statistiche ricercatore

MASERATI, EMANUELA

Distribuzione geografica

Continente	#
NA - Nord America	9.376
EU - Europa	9.366
AS - Asia	1.792
SA - Sud America	30
Continente sconosciuto - Info sul continente non disponibili	22
OC - Oceania	6
AF - Africa	2
Totale	20.594

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Nazione	#
US - Stati Uniti d'America	9.340
IT - Italia	5.249
UA - Ucraina	1.665
TR - Turchia	675
SE - Svezia	554
VN - Vietnam	537
CN - Cina	462
FI - Finlandia	437
FR - Francia	389
IE - Irlanda	371
DE - Germania	306
GB - Regno Unito	243
JP - Giappone	46
IN - India	42
PL - Polonia	34
BE - Belgio	29
EU - Europa	22
CA - Canada	20
CH - Svizzera	15
BR - Brasile	14
MX - Messico	14
SG - Singapore	11
NL - Olanda	9
ES - Italia	8
CZ - Repubblica Ceca	7
RU - Federazione Russa	7
AT - Austria	6
BG - Bulgaria	6
AR - Argentina	5
IL - Israele	5
AU - Australia	4
CL - Cile	4
EC - Ecuador	4
RO - Romania	4
RS - Serbia	4
AL - Albania	2
BN - Brunei Darussalam	2
HK - Hong Kong	2
HR - Croazia	2
IM - Isola di Man	2
KR - Corea	2
LU - Lussemburgo	2
MC - Monaco	2
MD - Moldavia	2
NO - Norvegia	2
NZ - Nuova Zelanda	2
OM - Oman	2
VE - Venezuela	2
AD - Andorra	1
AZ - Azerbaigian	1
BD - Bangladesh	1
BS - Bahamas	1
BY - Bielorussia	1
CO - Colombia	1
DK - Danimarca	1
EE - Estonia	1
GR - Grecia	1
LV - Lettonia	1
ME - Montenegro	1
MK - Macedonia	1
MU - Mauritius	1
MY - Malesia	1
NP - Nepal	1
PA - Panama	1
PK - Pakistan	1
SK - Slovacchia (Repubblica Slovacca)	1
TW - Taiwan	1
ZA - Sudafrica	1
Totale	20.594

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Città	#
Milan	3.439
Jacksonville	1.252
Chandler	1.173
Fairfield	1.046
Woodbridge	611
Ashburn	516
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	251
San Mateo	176
Beijing	169
Como	128
San Diego	87
Ogden	76
Tokyo	46
Hefei	44
New York	43
Helsinki	41
Kunming	39
Nanjing	37
Verona	35
Boardman	34
London	32
Redwood City	31
Los Angeles	27
Norwalk	26
Brussels	24
Radomsko	23
Nanchang	20
Washington	20
Guangzhou	19
Jinan	18
Falls Church	17
Phoenix	17
Düsseldorf	15
Edinburgh	13
Catania	11
Philadelphia	10
Redmond	10
Bari	9
Bologna	9
Frankfurt am Main	9
Kocaeli	9
Naples	9
Ottawa	9
Palermo	9
Shanghai	9
Auburn Hills	8
Brescia	8
Chengdu	8
Chiswick	8
Florence	8
Fuzhou	8
Pune	8
Singapore	8
Chicago	7
Genova	7
Hebei	7
Mcallen	7
Pavia	7
Reggio Nell'emilia	7
Shenyang	7
Torino	7
Berlin	6
Padova	6
Prague	6
Sofia	6
Vienna	6
Acton	5
Bangalore	5
Cagliari	5
Indiana	5
Islington	5
Monterrey	5
Monza	5
Pescara	5
Sassari	5
Shaoxing	5
Stockholm	5
Tappahannock	5
Tel Aviv	5
Warsaw	5
Zhengzhou	5
Zurich	5
Belgrade	4
Busto Arsizio	4
Catanzaro	4
Dallas	4
Goito	4
Hangzhou	4
Istanbul	4
Totale	14.106

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	293
MOSAICISMO PIGMENTARIO CON ASPETTO FILLOIDE IN UN CASO DI TRISOMIA 13 TOTALE E PARZIALE IN MOSAICISMO INCONSUETO	229
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	208
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	200
Sindrome di Patau con lunga sopravvivenza in un caso di trisomia 13 totale e parziale in mosaicismo inconsueto	199
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	185
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	175
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	172
JUMPING TRANSLOCATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA.	170
High variability of genomic instability and gene expression profiling in different HeLa clones	167
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	156
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	156
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	153
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers	151
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	149
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	148
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line.	144
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	144
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	144
Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia.	142
In situ hybridization by scanning electron microscopy for painting, centromeric, and YAC localization	142
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	141
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	140
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	139
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	138
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	138
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	138
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	137
Duplication of the der(14) chromosome of a translocation (8;14) in a case of Burkitt's type L3-ALL.	135
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	135
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	135
Ring chromosome 9 with a 9p22.3-p24.3 duplication	134
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	133
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	133
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	132
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.	131
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	131
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	131
Cadmium Impairs p53 Activity in HepG2 Cells	130
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	130
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	130
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	130
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	129
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.	128
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	128
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	127
Cytogenetics in autologous bone marrow transplantation.	126
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	126
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	126
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	125
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.	125
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp	125
INVOLVEMENT OF 9Q22.1-31.1 REGION IN PYLORIC STENOSIS.	123
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	122
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	122
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	118
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	118
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	117
Minimal residual disease and trisomy 8	116
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	116
Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome	116
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	115
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	113
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	112
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	111
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	110
Myelodysplastic syndromes: the pediatric point of view.	109
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	109
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	108
Cytogenetics of Kaposi Sarcoma, an analysis of 15 cases	108
Acquired Chromosome change in Cholesteatoma	107
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	107
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	105
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	105
Normative growth charts for Shwachman-Diamond syndrome from Italian cohort of 0-8 years old	104
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	102
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	102
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	102
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	102
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	101
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	100
BUSULFAN, CYCLOPHOSPHAMIDE AND MELPHALAN AS CONDITIONING REGIMEN FOR BONE MARROW TRANSPLANTATION IN CHILDREN WITH MYELODYSPLASTIC SYNDROMES.	99
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	98
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	97
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	97
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	97
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.	96
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	95
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	95
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	94
Clinical cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia.	94
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	94
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.	93
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	92
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	92
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	92
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	92
The 47,XXY karyotype and unrelated malformative patterns: an usual association	91
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	91
Involvement of dendritic cells in juvenile chronic myelomonocytic leukaemia shown by FISH on interphase nuclei	90
Totale	12.702

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Categoria	#
all - tutte	65.019
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	65.019

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	619	0	0	0	0	0	0	0	0	0	0	0	619
2019/2020	3.571	151	145	127	572	150	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	5.187	881	891	906	914	957	260	35	66	117	54	18	88
Totale													20.731