Lista de obras - Cinzia Ciccacci - Dominio Público Uruguay

A family study of asymptomatic small bowel Crohn's disease

artículo científico publicado en 2013

A large-scale study of the random variability of a coding sequence: a study on the CFTR gene

artículo científico publicado en 2005

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

artículo científico publicado en 2014

A pharmacogenetics study in Mozambican patients treated with nevirapine: full resequencing of TRAF3IP2 gene shows a novel association with SJS/TEN susceptibility

artículo científico publicado en 2015

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

artículo científico publicado en 2016

ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique

artículo científico publicado en 2013

ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn’s Disease or With Phenotype in an Italian Population

article

Advances in Exploring the Role of Micrornas in Inflammatory Bowel Disease.

artículo científico publicado en 2016

Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians.

artículo científico publicado en 2007

Altered expression of miR-142, miR-155, miR-499a and of their putative common target <i>MDM2</i> in systemic lupus erythematosus

artículo científico publicado en 2020

Anthropological features of the CFTR gene: Its variability in an African population

artículo científico publicado en 2010

Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study

artículo científico publicado en 2013

Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes.

artículo científico publicado en 2017

Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease

artículo científico publicado en 2015

CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population.

artículo científico publicado en 2009

Cannabinoid Poisoning by Hemp Seed Oil in a Child

artículo científico publicado en 2017

Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient

artículo científico publicado en 2011

Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes

article

Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes

artículo científico publicado en 2015

EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population

article

Evaluation of ATG5 polymorphisms in Italian patients with systemic lupus erythematosus: contribution to disease susceptibility and clinical phenotypes

scientific article published on 14 May 2018

Expression study of candidate miRNAs and evaluation of their potential use as biomarkers of diabetic neuropathy

artículo científico publicado en 2020

Genetic Factors in Systemic Lupus Erythematosus: Contribution to Disease Phenotype

artículo científico publicado en 2015

Genetics and Treatment Response in Parkinson's Disease: An Update on Pharmacogenetic Studies.

artículo científico publicado en 2018

HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique.

artículo científico publicado en 2013

Highly preferential association of NonF508del CF mutations with the M470 allele

artículo científico publicado en 2006

Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility

artículo científico publicado en 2017

Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis

artículo científico publicado en 2012

Interaction between microbiome and host genetics in psoriatic arthritis

artículo científico publicado en 2018

Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population

artículo científico publicado en 2007

MicroRNA genetic variations: association with type 2 diabetes

artículo científico publicado en 2013

Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique

artículo científico publicado en 2010

Pharmacogenetics of inflammatory bowel disease: a focus on Crohn's disease.

artículo científico publicado en 2017

Polymorphisms in MIR122, MIR196A2, and MIR124A Genes are Associated with Clinical Phenotypes in Inflammatory Bowel Diseases

artículo científico publicado en 2016

Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 Genes Are Associated with the Response to TNF Inhibitors in Patients with Rheumatoid Arthritis

artículo científico publicado en 2017

Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility.

artículo científico publicado en 2017

Population differences in allele frequencies at theOLR1locus may suggest geographic disparities in cardiovascular risk events

Recent advances in exploring the genetic susceptibility to diabetic neuropathy

artículo científico publicado en 2016

STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren’s Syndrome: Association with Disease Susceptibility and Clinical Aspects

artículo científico publicado en 2019

Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction

artículo científico publicado en 2015

TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy

article

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

artículo científico publicado en 2019

TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in inflammatory bowel disease.

artículo científico publicado en 2012

Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants.

artículo científico publicado en 2017

Lista de obras de Cinzia Ciccacci

A family study of asymptomatic small bowel Crohn's disease

A large-scale study of the random variability of a coding sequence: a study on the CFTR gene

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

A pharmacogenetics study in Mozambican patients treated with nevirapine: full resequencing of TRAF3IP2 gene shows a novel association with SJS/TEN susceptibility

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

ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique

ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn’s Disease or With Phenotype in an Italian Population

Advances in Exploring the Role of Micrornas in Inflammatory Bowel Disease.

Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians.

Altered expression of miR-142, miR-155, miR-499a and of their putative common target <i>MDM2</i> in systemic lupus erythematosus

Anthropological features of the CFTR gene: Its variability in an African population

Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study

Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes.

Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease

CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population.

Cannabinoid Poisoning by Hemp Seed Oil in a Child

Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient

Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes

Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes

EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population

Evaluation of ATG5 polymorphisms in Italian patients with systemic lupus erythematosus: contribution to disease susceptibility and clinical phenotypes

Expression study of candidate miRNAs and evaluation of their potential use as biomarkers of diabetic neuropathy

Genetic Factors in Systemic Lupus Erythematosus: Contribution to Disease Phenotype

Genetics and Treatment Response in Parkinson's Disease: An Update on Pharmacogenetic Studies.

HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique.

Highly preferential association of NonF508del CF mutations with the M470 allele

Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility

Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis

Interaction between microbiome and host genetics in psoriatic arthritis

Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population

MicroRNA genetic variations: association with type 2 diabetes

Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique

Pharmacogenetics of inflammatory bowel disease: a focus on Crohn's disease.

Polymorphisms in MIR122, MIR196A2, and MIR124A Genes are Associated with Clinical Phenotypes in Inflammatory Bowel Diseases

Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 Genes Are Associated with the Response to TNF Inhibitors in Patients with Rheumatoid Arthritis

Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility.

Population differences in allele frequencies at theOLR1locus may suggest geographic disparities in cardiovascular risk events

Recent advances in exploring the genetic susceptibility to diabetic neuropathy

STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren’s Syndrome: Association with Disease Susceptibility and Clinical Aspects

Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction

TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy

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

TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in inflammatory bowel disease.

Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants.