statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	14.641
EU - Europa	11.209
AS - Asia	6.463
SA - Sud America	798
AF - Africa	99
Continente sconosciuto - Info sul continente non disponibili	19
OC - Oceania	19
Totale	33.248

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Nazione	#
US - Stati Uniti d'America	14.444
IT - Italia	5.524
SG - Singapore	1.916
UA - Ucraina	1.863
CN - Cina	1.633
VN - Vietnam	1.011
TR - Turchia	766
SE - Svezia	700
HK - Hong Kong	688
BR - Brasile	674
FR - Francia	667
FI - Finlandia	639
DE - Germania	456
IE - Irlanda	455
GB - Regno Unito	368
RU - Federazione Russa	225
IN - India	122
JP - Giappone	99
MX - Messico	99
PL - Polonia	89
CA - Canada	78
BD - Bangladesh	70
AR - Argentina	40
ES - Italia	39
ZA - Sudafrica	37
IQ - Iraq	33
NL - Olanda	32
AT - Austria	30
BE - Belgio	28
EC - Ecuador	27
NG - Nigeria	25
CH - Svizzera	21
AU - Australia	18
EU - Europa	18
PK - Pakistan	16
VE - Venezuela	15
CO - Colombia	12
LT - Lituania	12
MA - Marocco	12
ID - Indonesia	11
PE - Perù	11
SA - Arabia Saudita	11
UZ - Uzbekistan	11
CZ - Repubblica Ceca	8
DK - Danimarca	8
IL - Israele	8
NP - Nepal	8
OM - Oman	8
PY - Paraguay	8
JO - Giordania	7
CL - Cile	6
MY - Malesia	6
PH - Filippine	6
AZ - Azerbaigian	5
BG - Bulgaria	5
JM - Giamaica	5
MD - Moldavia	5
RS - Serbia	5
SN - Senegal	5
AL - Albania	4
DZ - Algeria	4
EG - Egitto	4
KE - Kenya	4
LB - Libano	4
GE - Georgia	3
HU - Ungheria	3
KR - Corea	3
LU - Lussemburgo	3
TH - Thailandia	3
AE - Emirati Arabi Uniti	2
AO - Angola	2
BA - Bosnia-Erzegovina	2
BN - Brunei Darussalam	2
BY - Bielorussia	2
CR - Costa Rica	2
DO - Repubblica Dominicana	2
EE - Estonia	2
GR - Grecia	2
IM - Isola di Man	2
KZ - Kazakistan	2
LV - Lettonia	2
MC - Monaco	2
MK - Macedonia	2
NO - Norvegia	2
PA - Panama	2
SR - Suriname	2
TW - Taiwan	2
BO - Bolivia	1
BS - Bahamas	1
CG - Congo	1
DM - Dominica	1
GT - Guatemala	1
GY - Guiana	1
HN - Honduras	1
IR - Iran	1
KG - Kirghizistan	1
LY - Libia	1
MM - Myanmar	1
MN - Mongolia	1
MQ - Martinica	1
Totale	33.232

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Città	#
Milan	3.664
Jacksonville	1.389
San Jose	1.289
Fairfield	1.183
Chandler	1.136
Ashburn	1.075
Singapore	989
Hong Kong	680
Woodbridge	617
Houston	530
Wilmington	503
Princeton	470
Seattle	463
Dublin	453
Izmir	447
Nyköping	421
Beijing	415
Ann Arbor	413
Dearborn	411
Cambridge	396
Dallas	362
Dong Ket	318
Rome	276
Boardman	255
The Dalles	253
Council Bluffs	228
Lauterbourg	207
San Mateo	201
Chicago	169
Helsinki	161
New York	142
Ho Chi Minh City	141
Como	130
Los Angeles	126
Santa Clara	121
Hanoi	120
San Diego	102
Tokyo	98
Guangzhou	92
Orem	89
Ogden	76
São Paulo	73
Munich	66
London	63
Verona	61
Mexico City	59
Warsaw	54
Nanjing	51
Hefei	49
Shanghai	49
Kunming	45
Tianjin	45
Chennai	42
Phoenix	41
Brooklyn	32
Stockholm	32
Shenzhen	31
Denver	30
Montreal	30
Poplar	29
Redwood City	29
Washington	29
Johannesburg	28
Norwalk	28
Frankfurt am Main	27
Manchester	27
Rio de Janeiro	27
Turku	27
Abuja	25
Brussels	24
Hangzhou	24
Nanchang	24
Düsseldorf	23
Radomsko	23
Da Nang	22
Atlanta	21
Nuremberg	20
Amsterdam	19
Brasília	19
Jinan	19
San Francisco	18
Belo Horizonte	17
Boston	17
Catania	17
Toronto	17
Zhengzhou	17
Fuzhou	15
Mumbai	15
Quito	15
Auburn Hills	14
Haiphong	14
Naples	14
Biên Hòa	13
Bologna	13
Columbus	13
Kocaeli	13
Philadelphia	13
Ponte Lambro	13
Salt Lake City	13
Miami	12
Totale	22.271

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	376
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	276
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	247
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	239
High variability of genomic instability and gene expression profiling in different HeLa clones	237
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	237
The mammary gland and the homeobox gene Otx1	231
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	225
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	222
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	220
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	220
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	214
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	213
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	213
Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia	213
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	211
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	206
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	205
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	203
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	201
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	201
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	198
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	196
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	196
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	194
Otx2 and VegfA expression and P53-Otx1 differentiation pathway in proliferative vitreoretinopathy	192
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	190
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	190
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	190
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.	189
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	188
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	188
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	186
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	183
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	182
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	181
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	181
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	181
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	181
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	181
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	179
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	177
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	175
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	174
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	174
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	173
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	172
Mechanism of origin of the isochromosome i(7q).	171
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	170
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	170
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.	170
Incidence of Shwachman-Diamond syndrome	170
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	168
Cytogenetics in autologous bone marrow transplantation.	167
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	167
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	166
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	166
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	165
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	164
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	164
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	162
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	162
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	161
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	160
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	159
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	159
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families	159
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	158
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases	158
Complex chromosome rearrangements in chronic myelocytic leukemia	158
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	158
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	157
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	157
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	156
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	156
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	156
The 11q;22q translocation: a european collaborative analysis of 43 cases	156
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	155
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	155
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	155
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	154
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	153
Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation	152
Masked Philadelphia chromosome caused by translocation (9;11;22)	152
An attempt to demonstrate gene dosage effect for beta-glucuronidase in monosomy 7 patients	152
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	152
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	152
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	151
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	151
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	150
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	149
Minimal residual disease and trisomy 8	149
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	149
A liveborn triploid (69,XXY)	149
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	148
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	148
A 45, X male with a Yp/18 translocation.	148
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	148
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	146
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	145
Totale	17.934

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Categoria	#
all - tutte	125.239
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	125.239

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
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	8.096	604	364	337	1.194	734	585	1.772	547	815	569	364	211
2026/2027	107	107	0	0	0	0	0	0	0	0	0	0	0
Totale													33.365