VALLI, ROBERTO
 Distribuzione geografica
Continente #
NA - Nord America 6.626
EU - Europa 4.785
AS - Asia 2.427
SA - Sud America 366
AF - Africa 41
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 5
Totale 14.259
Nazione #
US - Stati Uniti d'America 6.501
IT - Italia 2.446
SG - Singapore 841
UA - Ucraina 676
CN - Cina 512
SE - Svezia 321
TR - Turchia 318
BR - Brasile 308
VN - Vietnam 304
HK - Hong Kong 276
DE - Germania 275
GB - Regno Unito 204
FI - Finlandia 200
IE - Irlanda 190
FR - Francia 158
RU - Federazione Russa 104
JP - Giappone 64
CA - Canada 61
PL - Polonia 58
MX - Messico 56
IN - India 43
NL - Olanda 30
AT - Austria 29
ZA - Sudafrica 28
AR - Argentina 22
ES - Italia 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
AZ - Azerbaigian 3
BA - Bosnia-Erzegovina 3
CO - Colombia 3
LB - Libano 3
NO - Norvegia 3
OM - Oman 3
PE - Perù 3
SA - Arabia Saudita 3
UY - Uruguay 3
DO - Repubblica Dominicana 2
IM - Isola di Man 2
JO - Giordania 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
KE - Kenya 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 14.259
Città #
Milan 1.453
Chandler 611
Fairfield 603
Ashburn 547
Jacksonville 509
Singapore 441
Woodbridge 421
Houston 302
Ann Arbor 290
Hong Kong 274
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 102
The Dalles 90
Rome 86
Munich 76
Tokyo 63
San Mateo 55
Santa Clara 51
Chicago 48
São Paulo 47
San Diego 40
Warsaw 40
London 38
Phoenix 32
Hefei 30
Ho Chi Minh City 30
Poplar 30
Mexico City 29
Stockholm 29
Turku 29
Helsinki 28
Ogden 28
Montreal 26
Brooklyn 25
Nanjing 23
Kunming 22
Varese 22
Hanoi 21
Johannesburg 21
Denver 20
Redwood City 19
Atlanta 17
Council Bluffs 17
Gavirate 16
Guangzhou 16
Kocaeli 16
Orem 16
Brussels 15
Frankfurt am Main 15
Jinan 15
Toronto 15
Washington 15
Nuremberg 14
San Francisco 14
Chennai 13
Rio de Janeiro 13
Vienna 13
Boston 12
Edinburgh 12
Redmond 12
Salt Lake City 12
Nanchang 11
Norwalk 11
Shanghai 11
Amsterdam 10
Verona 10
Assago 9
Belo Horizonte 9
Catania 9
Manchester 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 9.619
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 229
Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability 220
Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome. 215
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML 213
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis 211
Parental Origin of the Deletion Del(20q) in Shwachman-Diamond Patients and Loss of the Paternally Derived Allele of the Imprinted L3MBTL1 Gene 211
CHARACTERIZATION BY MOLECULAR CYTOGENETICS, ARRAY-CGH AND WHOLE TRANSCRIPTOME ANALYSIS OF DIFFERENT BATCHES OF HeLa CELLS: GENOMIC VARIABILITY AND DIVERGENT GENE EXPRESSION 210
A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling 200
High variability of genomic instability and gene expression profiling in different HeLa clones 199
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 191
Improving the definition of the structure of the isochromosome i(7)(q10) in Shwachman-Diamond Syndrome 190
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells 187
The human RNASET2 protein affects the polarization pattern of human macrophages in vitro 187
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR 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
Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms 186
Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning 186
Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498) 182
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 174
Caratterizzazione Molecolare della traslocazione t(10;21) in un paziente affetto da Ritorno Venoso Polmonare Anomalo Totale (TAPVR) 167
Homeoprotein OTX1 and OTX2 involvement in rat myenteric neuron adaptation after DNBS-induced colitis 167
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies. 165
Novel recurrent chromosome anomalies in Shwachman Diamond syndrome 165
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas 162
Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies 161
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies 161
Array-based Comparative Genomic Hybridization in Shwachman-Diamond syndrome: results in 24 patients 157
Clonal Chromosome Anomalies Affecting Fli1 Mimic Inherited Thrombocytopenia Of The Paris-Trousseau Type 156
Analysis of the 635T>C polymorphism in a gropu of 31 Shwachmann-Diamond patients 155
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 154
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
