IRIS
CICCACCI, CINZIA
 Distribuzione geografica
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Continente #
NA - Nord America 16.616
EU - Europa 1.666
AS - Asia 1.652
SA - Sud America 259
AF - Africa 35
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 4
Totale 20.241
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Nazione #
US - Stati Uniti d'America 16.544
SG - Singapore 884
IT - Italia 335
CN - Cina 329
DE - Germania 232
BR - Brasile 222
IE - Irlanda 185
UA - Ucraina 176
HK - Hong Kong 160
FR - Francia 134
PL - Polonia 125
GB - Regno Unito 120
RU - Federazione Russa 108
SE - Svezia 83
VN - Vietnam 72
FI - Finlandia 60
CA - Canada 46
KR - Corea 36
NL - Olanda 33
TR - Turchia 29
IN - India 25
IR - Iran 21
JP - Giappone 21
BE - Belgio 19
MX - Messico 19
ZA - Sudafrica 19
AR - Argentina 15
ID - Indonesia 13
KG - Kirghizistan 12
CZ - Repubblica Ceca 11
IQ - Iraq 11
AT - Austria 10
ES - Italia 9
UZ - Uzbekistan 9
BD - Bangladesh 7
CH - Svizzera 7
A2 - ???statistics.table.value.countryCode.A2??? 5
MA - Marocco 5
EC - Ecuador 4
EU - Europa 4
MY - Malesia 4
PY - Paraguay 4
RO - Romania 4
AU - Australia 3
CL - Cile 3
CO - Colombia 3
DZ - Algeria 3
LT - Lituania 3
PE - Perù 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
CG - Congo 2
EG - Egitto 2
GE - Georgia 2
GR - Grecia 2
HU - Ungheria 2
JM - Giamaica 2
KZ - Kazakistan 2
LB - Libano 2
PK - Pakistan 2
SA - Arabia Saudita 2
TN - Tunisia 2
AL - Albania 1
AM - Armenia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BW - Botswana 1
CR - Costa Rica 1
DM - Dominica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
HN - Honduras 1
IL - Israele 1
MK - Macedonia 1
NO - Norvegia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TJ - Tagikistan 1
TW - Taiwan 1
UY - Uruguay 1
Totale 20.241
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Città #
Wilmington 4.446
Houston 3.996
Woodbridge 3.900
Fairfield 620
Singapore 474
Chandler 361
Ashburn 317
Ann Arbor 306
New York 282
Cambridge 213
Seattle 209
Dublin 173
Beijing 162
Hong Kong 158
Rome 138
Jacksonville 129
Medford 129
Kraków 104
Santa Clara 90
Dallas 89
Dearborn 85
Los Angeles 75
Boardman 70
Lawrence 60
The Dalles 60
Council Bluffs 45
Menlo Park 39
Buffalo 31
Munich 26
London 25
San Diego 25
São Paulo 23
Ho Chi Minh City 21
Montreal 21
Moscow 21
Warsaw 19
Atlanta 18
Redwood City 17
Brussels 16
Palo Alto 16
Tokyo 16
Chicago 15
Hanoi 15
Helsinki 15
Denver 14
Hefei 14
Johannesburg 14
Milan 13
Norwalk 13
Redondo Beach 13
Toronto 13
Kunming 12
Phoenix 12
Mountain View 11
Nuremberg 11
Stockholm 11
Brooklyn 10
Poplar 10
Ankara 9
Chennai 9
Jakarta 9
Olomouc 9
Seoul 9
Shanghai 9
Amsterdam 8
Creede 8
Da Nang 8
Orem 8
Boston 7
Columbus 7
Mülheim 7
North Bergen 7
San Francisco 7
Belo Horizonte 6
Center 6
Fortaleza 6
Frankfurt am Main 6
Istanbul 6
Lappeenranta 6
Manchester 6
Paris 6
Querétaro 6
Turhal 6
Turku 6
University Park 6
Zhengzhou 6
Baghdad 5
Biên Hòa 5
Brasília 5
Charlotte 5
Guangzhou 5
Hebei 5
Kilburn 5
Mexico City 5
Mumbai 5
Nanjing 5
Pisa 5
Rio de Janeiro 5
Salt Lake City 5
Tashkent 5
Totale 17.510
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Nome #
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 508
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 492
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 478
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 475
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 469
A family study of asymptomatic small bowel Crohn's disease 468
Advances in exploring the role of micrornas in inflammatory bowel disease 466
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 465
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 464
A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene 458
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 455
HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons syndrome/toxic epidermal necrolysis susceptibility in a population from Mozambique 445
Genetic factors in systemic lupus erythematosus: Contribution to disease phenotype 445
Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient 439
Interleukin-23R Arg381Gln Is Associated With Susceptibility to Crohn's Disease But Not With Phenotype in an Italian Population 437
Recent advances in exploring the genetic susceptibility to diabetic neuropathy 432
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 431
Cannabinoid Poisoning by Hemp Seed Oil in a Child 425
Biomarkers to predict drug efficacy and safety in neurodegenerative diseases 423
Polymorphisms in MIR122, MIR196A2, and MIR124A genes are associated with clinical phenotypes in inflammatory bowel diseases 421
Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 genes are associated with the response to TNF inhibitors in patients with rheumatoid arthritis 420
TRAF3IP2 gene and systemic lupus erythematosus: association with disease susceptibility and pericarditis development 417
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis 416
Recent advances in the genetic susceptibility to osteoarthritis 407
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 400
EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population 396
ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique 396
Resequencing of VKORC1, CYP2C9 and CYP4F2 genes in Italian patients requiring extreme low and high warfarin doses 393
L’impatto sulla salute umana dell’arsenico presente in basse concentrazioni nelle acque. Proposta di uno studio caso controllo Nested nell’area del viterbese 379
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis 377
Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes 376
Genetic tests and genomic biomarkers: regulation, qualification and validation 369
