statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
NA - Nord America	15.491
EU - Europa	10.644
AS - Asia	5.859
SA - Sud America	745
Continente sconosciuto - Info sul continente non disponibili	159
AF - Africa	117
OC - Oceania	25
Totale	33.040

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Nazione	#
US - Stati Uniti d'America	15.220
IT - Italia	5.525
SG - Singapore	1.777
UA - Ucraina	1.676
CN - Cina	1.433
VN - Vietnam	906
TR - Turchia	690
FR - Francia	615
BR - Brasile	608
HK - Hong Kong	605
SE - Svezia	576
FI - Finlandia	571
DE - Germania	419
IE - Irlanda	375
GB - Regno Unito	366
RU - Federazione Russa	189
CA - Canada	122
IN - India	116
MX - Messico	100
JP - Giappone	86
PL - Polonia	83
BD - Bangladesh	78
ES - Italia	43
AR - Argentina	42
AT - Austria	37
ZA - Sudafrica	37
EC - Ecuador	34
BE - Belgio	33
NG - Nigeria	32
NL - Olanda	31
CH - Svizzera	27
IQ - Iraq	26
AU - Australia	23
EU - Europa	22
PK - Pakistan	20
CR - Costa Rica	15
VE - Venezuela	14
SA - Arabia Saudita	12
CO - Colombia	11
CZ - Repubblica Ceca	11
ID - Indonesia	11
PH - Filippine	11
PY - Paraguay	11
UZ - Uzbekistan	11
CL - Cile	10
MA - Marocco	10
PE - Perù	10
IL - Israele	9
JM - Giamaica	9
JO - Giordania	9
EG - Egitto	8
LT - Lituania	8
MY - Malesia	8
OM - Oman	8
BG - Bulgaria	7
RS - Serbia	7
AZ - Azerbaigian	6
DZ - Algeria	6
KE - Kenya	6
KR - Corea	6
NP - Nepal	6
RO - Romania	6
MD - Moldavia	5
SC - Seychelles	4
AE - Emirati Arabi Uniti	3
AL - Albania	3
BY - Bielorussia	3
DK - Danimarca	3
DO - Repubblica Dominicana	3
GT - Guatemala	3
KZ - Kazakistan	3
LB - Libano	3
NO - Norvegia	3
PA - Panama	3
PR - Porto Rico	3
TT - Trinidad e Tobago	3
TW - Taiwan	3
AO - Angola	2
BB - Barbados	2
BN - Brunei Darussalam	2
BS - Bahamas	2
EE - Estonia	2
ET - Etiopia	2
GE - Georgia	2
GR - Grecia	2
HN - Honduras	2
HR - Croazia	2
HU - Ungheria	2
IM - Isola di Man	2
IR - Iran	2
LU - Lussemburgo	2
MC - Monaco	2
MK - Macedonia	2
NZ - Nuova Zelanda	2
SN - Senegal	2
SR - Suriname	2
SV - El Salvador	2
AD - Andorra	1
BA - Bosnia-Erzegovina	1
BF - Burkina Faso	1
Totale	32.880

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Città	#
Milan	3.478
San Jose	1.449
Ashburn	1.288
Jacksonville	1.257
Chandler	1.173
Fairfield	1.046
Singapore	944
Council Bluffs	685
Woodbridge	611
Hong Kong	599
Houston	465
Wilmington	448
Princeton	424
Beijing	422
Seattle	403
Ann Arbor	389
Izmir	382
Dublin	371
Dallas	362
Nyköping	356
Cambridge	353
Dearborn	332
Dong Ket	316
Rome	277
Boardman	246
The Dalles	245
Lauterbourg	183
San Mateo	176
Chicago	171
New York	154
Helsinki	151
Ho Chi Minh City	132
Los Angeles	132
Santa Clara	131
Como	128
Hanoi	100
San Diego	87
Tokyo	83
Ogden	76
São Paulo	75
Orem	74
Guangzhou	67
Munich	58
London	54
Mexico City	52
Verona	50
Phoenix	46
Warsaw	46
Hefei	45
Shanghai	41
Kunming	40
Nanjing	40
Chennai	36
Atlanta	34
Brooklyn	33
Toronto	32
Abuja	31
Frankfurt am Main	31
Montreal	31
Redwood City	31
Brussels	28
Columbus	28
Norwalk	28
Johannesburg	27
Washington	26
Buffalo	25
Manchester	25
Stockholm	25
Turku	24
Poplar	23
Radomsko	23
Rio de Janeiro	23
Tianjin	23
Denver	22
Brasília	21
Nanchang	21
Shenzhen	21
Boston	20
Jinan	20
Miami	20
San Francisco	20
Catania	19
Nuremberg	19
Philadelphia	19
Zhengzhou	19
Naples	18
Amsterdam	17
Da Nang	17
Falls Church	17
Belo Horizonte	15
Düsseldorf	15
Biên Hòa	14
Brescia	14
Quito	14
Salt Lake City	14
Vienna	14
Bologna	13
Edinburgh	13
Hangzhou	13
Mumbai	13
Totale	21.762

