IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

RATTI, ANTONIA
 Distribuzione geografica
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Continente #
EU - Europa 8.435
NA - Nord America 5.889
AS - Asia 4.777
SA - Sud America 208
OC - Oceania 108
AF - Africa 48
Continente sconosciuto - Info sul continente non disponibili 11
Totale 19.476
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Nazione #
US - Stati Uniti d'America 5.559
CN - Cina 2.494
GB - Regno Unito 2.179
IT - Italia 1.814
DE - Germania 1.681
SG - Singapore 650
SE - Svezia 624
IN - India 497
RU - Federazione Russa 481
IE - Irlanda 287
CA - Canada 273
TR - Turchia 267
KR - Corea 240
UA - Ucraina 227
FR - Francia 202
JP - Giappone 180
FI - Finlandia 173
NL - Olanda 143
HK - Hong Kong 141
DK - Danimarca 109
IR - Iran 98
EU - Europa 96
AU - Australia 87
BE - Belgio 83
ES - Italia 82
PE - Perù 74
PL - Polonia 68
ID - Indonesia 64
CH - Svizzera 58
CO - Colombia 57
GR - Grecia 55
BR - Brasile 45
MX - Messico 45
TW - Taiwan 43
HU - Ungheria 41
VN - Vietnam 32
IL - Israele 24
CL - Cile 22
CZ - Repubblica Ceca 22
NZ - Nuova Zelanda 21
RO - Romania 21
EG - Egitto 19
PT - Portogallo 19
SI - Slovenia 14
AT - Austria 11
NO - Norvegia 10
TH - Thailandia 9
TN - Tunisia 8
SC - Seychelles 7
LU - Lussemburgo 6
MA - Marocco 6
NP - Nepal 6
LB - Libano 5
RS - Serbia 5
SK - Slovacchia (Repubblica Slovacca) 5
BD - Bangladesh 4
CU - Cuba 4
HR - Croazia 4
MY - Malesia 4
PH - Filippine 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AG - Antigua e Barbuda 3
EC - Ecuador 3
JO - Giordania 3
AR - Argentina 2
BG - Bulgaria 2
BS - Bahamas 2
ET - Etiopia 2
IS - Islanda 2
KE - Kenya 2
MT - Malta 2
PK - Pakistan 2
PY - Paraguay 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
ZA - Sudafrica 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AN - Antille olandesi 1
BO - Bolivia 1
BZ - Belize 1
EE - Estonia 1
FO - Isole Faroe 1
GH - Ghana 1
LT - Lituania 1
ME - Montenegro 1
NG - Nigeria 1
PR - Porto Rico 1
QA - Qatar 1
Totale 19.563
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Città #
Southend 1.713
Frankfurt am Main 755
Milan 658
Chandler 516
Singapore 466
Beijing 409
Seattle 404
Hanover 308
Dublin 278
Ashburn 272
Wilmington 266
Princeton 256
Fairfield 224
Ann Arbor 223
Dearborn 179
Nanjing 177
Toronto 169
Shanghai 166
Houston 160
Woodbridge 159
Jacksonville 158
Redmond 124
Redwood City 121
Mountain View 109
Bengaluru 107
Changsha 104
Santa Clara 102
Des Moines 98
Shenyang 96
Guangzhou 92
Boardman 91
Hangzhou 87
Cambridge 82
Jinan 82
Serra 80
Sakarya 70
Wuhan 68
Hong Kong 61
Helsinki 60
Rome 59
Somerville 57
Nanchang 55
Lima 54
New York 54
Jakarta 52
Fuzhou 49
Warsaw 49
Andover 47
Bogotá 47
Tianjin 47
London 46
Chicago 45
Zhengzhou 45
Phoenix 44
Athens 43
Istanbul 43
Berlin 41
Brussels 41
Hebei 41
Tokyo 40
Los Angeles 35
Kunming 32
Munich 30
Chengdu 29
Kent 28
Taipei 27
Xian 27
Medford 26
Hefei 24
Ottawa 24
San Diego 23
Central District 22
Roxbury 22
Turin 22
Atlanta 21
Bühl 21
Eitensheim 20
Falls Church 20
Norwalk 20
Szeged 20
Central 19
Grafing 19
Göttingen 19
Jiaxing 19
Montreal 19
Tehran 19
Chongqing 18
Ningbo 18
Paris 18
Philadelphia 18
Delhi 17
Dong Ket 17
Mumbai 17
Nuremberg 17
Pune 17
Rochester 17
Santiago 17
Kiez 16
Yongin-si 16
Auburn Hills 15
Totale 11.394
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Nome #
The long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis 3.237
Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis 404
Phosphorylated neurofilament heavy chain : a biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosis 347
TDP-43 real-time quaking induced conversion reaction optimization and detection of seeding activity in CSF of amyotrophic lateral sclerosis and frontotemporal dementia patients 319
Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis 238
A role for the ELAV RNA-binding proteins in neural stem cells : stabilization of Msi1 mRNA 236
Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts 235
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 220
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 212
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function 208
A comparative transcriptomic analysis of gastrocnemius and triceps muscles in an ALS mouse model 205
