BAGNOLI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 6.539
EU - Europa 3.475
AS - Asia 763
AF - Africa 5
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 10.789
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Nazione #
US - Stati Uniti d'America 6.523
PL - Polonia 1.365
IE - Irlanda 555
IT - Italia 540
SE - Svezia 479
HK - Hong Kong 271
CN - Cina 265
DE - Germania 161
UA - Ucraina 91
FI - Finlandia 90
GB - Regno Unito 73
JO - Giordania 73
RU - Federazione Russa 50
SG - Singapore 46
TR - Turchia 39
VN - Vietnam 30
IN - India 24
CH - Svizzera 16
BE - Belgio 15
CA - Canada 15
FR - Francia 13
BG - Bulgaria 7
ES - Italia 6
JP - Giappone 5
BR - Brasile 4
NL - Olanda 4
SC - Seychelles 4
IR - Iran 3
CZ - Repubblica Ceca 2
DK - Danimarca 2
GE - Georgia 2
IL - Israele 2
RO - Romania 2
AZ - Azerbaigian 1
EU - Europa 1
GR - Grecia 1
KH - Cambogia 1
KR - Corea 1
LI - Liechtenstein 1
MK - Macedonia 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
Totale 10.789
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Città #
Warsaw 1.365
Fairfield 1.050
Chandler 636
Dublin 554
Ashburn 542
Woodbridge 490
Seattle 458
Cambridge 453
Houston 421
Wilmington 346
Altamura 244
Dearborn 216
Lawrence 214
Ann Arbor 204
Hong Kong 166
Jacksonville 162
Princeton 145
Beijing 119
Florence 98
Buffalo 89
Boston 88
Bremen 75
Boardman 74
Medford 62
San Diego 58
Moscow 40
Izmir 39
New York 28
Dong Ket 24
Hefei 24
Shanghai 24
Norwalk 23
Pune 23
Singapore 20
Hillsboro 19
Falls Church 18
London 17
Kunming 16
Brussels 15
Toronto 15
Kent 13
Nanjing 13
Bern 12
West Jordan 12
Andover 11
Jinan 9
Phoenix 9
Redwood City 9
Auburn Hills 8
Milan 8
Sofia 7
Los Angeles 6
Rome 6
Stia 6
Wenzhou 6
Bari 5
Castelliri 5
Frankfurt Am Main 5
Guangzhou 5
Misano Adriatico 5
Prescot 5
Turin 5
Wuhan 5
Barcelona 4
Campi Bisenzio 4
Chengdu 4
Dallas 4
Fuzhou 4
Nanchang 4
Verona 4
Zurich 4
Castelfidardo 3
Catania 3
Hebei 3
Hounslow 3
Jamaica 3
Lucca 3
Salerno 3
Santa Maria A Monte 3
Siena 3
Xian 3
Zhengzhou 3
Afragola 2
Arezzo 2
Asciano 2
Baotou 2
Brentford 2
Casamarciano 2
Chicago 2
Copenhagen 2
Cosenza 2
Genoa 2
Harbin 2
Jenera 2
Lund 2
Modena 2
Monza 2
Naples 2
Napoli 2
Old Bridge 2
Totale 8.950
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Nome #
Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts 229
Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier 218
Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference 211
Lipid Rafts Mediate Amyloid-induced Calcium Dyshomeostasis and Oxidative Stress in Alzheimer's Disease. 200
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 189
Membrane cholesterol enrichment prevents Abeta-induced oxidative stress in Alzheimer's fibroblasts. 186
Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits 184
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians 177
Donor-specific anti-HLA antibodies in Huntington’s disease recipients of human fetal striatal grafts 176
Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases 155
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 147
Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane 118
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 116
Alzheimer's Disease Progression: Factors Influencing Cognitive Decline 115
Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons 110
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 109
PRESENILIN MUTATIONS LINKED TO FAMILIAL ALZHEIMER'S DISEASE REDUCE ENDOPLASMIC RETICULUM AND GOLGI APPARATUS CALCIUM LEVELS. 106
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 104
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. 100
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 99
Association between serotonin transporter gene polymorphism and eating disorders outcome: A 6-year follow-up study. 98
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study 97
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 96
Fragile X premutation with atypical symptoms at onset. 95
Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications. 95
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. 94
A new social-family model for eating disorders: A European multicentre project using a case-control design 94
Biomarkers study in atypical dementia: proof of a diagnostic work-up 93
Primary Progressive Aphasia: Natural History in an Italian Cohort 92
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease 91
KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment 91
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 91
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 91
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease. 91
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 90
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 90
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 89
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease 89
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. 89
Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease 88
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) 86
High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia 86
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 84
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 83
Semantic dementia associated with mutation V363I in the tau gene. 83
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis 83
Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients. 83
KIBRA gene variants are associated with episodic memory performance in subjective memory complaints. 82
Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity. 82
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 81
The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study 81
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 81
Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease 81
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia 81
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 80
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 80
DAPK1 is Associated with FTD and not with Alzheimer's Disease 79
Brain-derived neurotrophic factor genetic variants are notsusceptibility factors to Alzheimer's disease in Italy. 78
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration 78
Protective effect of new S-acylglutathione derivatives against amyloid induced oxidative stress 78
Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation 78
Contribution of Bilingualism to Cognitive Reserve of an Italian Literature Professor at High Risk for Alzheimer's Disease 78
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort 78
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease 76
Pattern and progression of cognitive decline in Alzheimer's disease:role of premorbid intelligence and ApoE genotype 76
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. 75
Suitability of neuropsychological tests in patients with vascular dementia (VaD). 75
Genetics of Alzheimer's Disease and Frontotemporal Dementia 75
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 74
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture 74
Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI). 73
The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts. 72
Novel GRN Mutations in Alzheimer's Disease and Frontotemporal Lobar Degeneration 72
Brain metabolic differences between sporadic and familial Alzheimer's disease. 72
Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. 72
Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships 72
Plasma Membrane Injury Depends on Bilayer Lipid Composition in Alzheimer’s Disease 71
Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner. 71
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 70
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients. 70
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 69
Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11-year follow-up study 69
Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis 68
Imaging and Cognitive Reserve Studies Predict Dementia in Presymptomatic Alzheimer's Disease Subjects. 68
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats 67
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 67
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia 67
Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients 65
Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease 65
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia 64
Human iPSC-Derived Hippocampal Spheroids: An Innovative Tool for Stratifying Alzheimer Disease Patient-Specific Cellular Phenotypes and Developing Therapies 63
Mitochondria and Alzheimer's disease. 62
Heterozygous TREM2 mutations in frontotemporal dementia 62
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis 60
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients 59
Epigenetic modifications in Alzheimer's disease: Cause or effect? 59
DNMT3B promoter polymorphisms and risk of late onset Alzheimer's disease. 58
CXCR4 involvement in neurodegenerative diseases 58
Contribution of mother tongue on cognitive reserve of an Italian bilingual literature Professor 58
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration 57
Totale 9.262
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Categoria #
all - tutte 34.538
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 34.538
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019747 0 0 0 0 0 0 0 0 0 0 410 337
2019/20202.847 181 166 67 196 337 416 445 353 285 185 165 51
2020/20211.332 141 144 82 132 55 113 61 117 127 188 78 94
2021/2022996 30 77 104 25 16 47 46 77 44 41 192 297
2022/20232.767 262 604 110 298 164 462 352 135 273 17 63 27
2023/2024977 52 107 160 52 84 119 60 233 30 62 18 0
Totale 10.970