VALLI, ROBERTO
 Distribuzione geografica
Continente #
NA - Nord America 5.296
EU - Europa 4.280
AS - Asia 1.007
SA - Sud America 40
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
AF - Africa 2
Totale 10.635
Nazione #
US - Stati Uniti d'America 5.274
IT - Italia 2.375
UA - Ucraina 672
TR - Turchia 307
SE - Svezia 295
CN - Cina 275
VN - Vietnam 226
IE - Irlanda 186
DE - Germania 183
FI - Finlandia 167
FR - Francia 147
SG - Singapore 139
GB - Regno Unito 118
RU - Federazione Russa 47
BR - Brasile 29
JP - Giappone 28
PL - Polonia 20
IN - India 18
BE - Belgio 15
MX - Messico 13
NL - Olanda 9
CA - Canada 8
AT - Austria 7
BG - Bulgaria 5
CZ - Repubblica Ceca 5
ES - Italia 5
EU - Europa 5
AR - Argentina 4
AU - Australia 4
DK - Danimarca 4
CH - Svizzera 3
EC - Ecuador 2
IM - Isola di Man 2
LU - Lussemburgo 2
LV - Lettonia 2
MC - Monaco 2
NO - Norvegia 2
OM - Oman 2
RS - Serbia 2
TW - Taiwan 2
VE - Venezuela 2
ZA - Sudafrica 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
IQ - Iraq 1
IR - Iran 1
KR - Corea 1
LT - Lituania 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
PK - Pakistan 1
RO - Romania 1
SA - Arabia Saudita 1
Totale 10.635
Città #
Milan 1.445
Chandler 611
Fairfield 603
Jacksonville 509
Woodbridge 421
Ashburn 330
Ann Arbor 290
Houston 289
Wilmington 237
Dearborn 210
Seattle 208
Nyköping 200
Cambridge 198
Princeton 189
Dublin 186
Izmir 152
Dong Ket 130
Singapore 125
Boardman 121
Como 116
Rome 84
San Mateo 55
Beijing 52
San Diego 40
New York 34
Hefei 30
Ogden 28
Tokyo 28
Chicago 25
Helsinki 24
Nanjing 23
Kunming 22
Santa Clara 22
London 19
Los Angeles 19
Redwood City 19
Gavirate 16
Kocaeli 16
Dallas 15
Guangzhou 15
Jinan 15
Brussels 14
Washington 14
Munich 13
Edinburgh 12
Redmond 12
Nanchang 11
Norwalk 11
Shanghai 11
Phoenix 10
Verona 10
Assago 9
Catania 9
Radomsko 9
São Paulo 9
Frankfurt am Main 8
Brescia 7
Vienna 7
Trento 6
Warsaw 6
Bangalore 5
Berlin 5
Bologna 5
Changsha 5
Chiswick 5
Falls Church 5
Florence 5
Lappeenranta 5
Maccagno 5
Shenyang 5
Sofia 5
Vigevano 5
Auburn Hills 4
Chengdu 4
Düsseldorf 4
Fuzhou 4
Islington 4
Istanbul 4
Magnago 4
Naples 4
Napoli 4
Padova 4
Palermo 4
Paris 4
Pavia 4
Pescara 4
Ponte Lambro 4
Shaoxing 4
Toronto 4
Turin 4
Zhengzhou 4
Acton 3
Ancona 3
Biassono 3
Brugherio 3
Cuneo 3
Estrela 3
Genzano Di Roma 3
Kilburn 3
Marsala 3
Totale 7.522
Nome #
La sindrome da aneuploidia variegata a mosaico (MVA) associata a neutropenia come condizione predisponente a displasia e neoplasia ematologia 311
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. 203
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene 189
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION 179
Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature 178
High variability of genomic instability and gene expression profiling in different HeLa clones 169
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability 167
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 164
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR 161
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro 157
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning 156
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis 154
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms 153
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis 151
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling 151
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498) 150
A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient 146
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome 141
Chromosome anomalies in bone marrow as primarycause of aplastic or hypoplastic conditions andperipheral cytopenia: disorders due to secondaryimpairment of RUNX1 and MPL genes 141
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells 140
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas 138
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies 137
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies 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 137
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome 136
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type 135
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 133
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 131
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
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies. 129
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis 123
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME 122
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR 119
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR) 116
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients 112
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES 111
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 111
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH 110
Acquisizione di anomalie cromosomiche clonali nel midollo osseo di pazienti con sindrome di Shwachman Diamond in relazione all’età 108
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients 108
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard 107