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 198
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression 190
Genetic and epigenetic disease modifiers in an Italian C9orf72 family expressing ALS, FTD or PD clinical phenotypes 190
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia 187
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 182
Dysregulation of axonal transport and motorneuron diseases 176
Identification and functional characterization of trans-acting factors involved in the post-transcriptional regulation of CDK5R1 174
Identification of post-transcriptional regulatory elements in CDK5R1 3’UTR gene involved in CNS development and functioning 166
Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations 164
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis 162
The validation of the Italian Edinburgh cognitive and behavioural ALS screen (ECAS) 160
Response to the commentary “The effect of C9orf72 intermediate repeat expansions in neurodegenerative and autoimmune diseases” by Biasiotto G and Zanella I. 158
Angiogenin: a novel candidate gene for ALS pathogenesis in the Italian Population 150
Characterization of SOD1-G93A mouse muscle by a combined genomic and proteomic approach 149
Identification of Angiogenin gene mutations in a large cohort of Italian ALS patients 147
Chronic stress induces formation of stress granules and pathological TDP-43 aggregates in human ALS fibroblasts and iPSC-motoneurons 142
Muscle proteomic profile in the transgenic SOD1G93A mouse and in ALS patients 141
C9ORF72 repeat expansion in a large Italian ALS cohort : evidence of a founder effect 139
Genetic variation in DPP6 gene is not associated with susceptibility to Amyotrophic Lateral Sclerosis in two European population 138
Post-trascriptional regulation of neuro-oncological ventral antigen 1 by the neuronal RNA-binding proteins ELAV 137
Proteomic profile of gastrocnemious muscle in a transgenic mouse model of familial amyotrophic lateral sclerosis 136
Molecular mechanisms in KIF5A-related neurodegeneration 134
ALS Genes: mutational analysis in a large cohort of Italian patients 132
Identification of new HSPB8 variants linked to familial Amiotrophic Lateral Sclerosis 132
SOD1 Gene mutations in Italian Amyotrophic Lateral Sclerosis Patients 131
TDP-43 is recruited to stress granules in conditions of oxidative insult 131
Cognitive-behavioral longitudinal assessment in ALS : the Italian Edinburgh Cognitive and Behavioral ALS screen (ECAS) 131
The human CDK5R1 3'UTR contains distinct subregions affecting transcript stability 130
Genetics of Familial Amyotrophic Lateral Sclerosis 128
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 128
C9orf72 ALS/FTD dipeptide repeat protein levels are reduced by small molecules that inhibit PKA or enhance protein degradation 126
Analysis of FUS Gene Mutation in Familial Amyotrophic Lateral Sclerosis within an Italian cohort 124
ALS genes: a mutational screening in a large cohort of Italian patients 124
Dendritic targeting of short and long 3' UTR BDNF mRNA is regulated by BDNF or NT-3 and distinct sets of RNA-binding proteins 122
Identification of new ANG gene mutations in a large cohort of Italian patients with Amyotrophic Lateral Sclerosis 121
Modulation of actin polymerization affects nucleocytoplasmic transport in multiple forms of amyotrophic lateral sclerosis 119
Mutation analysis of the VPS54 gene in ALS patients 118
Motor, cognitive and behavioural profiles of C9orf72 expansion-related amyotrophic lateral sclerosis 117
Angiogenin gene mutations in Italian patients with familial and sporadic ALS 116
Inter-species differences in regulation of the progranulin–sortilin axis in TDP-43 cell models of neurodegeneration 115
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 115
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis 115
C9orf72 ALS/FTD dipeptide repeat protein levels are reduced by small molecules that inhibit PKA or enhance protein degradation 114
Stem cell therapy for neurodegenerative diseases: the issue of transdifferentiation 114
Ubiquilin 2 mutations in Italians patients with amyotrophic lateral sclerosis and frontotemporal dementia 114
null 112
Paraoxonase gene mutations in amyotrophic lateral sclerosis 111
