IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 8.380
NA - Nord America 6.347
AS - Asia 4.744
SA - Sud America 961
AF - Africa 167
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 6
AN - Antartide 1
Totale 20.622
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Nazione #
US - Stati Uniti d'America 6.178
RU - Federazione Russa 2.093
IE - Irlanda 1.766
SG - Singapore 1.424
CN - Cina 1.180
DE - Germania 1.074
SE - Svezia 862
HK - Hong Kong 742
BR - Brasile 734
VN - Vietnam 726
IT - Italia 691
UA - Ucraina 644
FI - Finlandia 393
FR - Francia 315
GB - Regno Unito 186
IN - India 152
KR - Corea 116
AR - Argentina 88
CA - Canada 84
BJ - Benin 59
MX - Messico 59
ID - Indonesia 58
NL - Olanda 56
PL - Polonia 55
AT - Austria 54
BD - Bangladesh 52
CZ - Repubblica Ceca 47
IQ - Iraq 43
JP - Giappone 43
ZA - Sudafrica 41
TR - Turchia 38
ES - Italia 35
IR - Iran 34
CO - Colombia 29
EC - Ecuador 27
BE - Belgio 23
PK - Pakistan 21
CL - Cile 20
LT - Lituania 19
PE - Perù 17
PY - Paraguay 17
EE - Estonia 14
EG - Egitto 14
EU - Europa 14
PH - Filippine 13
UZ - Uzbekistan 13
VE - Venezuela 13
MA - Marocco 12
SA - Arabia Saudita 12
AE - Emirati Arabi Uniti 9
DO - Repubblica Dominicana 9
JO - Giordania 9
DZ - Algeria 8
IL - Israele 8
TH - Thailandia 8
TN - Tunisia 8
TW - Taiwan 8
AZ - Azerbaigian 7
BO - Bolivia 7
GR - Grecia 7
MY - Malesia 7
UY - Uruguay 7
AU - Australia 6
CH - Svizzera 6
DK - Danimarca 5
JM - Giamaica 5
LV - Lettonia 5
RO - Romania 5
ET - Etiopia 4
KE - Kenya 4
LY - Libia 4
SN - Senegal 4
AL - Albania 3
BG - Bulgaria 3
BY - Bielorussia 3
HN - Honduras 3
KW - Kuwait 3
LK - Sri Lanka 3
SI - Slovenia 3
AO - Angola 2
CU - Cuba 2
HR - Croazia 2
HU - Ungheria 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LB - Libano 2
MK - Macedonia 2
NG - Nigeria 2
NP - Nepal 2
PA - Panama 2
QA - Qatar 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
XK - ???statistics.table.value.countryCode.XK??? 2
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
CI - Costa d'Avorio 1
Totale 20.607
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Città #
Dublin 1.765
Jacksonville 1.127
Hong Kong 736
Singapore 546
Dearborn 513
San Jose 445
Beijing 397
Ashburn 396
Chandler 334
Moscow 280
Wilmington 244
Ho Chi Minh City 223
Lauterbourg 212
Lawrence 206
Princeton 206
Los Angeles 187
San Mateo 156
Hanoi 132
Bremen 120
Buffalo 117
Seoul 109
Ann Arbor 101
Andover 95
Piemonte 92
Munich 86
New York 84
Novara 77
Dallas 73
São Paulo 67
Boardman 62
Orem 62
Cotonou 59
Nuremberg 55
Houston 52
Helsinki 50
Warsaw 46
Brno 44
Frankfurt am Main 42
Nanjing 40
Rome 40
Denver 38
Redondo Beach 37
Guangzhou 36
Turin 36
Chennai 35
Santa Clara 35
Tianjin 35
Düsseldorf 34
The Dalles 34
Tokyo 34
Woodbridge 34
Milan 33
Haiphong 32
Strasbourg 32
Council Bluffs 28
Hefei 28
Monmouth Junction 28
Montreal 28
Vienna 28
Brooklyn 27
Rio de Janeiro 25
Boston 24
Kunming 24
Poplar 24
Da Nang 23
Mexico City 23
Toronto 23
Hangzhou 22
Johannesburg 22
Shanghai 21
Amsterdam 20
Atlanta 20
Falkenstein 20
London 19
Norwalk 19
Brussels 18
Manchester 18
Philadelphia 17
Porto Alegre 17
Stockholm 17
Chicago 16
Dong Ket 16
Hải Dương 16
Jakarta 16
Leawood 16
Mumbai 16
Ankara 15
Turku 15
Baghdad 14
Biên Hòa 14
Curitiba 13
Nanchang 13
Vercelli 13
Brasília 12
Fairfield 12
Kocaeli 12
Phoenix 12
Quận Bình Thạnh 12
Zanjan 12
Belo Horizonte 11
Totale 11.022
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 198
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 169
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 156
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 148
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 140
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 138
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 133
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 132
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 130
Concordance, disease progression, and heritability of coeliac disease in Italian twins 129
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 129
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 127
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 127
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 126
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 126
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 125
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 125
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 124
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 124
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 123
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 121
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 120
Association of osteopontin regulatory polymorphisms with systemic sclerosis 120
A polymorphic variation in a putative regulation box of the TNFA promoter region. 119
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 119
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 118
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 117
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 117
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 117
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 114
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 114
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 114
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 111
MICA and MICB microsatellite alleles in HLA extended haplotypes 111
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 111
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 111
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 110
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 110
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 110
Extensive genetics of ALS: a population-based study in Italy. 109
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 108
Locus for severity implicates CNS resilience in progression of multiple sclerosis 107
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 107
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 107
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 107
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 107
The multistep hypothesis of ALS revisited: The role of genetic mutations 107
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 106
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 106
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 106
Overexpression of the Cytokine BAFF and Autoimmunity Risk 105
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 105
null 105
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 105
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 104
A Large twins study in coeliac disease 104
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 104
HLA alleles modulate EBV viral load in multiple sclerosis 104
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 104
Cytokine gene polymorphism in human disease: on-line databases 103
A genome screen for multiple sclerosis in Sardinian multiplex families 103
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 102
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 102
A genome screen for multiple sclerosis in Italian families 100
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 100
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 100
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 100
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)) 100
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 99
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 99
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 99
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 98
Cognitive impairment across ALS clinical stages in a population-based cohort 98
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 97
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 97
Un ampio studio di concordanza per il morbo celiaco in gemelli 96
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 95
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 94
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 94
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 94
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 94
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 93
Evaluation of TRAF6 in a large multiancestral lupus cohort 93
Variations of the perforin gene in patients with multiple sclerosis 93
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 93
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 93
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 93
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 93
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 93
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 92
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 92
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 92
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 91
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 91
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 91
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 91
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 89
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 88
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 88
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 88
Totale 10.931
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Categoria #
all - tutte 101.538
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 101.538
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021290 0 0 0 0 0 0 0 0 0 21 225 44
2021/20221.502 63 28 224 220 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
2025/20268.127 434 361 693 1.334 768 626 1.223 1.481 635 572 0 0
Totale 20.874