statistiche ricercatore

PASQUALI, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	15.459
EU - Europa	11.251
AS - Asia	6.489
SA - Sud America	803
Continente sconosciuto - Info sul continente non disponibili	136
AF - Africa	99
OC - Oceania	19
Totale	34.256

Salva come PNG Salva come JPEG

Nazione	#
US - Stati Uniti d'America	15.213
IT - Italia	5.557
SG - Singapore	1.923
UA - Ucraina	1.863
CN - Cina	1.641
VN - Vietnam	1.011
TR - Turchia	766
SE - Svezia	704
HK - Hong Kong	689
BR - Brasile	676
FR - Francia	667
FI - Finlandia	639
DE - Germania	456
IE - Irlanda	455
GB - Regno Unito	369
RU - Federazione Russa	225
IN - India	123
CA - Canada	102
MX - Messico	101
JP - Giappone	99
PL - Polonia	89
BD - Bangladesh	78
AR - Argentina	40
ES - Italia	39
ZA - Sudafrica	37
IQ - Iraq	33
NL - Olanda	33
AT - Austria	30
BE - Belgio	30
EC - Ecuador	28
NG - Nigeria	25
CH - Svizzera	21
AU - Australia	18
EU - Europa	18
PK - Pakistan	17
VE - Venezuela	15
CO - Colombia	13
LT - Lituania	12
MA - Marocco	12
ID - Indonesia	11
PE - Perù	11
SA - Arabia Saudita	11
UZ - Uzbekistan	11
JM - Giamaica	9
CR - Costa Rica	8
CZ - Repubblica Ceca	8
DK - Danimarca	8
IL - Israele	8
NP - Nepal	8
OM - Oman	8
PY - Paraguay	8
CL - Cile	7
JO - Giordania	7
MY - Malesia	6
PH - Filippine	6
AZ - Azerbaigian	5
BG - Bulgaria	5
GT - Guatemala	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
DO - Repubblica Dominicana	3
GE - Georgia	3
GR - Grecia	3
HU - Ungheria	3
KR - Corea	3
LU - Lussemburgo	3
PR - Porto Rico	3
TH - Thailandia	3
AE - Emirati Arabi Uniti	2
AO - Angola	2
BA - Bosnia-Erzegovina	2
BN - Brunei Darussalam	2
BY - Bielorussia	2
EE - Estonia	2
HN - Honduras	2
IM - Isola di Man	2
KZ - Kazakistan	2
LV - Lettonia	2
MC - Monaco	2
MK - Macedonia	2
NI - Nicaragua	2
NO - Norvegia	2
PA - Panama	2
SR - Suriname	2
SV - El Salvador	2
TT - Trinidad e Tobago	2
TW - Taiwan	2
BB - Barbados	1
BO - Bolivia	1
BS - Bahamas	1
CG - Congo	1
DM - Dominica	1
GY - Guiana	1
HT - Haiti	1
Totale	34.121

Salva come PNG Salva come JPEG

Città	#
Milan	3.671
San Jose	1.461
Jacksonville	1.389
Fairfield	1.183
Chandler	1.136
Ashburn	1.103
Singapore	992
Hong Kong	681
Woodbridge	617
Houston	532
Wilmington	503
Princeton	470
Seattle	464
Council Bluffs	460
Dublin	453
Izmir	447
Nyköping	421
Beijing	420
Ann Arbor	413
Dearborn	411
Cambridge	397
Dallas	372
Dong Ket	318
Rome	282
Boardman	255
The Dalles	253
Lauterbourg	207
San Mateo	201
Chicago	172
New York	162
Helsinki	161
Los Angeles	153
Ho Chi Minh City	141
Santa Clara	140
Como	130
Hanoi	120
San Diego	103
Tokyo	98
Guangzhou	92
Orem	89
Ogden	76
São Paulo	73
Munich	66
London	64
Verona	61
Mexico City	60
Warsaw	54
Nanjing	51
Hefei	49
Shanghai	49
Kunming	45
Tianjin	45
Chennai	42
Phoenix	42
Brooklyn	34
Stockholm	32
Denver	31
Shenzhen	31
Montreal	30
Norwalk	30
Washington	30
Poplar	29
Redwood City	29
Buffalo	28
Johannesburg	28
Frankfurt am Main	27
Manchester	27
Rio de Janeiro	27
Turku	27
Brussels	26
Abuja	25
Toronto	25
Hangzhou	24
Nanchang	24
Düsseldorf	23
Radomsko	23
Atlanta	22
Da Nang	22
San Francisco	21
Nuremberg	20
Amsterdam	19
Brasília	19
Jinan	19
Catania	18
Belo Horizonte	17
Boston	17
Zhengzhou	17
Miami	16
Salt Lake City	16
Fuzhou	15
Mumbai	15
Quito	15
Auburn Hills	14
Haiphong	14
Naples	14
Philadelphia	14
Biên Hòa	13
Bologna	13
Columbus	13
Kocaeli	13
Totale	22.856

