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Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19.
Cantalupo S, Lasorsa VA, Russo R, Andolfo I, D'Alterio G, Rosato BE, Frisso G, Abete P, Cassese GM, Servillo G, Gentile I, Piscopo C, Della Monica M, Fiorentino G, Russo G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Cantalupo S, et al. Among authors: frisso g. Int J Mol Sci. 2021 May 20;22(10):5372. doi: 10.3390/ijms22105372. Int J Mol Sci. 2021. PMID: 34065289 Free PMC article.
Allelic Complexity in Long QT Syndrome: A Family-Case Study.
Zullo A, Frisso G, Detta N, Sarubbi B, Romeo E, Cordella A, Vanoye CG, Calabrò R, George AL, Salvatore F. Zullo A, et al. Among authors: frisso g. Int J Mol Sci. 2017 Jul 27;18(8):1633. doi: 10.3390/ijms18081633. Int J Mol Sci. 2017. PMID: 28749435 Free PMC article.
Molecular Basis of Inflammation in the Pathogenesis of Cardiomyopathies.
Monda E, Palmiero G, Rubino M, Verrillo F, Amodio F, Di Fraia F, Pacileo R, Fimiani F, Esposito A, Cirillo A, Fusco A, Moscarella E, Frisso G, Russo MG, Pacileo G, Calabrò P, Scudiero O, Caiazza M, Limongelli G. Monda E, et al. Among authors: frisso g. Int J Mol Sci. 2020 Sep 4;21(18):6462. doi: 10.3390/ijms21186462. Int J Mol Sci. 2020. PMID: 32899712 Free PMC article. Review.
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19.
Andolfo I, Russo R, Lasorsa VA, Cantalupo S, Rosato BE, Bonfiglio F, Frisso G, Abete P, Cassese GM, Servillo G, Esposito G, Gentile I, Piscopo C, Villani R, Fiorentino G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Andolfo I, et al. Among authors: frisso g. iScience. 2021 Apr 23;24(4):102322. doi: 10.1016/j.isci.2021.102322. Epub 2021 Mar 17. iScience. 2021. PMID: 33748697 Free PMC article.
The TNFRSF13C H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern Italy.
Russo R, Andolfo I, Lasorsa VA, Cantalupo S, Marra R, Frisso G, Abete P, Cassese GM, Servillo G, Esposito G, Gentile I, Piscopo C, Della Monica M, Fiorentino G, Russo G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Russo R, et al. Among authors: frisso g. Genes (Basel). 2021 Jun 8;12(6):881. doi: 10.3390/genes12060881. Genes (Basel). 2021. PMID: 34201032 Free PMC article.
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals.
D'Alterio G, Lasorsa VA, Bonfiglio F, Cantalupo S, Rosato BE, Andolfo I, Russo R, Esposito U, Frisso G, Abete P, Cassese GM, Servillo G, Gentile I, Piscopo C, Della Monica M, Fiorentino G, Boccia A, Paolella G, Ferrucci V, de Antonellis P, Siciliano R, Asadzadeh F, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. D'Alterio G, et al. Among authors: frisso g. Genet Med. 2022 Aug;24(8):1653-1663. doi: 10.1016/j.gim.2022.04.007. Epub 2022 May 5. Genet Med. 2022. PMID: 35511137 Free PMC article.
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy.
Mazzaccara C, Limongelli G, Petretta M, Vastarella R, Pacileo G, Bonaduce D, Salvatore F, Frisso G. Mazzaccara C, et al. Among authors: frisso g. J Cardiovasc Med (Hagerstown). 2018 Jul;19(7):344-350. doi: 10.2459/JCM.0000000000000670. J Cardiovasc Med (Hagerstown). 2018. PMID: 29782370 Free PMC article.
88 results