CINECA IRIS Institutional Research Information System

RUBINO, Elisa
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 9.911
EU - Europa 6.258
AS - Asia 3.441
OC - Oceania 136
SA - Sud America 111
AF - Africa 39
Continente sconosciuto - Info sul continente non disponibili 28
Totale 19.924
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 9.721
CN - Cina 1.777
IT - Italia 1.555
SG - Singapore 741
IE - Irlanda 689
SE - Svezia 680
FR - Francia 554
DE - Germania 455
AT - Austria 397
FI - Finlandia 377
GB - Regno Unito 358
UA - Ucraina 274
DK - Danimarca 252
KR - Corea 176
CA - Canada 167
VN - Vietnam 162
PL - Polonia 149
JP - Giappone 130
AU - Australia 122
ES - Italia 111
IN - India 101
BE - Belgio 93
ID - Indonesia 87
NL - Olanda 86
TR - Turchia 66
HK - Hong Kong 64
BR - Brasile 54
PT - Portogallo 31
TW - Taiwan 31
GR - Grecia 29
RU - Federazione Russa 29
EU - Europa 28
CH - Svizzera 27
RO - Romania 24
CO - Colombia 23
SI - Slovenia 22
MY - Malesia 18
AR - Argentina 17
RS - Serbia 17
IL - Israele 16
IR - Iran 14
MX - Messico 14
NZ - Nuova Zelanda 14
CL - Cile 13
SN - Senegal 12
CZ - Repubblica Ceca 11
IQ - Iraq 11
NO - Norvegia 10
PK - Pakistan 10
SA - Arabia Saudita 10
NG - Nigeria 8
BG - Bulgaria 7
TH - Thailandia 7
UZ - Uzbekistan 6
CY - Cipro 5
PR - Porto Rico 4
BA - Bosnia-Erzegovina 3
EG - Egitto 3
HU - Ungheria 3
LK - Sri Lanka 3
LT - Lituania 3
LV - Lettonia 3
MA - Marocco 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
ZA - Sudafrica 3
CI - Costa d'Avorio 2
HR - Croazia 2
LB - Libano 2
MD - Moldavia 2
PE - Perù 2
PH - Filippine 2
SD - Sudan 2
BD - Bangladesh 1
BO - Bolivia 1
BY - Bielorussia 1
CU - Cuba 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GL - Groenlandia 1
LU - Lussemburgo 1
NP - Nepal 1
PA - Panama 1
SC - Seychelles 1
SV - El Salvador 1
TG - Togo 1
VE - Venezuela 1
Totale 19.924
Salva come PNG Salva come JPEG
Città #
Chandler 1.041
Beijing 977
Dublin 679
Singapore 614
Fairfield 546
Santa Clara 535
Houston 515
Ashburn 490
Ann Arbor 485
Dearborn 439
Torino 397
Vienna 383
Wilmington 370
Woodbridge 334
Villeurbanne 328
Nyköping 307
Jacksonville 239
Seattle 238
Medford 218
Princeton 214
Cambridge 202
Redwood City 193
Columbus 188
Pisa 172
Guangzhou 139
Warsaw 138
Dong Ket 130
Turin 126
Milan 87
Jakarta 86
New York 77
Shanghai 69
Nanjing 62
Boston 60
London 57
Boardman 56
Brussels 51
Toronto 50
Helsinki 48
San Diego 46
Chengdu 43
Norwalk 41
Rome 41
Munich 40
Tokyo 39
Hangzhou 37
San Mateo 37
Fremont 34
Paris 33
Hefei 30
Jinan 30
Los Angeles 28
Washington 28
Chicago 26
Hong Kong 26
Kunming 25
Xian 24
Verona 23
Düsseldorf 21
Falls Church 21
Istanbul 21
Sydney 21
Frankfurt am Main 19
Madrid 19
Melbourne 19
Ottawa 19
Zhengzhou 19
Oxford 18
Villa Cortese 18
Brisbane 17
Phoenix 17
Piemonte 17
Silver Spring 17
Taipei 17
Nanchang 16
Philadelphia 16
Barcelona 15
Bologna 15
Edinburgh 15
Naples 15
Nuremberg 15
Buffalo 14
Central District 14
Duncan 14
Rotterdam 14
Southampton 14
Wuhan 14
Changsha 13
Ipoh 13
Tianjin 13
Berlin 12
Mountain View 12
Rochester 12
Bethesda 11
Grand Rapids 11
Leeds 11
Amsterdam 10
Athens 10
Atlanta 10
Belgrade 10
Totale 12.610
Salva come PNG Salva come JPEG
Nome #
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients. 578
Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy 513
Investigating the role of adipokines in chronic migraine 414
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers 365
Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia 322
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation. 321
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations 318
A review of the recent advances in neuroimaging of frontotemporal lobar degeneration 305
Association between Major Mood Disorders and the hypocretin receptor 1 gene 290
CXCR4 involvement in neurodegenerative diseases 288
Three novel missense mutations in SLC20A2 associated with idiopathic basal ganglia calcification 280
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS 277
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia 273
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia 259
Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis. 249
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification 246
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients. 233
Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report 227
Novel mutation of SLC20A2 in an Italian patient presenting with migraine. 210
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy 208
Genetic variants in the NOTCH4 gene influence the clinical features of migraine 204
A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10 201
Neuropsychological Correlates of Pre-Frailty in Neurocognitive Disorders: A Possible Role for Metacognitive Dysfunction and Mood Changes 201
Consistent effects of non-invasive vagus nerve stimulation (nVNS) for the acute treatment of migraine: Additional findings from the randomized, sham-controlled, double-blind PRESTO trial 11 Medical and Health Sciences 1103 Clinical Sciences 193
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia 190
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis 184
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 179
Noninvasive vagus nerve stimulation as acute therapy for migraine: The randomized PRESTO study 179
Neurofunctional Signature of Hyperfamiliarity for Unknown Faces 175
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population 174
High Risk of Suicide in Behavioral Variant Frontotemporal Dementia 161
Evidence for an association between migraine and the hypocretin receptor 1 gene 151
Genes and primary headaches: discovering new potential therapeutic targets 149
Polymorphisms in the Proinflammatory Cytokines Genes and Response to NSAIDs in Migraine Attacks 143
The hemochromatosis (HFE) gene influences the clinical features of migraine 139
Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum 138
Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration 137
Practical and clinical utility of non-invasive vagus nerve stimulation (nVNS) for the acute treatment of migraine: a post hoc analysis of the randomized, sham-controlled, double-blind PRESTO trial 135
O056. Migraine as presenting symptom of SLC20A2gene mutations 129
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases 128
Recent advances in the molecular genetics of frontotemporal lobar degeneration 128
Genetic risk for neurodegenerative disorders, and its overlap with cognitive ability and physical function 126
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 126
Focal gray matter decrease in the cerebral pain network of migraine patients 124
Behavioral and psychological effects of coronavirus disease-19 quarantine in patients with dementia 121
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. 117
The Impact of COVID-19 Quarantine on Patients With Dementia and Family Caregivers: A Nation-Wide Survey 115
Neural correlates of reduced awareness in instrumental activities of daily living in frontotemporal dementia 114
Association between Alzheimer's Disease and the hypocretin receptor 2 gene 111
Protein network analysis reveals selectively vulnerable regions and biological processes in FTD 109
Non-invasive vagal nerve stimulation in patients with chronic migraine and medication-overuse headache: a 9-month follow-up study 105
The My Active and Healthy Aging (My-AHA) ICT platform to detect and prevent frailty in older adults: Randomized control trial design and protocol 105
Prevalence of the placebo and nocebo responses in patients with migraine and tension- type headache 104
High dose intravenous methylprednisolone in cluster headache patients non responders to oral therapy 104
Late onset bipolar disorder preceding frontotemporal dementia with mutation in progranulin gene: a case report 102
Voxel-based Morphometry Reveals Gray Matter Loss in Patients with Paget's Disease of the Bone Carrying SQSTM1 Gene Mutations 99
Neuropsychological correlates of instrumental activities of daily living in neurocognitive disorders: a possible role for executive dysfunction and mood changes 97
Association of polymorphisms and haplotypes of hypocretin receptor 2 gene with cluster headache 94
