C. Ciccacci

P. Borgiani, C. Ciccacci, L. Biancone, 2014, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

VDR Polymorphisms in Autoimmune Connective Tissue Diseases: Focus on Italian Population

P. Borgiani, M. Chimenti, P. Conigliaro, 2021, Journal of immunology research.

TRAF3IP2 gene and systemic lupus erythematosus: association with disease susceptibility and pericarditis development

G. Novelli, P. Borgiani, G. Valesini, 2013, Immunogenetics.

Emerging Role of microRNAs and Long Non-Coding RNAs in Sjögren’s Syndrome

G. Novelli, P. Borgiani, A. Latini, 2021, Genes.

Impact of the CYP4F2 p.V433M Polymorphism on Coumarin Dose Requirement: Systematic Review and Meta‐Analysis

Mohamed H. Shahin, R. Altman, B. Horne, 2012, Clinical pharmacology and therapeutics.

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

Placido Bramanti, P. Bramanti, G. Novelli, 2009, Pharmacogenomics.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2013, Journal of Crohn's & colitis.

Recent advances in exploring the genetic susceptibility to diabetic neuropathy.

G. Novelli, P. Borgiani, C. Ciccacci, 2016, Diabetes research and clinical practice.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2015, Pharmacogenomics.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2017, Pharmacogenomics.

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

G. Novelli, P. Borgiani, P. Conigliaro, 2019, Journal of immunology research.

Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility

G. Novelli, P. Borgiani, A. Latini, 2017, Immunologic Research.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2015, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

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

G. Novelli, P. Borgiani, D. Lauro, 2018, Journal of diabetes and its complications.

CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa).

Rafal S. Sobota, Scott M. Williams, G. Sirugo, 2020, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

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

P. Pignatti, G. Modiano, M. Claustres, 2005, European Journal of Human Genetics.

Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single‐Patient Data Meta‐Analysis in More Than 15,000 Individuals

Mohamed H. Shahin, P. Deloukas, R. Altman, 2019, Clinical pharmacology and therapeutics.

Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations

P. Pignatti, G. Modiano, M. Claustres, 2006, European Journal of Human Genetics.

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

G. Novelli, P. Borgiani, R. Priori, 2019, Journal of immunology research.

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

G. Novelli, P. Borgiani, G. Valesini, 2014, PloS one.

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

G. Novelli, F. Sangiuolo, P. Borgiani, 2013, Acta Diabetologica.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2013, European Journal of Clinical Pharmacology.

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

P. Bramanti, G. Novelli, P. Borgiani, 2010, Pharmacogenomics.

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

G. Novelli, P. Borgiani, D. Lauro, 2020, Epigenomics.

MicroRNA genetic variations: association with type 2 diabetes

G. Novelli, F. Sangiuolo, P. Borgiani, 2013, Acta Diabetologica.

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

P. Pignatti, G. Modiano, C. Bombieri, 2011, Annals of human biology.

Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population

T. Beccari, C. Ciccacci, M. Bertelli, 2022, Frontiers in Nutrition.

Genetic tests and genomic biomarkers: regulation, qualification and validation.

Eric Abadie, G. Novelli, P. Borgiani, 2008, Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases.

Cannabinoid Poisoning by Hemp Seed Oil in a Child

P. Borgiani, C. Ciccacci, M. Calvani, 2017, Pediatric emergency care.

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

G. Marfia, G. Novelli, F. Sangiuolo, 2014, Acta Diabetologica.

Pharmacogenomics: Role in Medicines Approval and Clinical Use

G. Sirugo, G. Novelli, P. Borgiani, 2009, Public Health Genomics.

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

G. Novelli, P. Borgiani, C. Alessandri, 2017, Lupus.

A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes

G. Novelli, P. Borgiani, A. Latini, 2019, Acta Diabetologica.

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

G. Novelli, P. Borgiani, A. Latini, 2017, Molecular Diagnosis & Therapy.

Polymorphisms in STAT‐4, IL‐10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis

G. Novelli, P. Borgiani, P. Triggianese, 2016, Clinical and experimental immunology.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2018, NeuroMolecular Medicine.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2011, Clinical pharmacology and therapeutics.

