NACMIAS, BENEDETTA
 Distribuzione geografica
Continente #
NA - Nord America 14.509
EU - Europa 7.105
AS - Asia 1.570
AF - Africa 26
OC - Oceania 8
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 3
Totale 23.226
Nazione #
US - Stati Uniti d'America 14.473
PL - Polonia 2.203
IE - Irlanda 1.362
IT - Italia 1.117
SE - Svezia 1.016
HK - Hong Kong 625
CN - Cina 546
DE - Germania 351
UA - Ucraina 302
FI - Finlandia 212
GB - Regno Unito 200
JO - Giordania 122
AT - Austria 88
TR - Turchia 85
BE - Belgio 83
SG - Singapore 71
VN - Vietnam 52
IN - India 49
RU - Federazione Russa 39
CA - Canada 35
FR - Francia 31
CH - Svizzera 26
SC - Seychelles 20
ES - Italia 19
GR - Grecia 17
NL - Olanda 10
CZ - Repubblica Ceca 9
BG - Bulgaria 8
NZ - Nuova Zelanda 6
JP - Giappone 5
BR - Brasile 4
ID - Indonesia 4
MU - Mauritius 4
EU - Europa 3
IR - Iran 3
RO - Romania 3
AU - Australia 2
AZ - Azerbaigian 2
DK - Danimarca 2
GE - Georgia 2
IL - Israele 2
NG - Nigeria 2
NO - Norvegia 2
HU - Ungheria 1
KH - Cambogia 1
KR - Corea 1
LI - Liechtenstein 1
LT - Lituania 1
MK - Macedonia 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
Totale 23.226
Città #
Fairfield 2.323
Warsaw 2.203
Ashburn 1.403
Dublin 1.358
Chandler 1.287
Woodbridge 1.092
Seattle 998
Cambridge 927
Houston 870
Wilmington 769
Altamura 525
Jacksonville 502
Lawrence 485
Dearborn 450
Ann Arbor 395
Hong Kong 356
Princeton 343
Beijing 241
Boston 206
Florence 192
Boardman 191
Medford 165
Buffalo 158
San Diego 145
Bremen 119
Izmir 85
Brussels 83
New York 75
Norwalk 64
Vienna 62
Shanghai 55
Hefei 50
Falls Church 49
Dong Ket 40
London 40
Pune 40
Singapore 35
Hillsboro 34
Toronto 31
Andover 30
Kunming 28
Milan 28
Nanjing 28
Moscow 24
Auburn Hills 21
Guangzhou 21
Bern 20
Jinan 19
Rome 19
Los Angeles 17
Barcelona 16
Phoenix 15
Fuzhou 12
Redwood City 12
Frankfurt Am Main 11
Verona 10
Nanchang 8
Sofia 8
Umbertide 8
Bari 7
Brno 7
Chicago 7
Hounslow 7
Castelliri 6
Hanover 6
Lambeth 6
Laurel 6
Old Bridge 6
Prescot 6
Redmond 6
Stia 6
Wenzhou 6
Zhengzhou 6
Zurich 6
Cagliari 5
Chengdu 5
Chennai 5
Dallas 5
Kilburn 5
Misano Adriatico 5
Perugia 5
Turin 5
Washington 5
Wuhan 5
Campi Bisenzio 4
Chiswick 4
Cosenza 4
Genova 4
Hebei 4
Helsinki 4
San Mateo 4
Shenyang 4
Taizhou 4
Acton 3
Auckland 3
Baotou 3
Bologna 3
Brentford 3
Castelfidardo 3
Catania 3
Totale 19.002
Nome #
Clinical and neuroimaging profiles to identify C9orf72-FTD patients and serum Neurofilament to monitor the progression and the severity of the disease 278
Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts 229
Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population. 227
Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa 226
FDG PET and the genetics of dementia 221
Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier 219
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
Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease 199
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 191
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 185
Donor-specific anti-HLA antibodies in Huntington’s disease recipients of human fetal striatal grafts 178
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians 177
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia 168
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease 163
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 147
Impact of demography and population dynamics on the genetic architecture of human longevity 125
Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane 122
Genetics of vascular dementia - review from the ICVD working group 122
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 122
Alzheimer's Disease Progression: Factors Influencing Cognitive Decline 120
5-HT2A receptor gene polymorphism and eating disorders. 119
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy 113
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 111
Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons 110
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 106
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease 105
Age and ApoE genotype interaction in Alzheimer's disease: an FDG-PET study 102
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 102
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 101
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. 101
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort 99
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. 98
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 98
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study 97
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 97
Biomarkers study in atypical dementia: proof of a diagnostic work-up 97
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 96
A new social-family model for eating disorders: A European multicentre project using a case-control design 96
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 95
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. 95
Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors. 95
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
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: A cross-sectional analysis 94
5-HT2A promoter polymorphism in anorexia nervosa. 94
Tumor necrosis factor α influences phenotypic plasticity and promotes epigenetic changes in human basal forebrain cholinergic neuroblasts 94
A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene 93
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 93
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease 93
From Subjective Cognitive Decline to Alzheimer's Disease: The Predictive Role of Neuropsychological Assessment, Personality Traits, and Cognitive Reserve. A 7-Year Follow-Up Study 93
Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob disease. 92
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. 92
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 92
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 92
Primary Progressive Aphasia: Natural History in an Italian Cohort 92
PRNP P39L variant is a rare cause of frontotemporal dementia in Italian population 92
Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic 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
Molecular genetics of Alzheimer's disease in Italian families. 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
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 90
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 90
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease 90
The diagnosis of dementias: a practical tool not to miss rare causes 90
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease 89
Mutation analysis of patients with neurodegenerative disorders using NeuroX array 89
Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study. 89
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. 89
Genetic risk factors in familial Alzheimer's disease 89
Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease. 88
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. 88
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadicAlzheimer's disease. 87
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) 87
MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET 86
HLA A2 allele is associated with age at onset of Alzheimer's disease. 86
Semantic dementia associated with mutation V363I in the tau gene. 86
High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia 86
Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population. 86
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. 85
Genetics of familial and sporadic Alzheimer's disease. 85
Distinct neuroanatomical correlates of neuropsychiatric symptoms in the three main forms of genetic frontotemporal dementia in the GENFI Cohort 85
Metabolic interaction between ApoE genotype and onset age in Alzheimer's disease: implications for brain reserve. 84
Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI) 84
Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study 84
ApoE as a prognostic factor for post-traumatic coma. 84
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference 84
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 83
Molecular genetics of Alzheimer's disease. 83
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa 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
Novel S-acyl glutathione derivatives prevent amyloid oxidative stress and cholinergic dysfunction in Alzheimer disease models. Free Radic Biol Med. 83
The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death. 82
KIBRA gene variants are associated with episodic memory performance in subjective memory complaints. 82
ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. 82
Totale 11.195
Categoria #
all - tutte 71.319
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 71.319


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192.073 0 0 0 0 0 0 0 0 110 386 859 718
2019/20206.015 383 384 134 433 655 901 940 746 603 354 370 112
2020/20212.894 278 252 218 306 112 287 104 257 277 413 177 213
2021/20222.236 55 161 209 72 78 106 102 190 118 89 387 669
2022/20236.139 597 1.343 206 557 382 1.038 894 289 565 45 151 72
2023/20242.209 134 229 382 145 205 234 111 720 49 0 0 0
Totale 23.615