872
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 2
Totale 6.775
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Nazione #
US - Stati Uniti d'America 3.293
IE - Irlanda 678
UA - Ucraina 564
SE - Svezia 400
IT - Italia 384
HK - Hong Kong 328
SG - Singapore 252
FI - Finlandia 159
DE - Germania 144
CN - Cina 133
VN - Vietnam 110
RU - Federazione Russa 109
GB - Regno Unito 47
CZ - Repubblica Ceca 20
CH - Svizzera 17
FR - Francia 16
KR - Corea 16
BE - Belgio 14
TR - Turchia 12
UZ - Uzbekistan 10
AT - Austria 9
NL - Olanda 8
GR - Grecia 7
EU - Europa 6
LB - Libano 6
CA - Canada 5
PL - Polonia 5
ES - Italia 3
SK - Slovacchia (Repubblica Slovacca) 3
BG - Bulgaria 2
IL - Israele 2
MX - Messico 2
NZ - Nuova Zelanda 2
RO - Romania 2
A1 - Anonimo 1
BD - Bangladesh 1
DK - Danimarca 1
IN - India 1
JP - Giappone 1
NO - Norvegia 1
PA - Panama 1
Totale 6.775
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Città #
Chandler 718
Dublin 675
San Mateo 331
Hong Kong 328
Jacksonville 305
Boardman 210
Singapore 189
Perugia 155
Medford 140
Princeton 138
Altamura 117
Dong Ket 110
Lawrence 107
Wilmington 101
Ann Arbor 96
Andover 78
Beijing 61
Redmond 56
Dearborn 46
Helsinki 38
San Paolo di Civitate 35
Munich 33
Saint Petersburg 32
Ashburn 28
Norwalk 28
Des Moines 26
Los Angeles 23
New York 22
Woodbridge 20
Brno 18
Santa Clara 18
Seoul 15
Brussels 14
Moscow 14
Falls Church 13
Dallas 12
Houston 12
Izmir 12
San Diego 12
Auburn Hills 11
Redwood City 10
Rome 10
Chicago 5
Amsterdam 4
Bologna 4
Chengdu 4
Shanghai 4
Boston 3
Bratislava 3
Den Haag 3
Lappeenranta 3
Madrid 3
Milan 3
Ponte 3
Salerno 3
Simi Valley 3
Deruta 2
Edinburgh 2
Frankfurt Am Main 2
Fremont 2
Gualdo Tadino 2
Hadera 2
Indianapolis 2
Nanjing 2
Naples 2
New Haven 2
Ottawa 2
Philadelphia 2
Piraeus 2
Santarcangelo di Romagna 2
Toronto 2
Vienna 2
Aprilia 1
Athens 1
Auckland 1
Birmingham 1
Bucharest 1
Cambridge 1
Chelyabinsk 1
Fairfield 1
Falkenstein 1
Florence 1
Fossano 1
Frankfurt am Main 1
Guangzhou 1
Kingstree 1
Kunming 1
Lausanne 1
Leawood 1
London 1
Ludwigshafen 1
Macclesfield 1
Memphis 1
Montréal 1
Nuremberg 1
Nürnberg 1
Olomouc 1
Orbetello 1
Oslo 1
Padova 1
Totale 4.525
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Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 88
14q+ chromosome marker in a T-cell-rich B-cell lymphoma. 87
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies 87
Molecular cytogenetic analysis of the 5Q-chromosome in the HL60 cell-line and in the 5Q-Syndrome 85
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia 85
Acute lymphoblastic leukaemia in Noonan syndrome 80
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 76
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia 75
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 74
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells 73
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 73
Constitutive phosphorylation of Janus kinase2 in the GL15 glioblastoma derived human cell line 72
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 72
Genetic profile of acute myeloid leukemia 71
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation 71
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9) 71
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus. 71
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 70
Alterazioni strutturali del cromosoma 12p dei disordini mieloidi 70
Genetic pathways in low-and high-grade HCV-related lymphomas are different 67
t(4;11) translocation involving NUP98 and RAP1GDS1 genes. Characterisation of a new subset of T acute lymphoblastc leukaemia 65
RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications 65
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases 65
Cytogenetic and FISH investigations on Tetrasomy 8 in ALL. 64
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 64
Succeful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. 63
Prognostic impact of genetic characterization in the GIMEMA LAM99P study for newly diagnosed adult AML. Relevance of combined analysis of conventional karyotyping, FLT3 and NPM mutational status 61
The ETV6,CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. 61
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 61
Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia 60
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 60
4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset 60
New somatic TERT promoter variants enhance the Telomerase activity in Glioblastoma 60
MYB rearrangements and over-expression in T-cell acute lymphoblastic leukemia 60
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 59
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia 59
MN1-ETV6 fusion gene arising from MDS With 5q- 59
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 59
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder 58
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 58
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts 57
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML. 57
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 57