A polymorphism upstream MIR1279 gene is associated with pericarditis development in Systemic Lupus Erythematosus and contributes to definition of a genetic risk profile for this complication 355
Pharmacogenetics of inflammatory bowel disease: A focus on Crohn's disease 348
Genetics and Treatment Response in Parkinson’s Disease: An Update on Pharmacogenetic Studies 347
Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility 345
A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes 342
A multivariate genetic analysis confirms rs5010528 in the human leucocyte antigen-C locus as a significant contributor to Stevens-Johnson syndrome/toxic epidermal necrolysis susceptibility in a Mozambique HIV population treated with nevirapine 303
Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility 294
TNFAIP3 gene polymorphisms in three common autoimmune diseases: Systemic lupus erythematosus, rheumatoid arthritis, and primary sjogren syndrome - association with disease susceptibility and clinical phenotypes in Italian patients 283
Interaction between microbiome and host genetics in psoriatic arthritis 267
STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects 265
Evaluation of ATG5 polymorphisms in Italian patients with systemic lupus erythematosus: contribution to disease susceptibility and clinical phenotypes 260
Pharmacogenomics in Parkinson's disease: which perspective for developing a personalized medicine? 251
Anthropological features of the CFTR gene: Its variability in an African population 247
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 241
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals 235
miRNAs in drug response variability: potential utility as biomarkers for personalized medicine 191
LOW LEVEL EXPOSURE TO ARSENIC IN DRINKING WATER: A REVIEW ON ACTION MECHANISM, HEALTH EFFECTS AND BIOMARKERS 187
Mitochondrial DNA copy number in peripheral blood is reduced in type 2 diabetes patients with polyneuropathy and associated with a MIR499A gene polymorphism 162
Genetics and autoimmunity: recent news 147
Expression study of candidate miRNAs and evaluation of their potential use as biomarkers of diabetic neuropathy 124
The differential response to anti IL-6 treatment in COVID-19: the genetic counterpart 109
The Heart Matters: Contribution of Genetic Factors in Recurrent Pericarditis 105
Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population 96
Large-scale DNA sequencing identifies rare variants associated with Systemic Lupus Erythematosus susceptibility in known risk genes 94
Altered expression of miR-142, miR-155, miR-499a and of their putative common target MDM2 in systemic lupus erythematosus 87
Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy 73
Alteration of Mitochondrial DNA Copy Number and Increased Expression Levels of Mitochondrial Dynamics-Related Genes in Sjögren's Syndrome 69
A multilocus genetic study evidences the association of autoimmune-related genes with Psoriatic Arthritis in Italian patients 66
Alteration of telomere length and mtDNA copy number in interstitial lung disease associated with rheumatoid arthritis 62
mRNA expression analysis confirms CD44 splicing impairment in systemic lupus erythematosus patients 62
Genetics, epigenetics, and gender impact in axial-spondyloarthritis susceptibility: an update on genetic polymorphisms and their sex related associations 60
The rs11568820 Variant in the Promoter Region of Vitamin D Receptor Gene Is Associated with Clinical Remission in Rheumatoid Arthritis Patients Receiving Tumor Necrosis Factor Inhibitors 60
Fever in systemic lupus erythematosus: associated clinical features and genetic factors 56
Low expression levels of miRNA-155 and miRNA-499a are associated with obesity in Type 2 diabetes 55
VDR Polymorphisms in Autoimmune Connective Tissue Diseases: Focus on Italian Population 55
VDR Polymorphisms in Autoimmune Connective Tissue Diseases: Focus on Italian Population 55
Emerging role of microRNAs and long non-coding rnas in sjögren’s syndrome 55
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What Is in the Field for Genetics and Epigenetics of Diabetic Neuropathy: The Role of MicroRNAs 48
The Impacts of the Clinical and Genetic Factors on Chronic Damage in Caucasian Systemic Lupus Erythematosus Patients 47
ATG5 GENE EXPRESSION ANALYSIS SUPPORTS THE INVOLVEMENT OF AUTOPHAGY IN MICROANGIOPATHIC COMPLICATIONS OF TYPE 2 DIABETES 46
Impact of TRAF3IP2, IL10 and HCP5 Genetic Polymorphisms in the Response to TNF-i Treatment in Patients with Psoriatic Arthritis 43
PCSK3 Overexpression in Sjögren’s Syndrome Patients May Be Regulated by rs4932178 SNP in Its Promoter Region and Correlates with IFN-γ Gene Expression 25
Late-onset neonatal sepsis: genetic differences by sex and involvement of the NOTCH pathway 22
Modulation of cellular senescence in psoriatic arthritis: exploring the potential impact of bDMARDs on telomere length, mtDNA copy number, and oxidative damage 13
Correlation between Sirtuin 1 downregulation and reduced vitamin D receptor expression in patients with diabetic neuropathy 11
A genetic variant in the potassium channel (KCNJ11) gene is associated with diabetic retinopathy in type 2 diabetes patients 11
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Totale 20.574
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Categoria #
all - tutte 51.447
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 51.447
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.415 0 0 0 0 0 365 419 345 71 80 96 39
2021/2022693 44 58 34 29 31 81 28 28 60 78 55 167
2022/2023956 93 82 36 128 97 203 83 65 83 15 40 31
2023/2024559 46 11 26 18 26 259 10 27 5 4 13 114
2024/20251.643 54 394 180 136 33 67 102 96 185 131 120 145
2025/20261.442 288 91 340 317 313 93 0 0 0 0 0 0
Totale 20.574