statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	9.178
EU - Europa	5.272
AS - Asia	3.472
SA - Sud America	423
Continente sconosciuto - Info sul continente non disponibili	181
AF - Africa	64
OC - Oceania	23
Totale	18.613

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Nazione	#
US - Stati Uniti d'America	8.965
IT - Italia	2.688
SG - Singapore	1.159
CN - Cina	883
UA - Ucraina	678
VN - Vietnam	455
BR - Brasile	343
HK - Hong Kong	340
SE - Svezia	333
TR - Turchia	322
DE - Germania	290
FR - Francia	262
FI - Finlandia	243
GB - Regno Unito	232
IE - Irlanda	195
RU - Federazione Russa	106
CA - Canada	98
MX - Messico	74
JP - Giappone	72
BD - Bangladesh	67
IN - India	67
PL - Polonia	63
NL - Olanda	37
AT - Austria	31
ZA - Sudafrica	31
AR - Argentina	28
ES - Italia	28
AU - Australia	22
EC - Ecuador	19
BE - Belgio	17
PK - Pakistan	15
CH - Svizzera	13
CR - Costa Rica	12
IQ - Iraq	11
VE - Venezuela	10
ID - Indonesia	9
SA - Arabia Saudita	9
CZ - Repubblica Ceca	8
LT - Lituania	8
CO - Colombia	7
JO - Giordania	7
MA - Marocco	7
BG - Bulgaria	6
KE - Kenya	6
NG - Nigeria	6
PE - Perù	6
AE - Emirati Arabi Uniti	5
EU - Europa	5
IL - Israele	5
JM - Giamaica	5
MY - Malesia	5
UZ - Uzbekistan	5
AZ - Azerbaigian	4
DK - Danimarca	4
EG - Egitto	4
NP - Nepal	4
OM - Oman	4
PH - Filippine	4
PR - Porto Rico	4
SV - El Salvador	4
TH - Thailandia	4
BA - Bosnia-Erzegovina	3
DZ - Algeria	3
GR - Grecia	3
LB - Libano	3
NO - Norvegia	3
PA - Panama	3
PY - Paraguay	3
RS - Serbia	3
TW - Taiwan	3
UY - Uruguay	3
AO - Angola	2
BY - Bielorussia	2
CL - Cile	2
DO - Repubblica Dominicana	2
EE - Estonia	2
HN - Honduras	2
HU - Ungheria	2
IM - Isola di Man	2
KR - Corea	2
LU - Lussemburgo	2
LV - Lettonia	2
MC - Monaco	2
MD - Moldavia	2
SN - Senegal	2
AL - Albania	1
AM - Armenia	1
BB - Barbados	1
BM - Bermuda	1
BN - Brunei Darussalam	1
CG - Congo	1
CW - ???statistics.table.value.countryCode.CW???	1
GD - Grenada	1
GE - Georgia	1
GT - Guatemala	1
GY - Guiana	1
IR - Iran	1
KG - Kirghizistan	1
KY - Cayman, isole	1
KZ - Kazakistan	1
Totale	18.427

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Città	#
Milan	1.467
Ashburn	963
San Jose	804
Singapore	677
Chandler	611
Fairfield	603
Jacksonville	510
Woodbridge	421
Council Bluffs	412
Hong Kong	333
Houston	311
Ann Arbor	290
Beijing	250
Wilmington	241
Seattle	219
Dearborn	210
Dallas	207
Cambridge	200
Nyköping	200
Dublin	192
Princeton	190
Izmir	152
New York	141
Los Angeles	132
The Dalles	131
Dong Ket	130
Boardman	123
Como	121
Rome	108
Santa Clara	97
Lauterbourg	95
Chicago	78
Ho Chi Minh City	76
Munich	76
Helsinki	71
Tokyo	70
Hanoi	63
Orem	55
San Mateo	55
São Paulo	55
Warsaw	43
Mexico City	41
London	40
San Diego	40
Guangzhou	39
Phoenix	39
Brooklyn	33
Stockholm	33
Hefei	30
Poplar	30
Montreal	29
Turku	29
Ogden	28
Toronto	27
Varese	27
Verona	27
Atlanta	26
Chennai	25
Kunming	25
Frankfurt am Main	24
Nanjing	24
Denver	23
Johannesburg	22
Shanghai	21
Buffalo	20
Naples	19
Redwood City	19
San Francisco	19
Manchester	18
Washington	17
Brussels	16
Catania	16
Gavirate	16
Jinan	16
Kocaeli	16
Shenzhen	16
Amsterdam	15
Columbus	15
Miami	14
Nuremberg	14
Rio de Janeiro	13
Salt Lake City	13
Tianjin	13
Vienna	13
Zhengzhou	13
Boston	12
Edinburgh	12
Philadelphia	12
Redmond	12
San José	12
Bologna	11
Nanchang	11
Norwalk	11
Belo Horizonte	10
Da Nang	10
Florence	10
Haiphong	10
Turin	10
Vancouver	10
Assago	9
Totale	12.358

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	394
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	290
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	254
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	254
High variability of genomic instability and gene expression profiling in different HeLa clones	250
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	245
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	244
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	242
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	241
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	231
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	228
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	228
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	227
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	224
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	221
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	220
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	218
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	217
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	214
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	213
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	213
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	208
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	207
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	201
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	201
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	200
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	199
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	199
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	199
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	195
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	194
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	193
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	193
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	191
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	189
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	188
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	188
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	183
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	182
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	176
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	176
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	175
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	171
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	171
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	168
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	167
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	166
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	164
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	164
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	164
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	162
Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations	162
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	161
Chromosome anomalies as cause of congenital bone marrow failure syndromes	161
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	161
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	161
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	160
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	160
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	159
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	159
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	158
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	158
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	156
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	154
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	153
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	152
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	150
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	150
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	150
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	148
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	148
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	147
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	147
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	146
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	145
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	144
Expression studies in the bone marrow of patients with Shwachman Diamond Syndrome (SDS) and deletion of the long arm of chromosome 20 encompassing th3 EIF6 gene: relation with benign prognosis.	144
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	143
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	143
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	143
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	142
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	142
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	142
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	138
OTX genes in adult tissues	137
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	136
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	134
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	132
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	130
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	127
L’utilizzo della comparative genomic hybridization su microarray (a-CGH) per rilevare e definire sbilanci cromosomici nel midollo osseo di pazienti affetti dalla sindrome di Shwachman-Diamond	123
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	120
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	117
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	116
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	116
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	113
Donor cell acute myeloid leukemia after hematopoietic stem cell transplantation for chronic granulomatous disease: a case report and literature review	108
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale	108
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	105
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman–Diamond syndrome cells	104
Totale	17.515

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Categoria	#
all - tutte	72.227
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	72.227

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	662	0	0	0	34	26	85	51	68	61	118	98	121
2022/2023	1.589	117	121	79	205	109	316	1	235	208	54	89	55
2023/2024	2.347	372	362	361	398	455	151	14	56	63	20	24	71
2024/2025	1.865	16	36	270	54	103	116	116	129	206	162	202	455
2025/2026	5.129	413	208	209	816	573	344	986	385	408	362	257	168
2026/2027	1.409	131	249	675	354	0	0	0	0	0	0	0	0
Totale													18.613