IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 6.290
NA - Nord America 5.573
AS - Asia 3.547
SA - Sud America 881
AF - Africa 137
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 5
AN - Antartide 1
Totale 16.450
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Nazione #
US - Stati Uniti d'America 5.429
IE - Irlanda 1.760
SG - Singapore 1.208
DE - Germania 1.035
SE - Svezia 862
HK - Hong Kong 712
CN - Cina 697
BR - Brasile 695
UA - Ucraina 639
IT - Italia 630
RU - Federazione Russa 429
VN - Vietnam 426
FI - Finlandia 389
GB - Regno Unito 154
IN - India 111
KR - Corea 109
FR - Francia 85
CA - Canada 78
AR - Argentina 69
BJ - Benin 59
ID - Indonesia 54
AT - Austria 52
CZ - Repubblica Ceca 47
NL - Olanda 47
MX - Messico 44
PL - Polonia 44
BD - Bangladesh 42
IR - Iran 34
ZA - Sudafrica 34
JP - Giappone 30
TR - Turchia 29
ES - Italia 28
EC - Ecuador 26
IQ - Iraq 25
BE - Belgio 23
CO - Colombia 22
CL - Cile 17
LT - Lituania 17
PE - Perù 16
EU - Europa 14
PY - Paraguay 14
EE - Estonia 13
EG - Egitto 13
PK - Pakistan 12
MA - Marocco 11
VE - Venezuela 10
DO - Repubblica Dominicana 8
IL - Israele 8
UZ - Uzbekistan 8
GR - Grecia 7
AE - Emirati Arabi Uniti 6
AZ - Azerbaigian 6
JO - Giordania 6
SA - Arabia Saudita 6
UY - Uruguay 6
AU - Australia 5
DK - Danimarca 5
BO - Bolivia 4
JM - Giamaica 4
TN - Tunisia 4
CH - Svizzera 3
ET - Etiopia 3
KE - Kenya 3
KW - Kuwait 3
MY - Malesia 3
RO - Romania 3
AL - Albania 2
BY - Bielorussia 2
CU - Cuba 2
HN - Honduras 2
HR - Croazia 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LV - Lettonia 2
LY - Libia 2
NG - Nigeria 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
CR - Costa Rica 1
DZ - Algeria 1
GA - Gabon 1
GD - Grenada 1
GY - Guiana 1
HU - Ungheria 1
KZ - Kazakistan 1
LB - Libano 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
NI - Nicaragua 1
NP - Nepal 1
Totale 16.443
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Città #
Dublin 1.760
Jacksonville 1.126
Hong Kong 709
Dearborn 513
Singapore 431
Beijing 386
Chandler 334
Ashburn 275
Wilmington 244
Lawrence 206
Princeton 206
Los Angeles 183
Moscow 170
San Mateo 156
Ho Chi Minh City 145
Bremen 120
Buffalo 113
Seoul 108
Ann Arbor 101
Andover 95
Piemonte 92
Munich 85
Hanoi 78
Novara 76
New York 74
Dallas 65
São Paulo 65
Boardman 62
Cotonou 59
Nuremberg 50
Houston 49
Helsinki 47
Brno 44
Denver 38
Redondo Beach 37
Warsaw 36
Rome 35
Düsseldorf 34
Nanjing 34
Woodbridge 34
Strasbourg 32
Frankfurt am Main 30
Milan 29
Monmouth Junction 28
Turin 28
Brooklyn 27
Hefei 27
Montreal 27
Santa Clara 27
Vienna 27
Tianjin 25
Tokyo 25
Boston 24
Kunming 23
Orem 23
Rio de Janeiro 23
Chennai 22
Poplar 22
Toronto 21
Haiphong 19
Norwalk 19
Atlanta 18
Brussels 18
Johannesburg 18
Philadelphia 17
Stockholm 17
The Dalles 17
Dong Ket 16
Jakarta 16
Leawood 16
Mexico City 16
Porto Alegre 16
Chicago 15
Turku 15
Amsterdam 14
Ankara 14
Guangzhou 13
London 13
Vercelli 13
Brasília 12
Curitiba 12
Fairfield 12
Kocaeli 12
Manchester 12
Nanchang 12
Phoenix 12
Zanjan 12
Mülheim 11
Ribeirão Preto 11
Belo Horizonte 10
Biên Hòa 10
Campinas 10
Da Nang 10
Lima 10
Mumbai 10
Quito 10
Quận Bình Thạnh 10
Seattle 10
Borgomanero 9
Cologne 9
Totale 9.511
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 159
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 144
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 134
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 121
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 118
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 117
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 111
Concordance, disease progression, and heritability of coeliac disease in Italian twins 111
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 111
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 110
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 109
A polymorphic variation in a putative regulation box of the TNFA promoter region. 108
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 108
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 107
null 105
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 104
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 104
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 103
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 103
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 103
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 101
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 100
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 100
Association of osteopontin regulatory polymorphisms with systemic sclerosis 100
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 98
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 98
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 98
Extensive genetics of ALS: a population-based study in Italy. 97
MICA and MICB microsatellite alleles in HLA extended haplotypes 96
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 95
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 94
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 94
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 94
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 94
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 93
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 92
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 92
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 92
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 92
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 91
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 91
A genome screen for multiple sclerosis in Sardinian multiplex families 89
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 89
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 89
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 89
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 89
The multistep hypothesis of ALS revisited: The role of genetic mutations 88
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 88
Un ampio studio di concordanza per il morbo celiaco in gemelli 86
Overexpression of the Cytokine BAFF and Autoimmunity Risk 86
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 86
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 85
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 85
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 85
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 85
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 85
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 84
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 84
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 84
Cytokine gene polymorphism in human disease: on-line databases 83
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 83
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 83
HLA alleles modulate EBV viral load in multiple sclerosis 83
Cognitive impairment across ALS clinical stages in a population-based cohort 83
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 82
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 82
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)) 82
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 81
A genome screen for multiple sclerosis in Italian families 81
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 81
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 81
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 80
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 80
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 80
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 79
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 78
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 78
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 78
ACTIVATED HUMAN T-CELLS EXPRESS BETA-2-MICROGLOBULIN-ASSOCIATED HLA-A,B,C MOLECULES NOT RECOGNIZED BY W6/32 MAB 77
A Large twins study in coeliac disease 77
Locus for severity implicates CNS resilience in progression of multiple sclerosis 76
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 76
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 76
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 76
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 76
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 75
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 74
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 74
CHARACTERIZATION OF 4 MURINE MONOCLONAL-ANTIBODIES RECOGNIZING RESPECTIVELY HLA-A2 PLUS AW69, HLA-B13, HLA-BW4 AND HLA-A28 74
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes. 74
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 74
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 74
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 73
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 73
Serum neurofilament light chain levels are increased in patients with a clinically isolated syndrome. 73
Altered biosynthesis of tumour necrosis factor (TNF) alpha is involved in postburn hypertrophic scars. 72
Evaluation of TRAF6 in a large multiancestral lupus cohort 72
The impact of osteopontin gene variations on multiple sclerosis development and progression 72
HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe 72
Genetic burden of common variants in progressive and bout-onset multiple sclerosis. 72
Totale 9.018
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Categoria #
all - tutte 94.388
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 94.388
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021746 0 0 0 0 0 17 207 16 216 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
2025/20263.954 434 361 693 1.334 768 364 0 0 0 0 0 0
Totale 16.701