statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	7.968
EU - Europa	5.104
AS - Asia	3.432
SA - Sud America	408
AF - Africa	64
OC - Oceania	22
Continente sconosciuto - Info sul continente non disponibili	5
Totale	17.003

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Nazione	#
US - Stati Uniti d'America	7.810
IT - Italia	2.551
SG - Singapore	1.148
CN - Cina	872
UA - Ucraina	678
VN - Vietnam	455
HK - Hong Kong	337
BR - Brasile	333
SE - Svezia	323
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	75
JP - Giappone	72
MX - Messico	71
IN - India	66
PL - Polonia	63
BD - Bangladesh	58
NL - Olanda	36
AT - Austria	31
ZA - Sudafrica	31
AR - Argentina	27
ES - Italia	24
AU - Australia	21
EC - Ecuador	18
BE - Belgio	16
PK - Pakistan	14
CH - Svizzera	13
IQ - Iraq	11
VE - Venezuela	10
SA - Arabia Saudita	9
ID - Indonesia	8
LT - Lituania	8
JO - Giordania	7
MA - Marocco	7
BG - Bulgaria	6
CO - Colombia	6
KE - Kenya	6
NG - Nigeria	6
AE - Emirati Arabi Uniti	5
CZ - Repubblica Ceca	5
EU - Europa	5
IL - Israele	5
MY - Malesia	5
PE - Perù	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
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
RS - Serbia	2
SN - Senegal	2
AL - Albania	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
MN - Mongolia	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PS - Palestinian Territory	1
RO - Romania	1
SR - Suriname	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
TZ - Tanzania	1
Totale	17.003

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Città	#
Milan	1.457
San Jose	669
Singapore	669
Ashburn	663
Chandler	611
Fairfield	603
Jacksonville	510
Woodbridge	421
Hong Kong	330
Houston	305
Ann Arbor	290
Beijing	241
Wilmington	240
Seattle	216
Dearborn	210
Cambridge	200
Nyköping	200
Dallas	199
Dublin	192
Council Bluffs	190
Princeton	190
Izmir	152
Dong Ket	130
The Dalles	129
New York	122
Boardman	121
Como	121
Los Angeles	111
Lauterbourg	95
Rome	91
Chicago	76
Ho Chi Minh City	76
Munich	76
Helsinki	71
Tokyo	70
Santa Clara	67
Hanoi	63
Orem	55
San Mateo	55
São Paulo	50
Warsaw	43
Mexico City	40
San Diego	40
Guangzhou	39
London	38
Phoenix	36
Stockholm	31
Hefei	30
Poplar	30
Montreal	29
Turku	29
Brooklyn	28
Ogden	28
Varese	27
Chennai	25
Kunming	25
Frankfurt am Main	24
Nanjing	24
Denver	22
Johannesburg	22
Shanghai	21
Verona	21
Atlanta	20
Redwood City	19
Manchester	18
Toronto	18
Gavirate	16
Jinan	16
Kocaeli	16
Shenzhen	16
Washington	16
Amsterdam	15
Brussels	15
San Francisco	15
Nuremberg	14
Rio de Janeiro	13
Tianjin	13
Vienna	13
Zhengzhou	13
Boston	12
Edinburgh	12
Redmond	12
Salt Lake City	12
Buffalo	11
Columbus	11
Miami	11
Nanchang	11
Norwalk	11
Catania	10
Da Nang	10
Haiphong	10
Assago	9
Belo Horizonte	9
Biên Hòa	9
Bologna	9
Falkenstein	9
Querétaro	9
Radomsko	9
Trento	9
Vancouver	9
Totale	11.469

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	376
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	272
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	247
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	238
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	237
High variability of genomic instability and gene expression profiling in different HeLa clones	235
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	231
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	231
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	231
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	225
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	224
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	218
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	212
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	211
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	210
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	209
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	205
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	203
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	203
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	203
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	200
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
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	192
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	191
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	191
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	190
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	187
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	182
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	181
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	181
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	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
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	179
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	178
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	172
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	170
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	169
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	168
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	164
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	161
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	161
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
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	156
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	156
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	156
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	155
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	154
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	154
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	154
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	153
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	152
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	152
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	149
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	148
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	146
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	146
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	143
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	142
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	142
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	142
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	141
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	137
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	136
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	134
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	134
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	134
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	134
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	133
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	133
Chromosome anomalies as cause of congenital bone marrow failure syndromes	133
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	132
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	132
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.	131
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	129
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	128
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	128
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	127
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	126
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	126
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	126
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	124
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	123
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	123
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	123
OTX genes in adult tissues	119
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	119
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	118
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	117
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	109
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	108
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	105
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	103
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	102
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale	102
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	99
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	95
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman–Diamond syndrome cells	93
Donor cell acute myeloid leukemia after hematopoietic stem cell transplantation for chronic granulomatous disease: a case report and literature review	92
Totale	16.274

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Categoria	#
all - tutte	65.497
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	65.497

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	229	0	0	0	0	0	0	0	0	0	0	0	229
2021/2022	961	91	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	5.103	413	208	209	816	573	344	986	385	408	362	257	142
Totale													17.178