IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 8.547
NA - Nord America 7.928
AS - Asia 5.053
SA - Sud America 971
Continente sconosciuto - Info sul continente non disponibili 279
AF - Africa 169
OC - Oceania 6
AN - Antartide 1
Totale 22.954
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Nazione #
US - Stati Uniti d'America 7.702
RU - Federazione Russa 2.094
IE - Irlanda 1.767
SG - Singapore 1.531
CN - Cina 1.249
DE - Germania 1.074
SE - Svezia 862
IT - Italia 830
HK - Hong Kong 766
BR - Brasile 740
VN - Vietnam 729
UA - Ucraina 645
FI - Finlandia 393
FR - Francia 316
GB - Regno Unito 191
IN - India 153
BD - Bangladesh 145
KR - Corea 119
CA - Canada 106
AR - Argentina 88
MX - Messico 64
BJ - Benin 59
ID - Indonesia 59
NL - Olanda 59
PL - Polonia 56
AT - Austria 54
CZ - Repubblica Ceca 47
JP - Giappone 45
IQ - Iraq 43
ZA - Sudafrica 41
TR - Turchia 39
ES - Italia 38
IR - Iran 34
CO - Colombia 30
EC - Ecuador 30
BE - Belgio 24
PK - Pakistan 21
CL - Cile 20
JM - Giamaica 19
LT - Lituania 19
PE - Perù 17
PY - Paraguay 17
EE - Estonia 14
EG - Egitto 14
EU - Europa 14
PH - Filippine 14
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
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
CR - Costa Rica 7
GR - Grecia 7
LV - Lettonia 7
UY - Uruguay 7
AU - Australia 6
RO - Romania 6
DK - Danimarca 5
HN - Honduras 5
KE - Kenya 5
ET - Etiopia 4
LY - Libia 4
SN - Senegal 4
AL - Albania 3
BG - Bulgaria 3
BY - Bielorussia 3
HU - Ungheria 3
KW - Kuwait 3
LK - Sri Lanka 3
MK - Macedonia 3
NP - Nepal 3
RS - Serbia 3
SI - Slovenia 3
TT - Trinidad e Tobago 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
NG - Nigeria 2
NI - Nicaragua 2
PA - Panama 2
PR - Porto Rico 2
PT - Portogallo 2
QA - Qatar 2
SK - Slovacchia (Repubblica Slovacca) 2
Totale 22.669
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Città #
Dublin 1.765
Jacksonville 1.129
Hong Kong 759
San Jose 707
Singapore 561
Dearborn 513
Council Bluffs 475
Ashburn 449
Beijing 405
Chandler 334
Moscow 281
Wilmington 246
Los Angeles 233
Ho Chi Minh City 223
Lauterbourg 212
Columbus 210
Princeton 207
Lawrence 206
San Mateo 156
Hanoi 132
Buffalo 127
Bremen 120
Seoul 110
New York 105
Ann Arbor 101
Andover 95
Dallas 92
Novara 92
Piemonte 92
Munich 86
Santa Clara 73
São Paulo 69
Orem 66
Boardman 62
Cotonou 59
Houston 57
Nuremberg 55
Milan 54
Helsinki 50
Rome 47
Warsaw 46
Denver 45
Brno 44
Frankfurt am Main 42
Nanjing 40
Turin 40
Guangzhou 37
Redondo Beach 37
Chennai 35
Tianjin 35
Düsseldorf 34
The Dalles 34
Tokyo 34
Woodbridge 34
Brooklyn 33
Haiphong 33
Philadelphia 32
Strasbourg 32
Chicago 30
Montreal 30
Hefei 28
Mexico City 28
Monmouth Junction 28
Vienna 28
Atlanta 26
Hangzhou 26
Boston 25
Rio de Janeiro 25
Toronto 25
Kunming 24
Poplar 24
Da Nang 23
Shanghai 23
Johannesburg 22
Amsterdam 20
Falkenstein 20
London 20
Norwalk 20
Phoenix 20
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
Las Vegas 14
Curitiba 13
Nanchang 13
Vercelli 13
Brasília 12
Fairfield 12
Kocaeli 12
Totale 12.311
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 243
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 184
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 176
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 168
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 161
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 149
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 146
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 145
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 144
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 143
Concordance, disease progression, and heritability of coeliac disease in Italian twins 142
Locus for severity implicates CNS resilience in progression of multiple sclerosis 138
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 136
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 135
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 134
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 134
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 133
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 133
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 133
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 131
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 130
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 130
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 130
Association of osteopontin regulatory polymorphisms with systemic sclerosis 128
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 128
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 125
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 125
A polymorphic variation in a putative regulation box of the TNFA promoter region. 124
Overexpression of the Cytokine BAFF and Autoimmunity Risk 124
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 124
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 123
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 123
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 122
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 120
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 120
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 119
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 118
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 117
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 117
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 117
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 117
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 116
MICA and MICB microsatellite alleles in HLA extended haplotypes 115
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 114
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 114
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 114
The multistep hypothesis of ALS revisited: The role of genetic mutations 114
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 114
Extensive genetics of ALS: a population-based study in Italy. 113
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 112
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 112
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 112
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 111
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 111
A Large twins study in coeliac disease 110
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 110
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 109
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 109
Cytokine gene polymorphism in human disease: on-line databases 108
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 108
HLA alleles modulate EBV viral load in multiple sclerosis 108
Cognitive impairment across ALS clinical stages in a population-based cohort 108
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)) 108
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 107
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 107
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 107
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 107
A genome screen for multiple sclerosis in Sardinian multiplex families 106
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 106
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 105
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 105
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 105
null 105
Variations of the perforin gene in patients with multiple sclerosis 104
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 104
A genome screen for multiple sclerosis in Italian families 103
Un ampio studio di concordanza per il morbo celiaco in gemelli 103
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 102
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 102
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 102
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 102
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 101
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 101
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 99
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 99
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 99
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 99
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 98
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 98
Evaluation of TRAF6 in a large multiancestral lupus cohort 98
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 98
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 98
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 98
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 97
SLE candidate genes in the Italian population: evidence for a significant association of IL-10 97
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 96
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 96
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 96
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 96
BRAT1 Mutation Retrospective Diagnosis: A Case Report 95
Totale 11.780
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Categoria #
all - tutte 115.344
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 115.344
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.439 0 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
2025/20269.140 434 361 693 1.334 768 626 1.223 1.481 635 737 624 224
2026/20271.067 458 609 0 0 0 0 0 0 0 0 0 0
Totale 22.954