statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	14.349
EU - Europa	11.134
AS - Asia	6.417
SA - Sud America	785
AF - Africa	99
Continente sconosciuto - Info sul continente non disponibili	19
OC - Oceania	19
Totale	32.822

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Nazione	#
US - Stati Uniti d'America	14.161
IT - Italia	5.469
SG - Singapore	1.909
UA - Ucraina	1.862
CN - Cina	1.627
VN - Vietnam	1.010
TR - Turchia	765
SE - Svezia	699
HK - Hong Kong	688
BR - Brasile	667
FR - Francia	664
FI - Finlandia	639
DE - Germania	456
IE - Irlanda	453
GB - Regno Unito	368
RU - Federazione Russa	225
IN - India	122
JP - Giappone	99
MX - Messico	98
PL - Polonia	88
CA - Canada	76
BD - Bangladesh	40
AR - Argentina	38
ZA - Sudafrica	37
ES - Italia	33
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
LT - Lituania	12
MA - Marocco	12
ID - Indonesia	11
SA - Arabia Saudita	11
UZ - Uzbekistan	11
CO - Colombia	10
PE - Perù	10
DK - Danimarca	8
IL - Israele	8
OM - Oman	8
PY - Paraguay	8
JO - Giordania	7
NP - Nepal	7
MY - Malesia	6
PH - Filippine	6
AZ - Azerbaigian	5
BG - Bulgaria	5
CL - Cile	5
CZ - Repubblica Ceca	5
SN - Senegal	5
AL - Albania	4
DZ - Algeria	4
EG - Egitto	4
KE - Kenya	4
LB - Libano	4
MD - Moldavia	4
RS - Serbia	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
DO - Repubblica Dominicana	2
EE - Estonia	2
GR - Grecia	2
IM - Isola di Man	2
JM - Giamaica	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
CR - Costa Rica	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
MU - Mauritius	1
Totale	32.809

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Città	#
Milan	3.662
Jacksonville	1.388
San Jose	1.279
Fairfield	1.183
Chandler	1.136
Ashburn	1.059
Singapore	989
Hong Kong	680
Woodbridge	617
Houston	527
Wilmington	503
Princeton	469
Seattle	463
Dublin	453
Izmir	447
Nyköping	421
Beijing	415
Ann Arbor	413
Dearborn	411
Cambridge	396
Dallas	361
Dong Ket	318
Rome	272
Boardman	255
The Dalles	253
Lauterbourg	207
San Mateo	201
Chicago	167
Helsinki	161
Ho Chi Minh City	141
New York	137
Como	130
Los Angeles	124
Hanoi	119
Council Bluffs	104
Santa Clara	104
San Diego	102
Tokyo	98
Guangzhou	92
Orem	89
Ogden	76
São Paulo	73
Munich	66
London	63
Mexico City	58
Warsaw	53
Nanjing	51
Hefei	49
Shanghai	49
Verona	48
Kunming	45
Tianjin	44
Chennai	42
Phoenix	40
Stockholm	32
Brooklyn	31
Shenzhen	31
Denver	30
Montreal	30
Poplar	29
Redwood City	29
Johannesburg	28
Norwalk	28
Frankfurt am Main	27
Manchester	27
Rio de Janeiro	27
Turku	27
Washington	26
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
Catania	17
Zhengzhou	17
Belo Horizonte	16
Boston	16
Toronto	16
Fuzhou	15
Mumbai	15
Quito	15
San Francisco	15
Auburn Hills	14
Haiphong	14
Biên Hòa	13
Columbus	13
Kocaeli	13
Ponte Lambro	13
Salt Lake City	13
Bologna	12
Naples	12
Edinburgh	11
Miami	11
Totale	22.049

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	375
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	263
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	244
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	237
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	235
High variability of genomic instability and gene expression profiling in different HeLa clones	235
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	221
The mammary gland and the homeobox gene Otx1	220
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	219
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	215
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	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
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	211
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	210
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	208
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	207
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	203
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	201
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	200
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	199
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
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	195
Otx2 and VegfA expression and P53-Otx1 differentiation pathway in proliferative vitreoretinopathy	190
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	189
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.	187
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	187
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	186
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	186
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	184
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	181
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	181
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	181
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	180
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	180
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	179
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	177
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	177
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	177
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	176
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	176
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	175
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	175
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	173
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	172
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	171
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	170
Incidence of Shwachman-Diamond syndrome	170
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	169
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	169
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.	169
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	165
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	164
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	164
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	162
Mechanism of origin of the isochromosome i(7q).	161
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	161
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	161
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	160
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	160
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
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	158
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
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
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	157
Complex chromosome rearrangements in chronic myelocytic leukemia	157
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	156
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	156
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	156
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	155
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	155
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	155
The 11q;22q translocation: a european collaborative analysis of 43 cases	155
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	154
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
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	152
Masked Philadelphia chromosome caused by translocation (9;11;22)	152
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	152
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	151
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	150
An attempt to demonstrate gene dosage effect for beta-glucuronidase in monosomy 7 patients	150
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	149
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	149
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	149
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	148
Minimal residual disease and trisomy 8	148
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	148
A liveborn triploid (69,XXY)	148
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	146
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	146
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	145
A 45, X male with a Yp/18 translocation.	145
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	145
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	144
Totale	17.678

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Categoria	#
all - tutte	120.209
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	120.209

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	844	0	0	0	0	0	0	0	0	0	0	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	7.777	604	364	337	1.194	734	585	1.772	547	815	569	256	0
Totale													32.939