statistiche ricercatore

VALLI, ROBERTO

Distribuzione geografica

Continente	#
NA - Nord America	5.263
EU - Europa	4.199
AS - Asia	869
SA - Sud America	26
Continente sconosciuto - Info sul continente non disponibili	5
OC - Oceania	5
Totale	10.367

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Nazione	#
US - Stati Uniti d'America	5.244
IT - Italia	2.355
UA - Ucraina	672
TR - Turchia	306
SE - Svezia	295
VN - Vietnam	226
CN - Cina	222
IE - Irlanda	186
DE - Germania	174
FI - Finlandia	164
FR - Francia	147
GB - Regno Unito	117
SG - Singapore	60
JP - Giappone	28
PL - Polonia	19
BR - Brasile	16
IN - India	16
BE - Belgio	14
MX - Messico	11
AT - Austria	7
CA - Canada	7
NL - Olanda	6
RU - Federazione Russa	6
BG - Bulgaria	5
CZ - Repubblica Ceca	5
ES - Italia	5
EU - Europa	5
AR - Argentina	4
AU - Australia	4
CH - Svizzera	3
DK - Danimarca	3
EC - Ecuador	2
IM - Isola di Man	2
LU - Lussemburgo	2
MC - Monaco	2
NO - Norvegia	2
OM - Oman	2
RS - Serbia	2
VE - Venezuela	2
AL - Albania	1
BD - Bangladesh	1
BN - Brunei Darussalam	1
CL - Cile	1
CO - Colombia	1
GR - Grecia	1
HU - Ungheria	1
IL - Israele	1
KR - Corea	1
LT - Lituania	1
LV - Lettonia	1
MY - Malesia	1
NP - Nepal	1
NZ - Nuova Zelanda	1
PA - Panama	1
PK - Pakistan	1
RO - Romania	1
SA - Arabia Saudita	1
TW - Taiwan	1
Totale	10.367

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Città	#
Milan	1.441
Chandler	611
Fairfield	603
Jacksonville	509
Woodbridge	421
Ashburn	319
Ann Arbor	290
Houston	289
Wilmington	237
Dearborn	210
Seattle	208
Nyköping	200
Cambridge	198
Princeton	189
Dublin	186
Izmir	152
Dong Ket	130
Boardman	121
Como	116
Rome	81
Singapore	57
San Mateo	55
Beijing	52
San Diego	40
New York	34
Hefei	29
Ogden	28
Tokyo	28
Chicago	25
Nanjing	23
Santa Clara	22
Helsinki	21
Kunming	21
Redwood City	19
London	18
Los Angeles	17
Gavirate	16
Kocaeli	16
Dallas	15
Jinan	14
Washington	14
Brussels	13
Guangzhou	13
Edinburgh	12
Redmond	12
Nanchang	11
Norwalk	11
Phoenix	10
Verona	10
Assago	9
Catania	9
Radomsko	9
Munich	8
Brescia	7
Frankfurt am Main	7
São Paulo	7
Vienna	7
Trento	6
Bangalore	5
Bologna	5
Chiswick	5
Falls Church	5
Florence	5
Lappeenranta	5
Maccagno	5
Shanghai	5
Sofia	5
Vigevano	5
Warsaw	5
Auburn Hills	4
Berlin	4
Changsha	4
Düsseldorf	4
Islington	4
Istanbul	4
Magnago	4
Napoli	4
Padova	4
Paris	4
Pavia	4
Pescara	4
Ponte Lambro	4
Shaoxing	4
Toronto	4
Turin	4
Acton	3
Ancona	3
Biassono	3
Brugherio	3
Chengdu	3
Cuneo	3
Estrela	3
Fuzhou	3
Genzano Di Roma	3
Kilburn	3
Marsala	3
Mexico	3
Modena	3
Montreuil	3
Mountain View	3
Totale	7.400

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Nome	#
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia	305
Trisomia 8 costituzionale a mosaico nelle malattie mielodisplatiche e mieloproliferative: importanza per pratica clinica e per implicazioni teoriche	211
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.	202
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene	189
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature	177
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION	175
High variability of genomic instability and gene expression profiling in different HeLa clones	169
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR	160
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML	160
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability	160
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro	153
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis	151
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis	151
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms	150
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling	149
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)	148
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient	143
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome	140
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells	138
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas	138
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes	137
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome	136
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies	135
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies	133
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome	133
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning	132
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	132
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type	132
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation	131
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients	130
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.	128
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME	120
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR	116
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR)	114
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis	114
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients	111
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH	108
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES	107
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età	105
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients	105
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene	105
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard	104
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome	104
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula	102
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge.	101
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498)	99
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS	99
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	99
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells	98
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.	96
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale	94
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George	94
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients	94
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore	92
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients	89
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo	88
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene	88
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications	87
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow	87
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND	85
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis	84
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type	83
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman	82
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells	82
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	81
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms	81
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene.	79
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1	79
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	79
Chromosome anomalies as cause of congenital bone marrow failure syndromes	78
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	77
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME	77
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND	76
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome.	76
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21	75
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498)	75
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	74
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment?	71
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies	70
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED	70
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION	69
Chromosome missegregation in single human oocytes is related to the age and gene expression profile	69
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family	69
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498)	68
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide	68
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome	67
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale	67
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR)	66
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello	66
Novel evidence of karyotype instability in Shwachman Diamond Syndrome	66
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells	65
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects	62
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia	61
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis	60
NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES	53
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations	52
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing	50
Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces	36
Soybean meal-dependent intestinal inflammation induces different patterns of bone-loss in adult zebrafish scale	33
The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer	19
Totale	10.448

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Categoria	#
all - tutte	38.418
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	38.418

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	1.709	0	0	64	297	87	236	313	271	111	150	50	130
2020/2021	1.512	37	145	45	136	92	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	320	16	36	268	0	0	0	0	0	0	0	0	0
Totale													10.530