Borgiani P - Search Results

1

WWP1 germline variants are associated with normocephalic autism spectrum disorder.

Novelli G, Novelli A, Borgiani P, Cocciadiferro D, Biancolella M, Agolini E, Pietrosanto M, Casalone R, Helmer-Citterich M, Giardina E, Jain SK, Wei W, Eng C, Pandolfi PP. Novelli G, et al. Among authors: borgiani p. Cell Death Dis. 2020 Jul 23;11(7):529. doi: 10.1038/s41419-020-2681-z. Cell Death Dis. 2020. PMID: 32699206 Free PMC article. No abstract available.

2

Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population.

Borgiani P, Vallo L, D'Apice MR, Giardina E, Pucci S, Capon F, Nisticò S, Chimenti S, Pallone F, Novelli G. Borgiani P, et al. Eur J Dermatol. 2002 Nov-Dec;12(6):540-2. Eur J Dermatol. 2002. PMID: 12459523

3

Role of genetics in prevention of coronary atherosclerosis.

Novelli G, Borgiani P, Giardina E, Mango R, Contino G, Romeo F, Mehta JL. Novelli G, et al. Among authors: borgiani p. Curr Opin Cardiol. 2003 Sep;18(5):368-71. doi: 10.1097/00001573-200309000-00008. Curr Opin Cardiol. 2003. PMID: 12960469 Review.

4

Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population.

Giardina E, Novelli G, Costanzo A, Nisticò S, Bulli C, Sinibaldi C, Sorgi ML, Chimenti S, Pallone F, Taccari E, Borgiani P. Giardina E, et al. Among authors: borgiani p. J Invest Dermatol. 2004 May;122(5):1106-7. doi: 10.1111/j.0022-202X.2004.22524.x. J Invest Dermatol. 2004. PMID: 15140210 Free article.

5

Pharmacogenomics in cardiovascular disease: the role of single nucleotide polymorphisms in improving drug therapy.

Mango R, Vecchione L, Raso B, Borgiani P, Brunetti E, Mehta JL, Lauro R, Romeo F, Novelli G. Mango R, et al. Among authors: borgiani p. Expert Opin Pharmacother. 2005 Dec;6(15):2565-76. doi: 10.1517/14656566.6.15.2565. Expert Opin Pharmacother. 2005. PMID: 16316297 Review.

6

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. Pharmacogenomics. 2007 Nov;8(11):1545-50. doi: 10.2217/14622416.8.11.1545. Pharmacogenomics. 2007. PMID: 18034619 Clinical Trial.

7

Genotyping OLR1 gene: a genomic biomarker for cardiovascular diseases.

Vecchione L, Gargiul E, Borgiani P, Predazzi I, Mango R, Romeo F, Magnani M, Novelli G. Vecchione L, et al. Among authors: borgiani p. Recent Pat Cardiovasc Drug Discov. 2007 Jun;2(2):147-51. doi: 10.2174/157489007780832506. Recent Pat Cardiovasc Drug Discov. 2007. PMID: 18221114

8

Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice.

Cipollone D, Carsetti R, Tagliani A, Rosado MM, Borgiani P, Novelli G, D'Amati G, Fumagalli L, Marino B, Businaro R. Cipollone D, et al. Among authors: borgiani p. Cardiovasc Pathol. 2009 Mar-Apr;18(2):100-9. doi: 10.1016/j.carpath.2008.02.007. Epub 2008 Apr 15. Cardiovasc Pathol. 2009. PMID: 18417366

9

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. Pharmacogenomics. 2009 Feb;10(2):261-6. doi: 10.2217/14622416.10.2.261. Pharmacogenomics. 2009. PMID: 19207028

10

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: borgiani p. Public Health Genomics. 2010;13(5):284-91. doi: 10.1159/000245271. Epub 2009 Oct 6. Public Health Genomics. 2010. PMID: 19815999 Review.

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