Research Topics
Genomes and GenesSpecies | Paola BorgianiSummaryAffiliation: University of Rome Tor Vergata Country: Italy Publications
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Detail Information
Publications
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian populationPaola Borgiani
Department of Biopathology and Diagnostic Imaging, School of Medicine, Tor Vergata University, Rome, Italy
Pharmacogenomics 10:261-6. 2009..Numerous papers have shown the important contribution of CYP2C9 and VKORC1 genetic variants to this variability. Recently, a new SNP within the CYP4F2 gene was found associated with warfarin dose in the USA...
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in ItaliansPaola Borgiani
Tor Vergata University, Department of Biopathology and Diagnostic Imaging, Section of Genetics, School of Medicine, Via Montpellier 1, 00133 Rome, Italy
Pharmacogenomics 8:1545-50. 2007....
CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's diseasePiero Vavassori
Cattedra di Gastroenterologia, Centro d eccellenza per lo studio del rischio genomico in patologie complesse e multifattoriali, Universita Tor Vergata, Rome, Italy
Inflamm Bowel Dis 10:116-21. 2004..The purpose of this study was to evaluate the frequency of the main mutations of the CARD15 gene (Leu 1007fsinsC, Arg702Trp, and Gly908Arg) in Italian CD patients and to establish possible genotype-phenotype correlations...
Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from MozambiqueCinzia Ciccacci
Department of Biopathology and Diagnostic Imaging, Section of Genetics, Tor Vergata University, Rome, Italy
Pharmacogenomics 11:23-31. 2010..Aims: Nevirapine is widely used to treat HIV-1 infection to prevent mother-to-child transmission; unfortunately adverse drug reactions have been reported. Our aim was to identify genes/variants involved in nevirapine-induced hepatotoxicity...
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian populationEmiliano Giardina
Centre of Excellence for Genomic Risk Assessment in Multifactorial and Complex Diseases, School of Medicine, Tor Vergata University of Rome, Rome, Italy
J Invest Dermatol 122:1106-7. 2004....
Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patientCinzia Ciccacci
Department of Biopathology and Diagnostic Imaging, Section of Genetics, School of Medicine, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy
Pharmacogenet Genomics 21:344-6. 2011..374G>T, which produces the Arg125Leu substitution. We have observed, through an electrostatic analysis, that the new mutation produces an electrostatic alteration on the cytochrome surface...
Genotyping OLR1 gene: a genomic biomarker for cardiovascular diseasesLucia Vecchione
Department of Biopathology and Diagnostic Imaging, Centre of Excellence for Genomic Risk Assessment in Multifactorial and Complex Diseases, School of Medicine, University of Tor Vergata, Rome, Italy
Recent Pat Cardiovasc Drug Discov 2:147-51. 2007..The recent patents related to OLR1, SNPs and LOXIN are also discussed in this article...
Pharmacogenomics in cardiovascular disease: the role of single nucleotide polymorphisms in improving drug therapyRuggiero Mango
Department of Biopathology, University of Roma Tor Vergata, Rome, Italy
Expert Opin Pharmacother 6:2565-76. 2005..To improve this, there is a need of new technology and large prospective trials allowing for simultaneous analysis of multiple genetic variants in molecular pathways that could affect drug disposition and action...
Role of genetics in prevention of coronary atherosclerosisGiuseppe Novelli
Centre of Excellence for Genomic Risk Assessment in Multifactorial and Complex Diseases, School of Medicine, Tor Vergata University of Rome, Rome, Italy
Curr Opin Cardiol 18:368-71. 2003..Here, we review these advances with regard to genome scan results and candidate gene analysis...
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian populationPaola Borgiani
Centro di Eccellenza per lo Studio del Rischio Genomico in Patologie Complesse Multifattoriali, Facolta di Medicina, Universita di Roma Tor Vergata, Via Montpellier 1, Italy
Eur J Dermatol 12:540-2. 2002..We failed to observe any significant difference between patients and controls, thereby excluding the presence of a strong genetic association between CARD15 gene polymorphisms and psoriasis, in the Italian population...
Folic acid and methionine in the prevention of teratogen-induced congenital defects in miceDaria Cipollone
Department of Biopathology and Diagnostic Imaging, University Tor Vergata, Rome, Italy
Cardiovasc Pathol 18:100-9. 2009..Hereby, we analyzed the effects of nutritive therapy involving folic acid and methionine on teratogen-induced congenital defects in mice...
ATG16L1 Ala197Thr is not associated with susceptibility to Crohn's disease or with phenotype in an Italian populationCarlo Perricone
Gastroenterology 134:368-70. 2008
Neonatal screening, clinical features and genetic testing for galactosemiaMarco Zaffanello
Genet Med 7:211-2. 2005
Association of the ACP1 genotype with metabolic parameters upon initial diagnosis of type 1 diabetesGianfranco Meloni
Department of Pediatrics, University of Sassari, Italy
Med Sci Monit 9:CR105-8. 2003..The purpose of our research was to determine the relationship of ACP1 with glycemic level, ketoacidosis and HbA1C in children with Type 1 diabetes...
OLR1 gene and coronary artery disease/acute myocardial infarction: replication in an independently collected sampleGiuseppe Novelli
Eur J Hum Genet 14:894-5; author reply 895. 2006
