statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	6.664
EU - Europa	4.788
AS - Asia	2.467
SA - Sud America	368
AF - Africa	43
OC - Oceania	9
Continente sconosciuto - Info sul continente non disponibili	5
Totale	14.344

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Nazione	#
US - Stati Uniti d'America	6.537
IT - Italia	2.446
SG - Singapore	873
UA - Ucraina	676
CN - Cina	513
SE - Svezia	321
TR - Turchia	318
BR - Brasile	310
VN - Vietnam	304
HK - Hong Kong	277
DE - Germania	275
GB - Regno Unito	205
FI - Finlandia	200
IE - Irlanda	190
FR - Francia	158
RU - Federazione Russa	104
JP - Giappone	66
CA - Canada	63
PL - Polonia	59
MX - Messico	56
IN - India	46
NL - Olanda	30
AT - Austria	29
ZA - Sudafrica	29
ES - Italia	23
AR - Argentina	22
BD - Bangladesh	18
BE - Belgio	16
EC - Ecuador	16
CH - Svizzera	13
AU - Australia	8
LT - Lituania	8
VE - Venezuela	8
PK - Pakistan	7
BG - Bulgaria	5
CZ - Repubblica Ceca	5
EU - Europa	5
IQ - Iraq	5
AE - Emirati Arabi Uniti	4
DK - Danimarca	4
ID - Indonesia	4
IL - Israele	4
MA - Marocco	4
OM - Oman	4
AZ - Azerbaigian	3
BA - Bosnia-Erzegovina	3
CO - Colombia	3
LB - Libano	3
NO - Norvegia	3
PE - Perù	3
SA - Arabia Saudita	3
UY - Uruguay	3
DO - Repubblica Dominicana	2
IM - Isola di Man	2
JO - Giordania	2
KE - Kenya	2
LU - Lussemburgo	2
LV - Lettonia	2
MC - Monaco	2
MY - Malesia	2
NP - Nepal	2
PA - Panama	2
RS - Serbia	2
SN - Senegal	2
TW - Taiwan	2
UZ - Uzbekistan	2
AL - Albania	1
AO - Angola	1
BN - Brunei Darussalam	1
BY - Bielorussia	1
CG - Congo	1
CL - Cile	1
DZ - Algeria	1
EG - Egitto	1
GD - Grenada	1
GE - Georgia	1
GR - Grecia	1
HU - Ungheria	1
IR - Iran	1
JM - Giamaica	1
KR - Corea	1
MN - Mongolia	1
NI - Nicaragua	1
NZ - Nuova Zelanda	1
PY - Paraguay	1
RO - Romania	1
SR - Suriname	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
TZ - Tanzania	1
Totale	14.344

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Città	#
Milan	1.453
Chandler	611
Fairfield	603
Ashburn	557
Jacksonville	509
Singapore	466
Woodbridge	421
Houston	302
Ann Arbor	290
Hong Kong	275
Wilmington	239
Seattle	215
Dearborn	210
Beijing	204
Nyköping	200
Cambridge	198
Dallas	194
Dublin	190
Princeton	189
Izmir	152
Dong Ket	130
Boardman	121
Como	121
New York	107
Los Angeles	106
The Dalles	90
Rome	86
Munich	76
Tokyo	65
San Mateo	55
Santa Clara	52
Chicago	48
São Paulo	48
Warsaw	41
San Diego	40
London	38
Phoenix	34
Hefei	30
Ho Chi Minh City	30
Poplar	30
Mexico City	29
Stockholm	29
Turku	29
Helsinki	28
Montreal	28
Ogden	28
Brooklyn	25
Nanjing	23
Johannesburg	22
Kunming	22
Orem	22
Varese	22
Hanoi	21
Denver	20
Redwood City	19
Atlanta	18
Council Bluffs	17
Guangzhou	17
Chennai	16
Gavirate	16
Kocaeli	16
Brussels	15
Frankfurt am Main	15
Jinan	15
Toronto	15
Washington	15
Nuremberg	14
San Francisco	14
Rio de Janeiro	13
Vienna	13
Boston	12
Edinburgh	12
Redmond	12
Salt Lake City	12
Nanchang	11
Norwalk	11
Shanghai	11
Amsterdam	10
Manchester	10
Verona	10
Assago	9
Belo Horizonte	9
Catania	9
Radomsko	9
Trento	9
Cavaria con Premezzo	8
Falkenstein	8
Miami	8
Querétaro	8
Brasília	7
Brescia	7
Buffalo	7
Istanbul	7
San Jose	7
Ankara	6
Berlin	6
Cape Town	6
Florence	6
Naples	6
Paris	6
Totale	9.681

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	351
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	230
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	221
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	216
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	214
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	213
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	212
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	211
High variability of genomic instability and gene expression profiling in different HeLa clones	202
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	200
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	196
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	192
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	190
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	189
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	188
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	188
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	187
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	186
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	186
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	186
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	177
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	175
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	175
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	168
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	168
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	166
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	166
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	163
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	162
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	161
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	159
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	157
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	156
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	155
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	153
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	150
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	149
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	148
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	147
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	147
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	147
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	146
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	141
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	137
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	137
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	136
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	135
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	133
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	132
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	132
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	131
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	130
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	129
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	126
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	123
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	122
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	121
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	120
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.	120
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	119
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	119
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	119
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	118
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	117
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	117
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	115
Chromosome anomalies as cause of congenital bone marrow failure syndromes	115
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	115
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	114
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	112
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	112
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	112
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	110
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	110
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	108
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	108
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	107
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	105
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	104
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	102
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	102
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	100
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	100
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	99
OTX genes in adult tissues	96
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	96
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	95
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	93
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	91
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	89
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale	89
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	88
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	87
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	85
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	85
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	81
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	78
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	75
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman–Diamond syndrome cells	70
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome	68
Totale	13.983

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Categoria	#
all - tutte	58.113
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	58.113

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	1.057	0	0	0	0	0	175	44	138	203	133	135	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	2.444	413	208	209	816	573	225	0	0	0	0	0	0
Totale													14.519