IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 5.827
NA - Nord America 4.280
AS - Asia 1.699
SA - Sud America 22
AF - Africa 16
Continente sconosciuto - Info sul continente non disponibili 14
OC - Oceania 3
Totale 11.861
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Nazione #
US - Stati Uniti d'America 4.243
IE - Irlanda 1.759
DE - Germania 948
SE - Svezia 843
UA - Ucraina 627
HK - Hong Kong 609
SG - Singapore 576
IT - Italia 564
RU - Federazione Russa 413
FI - Finlandia 372
CN - Cina 341
GB - Regno Unito 82
IN - India 66
CZ - Repubblica Ceca 47
FR - Francia 42
NL - Olanda 39
CA - Canada 33
AT - Austria 31
IR - Iran 30
ID - Indonesia 25
BE - Belgio 22
VN - Vietnam 19
TR - Turchia 16
EU - Europa 14
EE - Estonia 13
BR - Brasile 10
CL - Cile 9
GR - Grecia 6
EG - Egitto 5
LT - Lituania 5
MA - Marocco 4
ZA - Sudafrica 4
AU - Australia 3
CH - Svizzera 3
IL - Israele 3
PK - Pakistan 3
AE - Emirati Arabi Uniti 2
CO - Colombia 2
CU - Cuba 2
ES - Italia 2
LK - Sri Lanka 2
LY - Libia 2
SK - Slovacchia (Repubblica Slovacca) 2
AZ - Azerbaigian 1
BY - Bielorussia 1
HR - Croazia 1
IQ - Iraq 1
JP - Giappone 1
KG - Kirghizistan 1
KR - Corea 1
LU - Lussemburgo 1
MK - Macedonia 1
NG - Nigeria 1
PA - Panama 1
PH - Filippine 1
PL - Polonia 1
PR - Porto Rico 1
RO - Romania 1
RS - Serbia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 11.861
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Città #
Dublin 1.759
Jacksonville 1.126
Hong Kong 606
Dearborn 513
Chandler 334
Wilmington 243
Singapore 217
Lawrence 206
Princeton 206
Beijing 170
Moscow 165
San Mateo 156
Bremen 120
Ann Arbor 101
Andover 95
Piemonte 92
Novara 75
Ashburn 67
Boardman 62
Helsinki 45
Brno 44
Nuremberg 36
Houston 35
Düsseldorf 34
Munich 34
Woodbridge 34
Strasbourg 32
Nanjing 31
Monmouth Junction 28
Hefei 27
Milan 26
Turin 26
Dallas 23
Kunming 23
Norwalk 19
Toronto 18
Brussels 17
Philadelphia 17
Vienna 17
Dong Ket 16
Leawood 16
Frankfurt am Main 13
Santa Clara 13
Fairfield 12
Guangzhou 12
Jakarta 12
Kocaeli 12
Nanchang 12
Zanjan 12
Mülheim 11
Rome 11
Vercelli 11
Borgomanero 9
Cologne 9
Falkenstein 9
Ardabil 8
Ottawa 8
Amsterdam 7
Genoa 7
Jinan 7
Los Angeles 7
Royal Leamington Spa 7
Trieste 7
Alessandria 6
Espoo 6
Grafing 6
Sacramento 6
Santiago 6
Seattle 6
Torino 6
Winnipeg 6
Goioerê 5
Mumbai 5
San Diego 5
Shenyang 5
Waanrode 5
Cambridge 4
Carate Brianza 4
Chennai 4
Concordia sulla Secchia 4
Dronten 4
Ningbo 4
Pisa 4
Shaoxing 4
Augusta 3
Baotou 3
Bologna 3
Castelnuovo Bormida 3
Charleston 3
Falls Church 3
Lissone 3
Mohammedia 3
Sermoneta 3
Tehran 3
Tel Aviv 3
Tortona 3
Wuhan 3
Zhengzhou 3
Albuzzano 2
Auburn Hills 2
Totale 7.278
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Nome #
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 118
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 109
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 95
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 94
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 92
A polymorphic variation in a putative regulation box of the TNFA promoter region. 91
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 87
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 87
Extensive genetics of ALS: a population-based study in Italy. 86
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 86
A case of late-onset OCD developing PLS and FTD 80
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 79
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 78
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 77
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 76
Un ampio studio di concordanza per il morbo celiaco in gemelli 75
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 74
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 74
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 73
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 73
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 72
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 71
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 71
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 71
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 70
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 70
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 70
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 70
Cytokine gene polymorphism in human disease: on-line databases 69
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 69
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 68
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 68
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 68
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 68
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 67
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 67
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 66
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 66
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 66
The multistep hypothesis of ALS revisited: The role of genetic mutations 66
Altered biosynthesis of tumour necrosis factor (TNF) alpha is involved in postburn hypertrophic scars. 65
A genome screen for multiple sclerosis in Sardinian multiplex families 65
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 65
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 65
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 65
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 65
CHARACTERIZATION OF 4 MURINE MONOCLONAL-ANTIBODIES RECOGNIZING RESPECTIVELY HLA-A2 PLUS AW69, HLA-B13, HLA-BW4 AND HLA-A28 64
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 64
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 64
HLA alleles modulate EBV viral load in multiple sclerosis 64
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 64
ATXN-2 CAG repeat expansions are interrupted in ALS patients 64
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 64
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 63
Concordance, disease progression, and heritability of coeliac disease in Italian twins 63
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 63
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 63
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 63
A genome screen for multiple sclerosis in Italian families 62
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. 62
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 62
Association between polymorphisms in the TNF region and Systemic Lupus Erythematosus in the Italian population 61
Evaluation of TRAF6 in a large multiancestral lupus cohort 61
Novel association of acid phosphatase locus l*C allele with systemic lupus erythematosus 61
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 61
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 61
Association of osteopontin regulatory polymorphisms with systemic sclerosis 61
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 61
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 61
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 60
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 60
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 60
Frequencies of HLA class II alleles in Piedmont (northern Italy). 59
The natural history of an HLA haplotype and its recombinants 59
Association study of IRAK-M and SIGIRR genes with SLE in a large European-descent population. 59
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 59
Vitamin D Supplementation modulates ICOS+ and ICOS- regulatory T cell in siblings of Children with Type 1 Diabetes 59
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes. 58
Two single-nucleotide polymorphisms in the 5' and 3' ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus 58
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 58
Overexpression of the Cytokine BAFF and Autoimmunity Risk 58
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 58
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 58
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 58
Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus. 57
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 57
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 57
An intragenic polymorphism in the human tumor necrosis factor alpha (TNFA) chain-encoding gene. 56
MICA and MICB microsatellite alleles in HLA extended haplotypes 56
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)) 56
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 56
Immunoglobulin and HLA-DP genes contribute to the susceptibility to juvenile dermatitis herpetiformis. 55
ACTIVATED HUMAN T-CELLS EXPRESS BETA-2-MICROGLOBULIN-ASSOCIATED HLA-A,B,C MOLECULES NOT RECOGNIZED BY W6/32 MAB 55
A Large twins study in coeliac disease 55
Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein. 55
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 55
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 55
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 55
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 55
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 55
Totale 6.675
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Categoria #
all - tutte 72.794
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 72.794
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020391 0 0 0 0 0 0 0 0 0 142 247 2
2020/20211.324 199 2 199 5 173 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
2024/20252.056 51 46 143 87 45 240 244 236 710 254 0 0
Totale 12.103