statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
NA - Nord America	9.864
EU - Europa	9.545
AS - Asia	2.055
SA - Sud America	59
Continente sconosciuto - Info sul continente non disponibili	22
OC - Oceania	6
AF - Africa	4
Totale	21.555

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Nazione	#
US - Stati Uniti d'America	9.823
IT - Italia	5.303
UA - Ucraina	1.665
TR - Turchia	677
SE - Svezia	554
VN - Vietnam	537
CN - Cina	520
FI - Finlandia	454
FR - Francia	389
IE - Irlanda	371
DE - Germania	313
GB - Regno Unito	244
SG - Singapore	200
RU - Federazione Russa	101
JP - Giappone	46
IN - India	45
BR - Brasile	38
PL - Polonia	35
BE - Belgio	30
EU - Europa	22
CA - Canada	21
MX - Messico	18
CH - Svizzera	15
NL - Olanda	11
ES - Italia	8
CZ - Repubblica Ceca	7
AT - Austria	6
BG - Bulgaria	6
AR - Argentina	5
IL - Israele	5
PE - Perù	5
AU - Australia	4
CL - Cile	4
EC - Ecuador	4
HK - Hong Kong	4
RO - Romania	4
RS - Serbia	4
KR - Corea	3
OM - Oman	3
ZA - Sudafrica	3
AL - Albania	2
AZ - Azerbaigian	2
BN - Brunei Darussalam	2
DK - Danimarca	2
HR - Croazia	2
IM - Isola di Man	2
LU - Lussemburgo	2
MC - Monaco	2
MD - Moldavia	2
NO - Norvegia	2
NZ - Nuova Zelanda	2
PK - Pakistan	2
VE - Venezuela	2
AD - Andorra	1
BD - Bangladesh	1
BS - Bahamas	1
BY - Bielorussia	1
CO - Colombia	1
EE - Estonia	1
GR - Grecia	1
ID - Indonesia	1
IQ - Iraq	1
IR - Iran	1
JO - Giordania	1
LT - Lituania	1
LV - Lettonia	1
ME - Montenegro	1
MK - Macedonia	1
MU - Mauritius	1
MY - Malesia	1
NP - Nepal	1
PA - Panama	1
SK - Slovacchia (Repubblica Slovacca)	1
TW - Taiwan	1
UZ - Uzbekistan	1
Totale	21.555

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Città	#
Milan	3.446
Jacksonville	1.252
Chandler	1.173
Fairfield	1.046
Woodbridge	611
Ashburn	554
Wilmington	447
Houston	443
Princeton	423
Seattle	392
Ann Arbor	389
Izmir	382
Dublin	370
Nyköping	356
Cambridge	350
Dearborn	332
Dong Ket	316
Rome	257
Boardman	246
San Mateo	176
Singapore	175
Beijing	172
Como	128
San Diego	87
Ogden	76
Chicago	75
Helsinki	58
Tokyo	46
Hefei	45
New York	43
Kunming	39
Nanjing	37
Santa Clara	37
Verona	35
London	32
Redwood City	31
Los Angeles	28
Norwalk	26
Brussels	25
Radomsko	23
Dallas	22
Guangzhou	22
Nanchang	20
Washington	20
Jinan	19
Falls Church	17
Phoenix	17
Düsseldorf	15
Shanghai	15
Catania	13
Edinburgh	13
Naples	12
Ottawa	10
Philadelphia	10
Redmond	10
Bari	9
Bologna	9
Brescia	9
Frankfurt am Main	9
Kocaeli	9
Palermo	9
São Paulo	9
Auburn Hills	8
Chengdu	8
Chiswick	8
Florence	8
Fuzhou	8
Pune	8
Berlin	7
Genova	7
Hebei	7
Mcallen	7
Pavia	7
Reggio Nell'emilia	7
Shenyang	7
Torino	7
Padova	6
Prague	6
Shaoxing	6
Sofia	6
Vienna	6
Warsaw	6
Zhengzhou	6
Acton	5
Bangalore	5
Cagliari	5
Indiana	5
Islington	5
Monterrey	5
Monza	5
Pescara	5
Sassari	5
Stockholm	5
Tappahannock	5
Tel Aviv	5
Zurich	5
Arequipa	4
Belgrade	4
Busto Arsizio	4
Catanzaro	4
Totale	14.704

