IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 8.488
NA - Nord America 6.983
AS - Asia 4.979
SA - Sud America 962
AF - Africa 168
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 6
AN - Antartide 1
Totale 21.604
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Nazione #
US - Stati Uniti d'America 6.785
RU - Federazione Russa 2.094
IE - Irlanda 1.766
SG - Singapore 1.516
CN - Cina 1.239
DE - Germania 1.074
SE - Svezia 862
IT - Italia 783
HK - Hong Kong 751
BR - Brasile 734
VN - Vietnam 728
UA - Ucraina 644
FI - Finlandia 393
FR - Francia 315
GB - Regno Unito 190
IN - India 153
BD - Bangladesh 117
KR - Corea 117
CA - Canada 96
AR - Argentina 88
MX - Messico 63
BJ - Benin 59
NL - Olanda 59
ID - Indonesia 58
PL - Polonia 55
AT - Austria 54
CZ - Repubblica Ceca 47
JP - Giappone 45
IQ - Iraq 43
ZA - Sudafrica 41
TR - Turchia 38
ES - Italia 37
IR - Iran 34
CO - Colombia 29
EC - Ecuador 28
BE - Belgio 24
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
JM - Giamaica 11
AE - Emirati Arabi Uniti 9
DO - Repubblica Dominicana 9
JO - Giordania 9
MY - Malesia 9
CH - Svizzera 8
DZ - Algeria 8
IL - Israele 8
TH - Thailandia 8
TN - Tunisia 8
TW - Taiwan 8
AZ - Azerbaigian 7
BO - Bolivia 7
GR - Grecia 7
LV - Lettonia 7
UY - Uruguay 7
AU - Australia 6
DK - Danimarca 5
RO - Romania 5
ET - Etiopia 4
HN - Honduras 4
KE - Kenya 4
LY - Libia 4
SN - Senegal 4
AL - Albania 3
BG - Bulgaria 3
BY - Bielorussia 3
CR - Costa Rica 3
KW - Kuwait 3
LK - Sri Lanka 3
NP - Nepal 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
MD - Moldavia 2
MK - Macedonia 2
NG - Nigeria 2
PA - Panama 2
QA - Qatar 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
XK - ???statistics.table.value.countryCode.XK??? 2
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
Totale 21.584
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Città #
Dublin 1.765
Jacksonville 1.129
Hong Kong 744
San Jose 672
Singapore 551
Dearborn 513
Ashburn 413
Beijing 401
Chandler 334
Moscow 281
Wilmington 246
Los Angeles 224
Ho Chi Minh City 223
Lauterbourg 212
Lawrence 206
Princeton 206
San Mateo 156
Council Bluffs 149
Hanoi 132
Buffalo 123
Bremen 120
Seoul 109
Ann Arbor 101
New York 101
Andover 95
Piemonte 92
Munich 86
Dallas 85
Novara 85
São Paulo 67
Orem 66
Boardman 62
Cotonou 59
Santa Clara 56
Nuremberg 55
Houston 53
Helsinki 50
Milan 49
Warsaw 46
Rome 45
Brno 44
Denver 43
Frankfurt am Main 42
Nanjing 40
Turin 39
Guangzhou 37
Redondo Beach 37
Chennai 35
Tianjin 35
Düsseldorf 34
The Dalles 34
Tokyo 34
Woodbridge 34
Haiphong 33
Strasbourg 32
Montreal 29
Brooklyn 28
Hefei 28
Monmouth Junction 28
Vienna 28
Mexico City 27
Hangzhou 26
Rio de Janeiro 25
Boston 24
Kunming 24
Poplar 24
Toronto 24
Da Nang 23
Atlanta 22
Columbus 22
Johannesburg 22
Chicago 21
Shanghai 21
Amsterdam 20
Falkenstein 20
London 20
Norwalk 19
Philadelphia 19
Brussels 18
Manchester 18
Porto Alegre 17
Stockholm 17
Tornaco 17
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
Totale 11.583
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 210
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 178
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 161
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 158
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 141
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 141
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 141
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 139
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 139
Concordance, disease progression, and heritability of coeliac disease in Italian twins 136
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 133
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 131
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 131
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 130
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 130
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 129
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 128
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 128
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 126
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 124
Locus for severity implicates CNS resilience in progression of multiple sclerosis 123
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 123
Association of osteopontin regulatory polymorphisms with systemic sclerosis 123
A polymorphic variation in a putative regulation box of the TNFA promoter region. 122
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 122
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 122
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 121
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 120
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 118
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 118
Overexpression of the Cytokine BAFF and Autoimmunity Risk 117
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 117
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 116
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 116
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 115
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 115
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 114
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 114
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 112
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 112
Extensive genetics of ALS: a population-based study in Italy. 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 multistep hypothesis of ALS revisited: The role of genetic mutations 111
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 110
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 110
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 110
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 109
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 109
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 109
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 109
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 108
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 107
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 107
HLA alleles modulate EBV viral load in multiple sclerosis 107
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 107
A Large twins study in coeliac disease 106
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 106
Cytokine gene polymorphism in human disease: on-line databases 105
null 105
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 105
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 105
Cognitive impairment across ALS clinical stages in a population-based cohort 104
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)) 104
A genome screen for multiple sclerosis in Sardinian multiplex families 103
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 102
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 102
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 102
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 101
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 101
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 101
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 100
A genome screen for multiple sclerosis in Italian families 100
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 100
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 99
Un ampio studio di concordanza per il morbo celiaco in gemelli 99
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 99
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 99
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 98
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 98
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 97
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 96
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 96
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 96
Evaluation of TRAF6 in a large multiancestral lupus cohort 96
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 95
Variations of the perforin gene in patients with multiple sclerosis 95
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 95
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 95
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 94
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 94
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 94
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 94
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 94
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 94
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 94
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 93
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 93
SLE candidate genes in the Italian population: evidence for a significant association of IL-10 91
Totale 11.349
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Categoria #
all - tutte 109.002
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 109.002
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202144 0 0 0 0 0 0 0 0 0 0 0 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
2025/20269.118 434 361 693 1.334 768 626 1.223 1.481 635 737 624 202
Totale 21.865