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome 106
Fenotipo di una paziente da microdelezione della regione 4q e avente di smorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di Gorge. 105
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula 103
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 103
Array-CGH used to monitor dysplastic/neoplastic disorders with unbalanced chromosome anomalies may detect as low as 8% abnormal cells 102
Fenotipo di una paziente affetta da microdelezione subtelomerica della regione 4q e avente dimorfismi facciali sovrapponibili con quelli della sindrome Velocardiofacciale/Di George 100
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
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. 97
The use of microarray-based comparative genomic hybridization (a-CGH) to detect and define chromosome imbalances in the bone marrow of SDS patients 96
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale 95
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore 92
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow 92
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients 91
Anomalie cromosomiche clonali e non-clonali in 32 casi di sindrome di Shwachman: valore prognostico e predittivo 90
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene 89
Cytogenetics in Shwachmann Syndrome: Chromosom changes and haematological implications 88
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND 86
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis 86
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 84
Acquiring an "inherited" thrombocitopenia: clonal chromosome anomalies affecting FLI1 mimic inherited thrombocitopenia of Paris-Trousseau type 84
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms 84
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman 83
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells 83
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1 81
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene. 80
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 80
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome. 80
Chromosome anomalies as cause of congenital bone marrow failure syndromes 80
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND 79
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME 78
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21 77
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498) 77
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 76
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIM #604498) 75
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment? 74
Chromosome missegregation in single human oocytes is related to the age and gene expression profile 74
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family 73
THE DEGREE OF KARYOTYPE INSTABILITY IN SDS EVALUATED BY a-CGH IS HIGHER THAN PREVIOUSLY ESTABLISHED 71
EXPRESSION STUDIES IN BONE MARROW OF PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME CARRYING A CHROMOSOME 20 LONG ARMS INTERSTITIAL DELETION 71
Shwachman sindrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies 70
Novel evidence of karyotype instability in Shwachman Diamond Syndrome 69
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello 68
Clonal chromosome anomalies in congenital amegakaryocytic thrombocytopenia (CAMT, OMIM #604498) 68
L’array-CGH per monitorare anomalie cromosomiche sbilanciate nelle malattie displastiche/neoplastiche puo’ rilevare fino all’8% di cellule anomale 68
Sindrome di shwachman: anomalie cromosomiche clonali nel midollo osseo e differenziamento della linea mieloide 68
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells 68
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects 68
Proteus instability of chromosomes 7 and 20 in Shwachman sindrome 67
Monitoraggio di anomalie sbilanciate acquisite del cromosoma 7 mediante citogenetica e real-time PCR quantitativa (RQ-PCR) 66
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis 65
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia 63
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations 55
Counteracting the Common Shwachman–Diamond Syndrome-Causing SBDS c.258+2T>C Mutation by RNA Therapeutics and Base/Prime Editing 54
NOVEL RECURRENT CHROMOSOMAL CHANGES AND GENE EXPRESSION RELATED TO CHROMOSOME ANOMALIES 53
Editorial: Inherited and acquired ribosomopathies: missing puzzle pieces 37
Soybean meal-dependent intestinal inflammation induces different patterns of bone-loss in adult zebrafish scale 35
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome 24
Totale 10.692
Categoria #
all - tutte 42.269
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 42.269


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.261 0 0 0 0 0 236 313 271 111 150 50 130
2020/20211.512 37 145 45 136 92 175 44 138 203 133 135 229
2021/2022961 91 139 69 34 26 85 51 68 61 118 98 121
2022/20231.589 117 121 79 205 109 316 1 235 208 54 89 55
2023/20242.347 372 362 361 398 455 151 14 56 63 20 24 71
2024/2025590 16 36 270 54 103 111 0 0 0 0 0 0
Totale 10.800