IRIS
BARIZZONE, NADIA
 Distribuzione geografica
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Continente #
EU - Europa 1.323
NA - Nord America 878
AS - Asia 218
Continente sconosciuto - Info sul continente non disponibili 6
AF - Africa 3
SA - Sud America 1
Totale 2.429
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Nazione #
US - Stati Uniti d'America 867
IE - Irlanda 454
SE - Svezia 246
DE - Germania 207
IT - Italia 165
UA - Ucraina 134
CN - Cina 92
FI - Finlandia 60
SG - Singapore 49
HK - Hong Kong 48
CZ - Repubblica Ceca 19
FR - Francia 16
IN - India 13
CA - Canada 11
GB - Regno Unito 7
IR - Iran 7
NL - Olanda 7
EU - Europa 6
VN - Vietnam 6
RU - Federazione Russa 4
MA - Marocco 3
TR - Turchia 3
GR - Grecia 2
BE - Belgio 1
BR - Brasile 1
RO - Romania 1
Totale 2.429
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Città #
Dublin 454
Jacksonville 262
Dearborn 122
Lawrence 53
Princeton 53
Wilmington 49
Hong Kong 48
Piemonte 46
Beijing 42
Bremen 41
Chandler 34
Singapore 28
San Mateo 23
Brno 17
Strasbourg 14
Monmouth Junction 13
Andover 10
Düsseldorf 10
Kunming 10
Leawood 9
Milan 9
Toronto 9
Ann Arbor 8
Boardman 8
Munich 8
Cologne 7
Nanjing 7
Norwalk 7
Novara 7
Ashburn 6
Dong Ket 6
Hefei 5
Helsinki 5
Torino 5
Dronten 4
Fairfield 4
Jinan 4
Mumbai 4
Nanchang 4
Turin 4
Carate Brianza 3
Grafing 3
Guangzhou 3
Gunzenhausen 3
Houston 3
Kocaeli 3
Lissone 3
Mohammedia 3
Sacramento 3
Tehran 3
Tortona 3
Trieste 3
Albuzzano 2
Baotou 2
Brindisi 2
Cassano Magnago 2
Concordia sulla Secchia 2
Des Moines 2
Jiaxing 2
Kolín 2
Menlo Park 2
Opera 2
Partinico 2
Savona 2
Shenyang 2
Varallo 2
Vercelli 2
Winnipeg 2
Ardabil 1
Augusta 1
Bangalore 1
Berlin 1
Bollate 1
Borgomasino 1
Boston 1
Brescia 1
Brussels 1
Caltignaga 1
Cambridge 1
Cascina 1
Changsha 1
Chaoyang 1
Chelyabinsk 1
Cilavegna 1
Dallas 1
Florence 1
Fuzhou 1
Grafenhausen 1
Hebei 1
Horia 1
Ningbo 1
Quzhou 1
Redwood City 1
Rio de Janeiro 1
Rome 1
Saluzzo 1
San Diego 1
San Marco dei Cavoti 1
Stresa 1
Tomsk 1
Totale 1.559
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Nome #
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 82
Variations in the High Mobility Group-A2 Gene (HMGA2) Are Associated With Idiopathic Short Stature (ISS) 80
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 67
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 66
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
HLA alleles modulate EBV viral load in multiple sclerosis 57
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 56
Periostin Circulating Levels and Genetic Variants in Patients with Non-Alcoholic Fatty Liver Disease 54
Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB1*15-positive individuals. 53
Two single-nucleotide polymorphisms in the 5' and 3' ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus 52
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 52
Association of osteopontin regulatory polymorphisms with systemic sclerosis 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
Overexpression of the Cytokine BAFF and Autoimmunity Risk 51
The impact of osteopontin gene variations on multiple sclerosis development and progression 49
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
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk 48
Variations of the perforin gene in patients with multiple sclerosis 47
Further evidence of subphenotype association with systemic lupus erythematosus susceptibility loci: a European cases only study. 47
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. 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
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 46
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis 46
The burden of multiple sclerosis variants in continental Italians and Sardinians 46
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 46
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 46
Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility 45
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis 45
Rare variants in the TREX1 gene and susceptibility to autoimmune diseases. 44
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 44
Targeted next-generation sequencing for the identification of genetic predictors of radiation-induced late skin toxicity in breast cancer patients: A preliminary study 44
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 43
Inverse correlation of genetic risk score with age at onset in bout-onset and progressiveonset multiple sclerosis 42
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus 42
Serum neurofilament light chain levels are increased in patients with a clinically isolated syndrome. 42
NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk 41
Genetic burden of common variants in progressive and bout-onset multiple sclerosis. 41
Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus 40
The impact of lifetime coffee and tea loads on Multiple Sclerosis severity 40
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. 38
Bias in effect size of systemic lupus erythematosus susceptibility loci across Europe: a case-control study. 38
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 38
The role of eight polymorphisms in three candidate genes in determining the susceptibility, phenotype, and response to anti-TNF therapy in patients with rheumatoid arthritis. 38
Opposed independent effects and epistasis in the complex association of IRF5 to SLE 37
Multiple sclerosis progression is not associated with birth timing in Italy 33
Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2018) 175 6 (1679-1687.e7) PII: S0092-8674(19)30679-8) 33
Kallikrein genes are associated with lupus and glomerular basement membrane-specific antibody-induced nephritis in mice and humans 32
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 32
Genetic analysis of perforin in two autoimmune diseases: systemic lupus erythematosus and systemic sclerosis 29
Influence of Sex on the Microbiota of the Human Face 10
Totale 2.518
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Categoria #
all - tutte 13.254
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 13.254
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020461 7 1 42 0 74 72 107 28 47 30 53 0
2020/2021323 44 0 45 0 45 15 48 1 56 8 51 10
2021/2022395 24 15 21 70 17 0 21 10 22 19 70 106
2022/2023839 58 46 51 0 50 58 24 50 455 4 28 15
2023/2024275 26 25 22 4 51 5 49 5 3 2 16 67
2024/20253 3 0 0 0 0 0 0 0 0 0 0 0
Totale 2.518