LA STARZA, Roberta
 Distribuzione geografica
Continente #
NA - Nord America 4.411
EU - Europa 3.310
AS - Asia 2.705
SA - Sud America 410
AF - Africa 42
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 4
Totale 10.890
Nazione #
US - Stati Uniti d'America 4.314
SG - Singapore 1.260
IE - Irlanda 681
UA - Ucraina 571
HK - Hong Kong 477
IT - Italia 456
SE - Svezia 422
CN - Cina 385
BR - Brasile 359
RU - Federazione Russa 318
DE - Germania 260
VN - Vietnam 231
FI - Finlandia 222
KR - Corea 160
GB - Regno Unito 95
CA - Canada 51
FR - Francia 48
PL - Polonia 45
AT - Austria 31
MX - Messico 31
TR - Turchia 31
CZ - Repubblica Ceca 30
NL - Olanda 28
ES - Italia 25
IN - India 24
JP - Giappone 22
IQ - Iraq 20
AR - Argentina 19
BE - Belgio 18
CH - Svizzera 18
UZ - Uzbekistan 16
ZA - Sudafrica 16
BD - Bangladesh 15
LT - Lituania 10
EC - Ecuador 9
DZ - Algeria 8
ID - Indonesia 8
LB - Libano 8
MA - Marocco 8
GR - Grecia 7
EU - Europa 6
PK - Pakistan 6
RO - Romania 6
AE - Emirati Arabi Uniti 5
CL - Cile 5
CO - Colombia 5
IL - Israele 4
VE - Venezuela 4
AZ - Azerbaigian 3
BG - Bulgaria 3
NP - Nepal 3
PY - Paraguay 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
UY - Uruguay 3
BB - Barbados 2
BH - Bahrain 2
BN - Brunei Darussalam 2
CR - Costa Rica 2
DK - Danimarca 2
GE - Georgia 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
KG - Kirghizistan 2
MN - Mongolia 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
TN - Tunisia 2
A1 - Anonimo 1
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BJ - Benin 1
BO - Bolivia 1
BY - Bielorussia 1
CG - Congo 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
HR - Croazia 1
HT - Haiti 1
HU - Ungheria 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MR - Mauritania 1
MY - Malesia 1
NI - Nicaragua 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
PS - Palestinian Territory 1
Totale 10.881
Città #
Singapore 818
Chandler 718
Dublin 678
Hong Kong 477
San Mateo 331
Jacksonville 306
Ashburn 212
Boardman 209
Perugia 190
Santa Clara 179
Seoul 159
Medford 140
Princeton 138
Altamura 117
Dong Ket 110
Lawrence 107
Munich 107
Beijing 104
Wilmington 101
Ann Arbor 96
Moscow 92
Los Angeles 88
Andover 78
New York 69
Piscataway 67
Helsinki 57
Redmond 56
Ho Chi Minh City 52
Dearborn 46
Turku 43
The Dalles 38
San Paolo di Civitate 35
Saint Petersburg 32
Warsaw 31
Norwalk 28
São Paulo 28
Des Moines 26
Orem 24
Brooklyn 22
Stockholm 22
Tokyo 21
Woodbridge 21
Amsterdam 20
Montreal 20
Hanoi 19
Brno 18
Brussels 18
Houston 18
London 18
Atlanta 17
Dallas 17
Denver 17
Chicago 15
Frankfurt am Main 15
Mexico City 15
Rome 15
Nuremberg 14
Toronto 14
Chennai 13
Falkenstein 13
Falls Church 13
Johannesburg 13
Shanghai 13
Baghdad 12
Izmir 12
San Diego 12
Auburn Hills 11
Phoenix 11
Vienna 11
Ankara 10
Boston 10
Redwood City 10
San Francisco 10
Council Bluffs 8
Rio de Janeiro 8
Belo Horizonte 7
Changsha 7
Hefei 7
Olomouc 7
Wroclaw 7
Campinas 6
Guangzhou 6
Haiphong 6
Poplar 6
Querétaro 6
São Vicente 6
Charlotte 5
Columbus 5
Forlì 5
Goiânia 5
Joinville 5
Manchester 5
Mumbai 5
Ribeirão Preto 5
Bologna 4
Brasília 4
Caxias do Sul 4
Chengdu 4
Da Nang 4
Guarulhos 4
Totale 6.868
Nome #
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 135
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 127
14q+ chromosome marker in a T-cell-rich B-cell lymphoma. 126
Acute lymphoblastic leukaemia in Noonan syndrome 119
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 119
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus. 110
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 110
Constitutive phosphorylation of Janus kinase2 in the GL15 glioblastoma derived human cell line 109
New somatic TERT promoter variants enhance the Telomerase activity in Glioblastoma 108
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia 107
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies 107
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 105
Alterazioni strutturali del cromosoma 12p dei disordini mieloidi 103
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 103
Genetic profile of acute myeloid leukemia 102
Molecular cytogenetic analysis of the 5Q-chromosome in the HL60 cell-line and in the 5Q-Syndrome 101
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 101
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia 98
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts 97
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation 97
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells 96
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 96
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 95
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases 95
MYB rearrangements and over-expression in T-cell acute lymphoblastic leukemia 95
Blockade of Oncogenic NOTCH1 With the SERCA Inhibitor CAD204520 in T Cell Acute Lymphoblastic Leukemia 94
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 92
Extramedullary molecular evidence of the 5'KIAA1509/3'PDGFRB fusion gene in chronic eosinophilic leukemia 92
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 91
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9) 90
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 90
4q12 translocations with GSX2 expression identify a CD7(+) acute myeloid leukaemia subset 89
