IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 6.275
NA - Nord America 5.490
AS - Asia 3.411
SA - Sud America 861
AF - Africa 126
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 5
AN - Antartide 1
Totale 16.185
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Nazione #
US - Stati Uniti d'America 5.355
IE - Irlanda 1.760
SG - Singapore 1.175
DE - Germania 1.033
SE - Svezia 861
HK - Hong Kong 712
BR - Brasile 680
CN - Cina 680
UA - Ucraina 638
IT - Italia 630
RU - Federazione Russa 429
FI - Finlandia 389
VN - Vietnam 376
GB - Regno Unito 151
KR - Corea 109
IN - India 108
FR - Francia 85
CA - Canada 74
AR - Argentina 67
BJ - Benin 59
ID - Indonesia 54
AT - Austria 50
CZ - Repubblica Ceca 47
NL - Olanda 46
PL - Polonia 42
MX - Messico 41
BD - Bangladesh 35
IR - Iran 33
JP - Giappone 30
ZA - Sudafrica 30
TR - Turchia 28
ES - Italia 27
EC - Ecuador 26
BE - Belgio 22
CO - Colombia 21
IQ - Iraq 18
CL - Cile 17
LT - Lituania 17
PE - Perù 15
EU - Europa 14
PY - Paraguay 14
EE - Estonia 13
EG - Egitto 12
MA - Marocco 10
VE - Venezuela 10
PK - Pakistan 9
DO - Repubblica Dominicana 8
IL - Israele 8
GR - Grecia 7
UY - Uruguay 6
AE - Emirati Arabi Uniti 5
AU - Australia 5
AZ - Azerbaigian 5
DK - Danimarca 5
SA - Arabia Saudita 5
UZ - Uzbekistan 5
TN - Tunisia 4
BO - Bolivia 3
CH - Svizzera 3
ET - Etiopia 3
JO - Giordania 3
KW - Kuwait 3
RO - Romania 3
AL - Albania 2
CU - Cuba 2
HN - Honduras 2
HR - Croazia 2
JM - Giamaica 2
LK - Sri Lanka 2
LV - Lettonia 2
LY - Libia 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
AQ - Antartide 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
BY - Bielorussia 1
CR - Costa Rica 1
DZ - Algeria 1
GD - Grenada 1
GY - Guiana 1
HU - Ungheria 1
KE - Kenya 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
MY - Malesia 1
NG - Nigeria 1
NI - Nicaragua 1
NP - Nepal 1
PA - Panama 1
PH - Filippine 1
PR - Porto Rico 1
QA - Qatar 1
Totale 16.182
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Città #
Dublin 1.760
Jacksonville 1.126
Hong Kong 709
Dearborn 513
Singapore 401
Beijing 386
Chandler 334
Ashburn 260
Wilmington 244
Lawrence 206
Princeton 206
Los Angeles 177
Moscow 170
San Mateo 156
Ho Chi Minh City 128
Bremen 120
Buffalo 113
Seoul 108
Ann Arbor 101
Andover 95
Piemonte 92
Munich 85
Novara 76
Hanoi 66
New York 66
Dallas 65
Boardman 62
São Paulo 61
Cotonou 59
Nuremberg 49
Houston 48
Helsinki 47
Brno 44
Redondo Beach 37
Rome 35
Düsseldorf 34
Nanjing 34
Warsaw 34
Woodbridge 34
Strasbourg 32
Denver 31
Frankfurt am Main 30
Milan 29
Monmouth Junction 28
Turin 28
Hefei 27
Santa Clara 26
Tokyo 25
Vienna 25
Kunming 23
Montreal 23
Boston 22
Brooklyn 22
Rio de Janeiro 22
Chennai 21
Toronto 21
Norwalk 19
Poplar 19
Atlanta 18
Brussels 17
Orem 17
Philadelphia 17
Tianjin 17
Dong Ket 16
Haiphong 16
Jakarta 16
Leawood 16
Mexico City 16
Porto Alegre 16
Stockholm 16
Turku 15
Chicago 14
Johannesburg 14
Amsterdam 13
Ankara 13
London 13
Vercelli 13
Brasília 12
Fairfield 12
Guangzhou 12
Kocaeli 12
Manchester 12
Nanchang 12
Phoenix 12
Zanjan 12
Curitiba 11
Mülheim 11
Ribeirão Preto 11
Belo Horizonte 10
Biên Hòa 10
Campinas 10
Lima 10
Mumbai 10
Quito 10
Quận Bình Thạnh 10
Seattle 10
The Dalles 10
Borgomanero 9
Cologne 9
Da Nang 9
Totale 9.353
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 155
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 143
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 132
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 119
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 116
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 116
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 110
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 109
Concordance, disease progression, and heritability of coeliac disease in Italian twins 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 107
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 107
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 107
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 106
null 105
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 102
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 102
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 101
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 101
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 101
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 99
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 99
Association of osteopontin regulatory polymorphisms with systemic sclerosis 98
Extensive genetics of ALS: a population-based study in Italy. 97
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 96
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 96
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 96
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 95
MICA and MICB microsatellite alleles in HLA extended haplotypes 94
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 94
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 93
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 92
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 92
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 92
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 92
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 92
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 90
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 90
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 89
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 88
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 88
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 88
A genome screen for multiple sclerosis in Sardinian multiplex families 87
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 87
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 87
Overexpression of the Cytokine BAFF and Autoimmunity Risk 86
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 86
The multistep hypothesis of ALS revisited: The role of genetic mutations 86
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 86
Un ampio studio di concordanza per il morbo celiaco in gemelli 85
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 85
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 84
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 84
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 84
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 84
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 83
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 83
Cytokine gene polymorphism in human disease: on-line databases 82
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 82
HLA alleles modulate EBV viral load in multiple sclerosis 82
[Viral genotype and HLA class II alleles influence on extra-hepatic manifestations of chronic HCV infection] 82
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 82
Cognitive impairment across ALS clinical stages in a population-based cohort 82
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 82
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 81
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 81
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)) 81
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 80
A genome screen for multiple sclerosis in Italian families 80
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 80
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 80
The impact of lifetime alcohol and cigarette smoking loads on multiple sclerosis severity 79
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 79
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 78
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 78
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 78
ACTIVATED HUMAN T-CELLS EXPRESS BETA-2-MICROGLOBULIN-ASSOCIATED HLA-A,B,C MOLECULES NOT RECOGNIZED BY W6/32 MAB 77
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 77
A Large twins study in coeliac disease 76
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 76
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 76
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 75
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 75
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. 75
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 75
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
Locus for severity implicates CNS resilience in progression of multiple sclerosis 73
CHARACTERIZATION OF 4 MURINE MONOCLONAL-ANTIBODIES RECOGNIZING RESPECTIVELY HLA-A2 PLUS AW69, HLA-B13, HLA-BW4 AND HLA-A28 73
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes. 73
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 72
Altered biosynthesis of tumour necrosis factor (TNF) alpha is involved in postburn hypertrophic scars. 72
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 72
Evaluation of TRAF6 in a large multiancestral lupus cohort 72
The impact of osteopontin gene variations on multiple sclerosis development and progression 72
Genetic burden of common variants in progressive and bout-onset multiple sclerosis. 72
Serum neurofilament light chain levels are increased in patients with a clinically isolated syndrome. 72
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 71
Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus 71
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 71
Totale 8.878
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Categoria #
all - tutte 93.282
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 93.282
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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
2025/20263.689 434 361 693 1.334 768 99 0 0 0 0 0 0
Totale 16.436