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia 111
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene 110
Musashi-1 is a target of the ELAV RNA-binding proteins in neural stem cells 109
High frequency of TARDBP gene mutations in Italian patients with Amyotrophic Lateral Sclerosis 109
Protein aggregation and defective RNA metabolism as mechanisms for motor neuron damage 109
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 109
Gene expression profiling of skeletal muscle from SOD1G93A transgenic mouse 106
Post-transcriptional regulation mediated by ELAV/Hu RNA-binding proteins in motor neuron-like NSC34 cells 106
A genome wide non-synonymous SNP Scan of Amyotrophic Lateral Sclerosis 105
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum 105
PON1 is a disease modifier gene in amyotrophic lateral sclerosis : association of the Q192R polymorphism with bulbar onset and reduced survival 105
Identification of FUS/TLS Gene mutations in a cohort of Italian FALS patients 103
Reprogramming fibroblasts and peripheral blood cells from a C9ORF72 patient : A proof-of-principle study 103
Concurrence of SOD1 and ANG mutations in an Italian ALS family 102
No C9orf72 repeat expansion in patients with primary progressive multiple sclerosis 102
Identification of FUS/TLS gene mutation in a cohort of Italian FALS patients 101
Recenti sviluppi nella genetica della Sclerosi Laterale Amiotrofica 101
TDP-43 protein forms stress granules in conditions of cellular isults 101
CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum 101
Concurrence of SOD1 and ANG Mutations in Italian ALS Family 100
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 100
Shaping the Neurovascular Unit Exploiting Human Brain Organoids 99
Discovery of small peptides derived from ELAV proteins structure showing RNA-stabilizing properties 99
RNA-binding proteins and RNA metabolism : a new scenario in the pathogenesis of Amyotrophic Lateral Sclerosis 99
From transcriptomic to protein level changes in TDP-43 and FUS loss-of-function cell models 99
Geldanamycin and spironolactone enhance the degradation­of­C9orf72­ALS/FTD­dipeptide­repeat­proteins 98
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 98
TDP-43 and FUS RNA-binding proteins binds distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transciptional fate in motoneuron-like cells 97
Optineurin gene mutations in a color of Italian amyotrophic lateral sclerosis patients 96
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis 96
Novel optineurin mutations in patients with familial and sporadic Amyotrophic Lateral Sclerosis 95
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories 95
High frequency of TARDBP Gene mutations in Italian Patients with Amyotrophic Lateral Sclerosis (ALS) 94
Elevated global DNA methylation is not exclusive to amyotrophic lateral sclerosis and is also observed in spinocerebellar ataxia types 1 and 2 94
Lower semantic fluency scores and a phonemic-over-semantic advantage predict abnormal CSF P-tau181 levels in Aβ + patients within the Alzheimer's disease clinical spectrum 93
Mutational analysis of VCP gene in familial Amyotrophic Lateral Sclerosis 93
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis 92
Lithium preserves F-actin from the disarrangement induced by either DNase I or cytochalasin D 92
Focus on the heterogeneity of amyotrophic lateral sclerosis 92
Rigenerazione e recupero: la frontiera delle cellule staminali. 91
Phosphorylated tau in plasma could be a biomarker of lower motor neuron impairment in amyotrophic lateral sclerosis 87
Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1 (G93A) mouse model 87
Totale 16.605
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Categoria #
all - tutte 61.404
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 61.404
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.712 0 0 0 0 129 244 249 132 359 319 182 98
2020/20212.318 228 184 163 113 222 197 177 180 187 171 363 133
2021/20222.488 135 92 144 172 222 175 256 146 397 264 147 338
2022/20232.557 266 237 206 218 255 439 92 187 264 71 208 114
2023/20242.957 125 172 182 281 560 219 199 196 109 229 340 345
2024/20251.842 321 524 204 566 227 0 0 0 0 0 0 0
Totale 20.614