Vecoli C - Search Results

1

Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility.

Borghini A, Vecoli C, Mercuri A, Turchi S, Andreassi MG. Borghini A, et al. Among authors: vecoli c. Cardiol Young. 2021 Jun;31(6):965-968. doi: 10.1017/S1047951120004874. Epub 2021 Jan 11. Cardiol Young. 2021. PMID: 33423710

2

T(-786)→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy.

Vecoli C, Andreassi MG, Liga R, Colombo MG, Coceani M, Carpeggiani C, L'Abbate A, Neglia D. Vecoli C, et al. BMC Med Genet. 2012 Oct 2;13:92. doi: 10.1186/1471-2350-13-92. BMC Med Genet. 2012. PMID: 23031426 Free PMC article.

3

Next generation sequencing in cardiovascular diseases.

Faita F, Vecoli C, Foffa I, Andreassi MG. Faita F, et al. Among authors: vecoli c. World J Cardiol. 2012 Oct 26;4(10):288-95. doi: 10.4330/wjc.v4.i10.288. World J Cardiol. 2012. PMID: 23110245 Free PMC article.

4

Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.

Cresci M, Vecoli C, Foffa I, Pulignani S, Ait-Ali L, Andreassi MG. Cresci M, et al. Among authors: vecoli c. Pediatr Cardiol. 2013 Apr;34(4):938-41. doi: 10.1007/s00246-012-0578-z. Epub 2012 Nov 15. Pediatr Cardiol. 2013. PMID: 23229290

5

Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve.

Foffa I, Ait Alì L, Panesi P, Mariani M, Festa P, Botto N, Vecoli C, Andreassi MG. Foffa I, et al. Among authors: vecoli c. BMC Med Genet. 2013 Apr 11;14:44. doi: 10.1186/1471-2350-14-44. BMC Med Genet. 2013. PMID: 23578328 Free PMC article.

6

Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.

Sabina S, Pulignani S, Rizzo M, Cresci M, Vecoli C, Foffa I, Ait-Ali L, Pitto L, Andreassi MG. Sabina S, et al. Among authors: vecoli c. J Mol Cell Cardiol. 2013 Jul;60:84-9. doi: 10.1016/j.yjmcc.2013.04.002. Epub 2013 Apr 11. J Mol Cell Cardiol. 2013. PMID: 23583740 Clinical Trial.

7

Genetic score based on high-risk genetic polymorphisms and early onset of ischemic heart disease in an Italian cohort of ischemic patients.

Vecoli C, Adlerstein D, Shehi E, Bigazzi F, Sampietro T, Foffa I, Carpeggiani C, L'abbate A, Andreassi MG. Vecoli C, et al. Thromb Res. 2014 May;133(5):804-10. doi: 10.1016/j.thromres.2014.03.006. Epub 2014 Mar 6. Thromb Res. 2014. PMID: 24656450

8

Stromal cell-derived factor-1-3'A polymorphism is associated with decreased risk of myocardial infarction and early endothelial disturbance.

Borghini A, Sbrana S, Vecoli C, Mercuri A, Turchi S, Carpeggiani C, L'Abbate A, Andreassi MG. Borghini A, et al. Among authors: vecoli c. J Cardiovasc Med (Hagerstown). 2014 Sep;15(9):710-6. doi: 10.2459/JCM.0000000000000068. J Cardiovasc Med (Hagerstown). 2014. PMID: 24751515

9

Genetic risk score and acute skin toxicity after breast radiation therapy.

Borghini A, Vecoli C, Mercuri A, Petruzzelli MF, D'Errico MP, Portaluri M, Andreassi MG. Borghini A, et al. Among authors: vecoli c. Cancer Biother Radiopharm. 2014 Sep;29(7):267-72. doi: 10.1089/cbr.2014.1620. Epub 2014 Aug 6. Cancer Biother Radiopharm. 2014. PMID: 25099761

10

Congenital heart disease: the crossroads of genetics, epigenetics and environment.

Vecoli C, Pulignani S, Foffa I, Andreassi MG. Vecoli C, et al. Curr Genomics. 2014 Oct;15(5):390-9. doi: 10.2174/1389202915666140716175634. Curr Genomics. 2014. PMID: 25435801 Free PMC article.

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