statistiche ricercatore

LO CURTO, FRANCESCO

Distribuzione geografica

Continente	#
NA - Nord America	9.168
EU - Europa	7.449
AS - Asia	3.965
SA - Sud America	388
AF - Africa	119
Continente sconosciuto - Info sul continente non disponibili	16
OC - Oceania	16
Totale	21.121

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Nazione	#
US - Stati Uniti d'America	9.040
IT - Italia	3.866
SG - Singapore	1.216
UA - Ucraina	1.151
CN - Cina	920
TR - Turchia	566
VN - Vietnam	564
SE - Svezia	443
HK - Hong Kong	398
FI - Finlandia	376
FR - Francia	341
BR - Brasile	317
GB - Regno Unito	312
DE - Germania	305
IE - Irlanda	271
RU - Federazione Russa	128
IN - India	103
JP - Giappone	85
PL - Polonia	71
NG - Nigeria	69
MX - Messico	67
CA - Canada	50
NL - Olanda	43
BE - Belgio	27
ES - Italia	26
BD - Bangladesh	23
ZA - Sudafrica	20
AR - Argentina	19
CH - Svizzera	17
EC - Ecuador	17
AT - Austria	16
AU - Australia	16
EU - Europa	16
IQ - Iraq	15
VE - Venezuela	12
IL - Israele	10
LT - Lituania	10
MA - Marocco	10
CO - Colombia	8
PK - Pakistan	8
PH - Filippine	7
AL - Albania	6
CZ - Repubblica Ceca	6
DK - Danimarca	6
UZ - Uzbekistan	6
AE - Emirati Arabi Uniti	5
BG - Bulgaria	5
EG - Egitto	5
JO - Giordania	5
NP - Nepal	5
OM - Oman	5
PE - Perù	5
PY - Paraguay	5
MY - Malesia	4
SN - Senegal	4
DO - Repubblica Dominicana	3
ID - Indonesia	3
KE - Kenya	3
LB - Libano	3
PA - Panama	3
RS - Serbia	3
SA - Arabia Saudita	3
AO - Angola	2
AZ - Azerbaigian	2
BA - Bosnia-Erzegovina	2
CL - Cile	2
DZ - Algeria	2
EE - Estonia	2
GR - Grecia	2
HU - Ungheria	2
IM - Isola di Man	2
JM - Giamaica	2
LU - Lussemburgo	2
MN - Mongolia	2
NO - Norvegia	2
SK - Slovacchia (Repubblica Slovacca)	2
TH - Thailandia	2
TW - Taiwan	2
UY - Uruguay	2
AM - Armenia	1
BO - Bolivia	1
BS - Bahamas	1
BY - Bielorussia	1
CG - Congo	1
GA - Gabon	1
GD - Grenada	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LY - Libia	1
MC - Monaco	1
MK - Macedonia	1
RO - Romania	1
TG - Togo	1
TT - Trinidad e Tobago	1
Totale	21.121

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Città	#
Milan	2.313
Chandler	957
Jacksonville	852
San Jose	693
Ashburn	650
Singapore	647
Fairfield	599
Hong Kong	392
Woodbridge	368
Izmir	293
Princeton	284
Wilmington	282
Dearborn	280
Dallas	273
Dublin	271
Houston	271
Ann Arbor	245
Seattle	242
Beijing	234
Cambridge	233
Nyköping	229
Rome	218
Dong Ket	188
Chicago	187
The Dalles	162
Boardman	149
San Mateo	128
Como	124
Lauterbourg	119
New York	105
Tokyo	84
Ho Chi Minh City	77
Helsinki	76
Los Angeles	72
Orem	71
Abuja	69
Redwood City	68
Santa Clara	68
Hanoi	65
San Diego	65
London	62
Ogden	61
Council Bluffs	60
Guangzhou	53
Munich	52
São Paulo	46
Mexico City	39
Warsaw	37
Nanjing	35
Hefei	33
Chennai	31
Verona	31
Kunming	28
Brussels	26
Frankfurt am Main	23
Phoenix	23
Radomsko	23
Shanghai	23
Philadelphia	22
Tianjin	20
Manchester	19
Norwalk	19
Turku	18
Düsseldorf	17
Brooklyn	16
Jinan	16
Johannesburg	16
Montreal	16
Naples	16
Shenzhen	16
Stockholm	16
Toronto	16
Catania	15
Denver	15
Nanchang	15
Amsterdam	14
Atlanta	14
Auburn Hills	14
Mumbai	13
Pavia	13
Poplar	13
Pune	13
Da Nang	11
Ponte Lambro	11
Washington	11
Fuzhou	10
Hangzhou	10
Rio de Janeiro	10
Zhengzhou	10
Boston	9
Brasília	9
Miami	9
Piemonte	9
Bangalore	8
Bari	8
Belo Horizonte	8
Edinburgh	8
Padova	8
San Francisco	8
Baghdad	7
Totale	13.935

