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Page 1
Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants.
Dell'Elice A, Cini G, Fornasarig M, Armelao F, Barana D, Bianchi F, Casalis Cavalchini GC, Maffè A, Mammi I, Pedroni M, Percesepe A, Sorrentini I, Tibiletti M, Maestro R, Quaia M, Viel A. Dell'Elice A, et al. Mol Genet Genomic Med. 2021 Dec;9(12):e1831. doi: 10.1002/mgg3.1831. Epub 2021 Oct 26. Mol Genet Genomic Med. 2021. PMID: 34704405 Free PMC article.
The Crucial Role of Hereditary Cancer Panel Testing in Unaffected Individuals with a Strong Family History of Cancer: A Retrospective Study of a Cohort of 103 Healthy Subjects.
Pilenzi L, Anaclerio F, Dell'Elice A, Minelli M, Giansante R, Cicirelli M, Tinari N, Grassadonia A, Pantalone A, Grossi S, Canale N, Bruno A, Calabrese G, Ballerini P, Stuppia L, Antonucci I. Pilenzi L, et al. Among authors: dell elice a. Cancers (Basel). 2024 Jun 25;16(13):2327. doi: 10.3390/cancers16132327. Cancers (Basel). 2024. PMID: 39001389 Free PMC article.
Detection of Germline Mutations in a Cohort of 250 Relatives of Mutation Carriers in Multigene Panel: Impact of Pathogenic Variants in Other Genes beyond BRCA1/2.
Di Rado S, Giansante R, Cicirelli M, Pilenzi L, Dell'Elice A, Anaclerio F, Rimoldi M, Grassadonia A, Grossi S, Canale N, Ballerini P, Stuppia L, Antonucci I. Di Rado S, et al. Among authors: dell elice a. Cancers (Basel). 2023 Dec 6;15(24):5730. doi: 10.3390/cancers15245730. Cancers (Basel). 2023. PMID: 38136276 Free PMC article.
Clinical usefulness of NGS multi-gene panel testing in hereditary cancer analysis.
Anaclerio F, Pilenzi L, Dell'Elice A, Ferrante R, Grossi S, Ferlito LM, Marinelli C, Gildetti S, Calabrese G, Stuppia L, Antonucci I. Anaclerio F, et al. Among authors: dell elice a. Front Genet. 2023 Feb 1;14:1060504. doi: 10.3389/fgene.2023.1060504. eCollection 2023. Front Genet. 2023. PMID: 37065479 Free PMC article.