statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	8.207
EU - Europa	5.157
AS - Asia	3.452
SA - Sud America	415
Continente sconosciuto - Info sul continente non disponibili	180
AF - Africa	64
OC - Oceania	23
Totale	17.498

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Nazione	#
US - Stati Uniti d'America	8.041
IT - Italia	2.587
SG - Singapore	1.154
CN - Cina	876
UA - Ucraina	678
VN - Vietnam	455
BR - Brasile	338
HK - Hong Kong	338
SE - Svezia	331
TR - Turchia	322
DE - Germania	290
FR - Francia	262
FI - Finlandia	243
GB - Regno Unito	224
IE - Irlanda	194
RU - Federazione Russa	106
CA - Canada	78
JP - Giappone	72
MX - Messico	71
IN - India	67
BD - Bangladesh	66
PL - Polonia	63
NL - Olanda	37
AT - Austria	31
ZA - Sudafrica	31
AR - Argentina	28
ES - Italia	28
AU - Australia	22
EC - Ecuador	18
BE - Belgio	16
PK - Pakistan	14
CH - Svizzera	13
IQ - Iraq	11
VE - Venezuela	10
SA - Arabia Saudita	9
CZ - Repubblica Ceca	8
ID - Indonesia	8
LT - Lituania	8
JO - Giordania	7
MA - Marocco	7
BG - Bulgaria	6
CO - Colombia	6
KE - Kenya	6
NG - Nigeria	6
PE - Perù	6
AE - Emirati Arabi Uniti	5
EU - Europa	5
IL - Israele	5
MY - Malesia	5
UZ - Uzbekistan	5
DK - Danimarca	4
EG - Egitto	4
NP - Nepal	4
OM - Oman	4
TH - Thailandia	4
AZ - Azerbaigian	3
BA - Bosnia-Erzegovina	3
DZ - Algeria	3
GR - Grecia	3
LB - Libano	3
NO - Norvegia	3
PA - Panama	3
PH - Filippine	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
HU - Ungheria	2
IM - Isola di Man	2
JM - Giamaica	2
KR - Corea	2
LU - Lussemburgo	2
LV - Lettonia	2
MC - Monaco	2
MD - Moldavia	2
SN - Senegal	2
AL - Albania	1
BB - Barbados	1
BM - Bermuda	1
BN - Brunei Darussalam	1
CG - Congo	1
GD - Grenada	1
GE - Georgia	1
GT - Guatemala	1
IR - Iran	1
KG - Kirghizistan	1
KY - Cayman, isole	1
KZ - Kazakistan	1
LC - Santa Lucia	1
MN - Mongolia	1
MQ - Martinica	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PR - Porto Rico	1
PS - Palestinian Territory	1
RO - Romania	1
Totale	17.319

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Città	#
Milan	1.461
San Jose	680
Ashburn	675
Singapore	673
Chandler	611
Fairfield	603
Jacksonville	510
Woodbridge	421
Hong Kong	331
Houston	307
Council Bluffs	292
Ann Arbor	290
Beijing	245
Wilmington	240
Seattle	216
Dearborn	210
Dallas	201
Cambridge	200
Nyköping	200
Dublin	192
Princeton	190
Izmir	152
Dong Ket	130
The Dalles	129
New York	124
Boardman	121
Como	121
Los Angeles	116
Rome	96
Lauterbourg	95
Santa Clara	84
Chicago	76
Ho Chi Minh City	76
Munich	76
Helsinki	71
Tokyo	70
Hanoi	63
Orem	55
San Mateo	55
São Paulo	50
Warsaw	43
Mexico City	40
San Diego	40
Guangzhou	39
London	38
Phoenix	37
Stockholm	31
Brooklyn	30
Hefei	30
Poplar	30
Montreal	29
Turku	29
Ogden	28
Varese	27
Verona	27
Chennai	25
Kunming	25
Frankfurt am Main	24
Nanjing	24
Denver	22
Johannesburg	22
Atlanta	21
Shanghai	21
Toronto	20
Redwood City	19
San Francisco	19
Manchester	18
Gavirate	16
Jinan	16
Kocaeli	16
Shenzhen	16
Washington	16
Amsterdam	15
Brussels	15
Columbus	14
Nuremberg	14
Rio de Janeiro	13
Tianjin	13
Vienna	13
Zhengzhou	13
Boston	12
Edinburgh	12
Miami	12
Redmond	12
Salt Lake City	12
Buffalo	11
Catania	11
Nanchang	11
Norwalk	11
Belo Horizonte	10
Bologna	10
Da Nang	10
Haiphong	10
Vancouver	10
Assago	9
Biên Hòa	9
Falkenstein	9
Querétaro	9
Radomsko	9
Trento	9
Totale	11.664

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	379
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	278
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	248
High variability of genomic instability and gene expression profiling in different HeLa clones	241
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	240
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	239
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	238
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	233
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	233
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	226
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	225
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	223
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	221
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	215
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	214
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	214
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	212
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	209
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	206
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	205
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	203
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	201
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	197
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	197
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	193
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	193
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	192
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	192
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	192
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	186
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	185
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	183
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	182
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	182
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	180
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	176
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	176
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	172
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	171
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	169
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	163
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	162
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	159
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	157
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	157
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	157
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	157
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	156
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	155
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	155
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	154
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	154
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	154
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	152
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	151
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	149
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	149
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	144
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	144
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	144
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	143
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	143
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	141
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	140
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	138
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	138
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	136
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	136
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	136
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	135
Chromosome anomalies as cause of congenital bone marrow failure syndromes	135
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	134
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	134
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	134
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.	132
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	131
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	130
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	129
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	129
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	129
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	127
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	127
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	127
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	126
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	126
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	125
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	125
OTX genes in adult tissues	124
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	118
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	111
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	110
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	106
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	105
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	103
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale	103
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	100
Soybean meal-dependent intestinal inflammation induces different patterns of bone-loss in adult zebrafish scale	98
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman–Diamond syndrome cells	96
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	96
Totale	16.539

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Categoria	#
all - tutte	68.162
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	68.162

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	870	0	139	69	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	294	131	163	0	0	0	0	0	0	0	0	0	0
Totale													17.498