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	371
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.	280
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	260
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	243
The mammary gland and the homeobox gene Otx1	217
Cd bands and centromeric function in dicentric chromosomes	217
A new chromosome instability disorder	217
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	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	210
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	209
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	205
OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas	205
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	199
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	198
Chronic Myeloid Leukemia: Molecular Monitoring of Residual Disease by Genomic DNA Compared to Conventional mRNA Analysis in Follow-Ups up to 8 Years	197
Acquired Chromosome change in Cholesteatoma	194
La trisomia 8 in leucemie acute e mielodisplasie e costituzionale nel 15-20% dei casi	193
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	193
48,XXXY/49,XXXXY Mosaicism in a month old infant.	191
Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.	184
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	184
Assessing residual disease in imatinib-treated CML patients by DNA compared to MRNA assays	183
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.	183
First trimester prenatal diagnosis of Sanfilippo disease (MPS III) type B.	182
Le basi genetiche della malattia linfoproliferativa.	181
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMIM 601399)	180
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	179
Acute lymphoblastic leukemia and a familial balanced translocation (12;15) involving ETV6	179
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	179
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	178
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	176
The syndrome of partial trisomy 14q.	175
Karyotypic variation in benign pleomorphic adenoma of the parotid and in normal salivary glands.	175
Analysis of cross-contamination in established tumour cell lines.	174
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	172
La citogenetica interfasica dimostra che le cellule dendritiche nella Leucemia Mielomonocitica Cronica Giovanile fanno parte del clone leucemico	170
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	168
Nuclear projections in tumour cells	167
Studio molecolare del differenziamento da cellule staminali in condrociti in vivo per lo sviluppo di un protocollo di trapianti di cartilagine umana	167
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	167
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.	166
Chromosomal analysis in cultured lymphocytes and fibroblasts of psoriatic patients before and after treatment.	165
The role of Yp in sex determination: new evidence from X/Y translocations.	165
Chromosome identification in a Chinese hamster pseudodiploid cell line (CHEF-125)	165
Anticentromeric antibodies and inactive centromeres.	164
A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.	163
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	162
Acute lymphoblastic leukemia and familial balanced translocation (12;15) involving ETV6	161
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia	161
Studio molecolare del differenziamento da cellule staminali in condrociti e osteoblasti in vivo per lo sviluppo di protocolli di trapianto	160
Mielodisplasia con monosomia 7 familiare: dati citogenetici e molecolari	159
Criobanca automatizzata di materiale biologico: stoccaggio e monitoraggio molecolare di cellule meniscali per il trapianto autologo	158
Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects	158
Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.	157
Microhomologiee and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.	154
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia.	154
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.	154
Mielodisplasia familiare con monosomia 7 e trisomia 8 associata a trombocitopenia ereditaria (OMOM 601399)	154
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	154
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	154
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	153
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	152
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	149
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	149
Citogenetica Umana: nuove metodiche ed applicazioni in medicina.	148
Myotonic Dystrophy: genetic aspects ; cytochemical findings.	147
Instabilità costituzionale del cariotipo all'origine di trisomia 8 acquisita midollare	147
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	145
Sindrome di Shwacham: instabilita del cromosoma 7 e rischio di patologia mielodisplastica e mieloproliferativa	143
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	143
Erratum: OTX1 expression in breast cancer is regulated by p53 (Oncogene (2011) 30 (3096-3103) doi:10.1038/onc.2011.31)	143
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	142
Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.	142
Growth Hormone and Estrogens in Patients with Turner Syndrome: in vivo and in vitro studies.	139
Chromosome size and nuclear projections	136
Variabilità cromosomica in linee cellulari derivate da melanomi.	135
Studio dei fibroblasti "in vitro" nella distrofia miotonica.	135
Nuclear projections and latent centromeres in primary culture and established cell lines.	135
Different reaction of inactive centromeres to anticentromeric antibodies.	134
La linea cellulare EUE deriva da una linea HeLa.	134
Diagnostica cromosomica	133
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	133
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento dei geni FLI1 e MPL	133
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	132
Chromosome identification and karyotypic evolution in a human melanoma cell line.	131
Leucemia linfoblastica acuta e traslocazione familiare (15-15) che coinvolge ETV6	131
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	131
Le basi genetiche della malattia linfoproliferativa legata al cromosoma X	130
Differente reazione dei centromeri inattivi agli anticorpi anticentromero.	129
Distrofia miotonica: genetica e citochimica	129
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	129
Insulin receptors in psoriasis.	128
Correlation between the numbers of sex chromosomes and the H-Y antigen titer.	127
Protrusioni nucleari dovute a cromosomi strutturalmente alterati.	126
Familial partial monosomy 7 and myelodysplasia: different paternal origin of the monosomy 7 suggests action of a mutator gene	126
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	126
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	125
Presenza di anomalie cromosomiche nelle cellule epiteliali della matrice del colesteatoma: studio citogenetico.	123
Chromosome 7 instability and myelodysplasia in Shwachman syndrome	123
Totale	16.612

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Categoria	#
all - tutte	73.326
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	73.326

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	564	0	0	0	0	0	0	0	0	0	63	169	332
2021/2022	1.265	104	177	137	76	38	26	44	77	70	194	98	224
2022/2023	2.356	186	143	200	279	156	472	2	336	322	90	101	69
2023/2024	3.566	594	611	591	636	630	189	23	74	94	26	11	87
2024/2025	2.094	12	39	395	71	141	111	106	140	197	140	147	595
2025/2026	4.515	393	234	207	625	508	376	1.062	277	602	231	0	0
Totale													21.164