IRIS
D'ALFONSO, Sandra
 Distribuzione geografica
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Continente #
EU - Europa 5.029
NA - Nord America 4.018
AS - Asia 801
Continente sconosciuto - Info sul continente non disponibili 14
AF - Africa 7
SA - Sud America 5
OC - Oceania 1
Totale 9.875
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Nazione #
US - Stati Uniti d'America 3.996
IE - Irlanda 1.757
SE - Svezia 843
DE - Germania 830
UA - Ucraina 598
IT - Italia 438
FI - Finlandia 338
CN - Cina 333
HK - Hong Kong 175
SG - Singapore 162
GB - Regno Unito 77
IN - India 66
CZ - Repubblica Ceca 46
FR - Francia 40
IR - Iran 30
NL - Olanda 25
CA - Canada 20
BE - Belgio 19
VN - Vietnam 16
TR - Turchia 15
EU - Europa 14
RU - Federazione Russa 7
GR - Grecia 5
MA - Marocco 3
CH - Svizzera 2
CL - Cile 2
CO - Colombia 2
CU - Cuba 2
IL - Israele 2
LY - Libia 2
AU - Australia 1
BR - Brasile 1
EG - Egitto 1
JP - Giappone 1
KR - Corea 1
MK - Macedonia 1
NG - Nigeria 1
PL - Polonia 1
RO - Romania 1
RS - Serbia 1
Totale 9.875
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Città #
Dublin 1.757
Jacksonville 1.126
Dearborn 513
Chandler 334
Wilmington 243
Lawrence 206
Princeton 206
Hong Kong 174
Beijing 169
San Mateo 156
Bremen 120
Ann Arbor 101
Andover 95
Piemonte 92
Singapore 89
Ashburn 63
Boardman 61
Brno 44
Houston 35
Düsseldorf 34
Woodbridge 34
Strasbourg 32
Nanjing 31
Monmouth Junction 28
Hefei 27
Turin 25
Kunming 23
Milan 22
Norwalk 19
Helsinki 18
Munich 18
Novara 18
Philadelphia 17
Dong Ket 16
Leawood 16
Brussels 14
Fairfield 12
Guangzhou 12
Kocaeli 12
Nanchang 12
Zanjan 12
Mülheim 11
Toronto 11
Cologne 9
Rome 9
Ardabil 8
Borgomanero 7
Dallas 7
Frankfurt am Main 7
Jinan 7
Royal Leamington Spa 7
Trieste 7
Vercelli 7
Grafing 6
Sacramento 6
Seattle 6
Torino 6
Winnipeg 6
Mumbai 5
San Diego 5
Shenyang 5
Waanrode 5
Alessandria 4
Cambridge 4
Chennai 4
Concordia sulla Secchia 4
Dronten 4
Ningbo 4
Shaoxing 4
Augusta 3
Baotou 3
Bologna 3
Carate Brianza 3
Castelnuovo Bormida 3
Falls Church 3
Lissone 3
Mohammedia 3
Tehran 3
Tortona 3
Wuhan 3
Zhengzhou 3
Albuzzano 2
Amsterdam 2
Auburn Hills 2
Benghazi 2
Brindisi 2
Caltignaga 2
Cassano Magnago 2
Changsha 2
Chengdu 2
Cureggio 2
Delft 2
Des Moines 2
Deventer 2
Fuzhou 2
Gunzenhausen 2
Havana 2
Hebei 2
Jiaxing 2
Kolín 2
Totale 6.285
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Nome #
Dissecting the Mechanism of Action of Spiperone— A Candidate for Drug Repurposing for Colorectal Cancer 95
HLA class I in Acute Promyelocytic Leukemia (APL): possible correlation with clinical outcome 86
A polymorphic variation in a putative regulation box of the TNFA promoter region. 83
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 82
Extensive genetics of ALS: a population-based study in Italy. 81
Liver infection and COVID-19: the electron microscopy proof and revision of the literature 80
. Linkage disequilibrium between intra-locus variants in the Aminopeptidase N gene and test of their association with coeliac disease 78
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 78
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 78
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 73
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 69
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 68
Quantitative expression of HLA class I molecules in acute non-lymphoblastic leukaemia cells. 67
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 67
A case of late-onset OCD developing PLS and FTD 67
Cytokine gene polymorphism in human disease: on-line databases 66
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 66
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 65
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 65
IEF ANALYSIS OF HLA MOLECULES IMMUNOPRECIPITATED BY PUTATIVE ANTICLASS-I-LIKE ALLOANTISERA 64
Un ampio studio di concordanza per il morbo celiaco in gemelli 64
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease 64
ALTERED EXPRESSION OF HLA-A,B SPECIFICITIES ON ACUTE LYMPHOID AND MYELOID-LEUKEMIA BLASTS 63
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function 63
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 62
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 62
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 62
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 62
Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5' regulatory region 61
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 61
Altered biosynthesis of tumour necrosis factor (TNF) alpha is involved in postburn hypertrophic scars. 60
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population. J. Neuroimmunology, 143: 97-100, 2003 60
CHARACTERIZATION OF 4 MURINE MONOCLONAL-ANTIBODIES RECOGNIZING RESPECTIVELY HLA-A2 PLUS AW69, HLA-B13, HLA-BW4 AND HLA-A28 59
Association of PPP2CA polymorphisms with systemic lupus erythematosus susceptibility in multiple ethnic groups. 59
Concordance, disease progression, and heritability of coeliac disease in Italian twins 59