UNCOMMON ACQUIRED CHROMOSOME ANOMALIES IN SHWACHMAN-DIAMOND SYNDROME 149
Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR 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 147
Comparative genomic hybridization su microarray (aCGH) in sindrome di Shwachman (OMIM 260400) e rischio di mielodisplasia: al di là della citogenetica standard 146
Evaluating chromosomal mosaicism by array-based CGH in relation to clinical issues: the proposal of a formula 146
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 146
BONE MARROW FAILURE CONDITIONS DUE TO CHROMOSOME ANOMALIES 145
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 139
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
Age related acquisition of clonal chromosome anomalies in bone marrow cells of SDS patients 134
MONITORING SHWACHMAN-DIAMOND SYNDROME BY CYTOGENETICS AND a-CGH 133
Aplasia midollare da perdita del gene RUNX1 acquisita a causa di un riarrangiamento strutturale clonale del cromosoma 21 132
Karyotype instability evaluated by array-CGH and risk of myeloid malignancy in Shwachman Diamond syndrome 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. 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
Different patterns of chromosome 20 interstitial deletion in Shwachman-Diamond syndrome and in myeloid neoplasms 128
A new recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of the short arms of chromosome 6 124
Expression studies in patients with Shwachman Diamond syndrome in relation to clonal chromosome anomalies in bone marrow 121
Cytogenetic and a-CGH monitoring in Shwachman-Diamond syndrome. 120
Chromosome anomalies in bone marrow of patients with Shwachman-Diamond syndrome as successful or unsuccessful attempts to improve ribosome biogenesis 120
Clonal bone marrow cytogenetic abnormalities in SDS patients persist in peripheral blood mature cells 119
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. 119
Paracrine effect of human Adipose-derived Stem Cells on Lymphatic Endothelial Cells 119
Traslocazione complessa che coinvolge MLL in leucemia mielomonocitica acuta connatale 118
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
STRUCTURAL VARIATION IN SBDS GENE, WITH LOSS OF EXON 3, IN TWO NEW SHWACHMAN-DIAMOND PATIENTS 117
Predisposizione ereditaria allo sviluppo di neoplasie pediatriche: anomalie cromosomiche clonali nella trombocitopenia amegacariocitica congenita (CAMT, OMIN #604498) 115
DIFFERENTE PERDITA DI MATERIALE NELLE DELEZIONI INTERSTIZIALI DEL CROMOSOMA 20 NELLE DISPLASIE/NEOPLASIE MIELOIDI E NELLA SINDROME DI SHWACHMAN-DIAMOND 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 113
Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family 113
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene 112
Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia 112
Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman–Diamond Syndrome Subjects 110
Instabilità del cariotipo e mielodisplasie nella Sindrome di Shwachman 108
Mielodisplasia familiare, monosomia 7 / trisomia 8 ed effetto mutatore 108
MONITORAGGIO CITOGENETICO E MEDIANTE a-CGH DELLA SINDROME DI SHWACHMAN-DIAMOND 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 107
Bone defects in Shwachman-diamond Syndrome: cellular oe systemic impairment? 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
DIFFERENT PATTERNS OF CHROMOSOME 20 INTERSTITIAL DELETIONS BETWEEN MYELOID NEOPLASMS AND SHWACHMAN-DIAMOND SYNDROME 103
Caratterizzazione molecolare di un caso di cromosoma 22 ad anello 101
Severe aplastic anemia (SAA) due to chromosome 21 acquired chromosome anomaly and haploinsufficiency of RUNX1 gene. 100
Novel evidence of karyotype instability in Shwachman Diamond Syndrome 100
Le anomalie cromosomiche nel midollo come causa primaria di aplasia o ipoplasia a rischio di mielodisplasia e leucemia acuta: coinvolgimento del gene RUNX1 99
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations 99
Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis 96
OTX genes in adult tissues 95
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 69
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman–Diamond Syndrome 68
Totale 13.899
Categoria #
all - tutte 57.921
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 57.921


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.057 0 0 0 0 0 175 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
2024/20251.865 16 36 270 54 103 116 116 129 206 162 202 455
2025/20262.359 413 208 209 816 573 140 0 0 0 0 0 0
Totale 14.434