MATTEUCCI, Caterina
 Distribuzione geografica
Continente #
NA - Nord America 1.398
EU - Europa 978
AS - Asia 463
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 1
Totale 2.843
Nazione #
US - Stati Uniti d'America 1.395
IE - Irlanda 271
IT - Italia 183
UA - Ucraina 174
HK - Hong Kong 160
SG - Singapore 149
CN - Cina 92
SE - Svezia 88
DE - Germania 62
FI - Finlandia 58
RU - Federazione Russa 54
VN - Vietnam 41
CZ - Repubblica Ceca 21
GB - Regno Unito 17
BE - Belgio 14
KR - Corea 10
AT - Austria 7
NL - Olanda 7
TR - Turchia 7
PL - Polonia 6
CH - Svizzera 5
GR - Grecia 5
FR - Francia 4
EU - Europa 3
CA - Canada 2
LB - Libano 2
UZ - Uzbekistan 2
BG - Bulgaria 1
MX - Messico 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 2.843
Città #
Chandler 343
Dublin 271
Hong Kong 160
San Mateo 134
Singapore 127
Jacksonville 97
Boardman 78
Perugia 66
Santa Clara 62
Ann Arbor 61
Medford 52
Princeton 51
Altamura 46
Lawrence 43
Dong Ket 41
Beijing 37
Wilmington 37
Andover 27
Redmond 27
Dearborn 23
Saint Petersburg 22
Munich 21
Brno 17
Helsinki 17
New York 15
Brussels 14
Norwalk 13
San Paolo di Civitate 12
Seoul 10
Woodbridge 10
Los Angeles 9
Falls Church 8
Izmir 7
Rome 7
Dallas 6
Moscow 6
San Diego 5
Amsterdam 4
Ashburn 4
Como 4
Florence 4
Chengdu 3
Des Moines 3
Houston 3
Padova 3
Ponte 3
Reggio Nell'emilia 3
Shanghai 3
Vienna 3
Bologna 2
Chicago 2
Collazzone 2
Gualdo Tadino 2
Lausanne 2
Nanjing 2
Naples 2
Piraeus 2
Prague 2
Redwood City 2
Santarcangelo di Romagna 2
Athens 1
Auburn Hills 1
Auckland 1
Birmingham 1
Den Haag 1
Düsseldorf 1
Edinburgh 1
Falkenstein 1
Forlì 1
Frankfurt Am Main 1
Groningen 1
Guangzhou 1
Lappeenranta 1
Memphis 1
Mexico City 1
Montréal 1
Nantong 1
Olomouc 1
Orbetello 1
Piazza 1
Romola 1
San Francisco 1
Shenzhen 1
Shijiazhuang 1
Simi Valley 1
Tappahannock 1
Toronto 1
Umbertide 1
Wuhan 1
Totale 2.073
Nome #
Role of BCL2L10 methylation and TET2 mutations in higher risk myelodysplastic syndromes treated with 5-Azacytidine 107
Design of a Comprehensive Fluorescence in Situ Hybridization Assay for Genetic Classification of T-Cell Acute Lymphoblastic Leukemia 91
Activating somatic and germline TERT promoter variants in myeloid malignancies 82
NPM1 deletion is associated with gross chromosomal rearrangements in leukemia 77
Detection of the NUP214-ABL rearrangement in T-ALL by high-density oligonucleotide arrays: Evidence of the value of this approach in the identification of gene amplifications 76
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia 76
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma 75
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia. 73
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer 67
A novel mutation of indoleamine 2,3-dioxygenase 1 causes a rapid proteasomal degradation and compromises protein function 65
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement 64
Highly aggressive T-cell acute lymphoblastic leukemia with t(8;14)(q24;q11): extensive genetic characterization and achievement of early molecular remission and long-term survival in an adult patient. 63
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. 63
Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults 62
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study 60
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 60
MN1-ETV6 fusion gene arising from MDS With 5q- 60
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia 60
DDX3X-MLLT10 fusion in adults with NOTCH1 positive T-cell acute lymphoblastic leukemia. 58
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study 58
Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome 57
Different genomic imbalances in low- and high-grade HCV-related lymphomas 55
NUP98/11p15 translocations affect CD34+ cells in myeloid and T lymphoid leukemias 55
Submicroscopic deletions in 5q- associated malignancies 55
Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis 54
14q32 rearrangements deregulating BCL11B mark a distinct subgroup of T and myeloid immature acute leukemia 54
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia 53
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia 53
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia. 52
Germline GATA2 variant disrupting endothelial eNOS cell function and angiogenesis can be restored by c-Jun/AP-1 upregulation 52
Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations. 51
The GNAS1 gene in myelodysplastic syndromes (MDS). 51
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 51
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia 49
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia 49
Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults 47
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13) 47
Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas 46
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 45
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia. 44
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 44
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumor. 43
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 42
FISH analysis reveals frequent co-occurrence of 4q24/TET2 and 5q and/or 7q deletions. 41
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification? 40
The EMT transcription factor Zeb2 controls adult murine hematopoietic differentiation by regulating cytokine signaling 36
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants. 34
Comparison between Sickle Cell Disease Patients and Healthy Donors: Untargeted Lipidomic Study of Erythrocytes 33
Typical genomic imbalances in primary MALT lymphoma of the orbit 33
Regression of lymphoproliferative disorder after treatment for hepatitis C virus infection in a patient with partial trisomy 3, Bcl-2 overexpression, and type II cryoglobulinemia 32
Genomic and clinical findings in myeloid neoplasms with PDGFRB rearrangement 32
Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes. 31
A Novel t(5;7)(q31;q21)/CDK6::IL3 in Immature T-cell Acute Lymphoblastic Leukemia With IL3 Expression and Eosinophilia 30
New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia 29
One disease, two faces: clonally-related AML and MPDCP with skin involvement 21
Correction to: One disease, two faces: clonally-related AML and MPDCP with skin involvement 17
A novel t(X;21)(p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in myelodysplastic syndromes and acute myeloid leukemias 15
null 11
Totale 2.981
Categoria #
all - tutte 13.274
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 13.274


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020211 0 0 0 0 27 17 28 12 29 38 35 25
2020/2021379 2 35 9 30 117 15 32 3 34 22 33 47
2021/2022448 19 99 8 19 13 8 3 138 14 14 57 56
2022/2023982 56 188 15 105 88 89 0 44 370 2 20 5
2023/2024450 37 37 23 9 8 1 110 2 70 8 72 73
2024/2025277 31 85 48 39 74 0 0 0 0 0 0 0
Totale 2.981