A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86. 58
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 58
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 58
The multistep hypothesis of ALS revisited: The role of genetic mutations 58
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 57
HLA alleles modulate EBV viral load in multiple sclerosis 57
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 57
ATXN-2 CAG repeat expansions are interrupted in ALS patients 57
Association between polymorphisms in the TNF region and Systemic Lupus Erythematosus in the Italian population 56
A genome screen for multiple sclerosis in Sardinian multiplex families 56
Cytokine gene polymorphism in human disease: on-line databases, supplement 1 56
Evaluation of TRAF6 in a large multiancestral lupus cohort 56
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 56
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes. 55
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 55
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 55
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 55
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression 55
Cytokine gene polymorphism in human disease: on-line databases, supplement 2 54
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 54
Frequencies of HLA class II alleles in Piedmont (northern Italy). 53
Association study of IRAK-M and SIGIRR genes with SLE in a large European-descent population. 53
Novel association of acid phosphatase locus l*C allele with systemic lupus erythematosus 53
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. 53
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 53
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 53
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies 53
Association of osteopontin regulatory polymorphisms with systemic sclerosis 53
An intragenic polymorphism in the human tumor necrosis factor alpha (TNFA) chain-encoding gene. 52
A genome screen for multiple sclerosis in Italian families 52
MICA and MICB microsatellite alleles in HLA extended haplotypes 52
Fas gene polymorphisms are not associated with Systemic Lupus Erythematosus, Multiple Sclerosis and HIV infection 52
Two single-nucleotide polymorphisms in the 5' and 3' ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus 52
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 52
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 52
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 52
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy 52
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility 52
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. 52
The natural history of an HLA haplotype and its recombinants 51
Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis 51
Overexpression of the Cytokine BAFF and Autoimmunity Risk 51
A Large twins study in coeliac disease 50
A whole genome screen for linkage disequilibrium in multiple sclerosis performed in a continental Italian population 50
ACTIVATED HUMAN T-CELLS EXPRESS BETA-2-MICROGLOBULIN-ASSOCIATED HLA-A,B,C MOLECULES NOT RECOGNIZED BY W6/32 MAB 49
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 49
The impact of osteopontin gene variations on multiple sclerosis development and progression 49
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis 49
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 49
Association study of a new polymorphism in the PECAM-1 gene in multiple sclerosis 48
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. 48
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population 48
Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study 48
Association of Systemic Lupus Erythematosus Clinical Features with European Population Genetic Substructure 48
Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus. 47
Variations of the perforin gene in patients with multiple sclerosis 47
Nonparametric linkage analysis of alcohol dependence with chromosome 1 and 7 markers. 47
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 47
Linkage analysis of Multiple Sclerosis with candidate region markers in Sardinian and Continental Italian families 47
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)) 47
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes 46
Immunoglobulin and HLA-DP genes contribute to the susceptibility to juvenile dermatitis herpetiformis. 46
HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe 46
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families 46
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 46
Totale 5.768
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Categoria #
all - tutte 53.187
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 53.187
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.955 10 1 181 3 325 323 406 96 219 142 247 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
2024/202537 37 0 0 0 0 0 0 0 0 0 0 0
Totale 10.084