IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 9.319
EU - Europa 8.723
AS - Asia 5.073
SA - Sud America 989
Continente sconosciuto - Info sul continente non disponibili 286
AF - Africa 169
OC - Oceania 6
AN - Antartide 1
Totale 24.566
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.982
RU - Federazione Russa 2.094
IE - Irlanda 1.767
SG - Singapore 1.535
CN - Cina 1.250
DE - Germania 1.083
IT - Italia 940
SE - Svezia 862
HK - Hong Kong 767
BR - Brasile 751
VN - Vietnam 732
UA - Ucraina 645
FI - Finlandia 393
FR - Francia 323
GB - Regno Unito 228
CA - Canada 166
IN - India 154
BD - Bangladesh 148
KR - Corea 120
AR - Argentina 91
MX - Messico 66
NL - Olanda 61
BJ - Benin 59
ID - Indonesia 59
PL - Polonia 56
AT - Austria 54
CZ - Repubblica Ceca 47
JP - Giappone 47
IQ - Iraq 44
ZA - Sudafrica 41
TR - Turchia 39
ES - Italia 38
IR - Iran 34
CO - Colombia 32
EC - Ecuador 31
BE - Belgio 26
JM - Giamaica 22
CL - Cile 21
PK - Pakistan 21
EE - Estonia 19
LT - Lituania 19
PE - Perù 17
PY - Paraguay 17
CR - Costa Rica 15
PH - Filippine 15
EG - Egitto 14
EU - Europa 14
UZ - Uzbekistan 13
VE - Venezuela 13
HN - Honduras 12
MA - Marocco 12
SA - Arabia Saudita 12
DO - Repubblica Dominicana 10
PR - Porto Rico 10
AE - Emirati Arabi Uniti 9
JO - Giordania 9
MY - Malesia 9
CH - Svizzera 8
DZ - Algeria 8
IL - Israele 8
SV - El Salvador 8
TH - Thailandia 8
TN - Tunisia 8
TT - Trinidad e Tobago 8
TW - Taiwan 8
AZ - Azerbaigian 7
BO - Bolivia 7
DK - Danimarca 7
GR - Grecia 7
LV - Lettonia 7
UY - Uruguay 7
AU - Australia 6
NI - Nicaragua 6
RO - Romania 6
KE - Kenya 5
CW - ???statistics.table.value.countryCode.CW??? 4
ET - Etiopia 4
HU - Ungheria 4
LY - Libia 4
RS - Serbia 4
SN - Senegal 4
AL - Albania 3
BG - Bulgaria 3
BY - Bielorussia 3
GP - Guadalupe 3
GT - Guatemala 3
KW - Kuwait 3
LK - Sri Lanka 3
MK - Macedonia 3
NP - Nepal 3
QA - Qatar 3
SI - Slovenia 3
AO - Angola 2
BS - Bahamas 2
CU - Cuba 2
HR - Croazia 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
MD - Moldavia 2
Totale 24.270
Salva come PNG Salva come JPEG
Città #
Dublin 1.765
Jacksonville 1.129
San Jose 886
Hong Kong 760
Singapore 564
Council Bluffs 535
Dearborn 513
Ashburn 500
Beijing 406
Chandler 335
Moscow 281
Los Angeles 256
Wilmington 246
Ho Chi Minh City 225
Columbus 212
Lauterbourg 212
Princeton 208
Lawrence 207
San Mateo 156
Hanoi 132
Buffalo 128
Bremen 120
New York 119
Phoenix 115
Seoul 110
Dallas 106
Ann Arbor 101
Novara 101
Santa Clara 99
Andover 95
Piemonte 92
Munich 86
São Paulo 70
Orem 67
Houston 64
Boardman 62
Milan 60
Cotonou 59
Rome 58
Nuremberg 55
Denver 54
Helsinki 50
Warsaw 46
Montreal 45
Brno 44
Brooklyn 44
Chicago 43
Frankfurt am Main 42
Turin 42
Philadelphia 41
Atlanta 40
Nanjing 40
Guangzhou 37
Redondo Beach 37
Tokyo 36
Chennai 35
Tianjin 35
Woodbridge 35
Düsseldorf 34
The Dalles 34
Toronto 34
Haiphong 33
Strasbourg 32
Boston 31
Hefei 28
Mexico City 28
Monmouth Junction 28
Vienna 28
Hangzhou 26
Rio de Janeiro 26
Carrboro 25
Kunming 24
Poplar 24
Da Nang 23
Shanghai 23
Johannesburg 22
London 22
Amsterdam 21
Falkenstein 20
Norwalk 20
Las Vegas 19
Manchester 19
Schaumburg 19
Brussels 18
North Bergen 17
Porto Alegre 17
Stockholm 17
Tornaco 17
Dong Ket 16
Hải Dương 16
Jakarta 16
Leawood 16
Mumbai 16
Ankara 15
Baghdad 15
Queens 15
Turku 15
Biên Hòa 14
Brasília 14
Curitiba 14
Totale 12.952
Salva come PNG Salva come JPEG
Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 250
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 189
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 184
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 176
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 171
Locus for severity implicates CNS resilience in progression of multiple sclerosis 158
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 155
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 153
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 152
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 150
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 149
Concordance, disease progression, and heritability of coeliac disease in Italian twins 148
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 146
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 143
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 142
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 142
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 141
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 141
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 139
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 138
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 138
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 137
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 137
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 136
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 136
Overexpression of the Cytokine BAFF and Autoimmunity Risk 135
Association of osteopontin regulatory polymorphisms with systemic sclerosis 135
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 133
