RIVA, PAOLA VANDA
 Distribuzione geografica
Continente #
EU - Europa 9.242
NA - Nord America 6.335
AS - Asia 4.597
SA - Sud America 235
OC - Oceania 59
AF - Africa 34
Continente sconosciuto - Info sul continente non disponibili 15
Totale 20.517
Nazione #
US - Stati Uniti d'America 6.095
GB - Regno Unito 3.217
CN - Cina 2.478
IT - Italia 1.985
DE - Germania 1.231
SE - Svezia 1.002
IN - India 453
TR - Turchia 342
SG - Singapore 329
UA - Ucraina 278
KR - Corea 276
HK - Hong Kong 227
IE - Irlanda 217
FR - Francia 212
CA - Canada 172
FI - Finlandia 159
RU - Federazione Russa 157
NL - Olanda 150
JP - Giappone 142
DK - Danimarca 118
IR - Iran 112
EU - Europa 111
BE - Belgio 89
PL - Polonia 85
PE - Perù 80
GR - Grecia 79
ES - Italia 78
CO - Colombia 68
MX - Messico 64
ID - Indonesia 62
TW - Taiwan 57
CH - Svizzera 54
BR - Brasile 45
VN - Vietnam 45
AU - Australia 42
IL - Israele 26
PT - Portogallo 24
RO - Romania 19
NO - Norvegia 18
CL - Cile 17
NZ - Nuova Zelanda 17
EG - Egitto 16
HU - Ungheria 14
BA - Bosnia-Erzegovina 11
AR - Argentina 10
AT - Austria 10
CZ - Repubblica Ceca 9
TH - Thailandia 9
SI - Slovenia 8
SA - Arabia Saudita 7
SC - Seychelles 7
EC - Ecuador 6
MA - Marocco 6
MO - Macao, regione amministrativa speciale della Cina 5
UZ - Uzbekistan 5
BD - Bangladesh 4
CU - Cuba 4
LU - Lussemburgo 4
MY - Malesia 4
SK - Slovacchia (Repubblica Slovacca) 4
BG - Bulgaria 3
JO - Giordania 3
KE - Kenya 3
PH - Filippine 3
RS - Serbia 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
FK - Isole Falkland (Malvinas) 2
HR - Croazia 2
LK - Sri Lanka 2
PK - Pakistan 2
PY - Paraguay 2
UY - Uruguay 2
A1 - Anonimo 1
A2 - ???statistics.table.value.countryCode.A2??? 1
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AZ - Azerbaigian 1
MD - Moldavia 1
NG - Nigeria 1
ZA - Sudafrica 1
Totale 20.615
Città #
Southend 2.894
Milan 815
Chandler 736
Beijing 436
Seattle 414
Hanover 360
Fairfield 319
Wilmington 310
Ashburn 265
Princeton 262
Ann Arbor 261
Dearborn 254
Frankfurt am Main 221
Houston 221
Woodbridge 218
Dublin 216
Nanjing 182
Jacksonville 179
Redwood City 169
Shanghai 169
Singapore 161
Mountain View 152
Redmond 142
Cambridge 117
Hong Kong 113
Guangzhou 111
Shenyang 111
Boardman 104
Toronto 98
Jinan 93
Hangzhou 90
Istanbul 90
Des Moines 89
Changsha 88
Bengaluru 87
Sakarya 86
Somerville 79
Serra 70
Rome 68
Wuhan 68
Nanchang 66
Athens 65
Zhengzhou 62
Andover 61
Warsaw 59
Lima 58
Bogotá 55
Tianjin 52
Bühl 48
Hebei 48
Phoenix 48
Berlin 45
Helsinki 43
Fuzhou 41
Kunming 41
Brussels 39
Jakarta 39
New York 39
Falls Church 38
London 36
Taipei 36
Hefei 35
Roxbury 35
Chengdu 33
Chicago 32
Tokyo 32
Ningbo 31
Xian 30
San Diego 29
Zogno 29
Medford 27
Eitensheim 26
Los Angeles 24
Verona 24
Monza 23
Dong Ket 21
Mumbai 21
Changchun 20
Hyderabad 20
Tehran 20
Göttingen 19
Jiaxing 18
Lanzhou 18
Auburn Hills 17
Bologna 17
Central District 17
Chongqing 17
Ottawa 17
Philadelphia 17
Zurich 17
Atlanta 16
Birmingham 16
Paris 16
Seoul 16
Torino 16
Washington 16
Boston 15
Hamburg 15
Padova 15
Ankara 14
Totale 12.778
Nome #
The long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis 3.199
The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer’s Disease Pathogenesis 628
HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles 566
NIPBL: a new player in myeloid cells differentiation 507
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with nonsyndromic mental retardation 386
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 270
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 266
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? 242
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies 221
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 209
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 208
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2 206
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2) 200
NIPBL a new player with NPMc+ in the onset of acute myeloid leukemia 198
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases 194
The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration 191
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 189
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 185
Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene 184
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression 180
Ruolo del complesso FAS-FASL nelle alterazioni delle notocorda e nello sviluppo del cordoma 176
IDENTIFICAZIONE DEI GENI TARGET DEL miR-182 NELLA LINEA CELLULARE KASUMI-1, MODELLO DI LEUCEMIA MIELOIDE ACUTA (AML), E NELLE SUE SOTTOPOPOLAZIONI 175
Dysregulation of apoptotic pathways in chordoma involving FAS and FASL: implications on notochord regression in zebrafish model 169
Identification and functional characterization of trans-acting factors involved in the post-transcriptional regulation of CDK5R1 168
Centa2 is expressed during heart development and is a candidate gene for CVMs 163
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability 161
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1 160
Identification of post-transcriptional regulatory elements in CDK5R1 3’UTR gene involved in CNS development and functioning 159
Characterization of breakpoint boundaries in 19 Neurofibromatosis type 1 microdeletions 158
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements 156
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 156
Centa2 è espresso durante lo sviluppo del cuore ed è un gene candidato per le malformazioni cardiovascolari 155
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients 155
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation 154
Expression study of receptor tyrosine kinase targets of Imatinib mesylate in skull base chordomas 151
Functional study of transcription cis-regulatory elements predicted in the CDK5R1 3’UTR 150
The discovery of a new role of HDAC8 in skeletal muscle differentiation and in centronuclear myopathy insurgence 150
