statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	12.152
EU - Europa	10.646
AS - Asia	4.805
SA - Sud America	723
AF - Africa	51
Continente sconosciuto - Info sul continente non disponibili	18
OC - Oceania	5
Totale	28.400

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Nazione	#
US - Stati Uniti d'America	12.012
IT - Italia	5.429
UA - Ucraina	1.860
SG - Singapore	1.538
CN - Cina	879
TR - Turchia	761
VN - Vietnam	734
SE - Svezia	696
BR - Brasile	634
HK - Hong Kong	601
FI - Finlandia	539
IE - Irlanda	453
DE - Germania	436
FR - Francia	430
GB - Regno Unito	332
RU - Federazione Russa	217
JP - Giappone	95
IN - India	84
PL - Polonia	80
MX - Messico	68
CA - Canada	62
AR - Argentina	34
ZA - Sudafrica	31
BD - Bangladesh	28
BE - Belgio	28
AT - Austria	26
ES - Italia	26
EC - Ecuador	23
CH - Svizzera	21
NL - Olanda	19
EU - Europa	18
IQ - Iraq	17
LT - Lituania	12
VE - Venezuela	9
ID - Indonesia	8
MA - Marocco	8
PE - Perù	8
PK - Pakistan	8
IL - Israele	7
OM - Oman	6
UZ - Uzbekistan	6
AZ - Azerbaigian	5
CO - Colombia	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
EE - Estonia	2
HU - Ungheria	2
IM - Isola di Man	2
KR - Corea	2
LV - Lettonia	2
MC - Monaco	2
MK - Macedonia	2
MY - Malesia	2
NO - Norvegia	2
SA - Arabia Saudita	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
DZ - Algeria	1
EG - Egitto	1
GE - Georgia	1
GR - Grecia	1
GY - Guiana	1
HN - Honduras	1
JM - Giamaica	1
KE - Kenya	1
KZ - Kazakistan	1
MN - Mongolia	1
MU - Mauritius	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PA - Panama	1
PR - Porto Rico	1
RO - Romania	1
SR - Suriname	1
SY - Repubblica araba siriana	1
TG - Togo	1
TL - Timor Orientale	1
TT - Trinidad e Tobago	1
TW - Taiwan	1
TZ - Tanzania	1
UY - Uruguay	1
Totale	28.400

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Città	#
Milan	3.661
Jacksonville	1.386
Fairfield	1.183
Chandler	1.136
Ashburn	877
Singapore	749
Woodbridge	617
Hong Kong	601
Houston	522
Wilmington	502
Princeton	469
Seattle	462
Dublin	453
Izmir	447
Nyköping	421
Ann Arbor	413
Dearborn	411
Cambridge	394
Beijing	362
Dallas	354
Dong Ket	318
Rome	269
Boardman	255
San Mateo	201
The Dalles	137
Como	130
New York	113
Los Angeles	104
San Diego	101
Tokyo	94
Chicago	93
Santa Clara	85
Ogden	76
São Paulo	71
Munich	66
Helsinki	61
London	60
Ho Chi Minh City	55
Hefei	49
Verona	48
Nanjing	47
Warsaw	47
Hanoi	45
Kunming	44
Phoenix	35
Mexico City	34
Stockholm	30
Redwood City	29
Guangzhou	28
Norwalk	28
Poplar	28
Rio de Janeiro	27
Turku	27
Brooklyn	26
Washington	25
Brussels	24
Montreal	24
Nanchang	24
Denver	23
Düsseldorf	23
Johannesburg	23
Radomsko	23
Chennai	19
Brasília	18
Jinan	18
Nuremberg	18
Belo Horizonte	16
Catania	16
Orem	16
Atlanta	15
Quito	15
Toronto	15
Auburn Hills	14
Boston	14
Frankfurt am Main	14
San Francisco	14
Council Bluffs	13
Kocaeli	13
Ponte Lambro	13
Salt Lake City	13
Shanghai	13
Fuzhou	12
Manchester	12
Edinburgh	11
Redmond	11
San Jose	11
Columbus	10
Mumbai	9
Naples	9
Ribeirão Preto	9
Shenyang	9
Amsterdam	8
Bangalore	8
Baotou	8
Berlin	8
Chengdu	8
Pune	8
Querétaro	8
Salvador	8
Thái Bình	8
Totale	18.932

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	350
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	228
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	219
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	211
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	210
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	210
High variability of genomic instability and gene expression profiling in different HeLa clones	199
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	195
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	194
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	186
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	186
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	185
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	185
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	184
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	183
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	183
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	182
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	177
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	176
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	174
The mammary gland and the homeobox gene Otx1	173
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	172
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	171
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	169
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	168
Otx2 and VegfA expression and P53-Otx1 differentiation pathway in proliferative vitreoretinopathy	168
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	166
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	164
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	164
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	163
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	163
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	162
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	161
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	161
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	160
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	160
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.	156
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	156
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	156
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	156
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	155
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	155
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	154
Cytogenetics in autologous bone marrow transplantation.	153
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	152
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.	151
Complex chromosome rearrangements in chronic myelocytic leukemia	150
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	149
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	149
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	148
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases	147
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	146
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	146
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	146
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	145
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	145
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	144
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	144
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	144
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families	144
Masked Philadelphia chromosome caused by translocation (9;11;22)	144
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	144
Mechanism of origin of the isochromosome i(7q).	143
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	143
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	143
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	142
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	142
Incidence of Shwachman-Diamond syndrome	142
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	141
The 11q;22q translocation: a european collaborative analysis of 43 cases	141
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	139
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	139
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	139
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	139
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	138
Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation	138
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	136
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	136
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	136
Minimal residual disease and trisomy 8	135
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	135
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	133
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	133
A liveborn triploid (69,XXY)	133
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	133
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	132
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	132
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	132
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	131
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	131
Involvement of chromosome no. 20 in a complex Ph' translocation	131
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	130
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	129
Male infertility and 13/14 translocation	129
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	128
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	128
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	128
An attempt to demonstrate gene dosage effect for beta-glucuronidase in monosomy 7 patients	127
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	127
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	126
Totale	15.661

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Categoria	#
all - tutte	109.984
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	109.984

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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	3.355	604	364	337	1.194	734	122	0	0	0	0	0	0
Totale													28.517