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	394
MOSAICISMO PIGMENTARIO CON ASPETTO FILLOIDE IN UN CASO DI TRISOMIA 13 TOTALE E PARZIALE IN MOSAICISMO INCONSUETO	355
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	284
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	253
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	251
High variability of genomic instability and gene expression profiling in different HeLa clones	249
Myelodysplastic syndromes: the pediatric point of view.	245
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	245
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	244
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers	242
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	239
Sindrome di Patau con lunga sopravvivenza in un caso di trisomia 13 totale e parziale in mosaicismo inconsueto	237
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	236
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	231
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	228
JUMPING TRANSLOCATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA.	227
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	227
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	226
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	221
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	220
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	218
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	217
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	213
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES.	212
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	210
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	209
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	208
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	207
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	205
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.	204
Acquired Chromosome change in Cholesteatoma	203
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.	203
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	203
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	201
In situ hybridization by scanning electron microscopy for painting, centromeric, and YAC localization	199
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	198
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	198
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	195
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	193
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	193
A new recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of the short arms of chromosome 6	193
Cadmium Impairs p53 Activity in HepG2 Cells	193
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.	192
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	191
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	191
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line.	189
Ring chromosome 9 with a 9p22.3-p24.3 duplication	189
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	189
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	188
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.	188
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	187
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	187
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	186
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	183
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	182
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	180
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	179
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	176
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.	176
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	176
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	175
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	174
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	174
Cytogenetics in autologous bone marrow transplantation.	173
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	173
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	172
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	171
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	171
ANALISI DI MUTAZIONE DEL GENE SBDS IN UN GRUPPO DI PAZIENTI ITALIANI AFFETTI DALLA SINDROME DI SHWACHMAN	170
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	170
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	169
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	169
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	168
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	167
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome	167
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	164
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	164
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp	164
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	164
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	163
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	163
INVOLVEMENT OF 9Q22.1-31.1 REGION IN PYLORIC STENOSIS.	162
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	162
AML1-MTG16 gene rearrangement in a pediatric therapy related AML after Ewing sarcoma: a case discussion and review of literature	160
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	160
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	160
A 45, X male with a Yp/18 translocation.	159
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	159
CYTOGENETIC AND MOLECULAR DETERMINANTS OF TRASFORMATION IN SCHWACHMAN DIAMOND SYNDROME	159
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	159
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	158
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	158
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	157
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	155
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	154
Minimal residual disease and trisomy 8	154
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	154
RESTRICTED TCR REPERTOIRE AND LONG-TERM PERSISTENCE OF DONOR-DERIVED ANTIGEN-EXPERIENCED CD4+ T CELLS IN ALLOGENEIC BONE MARROW TRANSPLANTATION RECIPIENTS.	153
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	153
i(7)(q10) carring c.258+2T>C mutazion and risk of myeloid malignancies in patients with SDS	153
Totale	19.392

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Categoria	#
all - tutte	125.386
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	125.386

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	1.178	0	0	0	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	2.942	22	43	541	60	119	177	122	204	322	240	259	833
2025/2026	7.368	568	346	330	1.012	663	501	1.630	491	758	512	344	213
2026/2027	1.998	184	372	1.231	211	0	0	0	0	0	0	0	0
Totale													33.040