IRIS
Ciccacci, Cinzia
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 112
EU - Europa 86
NA - Nord America 14
AF - Africa 1
Totale 213
Salva come PNG Salva come JPEG
Nazione #
SG - Singapore 93
IT - Italia 74
HK - Hong Kong 17
US - Stati Uniti d'America 11
DE - Germania 7
MX - Messico 3
NL - Olanda 3
CZ - Repubblica Ceca 1
DZ - Algeria 1
ID - Indonesia 1
JP - Giappone 1
UA - Ucraina 1
Totale 213
Salva come PNG Salva come JPEG
Città #
Rome 71
Singapore 45
Hong Kong 15
Mexico City 3
Boardman 1
Chlef 1
Ichikawa 1
Totale 137
Salva come PNG Salva come JPEG
Nome #
A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes. 16
Genetics and Autoimmunity: Recent News 12
Sjogren's syndrome: Everything you always wanted to know about genetic and epigenetic factors 12
A multilocus genetic study evidences the association of autoimmune-related genes with Psoriatic Arthritis in Italian patients 9
Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy 8
Role of the Vitamin D Receptor (VDR) in the Pathogenesis of Osteoporosis: A Genetic, Epigenetic and Molecular Pilot Study 7
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 7
ATG5 gene expression analysis supports the involvement of autophagy in microangiopathic complications of type 2 diabetes 6
Low expression levels of miRNA-155 and miRNA-499a are associated with obesity in Type 2 diabetes 6
The dysregulation of mitochondrial homeostasis-related genes could be involved in the decrease of mtDNA copy number in systemic lupus erythematosus patients 6
Alteration of Mitochondrial DNA Copy Number and Increased Expression Levels of Mitochondrial Dynamics-Related Genes in Sjögren's Syndrome 5
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene 5
Altered expression of miR-142, miR-155, miR-499a and of their putative common target MDM2 in systemic lupus erythematosus 5
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 4
A pharmacogenetics study in Mozambican patients treated with nevirapine: full resequencing of TRAF3IP2 gene shows a novel association with SJS/TEN susceptibility. 4
Expression study of candidate miRNAs and evaluation of their potential use as biomarkers of diabetic neuropathy 4
Mitochondrial DNA Copy Number in Peripheral Blood Is Reduced in Type 2 Diabetes Patients with Polyneuropathy and Associated with a MIR499A Gene Polymorphism 4
Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 Genes Are Associated with the Response to TNF Inhibitors in Patients with Rheumatoid Arthritis. 4
Large-scale DNA sequencing identifies rare variants associated with Systemic Lupus Erythematosus susceptibility in known risk genes 4
Late-onset neonatal sepsis: genetic differences by sex and involvement of the NOTCH pathway 4
CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa) 4
VDR Polymorphisms in Autoimmune Connective Tissue Diseases: Focus on Italian Population 4
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. 3
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants. 3
miRNAs in drug response variability: potential utility as biomarkers for personalized medicine 3
Biomarkers to predict drug efficacy and safety in neurodegenerative diseases 3
What Is in the Field for Genetics and Epigenetics of Diabetic Neuropathy: The Role of MicroRNAs 3
Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population 3
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 3
Advances in exploring the role of micrornas in inflammatory bowel disease 3
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population 3
Emerging Role of microRNAs and Long Non-Coding RNAs in Sjögren's Syndrome 3
Anthropological features of the CFTR gene: Its variability in an African population 3
The Impacts of the Clinical and Genetic Factors on Chronic Damage in Caucasian Systemic Lupus Erythematosus Patients 3
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study. 3
Discovering the genetic contribution to cardiovascular diseases in patients affected by autoimmune diseases. 3
Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations 3
A family study of asymptomatic small bowel Crohn's disease 2
STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects 2
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes. 2
ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique 2
ATG16L1 Ala197Thr is not associated with susceptibility to Crohn's disease or with phenotype in an Italian population 2
MicroRNA genetic variations: association with type 2 diabetes. 2
Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes. 2
Evaluation of ATG5 polymorphisms in Italian patients with systemic lupus erythematosus: contribution to disease susceptibility and clinical phenotypes. 2
TRAF3IP2 gene and systemic lupus erythematosus: association with disease susceptibility and pericarditis development 2
Impact of TRAF3IP2, IL10 and HCP5 Genetic Polymorphisms in the Response to TNF-i Treatment in Patients with Psoriatic Arthritis 2
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 2
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes. 2
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 2
Genetics and Treatment Response in Parkinson's Disease: An Update on Pharmacogenetic Studies. 2
mRNA expression analysis confirms CD44 splicing impairment in systemic lupus erythematosus patients 2
PCSK3 Overexpression in Sjögren's Syndrome Patients May Be Regulated by rs4932178 SNP in Its Promoter Region and Correlates with IFN-γ Gene Expression 2
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 2
The differential response to anti IL-6 treatment in COVID-19: the genetic counterpart 2
EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population 2
Interaction between microbiome and host genetics in psoriatic arthritis. 2
Pharmacogenomics: role in medicines approval and clinical use 1
Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility. 1
Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility. 1
Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient 1
Genetic tests and genomic biomarkers: regulation, qualification and validation 1
Recent advances in exploring the genetic susceptibility to diabetic neuropathy. 1
Recent advances in the genetic susceptibility to osteoarthritis 1
Nevirapine-induced hepatotoxicity and Pharmacogenetics: a retrospective study in a population of Mozambique 1
Resequencing of VKORC1, CYP2C9 and CYP4F2 genes in Italian patients requiring extreme low and high warfarin doses 1
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals. 1
Pharmacogenetics of inflammatory bowel disease: a focus on Crohn's disease. 1
Highly preferential association of NonF508del CF mutations with the M470 allele 1
Genetics, Epigenetics, and Gender Impact in Axial-Spondyloarthritis Susceptibility: An Update on Genetic Polymorphisms and Their Sex Related Associations 1
TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy. 1
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 1
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events 1
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis 1
Polymorphisms in MIR122, MIR196A2, and MIR124A Genes are Associated with Clinical Phenotypes in Inflammatory Bowel Diseases. 1
Pharmacogenomics in Parkinson's disease: which perspective for developing a personalized medicine? 1
Genetic Factors in Systemic Lupus Erythematosus: Contribution to Disease Phenotype. 1
Cannabinoid Poisoning by Hemp Seed Oil in a Child. 1
HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons syndrome/toxic epidermal necrolysis susceptibility in a population from Mozambique 1
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction. 1
Fever in systemic lupus erythematosus: associated clinical features and genetic factors. 1
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis 1
The Heart Matters: Contribution of Genetic Factors in Recurrent Pericarditis. 1
Totale 251
Salva come PNG Salva come JPEG
Categoria #
all - tutte 1.482
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 1.482
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/2025251 2 0 1 9 41 3 84 83 23 5 0 0
Totale 251