statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	7.648
EU - Europa	5.035
AS - Asia	3.345
SA - Sud America	407
AF - Africa	64
OC - Oceania	22
Continente sconosciuto - Info sul continente non disponibili	5
Totale	16.526

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Nazione	#
US - Stati Uniti d'America	7.499
IT - Italia	2.489
SG - Singapore	1.131
CN - Cina	845
UA - Ucraina	678
VN - Vietnam	454
BR - Brasile	332
HK - Hong Kong	331
SE - Svezia	323
TR - Turchia	321
DE - Germania	288
FR - Francia	262
FI - Finlandia	243
GB - Regno Unito	224
IE - Irlanda	192
RU - Federazione Russa	106
JP - Giappone	72
CA - Canada	70
MX - Messico	69
IN - India	66
PL - Polonia	62
NL - Olanda	36
AT - Austria	31
ZA - Sudafrica	31
AR - Argentina	27
BD - Bangladesh	26
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
PE - Perù	5
UZ - Uzbekistan	5
DK - Danimarca	4
EG - Egitto	4
MY - Malesia	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
NP - Nepal	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
LU - Lussemburgo	2
LV - Lettonia	2
MC - Monaco	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
JM - Giamaica	1
KG - Kirghizistan	1
KR - Corea	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	16.526

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Città	#
Milan	1.455
Singapore	664
Ashburn	658
Chandler	611
Fairfield	603
San Jose	590
Jacksonville	510
Woodbridge	421
Hong Kong	324
Houston	303
Ann Arbor	290
Wilmington	239
Beijing	231
Seattle	216
Dearborn	210
Nyköping	200
Cambridge	199
Dallas	196
Dublin	192
Princeton	189
Izmir	152
Dong Ket	130
The Dalles	129
Boardman	121
Como	121
New York	114
Council Bluffs	113
Los Angeles	108
Lauterbourg	95
Rome	89
Munich	76
Ho Chi Minh City	75
Chicago	73
Helsinki	71
Tokyo	70
Hanoi	63
Santa Clara	60
San Mateo	55
Orem	54
São Paulo	50
Warsaw	43
San Diego	40
Guangzhou	39
London	38
Mexico City	38
Phoenix	34
Stockholm	31
Hefei	30
Poplar	30
Montreal	29
Turku	29
Ogden	28
Brooklyn	27
Varese	27
Chennai	25
Frankfurt am Main	24
Kunming	24
Nanjing	24
Johannesburg	22
Denver	21
Shanghai	20
Atlanta	19
Redwood City	19
Manchester	18
Toronto	17
Gavirate	16
Jinan	16
Kocaeli	16
Shenzhen	16
Amsterdam	15
Brussels	15
San Francisco	15
Washington	15
Nuremberg	14
Rio de Janeiro	13
Verona	13
Vienna	13
Zhengzhou	13
Boston	12
Edinburgh	12
Redmond	12
Salt Lake City	12
Tianjin	12
Nanchang	11
Norwalk	11
Catania	10
Da Nang	10
Haiphong	10
Assago	9
Belo Horizonte	9
Biên Hòa	9
Columbus	9
Falkenstein	9
Querétaro	9
Radomsko	9
Trento	9
Bologna	8
Buffalo	8
Cavaria con Premezzo	8
Istanbul	8
Totale	11.222

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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
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
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	235
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	232
High variability of genomic instability and gene expression profiling in different HeLa clones	230
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	229
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	228
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	227
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	220
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	217
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	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
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	204
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	202
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
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	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	195
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	193
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	190
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	189
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	189
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	189
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	184
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
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	178
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	176
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	175
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	174
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	172
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	171
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	168
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	168
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	167
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	166
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	163
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	157
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	157
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
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	153
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	153
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	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
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	147
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	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
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	143
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	142
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	140
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	139
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	138
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	137
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	136
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	136
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	135
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
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	133
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	132
Chromosome anomalies as cause of congenital bone marrow failure syndromes	132
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	131
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
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	129
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	126
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	126
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	126
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	125
A Distinctive Type of Mosaic Variegated Aneuploidy: Case Report and Review of the Literature	125
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	124
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	124
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	123
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	122
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	122
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	122
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	121
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	120
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	118
OTX genes in adult tissues	116
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	112
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	106
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	106
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	104
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	101
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	100
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	97
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	95
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	93
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman–Diamond syndrome cells	91
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome	86
Totale	15.877

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Categoria	#
all - tutte	61.958
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	61.958

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	497	0	0	0	0	0	0	0	0	0	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	4.626	413	208	209	816	573	344	986	385	408	284	0	0
Totale													16.701