Salva come PNG Salva come JPEG

Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	383
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	279
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	250
High variability of genomic instability and gene expression profiling in different HeLa clones	242
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	241
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	240
The mammary gland and the homeobox gene Otx1	237
MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity	230
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	227
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	224
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	223
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	216
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	215
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	215
8/21 translocation, loss of the Y chromosome and Philadelphia chromosome	213
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	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
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	209
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	206
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	206
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	202
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	201
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases	201
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	200
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	198
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	196
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.	196
17Q21-QTER TRYSOMY IS AN INDICATOR OF POOR PROGNOSIS IN ACUTE MYELOGENOUS LEUKAEMIA	195
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	195
Otx2 and VegfA expression and P53-Otx1 differentiation pathway in proliferative vitreoretinopathy	193
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	191
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	190
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	189
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	189
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	189
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	187
CONSTITUTIONAL TRISOMY 8 MOSAICISM: MECHANISM OF ORIGIN, PHENOTYPE VARIABILITY, AND RISK OF MALIGNANCIES.	186
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	185
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	184
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	183
Trisomy 8 in Philadelphia Chromosome (Ph1)- Negative Cells in the Course of Ph1-Positive Chronic Myelocytic Leukemia	182
The strange case of the lost NRAS mutation in a child with juvenile myelomonocytic leukemia	182
Derangements of immunoglobulin levels, phytohemagglutinin responsiveness and T and B cell markers in Down's syndrome at different ages	180
A translocation t(4;13)(q21; q14) as single clonal chromosomal abnormality in a parathyroid adenoma	179
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	178
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase	176
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	175
Incidence of Shwachman-Diamond syndrome	174
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	173
Mechanism of origin of the isochromosome i(7q).	173
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.	173
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	172
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	172
Constitutional trisomy 8 mosaicism: mechanism of origin, phenotype variability, and risk of malignancies.	171
Cytogenetics in autologous bone marrow transplantation.	169
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	169
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	169
MEIOTIC ORIGIN OF TRISOMY IN NEOPLASM: EVIDENCE IN A CASE OF ERYTROLEUKAEMIA	169
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	168
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	168
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	167
ATAXIA WITHOUT TELANGIECTASIA IN TWO SISTERS WITH REARRANGEMENTS OF CHROMOSOMES 7 AND 14.	165
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	165
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	165
Cytogenetics of Kaposi sarcoma: an analysis of 15 cases	165
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families	162
Complex chromosome rearrangements in chronic myelocytic leukemia	162
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	161
SPONTANEOUS REMISSION FROM RAEB IN A CHILD	161
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	161
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia	161
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	160
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	160
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	160
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases	160
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	160
Sindrome di Shwachman con isocromosoma i(7q) e ruolo delle anomalie del cromosoma 7 nelle malattie mieloproliferative	159
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	159
The 11q;22q translocation: a european collaborative analysis of 43 cases	159
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	158
Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation	157
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	157
Masked Philadelphia chromosome caused by translocation (9;11;22)	157
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile	157
Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemia	156
An attempt to demonstrate gene dosage effect for beta-glucuronidase in monosomy 7 patients	156
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	156
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma	155
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	155
Gene dosage effect in acquired monosomy 7: distinct behaviour of β-glucuronidase and phosphoserine phosphatase.	154
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	154
A liveborn triploid (69,XXY)	154
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	153
A 45, X male with a Yp/18 translocation.	152
Translocation 8/21 in two cases of refractory anaemia with excess of blasts in trasformation.	151
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	151
Minimal residual disease and trisomy 8	150
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome	150
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	150
Isochromosome (17q) in Philadelphia chromosome (Ph') - negative juvenile chronic myelocytic leukemia	148
Totale	18.307

Salva come PNG Salva come JPEG

Categoria	#
all - tutte	130.873
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	130.873

Salva come PNG Salva come JPEG

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	1.525	0	0	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	998	172	406	420	0	0	0	0	0	0	0	0	0
Totale													34.256