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A Novel Pathogenic BRCA1 Splicing Variant Produces Partial Intron Retention in the Mature Messenger RNA.
Int J Mol Sci. 2016 Dec 21;17(12):2145. doi: 10.3390/ijms17122145.
Int J Mol Sci. 2016.
PMID: 28009814
Free PMC article.
The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches.
D'Argenio V, Esposito MV, Telese A, Precone V, Starnone F, Nunziato M, Cantiello P, Iorio M, Evangelista E, D'Aiuto M, Calabrese A, Frisso G, D'Aiuto G, Salvatore F.
D'Argenio V, et al. Among authors: starnone f.
Clin Chim Acta. 2015 Jun 15;446:221-5. doi: 10.1016/j.cca.2015.03.045. Epub 2015 Apr 17.
Clin Chim Acta. 2015.
PMID: 25896959
Free article.
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Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report.
Nunziato M, Starnone F, Lombardo B, Pensabene M, Condello C, Verdesca F, Carlomagno C, De Placido S, Pastore L, Salvatore F, D'Argenio V.
Nunziato M, et al. Among authors: starnone f.
Int J Mol Sci. 2017 Nov 22;18(11):2487. doi: 10.3390/ijms18112487.
Int J Mol Sci. 2017.
PMID: 29165356
Free PMC article.
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A multi-gene panel beyond BRCA1/BRCA2 to identify new breast cancer-predisposing mutations by a picodroplet PCR followed by a next-generation sequencing strategy: a pilot study.
Nunziato M, Esposito MV, Starnone F, Diroma MA, Calabrese A, Del Monaco V, Buono P, Frasci G, Botti G, D'Aiuto M, Salvatore F, D'Argenio V.
Nunziato M, et al. Among authors: starnone f.
Anal Chim Acta. 2019 Jan 10;1046:154-162. doi: 10.1016/j.aca.2018.09.032. Epub 2018 Sep 18.
Anal Chim Acta. 2019.
PMID: 30482293
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Multi-gene panel testing increases germline predisposing mutations' detection in a cohort of breast/ovarian cancer patients from Southern Italy.
Nunziato M, Di Maggio F, Pensabene M, Esposito MV, Starnone F, De Angelis C, Calabrese A, D'Aiuto M, Botti G, De Placido S, D'Argenio V, Salvatore F.
Nunziato M, et al. Among authors: starnone f.
Front Med (Lausanne). 2022 Aug 11;9:894358. doi: 10.3389/fmed.2022.894358. eCollection 2022.
Front Med (Lausanne). 2022.
PMID: 36035419
Free PMC article.
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Evaluation of a Four-Gene Panel for Hereditary Cancer Risk Assessment.
Secondino A, Starnone F, Veneruso I, Di Tella MA, Conato S, De Angelis C, De Placido S, D'Argenio V.
Secondino A, et al. Among authors: starnone f.
Genes (Basel). 2022 Apr 13;13(4):682. doi: 10.3390/genes13040682.
Genes (Basel). 2022.
PMID: 35456488
Free PMC article.
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One-step NGS molecular analysis of the CFTR gene on newborn dried blood spots gives a higher diagnostic sensitivity in affected and carrier subjects: A pilot study.
Nunziato M, Starnone F, Giordano S, D'Antonio M, Scognamiglio D, Esposito MV, Correra A, Di Maggio F, D'Argenio V, Scaglione GL, Castaldo G, Salvatore F.
Nunziato M, et al. Among authors: starnone f.
Clin Chim Acta. 2024 Jan 1;552:117625. doi: 10.1016/j.cca.2023.117625. Epub 2023 Nov 3.
Clin Chim Acta. 2024.
PMID: 37923102
Free article.
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