statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	12.360
EU - Europa	10.672
AS - Asia	4.951
SA - Sud America	731
AF - Africa	56
Continente sconosciuto - Info sul continente non disponibili	19
OC - Oceania	5
Totale	28.794

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Nazione	#
US - Stati Uniti d'America	12.210
IT - Italia	5.430
UA - Ucraina	1.860
SG - Singapore	1.638
CN - Cina	902
TR - Turchia	763
VN - Vietnam	737
SE - Svezia	698
BR - Brasile	638
HK - Hong Kong	606
FI - Finlandia	539
IE - Irlanda	453
DE - Germania	436
FR - Francia	430
GB - Regno Unito	337
RU - Federazione Russa	222
JP - Giappone	97
IN - India	89
PL - Polonia	87
MX - Messico	72
CA - Canada	68
AR - Argentina	36
ZA - Sudafrica	33
BD - Bangladesh	29
ES - Italia	29
AT - Austria	28
BE - Belgio	28
EC - Ecuador	23
CH - Svizzera	21
NL - Olanda	20
EU - Europa	18
IQ - Iraq	18
LT - Lituania	12
PK - Pakistan	9
VE - Venezuela	9
ID - Indonesia	8
MA - Marocco	8
PE - Perù	8
IL - Israele	7
OM - Oman	7
CO - Colombia	6
UZ - Uzbekistan	6
AZ - Azerbaigian	5
CZ - Repubblica Ceca	5
DK - Danimarca	5
JO - Giordania	5
PY - Paraguay	5
AL - Albania	4
AU - Australia	4
BG - Bulgaria	4
LB - Libano	4
NP - Nepal	4
SN - Senegal	4
LU - Lussemburgo	3
RS - Serbia	3
BN - Brunei Darussalam	2
CL - Cile	2
DZ - Algeria	2
EE - Estonia	2
EG - Egitto	2
HU - Ungheria	2
IM - Isola di Man	2
KE - Kenya	2
KR - Corea	2
LV - Lettonia	2
MC - Monaco	2
MK - Macedonia	2
MY - Malesia	2
NO - Norvegia	2
SA - Arabia Saudita	2
SR - Suriname	2
AE - Emirati Arabi Uniti	1
AO - Angola	1
BA - Bosnia-Erzegovina	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
CR - Costa Rica	1
DM - Dominica	1
DO - Repubblica Dominicana	1
GE - Georgia	1
GR - Grecia	1
GY - Guiana	1
HN - Honduras	1
IR - Iran	1
JM - Giamaica	1
KZ - Kazakistan	1
MM - Myanmar	1
MN - Mongolia	1
MU - Mauritius	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PA - Panama	1
PR - Porto Rico	1
RO - Romania	1
SY - Repubblica araba siriana	1
TG - Togo	1
TL - Timor Orientale	1
TT - Trinidad e Tobago	1
TW - Taiwan	1
Totale	28.791

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Città	#
Milan	3.661
Jacksonville	1.386
Fairfield	1.183
Chandler	1.136
Ashburn	933
Singapore	838
Woodbridge	617
Hong Kong	606
Houston	526
Wilmington	502
Princeton	469
Seattle	463
Dublin	453
Izmir	447
Nyköping	421
Ann Arbor	413
Dearborn	411
Cambridge	394
Beijing	362
Dallas	357
Dong Ket	318
Rome	269
Boardman	255
San Mateo	201
The Dalles	143
Como	130
New York	124
Los Angeles	120
San Diego	101
Tokyo	96
Chicago	93
Santa Clara	89
Ogden	76
São Paulo	71
Munich	66
Helsinki	61
London	61
Ho Chi Minh City	55
Warsaw	52
Hefei	49
Verona	48
Hanoi	47
Nanjing	47
Council Bluffs	44
Kunming	44
Mexico City	37
Phoenix	37
Stockholm	32
Guangzhou	31
Orem	31
Denver	29
Montreal	29
Poplar	29
Redwood City	29
Norwalk	28
Rio de Janeiro	27
Turku	27
Brooklyn	26
Johannesburg	25
Washington	25
Brussels	24
Chennai	24
Nanchang	24
Düsseldorf	23
Radomsko	23
Atlanta	20
Brasília	18
Jinan	18
Nuremberg	18
Belo Horizonte	16
Catania	16
Boston	15
Manchester	15
Quito	15
Toronto	15
Auburn Hills	14
Frankfurt am Main	14
San Francisco	14
San Jose	14
Shanghai	14
Kocaeli	13
Ponte Lambro	13
Salt Lake City	13
Fuzhou	12
Edinburgh	11
Redmond	11
Columbus	10
Ribeirão Preto	10
Amsterdam	9
Ankara	9
Mumbai	9
Naples	9
Shenyang	9
Bangalore	8
Baotou	8
Berlin	8
Chengdu	8
Miami	8
Pune	8
Querétaro	8
Totale	19.228

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	351
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	231
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	221
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	217
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	212
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	212
High variability of genomic instability and gene expression profiling in different HeLa clones	202
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	197
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	197
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	190
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	189
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	188
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	188
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	186
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	186
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	186
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	186
The mammary gland and the homeobox gene Otx1	179
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	179
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	178
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	175
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	173
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	173
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	171
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	169
Otx2 and VegfA expression and P53-Otx1 differentiation pathway in proliferative vitreoretinopathy	169
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	167
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	167
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	167
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	165
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	164
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	163
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	163
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	162
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	162
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	161
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	161
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	159
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.	158
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	158
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	158
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	157
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	156
Cytogenetics in autologous bone marrow transplantation.	154
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	153
Complex chromosome rearrangements in chronic myelocytic leukemia	153
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.	152
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	151
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	150
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	150
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	150
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	149
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	148
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases	148
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	147
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	147
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	147
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	147
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families	146
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	146
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	145
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	145
Masked Philadelphia chromosome caused by translocation (9;11;22)	145
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	145
Mechanism of origin of the isochromosome i(7q).	144
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	144
Incidence of Shwachman-Diamond syndrome	144
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	143
The 11q;22q translocation: a european collaborative analysis of 43 cases	143
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	142
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	141
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	141
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	141
Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation	139
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	139
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	139
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	138
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	138
Minimal residual disease and trisomy 8	137
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	137
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	136
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	136
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	135
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	135
A liveborn triploid (69,XXY)	135
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	134
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	134
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	134
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	133
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	133
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	132
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	132
Involvement of chromosome no. 20 in a complex Ph' translocation	132
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	130
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	130
Male infertility and 13/14 translocation	130
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	130
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	129
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	128
An attempt to demonstrate gene dosage effect for beta-glucuronidase in monosomy 7 patients	128
Totale	15.867

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Categoria	#
all - tutte	111.474
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	111.474

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	2.273	0	0	0	0	0	414	89	285	520	121	289	555
2021/2022	1.987	189	273	213	109	56	76	61	136	103	282	184	305
2022/2023	3.004	284	159	207	332	257	659	3	392	427	98	98	88
2023/2024	5.511	946	946	963	962	1.053	288	30	54	126	39	15	89
2024/2025	3.052	20	30	587	54	108	187	120	215	340	243	237	911
2025/2026	3.749	604	364	337	1.194	734	516	0	0	0	0	0	0
Totale													28.911