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	311
MOSAICISMO PIGMENTARIO CON ASPETTO FILLOIDE IN UN CASO DI TRISOMIA 13 TOTALE E PARZIALE IN MOSAICISMO INCONSUETO	254
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	211
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	203
Sindrome di Patau con lunga sopravvivenza in un caso di trisomia 13 totale e parziale in mosaicismo inconsueto	201
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	189
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	179
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	178
JUMPING TRANSLOCATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA.	175
High variability of genomic instability and gene expression profiling in different HeLa clones	169
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	167
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	164
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	161
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers	159
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	156
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	154
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	153
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	150
Sindrome di Shwachman: isocromosoma i(7)(q10), rischio di MDS/AML ed effetto da dosaggio genico della mutazione c.258+2T→C associata al gene SBDS	149
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	149
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	149
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line.	147
In situ hybridization by scanning electron microscopy for painting, centromeric, and YAC localization	147
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	146
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.	144
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	143
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	141
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	141
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	141
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	141
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	140
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.	139
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.	137
Ring chromosome 9 with a 9p22.3-p24.3 duplication	137
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	137
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	137
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	136
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	136
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	135
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	135
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.	134
Cadmium Impairs p53 Activity in HepG2 Cells	134
Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations	133
Cytogenetics in autologous bone marrow transplantation.	132
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	132
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	131
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	131
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.	130
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	129
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	129
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	128
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp	128
INVOLVEMENT OF 9Q22.1-31.1 REGION IN PYLORIC STENOSIS.	127
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	126
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	125
Myelodysplastic syndromes: the pediatric point of view.	123
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	122
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	122
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	122
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	122
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	121
Minimal residual disease and trisomy 8	119
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	119
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome	118
Acquired Chromosome change in Cholesteatoma	116
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	116
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	116
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	115
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	113
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	112
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	112
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	111
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	111
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES.	110
Cytogenetics of Kaposi Sarcoma, an analysis of 15 cases	110
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	110
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	108
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	108
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	108
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	107
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	106
Normative growth charts for Shwachman-Diamond syndrome from Italian cohort of 0-8 years old	106
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	105
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	103
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	103
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype	103
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	102
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	102
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	100
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	99
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	99
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.	99
RESTRICTED TCR REPERTOIRE AND LONG-TERM PERSISTENCE OF DONOR-DERIVED ANTIGEN-EXPERIENCED CD4+ T CELLS IN ALLOGENEIC BONE MARROW TRANSPLANTATION RECIPIENTS.	98
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	98
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	97
Expression studies in the bone marrow of patients with Shwachman Diamond Syndrome (SDS) and deletion of the long arm of chromosome 20 encompassing th3 EIF6 gene: relation with benign prognosis.	97
Clinical cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia.	96
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	96
The 47,XXY karyotype and unrelated malformative patterns: an usual association	95
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	95
Totale	13.260

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Categoria	#
all - tutte	78.495
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	78.495

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	2.426	0	0	0	0	0	371	580	533	216	352	72	302
2020/2021	2.942	44	306	68	303	129	361	60	280	460	136	270	525
2021/2022	1.844	177	301	188	93	40	50	66	124	108	230	176	291
2022/2023	2.968	272	168	224	338	244	628	5	391	391	93	125	89
2023/2024	5.188	881	891	906	914	957	260	35	66	117	54	18	89
2024/2025	960	22	43	541	60	119	175	0	0	0	0	0	0
Totale													21.692