PIACERI, IRENE
 Distribuzione geografica
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Continente #
NA - Nord America 5.865
EU - Europa 3.629
AS - Asia 2.319
SA - Sud America 361
AF - Africa 46
OC - Oceania 28
Continente sconosciuto - Info sul continente non disponibili 1
Totale 12.249
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Nazione #
US - Stati Uniti d'America 5.811
RU - Federazione Russa 1.147
IT - Italia 776
PL - Polonia 743
SG - Singapore 709
CN - Cina 520
HK - Hong Kong 379
BR - Brasile 279
IE - Irlanda 279
VN - Vietnam 249
SE - Svezia 213
KR - Corea 170
DE - Germania 114
FR - Francia 102
IN - India 97
FI - Finlandia 69
GB - Regno Unito 66
UA - Ucraina 45
JO - Giordania 42
AR - Argentina 34
AU - Australia 28
CA - Canada 28
ID - Indonesia 26
BD - Bangladesh 19
ES - Italia 18
IQ - Iraq 17
JP - Giappone 17
MX - Messico 16
TR - Turchia 15
NL - Olanda 14
EC - Ecuador 12
ZA - Sudafrica 11
CI - Costa d'Avorio 10
BE - Belgio 9
AT - Austria 8
CH - Svizzera 8
CO - Colombia 8
PK - Pakistan 8
CL - Cile 7
PH - Filippine 7
UZ - Uzbekistan 7
KE - Kenya 6
SA - Arabia Saudita 6
UY - Uruguay 6
VE - Venezuela 6
IL - Israele 5
TN - Tunisia 5
EG - Egitto 4
JM - Giamaica 4
MA - Marocco 4
NG - Nigeria 4
AE - Emirati Arabi Uniti 3
CZ - Repubblica Ceca 3
GR - Grecia 3
KZ - Kazakistan 3
LB - Libano 3
OM - Oman 3
PE - Perù 3
AL - Albania 2
BO - Bolivia 2
GE - Georgia 2
GY - Guiana 2
KW - Kuwait 2
NI - Nicaragua 2
NP - Nepal 2
PY - Paraguay 2
RS - Serbia 2
AM - Armenia 1
BG - Bulgaria 1
BY - Bielorussia 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EU - Europa 1
HN - Honduras 1
HR - Croazia 1
IR - Iran 1
KG - Kirghizistan 1
KH - Cambogia 1
LT - Lituania 1
LY - Libia 1
MY - Malesia 1
PA - Panama 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TH - Thailandia 1
YE - Yemen 1
Totale 12.249
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Città #
Ashburn 926
Santa Clara 827
Warsaw 743
Fairfield 551
Singapore 529
Hong Kong 327
Dublin 275
Chandler 274
Woodbridge 270
Houston 255
Seattle 255
Cambridge 227
Wilmington 173
Seoul 165
Beijing 159
San Jose 156
Milan 135
Dallas 131
Altamura 123
Ann Arbor 122
Lawrence 118
Dearborn 82
Buffalo 78
Princeton 78
Moscow 74
Florence 73
Ho Chi Minh City 73
The Dalles 70
Hanoi 60
Lauterbourg 56
Boston 55
Rome 53
Los Angeles 51
Mumbai 49
Hefei 42
Munich 42
Council Bluffs 41
New York 37
San Diego 35
Shanghai 32
Bremen 31
Clifton 28
São Paulo 27
Medford 26
Melbourne 26
Boardman 25
Paris 25
Kent 23
Pune 23
Jacksonville 22
Jakarta 20
Turin 20
Redondo Beach 19
Turku 19
Naples 15
Orem 15
Helsinki 14
Dong Ket 13
Falls Church 13
Norwalk 13
Chennai 12
London 12
Barcelona 11
Guangzhou 11
Hillsboro 11
Montreal 11
Tokyo 11
Abidjan 10
Izmir 10
Phoenix 10
Tianjin 10
Toronto 10
West Jordan 10
Atlanta 9
Bari 9
Bologna 9
Brussels 9
Chicago 9
Frankfurt am Main 9
Haiphong 9
Jinan 9
Rio de Janeiro 9
Cagliari 8
Miano 8
Nanjing 8
Andover 7
Belo Horizonte 7
Bern 7
Catania 7
Figino 7
Guayaquil 7
Johannesburg 7
Kunming 7
Redwood City 7
Tashkent 7
Brasília 6
Da Nang 6
Erbil 6
Genoa 6
Hải Dương 6
Totale 8.583
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Nome #
Clinical and neuroimaging profiles to identify C9orf72-FTD patients and serum Neurofilament to monitor the progression and the severity of the disease 400
Profilo Genetico ed Epigenetico in pazienti con Demenza Frontotemporale 389
Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier 335
FDG PET and the genetics of dementia 295
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 293
Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases 269
Alzheimer's Disease Progression: Factors Influencing Cognitive Decline 256
Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study. 251
Tumor necrosis factor α influences phenotypic plasticity and promotes epigenetic changes in human basal forebrain cholinergic neuroblasts 245
A PALB2 germline mutation associated with hereditary breast cancer in Italy. 231
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study 229
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 221
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 219
Challenges in Alzheimer's Disease Diagnostic Work-Up: Amyloid Biomarker Incongruences 214
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration 212
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 210
Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11-year follow-up study 209
