Ciccacci C - Search Results

1

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

Cascella R, Strafella C, Longo G, Ragazzo M, Manzo L, De Felici C, Errichiello V, Caputo V, Viola F, Eandi CM, Staurenghi G, Cusumano A, Mauriello S, Marsella LT, Ciccacci C, Borgiani P, Sangiuolo F, Novelli G, Ricci F, Giardina E. Cascella R, et al. Among authors: ciccacci c. Oncotarget. 2017 Dec 12;9(8):7812-7821. doi: 10.18632/oncotarget.23241. eCollection 2018 Jan 30. Oncotarget. 2017. PMID: 29487693 Free PMC article.

2

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

Borgiani P, Ciccacci C, Forte V, Romano S, Federici G, Novelli G. Borgiani P, et al. Among authors: ciccacci c. Pharmacogenomics. 2007 Nov;8(11):1545-50. doi: 10.2217/14622416.8.11.1545. Pharmacogenomics. 2007. PMID: 18034619 Clinical Trial.

3

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

Borgiani P, Ciccacci C, Forte V, Sirianni E, Novelli L, Bramanti P, Novelli G. Borgiani P, et al. Among authors: ciccacci c. Pharmacogenomics. 2009 Feb;10(2):261-6. doi: 10.2217/14622416.10.2.261. Pharmacogenomics. 2009. PMID: 19207028

4

Pharmacogenomics: role in medicines approval and clinical use.

Novelli G, Borgiani P, Ciccacci C, Di Daniele N, Sirugo G, Papaluca Amati M. Novelli G, et al. Among authors: ciccacci c. Public Health Genomics. 2010;13(5):284-91. doi: 10.1159/000245271. Epub 2009 Oct 6. Public Health Genomics. 2010. PMID: 19815999 Review.

5

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

Ciccacci C, Borgiani P, Ceffa S, Sirianni E, Marazzi MC, Altan AM, Paturzo G, Bramanti P, Novelli G, Palombi L. Ciccacci C, et al. Pharmacogenomics. 2010 Jan;11(1):23-31. doi: 10.2217/pgs.09.142. Pharmacogenomics. 2010. PMID: 20017669

6

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

Ciccacci C, Falconi M, Paolillo N, Oteri F, Forte V, Novelli G, Desideri A, Borgiani P. Ciccacci C, et al. Pharmacogenet Genomics. 2011 Jun;21(6):344-6. doi: 10.1097/FPC.0b013e328344c340. Pharmacogenet Genomics. 2011. PMID: 21451434

7

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

Ciccacci C, Biancone L, Di Fusco D, Ranieri M, Condino G, Giardina E, Onali S, Lepre T, Pallone F, Novelli G, Borgiani P. Ciccacci C, et al. J Crohns Colitis. 2013 Feb;7(1):44-52. doi: 10.1016/j.crohns.2012.02.020. Epub 2012 Mar 24. J Crohns Colitis. 2013. PMID: 22445837

8

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

Novelli G, Ciccacci C, Borgiani P, Papaluca Amati M, Abadie E. Novelli G, et al. Among authors: ciccacci c. Clin Cases Miner Bone Metab. 2008 May;5(2):149-54. Clin Cases Miner Bone Metab. 2008. PMID: 22460999 Free PMC article.

9

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

Ciccacci C, Di Fusco D, Cacciotti L, Morganti R, D'Amato C, Novelli G, Sangiuolo F, Spallone V, Borgiani P. Ciccacci C, et al. Acta Diabetol. 2013 Oct;50(5):789-99. doi: 10.1007/s00592-012-0418-x. Epub 2012 Jul 28. Acta Diabetol. 2013. PMID: 22843023

10

MicroRNA genetic variations: association with type 2 diabetes.

Ciccacci C, Di Fusco D, Cacciotti L, Morganti R, D'Amato C, Greco C, Rufini S, Novelli G, Sangiuolo F, Spallone V, Borgiani P. Ciccacci C, et al. Acta Diabetol. 2013 Dec;50(6):867-72. doi: 10.1007/s00592-013-0469-7. Epub 2013 Mar 27. Acta Diabetol. 2013. PMID: 23532299

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