C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone 94
Aquaporin 4 gene and migraine: an association study 93
Insulin sensitivity is impaired in Frontotemporal Lobar Degeneration 92
Insulin Resistance in Dementia: A Comparison between Alzheimer's Disease and Frontotemporal Lobar Degeneration 92
Prediction of Alzheimer's disease in patients with mild cognitive impairment using CSF biomarkers 92
Mutation Screening of Neuromedin B (NMB) gene in behavioral variant Frontotemporal Dementia 92
Haemochromatosis gene (HFE) polymorphisms and migraine: an association study 91
Vascular endothelial growth factor gene polymorphisms and intracranial aneurysms. 90
Investigating the Placebo/Nocebo Responses and the Natural History of the Disease in Patients with Migraine 90
Investigating involvement of Von Economo neurons in behavioral variant frontotemporal dementia 89
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache 88
Association between polymorphisms and haplotypes of the HCRTR2 gene and cluster headache 88
Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene 87
Placebo and Nocebo Responses in Patients with Migraine 87
SQSTM1/p62 gene sequencing in Frontotemporal Lobar Degeneration 87
Increased p62 levels in cerebrospinal fluid of patients with Alzheimer’s disease and Frontotemporal dementia. 87
Subclinical hypothyroidism is associated with migraine: A case-control study 87
The Carers’ Needs Assessment for Dementia (CNA-D): a validation study in the Italian population 85
Association between interleukin-1α gene polymorphisms and Alzheimer’s Disease: a meta-analytic study 83
La sensibilità all'insulina è alterata nei pazienti con emicrania cronica 83
A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine 83
Lack of association between the 3092 T→C Clock gene polymorphism and cluster headache 83
Investigating Neuroimaging Correlates of Early Frailty in Patients With Behavioral Variant Frontotemporal Dementia: A MRI and FDG-PET Study 83
Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache: a meta-analysis 82
Insulin Resistance in dementia: A comparison between Alzheimer’s Disease and Fronto-Temporal Lobar Degeneration 82
Prevalence of placebo and nocebo effects in migraine patients attending a specialty headache center 82
HLA-DRB1 genotyping in Italian migraine patients 81
A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura 81
Migraine: Genetic Variants and Clinical Phenotypes 81
Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: A comprehensive meta-analysis. 81
Meta-analysis of the association between ApoE gene polymorphisms and frontotemporal dementia 80
Genetic polymorphism at the Clock gene locus and cluster headache 80
Association analyses of genetic variants of the HCTR1 gene in migraine 79
APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis 79
Predictive value of CSF biomarkers for Alzheimer's Disease in a cohort of patients with Mild Cognitive Impairment 79
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 79
Investigating the role of adipokines in Alzheimer's disease 79
Association between Tumor Necrosis Factor-α and aneurismal subarachnoid hemorrhage 79
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores 79
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation 78
Association study between intracranial aneurysms and polymorphisms of IL-1 alfa, IL-1 beta, IL-1RN genes 78
Cardiac homeobox gene CSK/NKX2-5 in patients wtih cluster headache 78
Totale 15.010
Salva come PNG Salva come JPEG
Categoria #
all - tutte 56.662
article - articoli 0
book - libri 0
conference - conferenze 18.344
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 75.006
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.300 0 0 0 0 0 563 411 269 337 328 232 160
2020/20212.421 267 225 236 188 178 162 189 105 243 238 141 249
2021/20222.497 161 101 109 216 143 149 146 154 101 177 593 447
2022/20233.408 325 348 76 344 300 795 219 188 418 109 167 119
2023/20241.780 207 270 127 106 157 227 76 109 25 112 144 220
2024/20252.140 91 182 222 336 1.003 306 0 0 0 0 0 0
Totale 20.569