The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study 197
Brain functional network integrity sustains cognitive function despite atrophy in presymptomatic genetic frontotemporal dementia 191
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture 191
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats 189
Biomarkers study in atypical dementia: proof of a diagnostic work-up 189
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study 189
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 188
High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia 183
Influence of apoe genotype and clock t3111c interaction with cardiovascular risk factors on the progression to alzheimer’s disease in subjective cognitive decline and mild cognitive impairment patients 182
Per2 C111G polymorphism influences cognition in Subjective Cognitive Decline and Mild Cognitive Impairment. A 10-year follow-up study 182
Primary Progressive Aphasia: Natural History in an Italian Cohort 182
Linguistic profiles, brain metabolic patterns and rates of amyloid-β biomarker positivity in patients with mixed primary progressive aphasia 182
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 176
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 174
Data-driven staging of genetic frontotemporal dementia using multi-modal MRI 173
Imaging and Cognitive Reserve Studies Predict Dementia in Presymptomatic Alzheimer's Disease Subjects. 173
Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications. 171
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia 168
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia 165
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. 161
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z) 161
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia 160
Genetics of familial and sporadic Alzheimer's disease. 158
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 153
DAPK1 is Associated with FTD and not with Alzheimer's Disease 152
"stato dell'arte" della ricerca 151
Genetics of Alzheimer's Disease and Frontotemporal Dementia 150
Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation 150
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis 142
Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease 141
Suitability of neuropsychological tests in patients with vascular dementia (VaD). 140
Novel GRN Mutations in Alzheimer's Disease and Frontotemporal Lobar Degeneration 136
Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease 136
Folate, Homocysteine, Vitamin B12, and Polymorphisms of Genes Participating in One-Carbon Metabolism in Late-Onset Alzheimer's Disease Patients and Healthy Controls 133
Epigenetic modifications in Alzheimer's disease: Cause or effect? 132
Heterozygous TREM2 mutations in frontotemporal dementia 130
Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships 128
Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis 127
CXCR4 involvement in neurodegenerative diseases 127
Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients 127
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol 127
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts 126
Cholesteryl ester transfer protein (CETP) I405V polymorphism in Italian memory complainers 125
Mitochondria and Alzheimer's disease. 123
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases 119
Frontotemporal dementia and its subtypes: a genome-wide association study 118
Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation 111
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients 109
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease 106
MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementia 105
Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes 97
Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians 92
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia 86
Totale 12.362
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Categoria #
all - tutte 34.151
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 34.151
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202139 0 0 0 0 0 0 0 0 0 0 0 39
2021/2022521 16 30 50 22 13 28 16 42 27 22 92 163
2022/20231.288 136 307 47 120 68 213 167 58 125 9 25 13
2023/2024759 30 52 75 26 32 69 25 334 10 42 45 19
2024/20252.880 87 334 220 476 752 326 26 225 143 94 91 106
2025/20263.642 356 431 305 357 495 127 408 185 206 232 75 465
Totale 12.362