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Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma.
EBioMedicine. 2023 Jan;87:104395. doi: 10.1016/j.ebiom.2022.104395. Epub 2022 Dec 6.
EBioMedicine. 2023.
PMID: 36493725
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.
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.
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Wee1 Rather Than Plk1 Is Inhibited by AZD1775 at Therapeutically Relevant Concentrations.
Serpico AF, D'Alterio G, Vetrei C, Della Monica R, Nardella L, Visconti R, Grieco D.
Serpico AF, et al. Among authors: d alterio g.
Cancers (Basel). 2019 Jun 13;11(6):819. doi: 10.3390/cancers11060819.
Cancers (Basel). 2019.
PMID: 31200459
Free PMC article.
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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: d alterio 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.
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A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis.
De Falco A, De Brasi D, Della Monica M, Cesario C, Petrocchi S, Novelli A, D'Alterio G, Iolascon A, Capasso M, Piscopo C.
De Falco A, et al. Among authors: d alterio g.
Genes (Basel). 2023 Jan 1;14(1):119. doi: 10.3390/genes14010119.
Genes (Basel). 2023.
PMID: 36672860
Free PMC article.
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