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 132
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 132
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 131
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 131
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 130
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 129
A polymorphic variation in a putative regulation box of the TNFA promoter region. 128
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 126
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 126
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 125
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 125
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 125
Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis 124
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 123
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 123
The multistep hypothesis of ALS revisited: The role of genetic mutations 123
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 122
MICA and MICB microsatellite alleles in HLA extended haplotypes 122
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 121
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 120
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 119
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 118
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 118
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 117
Extensive genetics of ALS: a population-based study in Italy. 117
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 117
Cytokine gene polymorphism in human disease: on-line databases 116
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 116
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 116
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 116
A Large twins study in coeliac disease 115
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 115
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 115
HLA alleles modulate EBV viral load in multiple sclerosis 114
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 114
A 3'-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus 114
Cognitive impairment across ALS clinical stages in a population-based cohort 114
Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2019) 178(1) (262), (S0092867419306798), (10.1016/j.cell.2019.06.016)) 114
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 113
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 113
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 112
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 112
A genome screen for multiple sclerosis in Sardinian multiplex families 111
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 110
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 110
Variations of the perforin gene in patients with multiple sclerosis 110
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 110
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 110
A genome screen for multiple sclerosis in Italian families 109
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 109
Validation of an Algorithm to Detect Multiple Sclerosis Cases in Administrative Health Databases in Piedmont (Italy): An Application to the Estimate of Prevalence by Age and Urbanization Level 109
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 108
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 107
A case of early-onset Parkinson's disease in a patient with KBG syndrome 107
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 107
A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis 106
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 106
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 106
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 105
null 105
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 104
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 104
Un ampio studio di concordanza per il morbo celiaco in gemelli 104
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 104
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 104
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 103
Evaluation of TRAF6 in a large multiancestral lupus cohort 102
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 101
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. 101
SLE candidate genes in the Italian population: evidence for a significant association of IL-10 101
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 101
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes. 100
Totale 12.481
Salva come PNG Salva come JPEG
Categoria #
all - tutte 124.213
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 124.213
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.187 0 0 0 220 65 3 109 28 98 31 310 323
2022/20233.293 239 150 123 71 256 255 86 169 1.775 13 100 56
2023/2024973 68 70 107 35 185 20 181 18 16 12 68 193
2024/20252.700 51 46 143 87 45 240 244 236 710 291 134 473
2025/20269.140 434 361 693 1.334 768 626 1.223 1.481 635 737 624 224
2026/20272.679 458 790 643 788 0 0 0 0 0 0 0 0
Totale 24.566