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 56
The hereditary hyperferritinemia-cataract syndrome in 2 italian families 56
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion 55
CALM/AF10-positive leukemias show upregulation of genes involved in chromatin assembly and DNA repair processes and of genes adjacent to the breakpoint at 10p12. 55
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 55
Metachronous cardiac and cerebral sarcomas: case report with focus on molecular findings and review of the literature 54
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 54
MYB deregulation from a EWSR1-MYB fusion at leukemic evolution of a JAK2 V617F positive primary myelofibrosis 54
Acute myeloid leukemia 54
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene 54
Blockade of Oncogenic NOTCH1 With the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia 54
Different genomic imbalances in low- and high-grade HCV-related lymphomas 53
Submicroscopic deletions in 5q- associated malignancies 53
Haplo-identical haematopoietic stem cell transplantation for secondary leukaemia 52
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 51
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 51
The Italian external quality assessment scheme in classical cytogenetics: four years of activity. 51
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 51
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia 51
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 50
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients 49
New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia. 49
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 49
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies. 48
Rapid reversion of Loeffler's endocarditis by imatinib in early stage clonal hypereosinophilic syndrome 48
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 48
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 48
Philadelphia-like acute lymphoblastic leukemia is associated with minimal residual disease persistence and poor outcome. First report of the minimal residual disease-oriented GIMEMA LAL1913 48
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with (8;11) (p11,2;p15) 48
Prognostic impact of genetic characterization in the GIMEMA LAM99P multicenter study for newly diagnosed acute myeloid leukemia 47
Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia 47
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia. 47
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome 47
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 47
Partial duplication of the MLL oncogene in patients with aggressive aute myeloid leukemia 46
Characterization of 12p molecular events outside ETV6 in complex karyotypes of acute myeloid malignancies 46
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia 46
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia 46
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 45
Philadelphia-positive acute lymphoblastic leukemia with multiple subclones including duplication of the Philadelphia chromosome and Abelson oncogene 45
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 44
Fluorescence In Situ Hybridization characterization of new translocation involving TEL (ETV6) in a wide spectrum of hematologic malignancies. 44
Le sindromi mielodisplastiche: citogenetica e biologia molecolare 44
MLL tandem duplication in two cases of acute myelocytic leukemia with unbalanced translocations: der(16)t(11;16)(q23;p13) and der(18)t(11;18)(q22;p11.2) 44
Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints. 44
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype 43
Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML-M1) 42
Leukemogenic mechanisms and targets of a NUP98/HHEX fusion in acute myeloid leukemia 42
H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22) 42
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 42
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. 42
A novel germline mutation in CDK4 codon 24 associated to familial melanoma 42
Targeting Cytokine- And Therapy-Induced PIM1 Activation in Preclinical Models of T-cell Acute Lymphoblastic Leukemia and Lymphoma 42
Interpretation of the complex karyotipe and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line 41
RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome 40
SQSTM1-NUP214: a new gene fusion in adult T-cell acute lymphoblastic leukemia 40
Involvement of a member of the histone cluster 1 at 6p21 in NUP98-positive MDS/AML 40
Totale 5.636
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Categoria #
all - tutte 30.334
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 30.334
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020488 0 0 0 3 81 34 84 11 90 70 33 82
2020/20211.206 3 85 47 110 335 73 90 20 130 73 111 129
2021/20221.170 25 236 15 76 35 10 14 367 11 47 161 173
2022/20232.261 147 398 18 206 182 210 3 125 883 1 71 17
2023/2024940 79 93 48 14 9 1 199 10 163 23 118 183
2024/2025371 35 219 112 5 0 0 0 0 0 0 0 0
Totale 7.119