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene 89
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 89
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML. 88
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia 88
The ETV6,CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignancies. 87
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 87
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 86
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 86
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype 86
Submicroscopic deletions in 5q- associated malignancies 86
The hereditary hyperferritinemia-cataract syndrome in 2 italian families 86
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 85
Different genomic imbalances in low- and high-grade HCV-related lymphomas 85
Genetic pathways in low-and high-grade HCV-related lymphomas are different 85
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome 85
t(4;11) translocation involving NUP98 and RAP1GDS1 genes. Characterisation of a new subset of T acute lymphoblastc leukaemia 84
Acute myeloid leukemia 84
Targeting Cytokine- And Therapy-Induced PIM1 Activation in Preclinical Models of T-cell Acute Lymphoblastic Leukemia and Lymphoma 84
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 84
Cytogenetic and FISH investigations on Tetrasomy 8 in ALL. 83
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 83
MYB deregulation from a EWSR1-MYB fusion at leukemic evolution of a JAK2 V617F positive primary myelofibrosis 83
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 82
Metachronous cardiac and cerebral sarcomas: case report with focus on molecular findings and review of the literature 82
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 81
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder 81
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 81
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. 81
MN1-ETV6 fusion gene arising from MDS With 5q- 80
RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications 80
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia 79
Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes 78
Succeful use of the same slide for consecutive fluorescence in situ hybridization (FISH) experiments. 78
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia 78
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 75
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies. 74
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion 74
A novel dic(1;10) in a patient with myelodysplastic syndrome 74
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 73
New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia. 73
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 73
Involvement of a member of the histone cluster 1 at 6p21 in NUP98-positive MDS/AML 73
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with (8;11) (p11,2;p15) 73
A novel germline mutation in CDK4 codon 24 associated to familial melanoma 72
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients 71
SQSTM1-NUP214: a new gene fusion in adult T-cell acute lymphoblastic leukemia 71
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 71
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 70
T-Cell Acute Lymphoblastic Leukemia: Biomarkers and Their Clinical Usefulness 70
Le sindromi mielodisplastiche: citogenetica e biologia molecolare 69
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia. 69
Molecular Cytogenetics Detect an Unbalanced t(2;13)(q36;q14) and PAX3-FOXO1 Fusion in Rhabdomyosarcoma With Mixed Embryonal/Alveolar Features 69
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 69
Haplo-identical haematopoietic stem cell transplantation for secondary leukaemia 68
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 68
Case report: Ponatinib as a bridge to CAR-T cells and subsequent maintenance in a patient with relapsed/refractory Philadelphia-like acute lymphoblastic leukemia 67
A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia 67
Rapid reversion of Loeffler's endocarditis by imatinib in early stage clonal hypereosinophilic syndrome 67
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 67
High PIM1 expression is a biomarker of T-cell acute lymphoblastic leukemia with JAK/STAT activation or t(6;7)(p21;q34)/TRB@-PIM1 rearrangement 67
Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement 66
Prognostic impact of genetic characterization in the GIMEMA LAM99P multicenter study for newly diagnosed acute myeloid leukemia 65
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 65
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 65
Fluorescence In Situ Hybridization characterization of new translocation involving TEL (ETV6) in a wide spectrum of hematologic malignancies. 64
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? 64
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) 63
RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome 63
Totale 8.492
Categoria #
all - tutte 52.379
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 52.379


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021626 0 0 0 0 0 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
2024/20252.039 35 218 112 69 284 101 81 162 376 113 309 179
2025/20262.472 331 334 186 601 728 292 0 0 0 0 0 0
Totale 11.259