FISH with locus-specific probes on stretched chromosomes : a useful tool for genome organization studies 149
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 149
19p deletion in recurring leiomyosarcoma lesions from the same patient 149
Monosomia del cromosoma 22 e perdita allelica al locus polimorfico c-sis nel meningioma. 149
The regulation of CDK5R1 gene expression by miRNAs may have a role in Alzheimer’s disease 148
miR-103 and miR-107 are involved in the regulation of CDK5R1/p35 expression 148
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth 148
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure 147
Centaurin-α2 and tubulin interaction increases microtubule stability 147
FAS/FASL are dysregulated in chordoma and their loss-of-function impairs zebrafish notochord formation 147
Studio comparativo di LOH e di espressione in linee cellulari di cordoma e nei tumori di origine 145
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes. Clues to the mechanisms of formation 144
Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study 144
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 144
Hyper conserved elements in vertebrate mRNA 3’-UTRs reveal a translational network of RNA-binding proteins controlled by HUR 144
Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child 143
Morpholino knockdown of the zebrafish CENTA2 orthologue results in cardiovascular defects 143
Dysregulation of apoptotic pathway/s in chordoma: searching for prognostic markers and study of fas and fasl involvement in zebrafish model 143
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells 142
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms 142
The role of p35/CDK5 regulation by miR-15/107 family in Alzheimer’s disease 142
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases 141
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 140
First cytogenetic study of a recurrent familial chordoma of the clivus 140
NF1 exon 7 skipping by disruption of exonic splice enhancers (ESEs) in neurofibromatosis 1 136
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 134
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas 133
Ricerca di interattori molecolari della centaurina-α2 : evidenze di associazione con la tubulina β 128
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 128
Tandem duplication of the NF1 gene detected by high resolution FISH in 17q11.2 region 127
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 126
The human CDK5R1 3'UTR contains distinct subregions affecting transcript stability 125
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations 125
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 125
Identification of a potential regulatory element forming a hairpin structure within the 3’UTR of CDK5R1 123
Expression of Centa2 and Suz12 during mammalian heart development 120
Update on the Cytogenetics and Molecular Genetics of Chordoma 119
Extensive mutational analysis of CDK5 and CDK5R1 in patients with non-syndromic mental retardation reveals novel variants in CDK5R1 3’-UTR 118
Expression of Centa2 during early heart development : a new candidate gene for the onset of cardiovascular malformations 117
Studio di espressione dei recettori tirosin-kinasici target dell’Imatinib mesilato in cordomi della base cranica 116
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 116
Thompson & Thompson : Genetica in medicina 116
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis 115
Identification of a chromosome 21 tandem duplication in a newborn 115
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 115
Un metodo rapido e semplice per generare sonde locus-specifiche per l’analisi mediante FISH 115
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval 114
Evidence on microRNA-mediated regulation of CDK5R1 gene expression 114
Dysregulation of Fas-Fasl in chordoma and implications on zebrafish notochord development/regression 114
Studio di LOH e espressione in geni apoptotici in 1p36 : ricerca di marcatori genetico-molecolari prognostici in cordomi della base cranica 110
HEBE project: Healthy aging versus inflamm-aging: The role of physical exercise in modulating the biomarkers of age-associated and environmentally determined chronic diseases, study protocol 106
Search of candidate genes for cardiovascular malformation in NF1 microdeletion syndrome 106
Differential allelic expression of the SOS1 c.755C activating variant in a Noonan syndrome family 106
Dysregulation of apoptotic pathway/s in chordoma : study of fas and fasl role in zebrafish notochord regression 104
Searching for centaurin-α2 interacting proteins: evidence of interaction with tubulin-β 103
Strumento per didattica scientifica 102
Genetica Quantitativa 102
Identification of a new Jnk-activating familial SOS1 and a de novo RAF1 mutations in a Noonan syndrome patient 102
Expression study of receptor tyrosine kinase targets of Imatinib mesylate in skull base chordomas 100
Evaluation of 1p36 LOH, apoptotic genes’ expression and clinical outcome in a skull base chordoma prospective study 100
Genomic organization study of NF1 duplicon by high resolution FISH 98
Skull base chordomas : clinical outcome in a consecutive series of 45 patients with long-term follow-up and evaluation of clinical and biological prognostic factors 97
NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder? 96
Totale 19.089
Categoria #
all - tutte 48.014
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 48.014


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.046 348 171 146 220 215 351 338 171 392 377 206 111
2020/20213.119 203 281 244 145 265 187 185 231 308 279 549 242
2021/20222.867 181 138 232 213 249 188 230 150 356 345 186 399
2022/20232.803 324 315 230 284 298 444 83 235 253 82 166 89
2023/20242.289 99 140 138 178 489 181 159 169 109 130 252 245
2024/2025179 179 0 0 0 0 0 0 0 0 0 0 0
Totale 21.561