Alteration of Mitochondrial DNA Copy Number and Increased Expression Levels of Mitochondrial Dynamics-Related Genes in Sjögren’s Syndrome

P. Borgiani, R. Priori, A. Latini, 2022, Biomedicines.

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

G. Novelli, P. Borgiani, A. Latini, 2017, European Journal of Clinical Pharmacology.

Role of the Vitamin D Receptor (VDR) in the Pathogenesis of Osteoporosis: A Genetic, Epigenetic and Molecular Pilot Study

M. Brandi, C. Ciccacci, A. Botta, 2023, Genes.

Late-onset neonatal sepsis: genetic differences by sex and involvement of the NOTCH pathway

Timothy H. Ciesielski, Scott M. Williams, G. Sirugo, 2022, Pediatric Research.

Genetic study of late-onset neonatal sepsis reveals significant differences by sex

Timothy H. Ciesielski, Scott M. Williams, G. Sirugo, 2021, medRxiv.

Genetics, Epigenetics, and Gender Impact in Axial-Spondyloarthritis Susceptibility: An Update on Genetic Polymorphisms and Their Sex Related Associations

P. Borgiani, M. Chimenti, P. Triggianese, 2021, Frontiers in Genetics.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2014, European Journal of Clinical Pharmacology.

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

G. Novelli, F. Sangiuolo, P. Borgiani, 2017, Oncotarget.

Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events

M. Crawford, R. Mango, G. Novelli, 2010, Annals of human biology.

The differential response to anti IL-6 treatment in COVID-19: the genetic counterpart.

G. Novelli, P. Borgiani, P. Conigliaro, 2020, Clinical and experimental rheumatology.

A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility

G. Novelli, P. Borgiani, C. Ciccacci, 2015, International journal of molecular sciences.

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

G. Novelli, P. Borgiani, A. Latini, 2020, Epigenomics.

miRNAs in drug response variability: potential utility as biomarkers for personalized medicine.

G. Novelli, P. Borgiani, A. Latini, 2019, Pharmacogenomics.

mRNA expression analysis confirms CD44 splicing impairment in systemic lupus erythematosus patients

G. Novelli, P. Borgiani, A. Latini, 2021, Lupus.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2007, Gastroenterology.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2013, European Journal of Clinical Pharmacology.

Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility

G. Novelli, P. Borgiani, A. Latini, 2017, Immunologic Research.

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

G. Novelli, P. Borgiani, C. Ciccacci, 2018, NeuroMolecular Medicine.

PCSK3 Overexpression in Sjögren’s Syndrome Patients May Be Regulated by rs4932178 SNP in Its Promoter Region and Correlates with IFN-γ Gene Expression

G. Novelli, P. Borgiani, R. Priori, 2023, Genes.

Study of lncRNAs expression profile in the response to biological drugs in Psoriatic Arthritis: MEG3 could be a potential genomic biomarker of therapy efficacy.

P. Borgiani, M. Chimenti, P. Triggianese, 2024, International immunopharmacology.

Polymorphisms in STAT‐4, IL‐10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis

P. Borgiani, P. Triggianese, P. Conigliaro, 2016, Clinical and experimental immunology.

The Heart Matters: Contribution of Genetic Factors in Recurrent Pericarditis.

Y. Shoenfeld, P. Borgiani, G. Valesini, 2019, The Israel Medical Association journal : IMAJ.

The dysregulation of mitochondrial homeostasis-related genes could be involved in the decrease of mtDNA copy number in systemic lupus erythematosus patients.

P. Borgiani, A. Latini, C. Ciccacci, 2024, Immunologic research.