statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	10.034
EU - Europa	9.930
AS - Asia	1.889
SA - Sud America	20
Continente sconosciuto - Info sul continente non disponibili	18
OC - Oceania	3
AF - Africa	2
Totale	21.896

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Nazione	#
US - Stati Uniti d'America	10.010
IT - Italia	5.352
UA - Ucraina	1.854
TR - Turchia	748
SE - Svezia	671
VN - Vietnam	571
CN - Cina	500
FI - Finlandia	496
IE - Irlanda	452
FR - Francia	410
DE - Germania	332
GB - Regno Unito	240
IN - India	42
PL - Polonia	34
BE - Belgio	27
EU - Europa	18
CA - Canada	12
CH - Svizzera	12
BR - Brasile	11
MX - Messico	10
NL - Olanda	9
SG - Singapore	9
AT - Austria	5
ES - Italia	5
JP - Giappone	5
AR - Argentina	4
BG - Bulgaria	4
CZ - Repubblica Ceca	4
IL - Israele	4
LU - Lussemburgo	3
AL - Albania	2
AU - Australia	2
BN - Brunei Darussalam	2
DK - Danimarca	2
EE - Estonia	2
IM - Isola di Man	2
MC - Monaco	2
OM - Oman	2
RU - Federazione Russa	2
VE - Venezuela	2
AZ - Azerbaigian	1
BD - Bangladesh	1
BS - Bahamas	1
BY - Bielorussia	1
CL - Cile	1
CO - Colombia	1
EC - Ecuador	1
GR - Grecia	1
HU - Ungheria	1
LT - Lituania	1
LV - Lettonia	1
MU - Mauritius	1
MY - Malesia	1
NO - Norvegia	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PA - Panama	1
PK - Pakistan	1
RO - Romania	1
RS - Serbia	1
TW - Taiwan	1
ZA - Sudafrica	1
Totale	21.896

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Città	#
Milan	3.647
Jacksonville	1.386
Fairfield	1.183
Chandler	1.136
Woodbridge	617
Ashburn	592
Houston	514
Wilmington	502
Princeton	469
Seattle	455
Dublin	452
Izmir	447
Nyköping	421
Ann Arbor	413
Dearborn	411
Cambridge	394
Dong Ket	318
Rome	264
San Mateo	201
Beijing	157
Como	128
San Diego	101
Ogden	76
Hefei	48
Nanjing	47
Verona	46
Helsinki	45
New York	45
Kunming	44
London	37
Redwood City	29
Norwalk	28
Washington	25
Nanchang	24
Brussels	23
Düsseldorf	23
Guangzhou	23
Los Angeles	23
Radomsko	23
Boardman	18
Phoenix	17
Jinan	16
Auburn Hills	14
Kocaeli	13
Ponte Lambro	13
Edinburgh	11
Redmond	11
Catania	10
Fuzhou	10
Shanghai	9
Shenyang	9
Bangalore	8
Baotou	8
Pune	8
Bologna	7
Chengdu	7
Chongqing	7
Hebei	7
Mcallen	7
Pavia	7
Philadelphia	7
Singapore	7
Berlin	6
Indiana	6
Mountain View	6
Naples	6
Acton	5
Bari	5
Brescia	5
Chiswick	5
Frankfurt am Main	5
Genova	5
Napoli	5
Ottawa	5
Palermo	5
Reggio Nell'emilia	5
Shaoxing	5
Stockholm	5
Tokyo	5
Vienna	5
Warsaw	5
Zhengzhou	5
Cagliari	4
Dallas	4
Enterprise	4
Goito	4
Hangzhou	4
Islington	4
Istanbul	4
Padova	4
Prague	4
Sofia	4
Tel Aviv	4
Turin	4
Ancona	3
Atlanta	3
Bergamo	3
Castelnuovo Rangone	3
Changsha	3
Chicago	3
Totale	15.218

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	283
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	208
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	170
High variability of genomic instability and gene expression profiling in different HeLa clones	166
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	166
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	156
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	155
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	155
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	148
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	146
Otx2 And VegfA Expression And P53-Otx1 Differentiation Pathway In Proliferative Vitreoretinopathy	145
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	143
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	141
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	138
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	138
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	138
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	138
The mammary gland and the homeobox gene Otx1	137
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	137
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	137
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	134
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	134
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	134
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	133
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	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
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	132
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	131
Complex chromosome rearrangements in chronic myelocytic leukemia	131
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	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
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	127
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	126
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
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	126
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	126
Incidence of Shwachman-Diamond syndrome	126
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
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	124
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families	124
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	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
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	122
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	120
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	120
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	118
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	118
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	117
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	117
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	117
Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation	116
Mechanism of origin of the isochromosome i(7q).	115
Minimal residual disease and trisomy 8	115
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	115
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	115
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	115
Involvement of chromosome no. 20 in a complex Ph' translocation	113
Masked Philadelphia chromosome caused by translocation (9;11;22)	113
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
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	112
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	111
Male infertility and 13/14 translocation	111
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	110
Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	109
Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies	108
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	108
Cytogenetics of Kaposi Sarcoma, an analysis of 15 cases	108
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	108
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	107
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	106
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	106
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	106
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases	105
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	105
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	104
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	104
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	102
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	102
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	101
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	101
The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution	101
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	100
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	100
Monozygotic twins discordant for cutaneous mastocytosis	100
The 11q;22q translocation: a european collaborative analysis of 43 cases	99
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	97
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	97
cytogenetic findings in a case of anaplastic carcinoma of the pancreas	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
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	96
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)	94
Clinical cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia.	94
Totale	12.433

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Categoria	#
all - tutte	64.775
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	64.775

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	1.094	0	0	0	0	0	0	0	0	0	0	384	710
2019/2020	3.999	170	152	125	663	173	419	717	584	238	368	73	317
2020/2021	3.124	44	323	43	330	111	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	5.410	946	946	963	962	1.053	288	30	54	126	39	3	0
Totale													22.009