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CDH1 Genotype Exploration in Women With Hereditary Lobular Breast Cancer Phenotype.
Corso G, Marino E, Zanzottera C, Oliveira C, Bernard L, Macis D, Figueiredo J, Pereira J, Carneiro P, Massari G, Barberis M, De Scalzi AM, Taormina SV, Sajjadi E, Sangalli C, Gandini S, D'Ecclesiis O, Trovato CM, Rotili A, Pesapane F, Nicosia L, La Vecchia C, Galimberti V, Guerini-Rocco E, Bonanni B, Veronesi P. Corso G, et al. Among authors: bonanni b. JAMA Netw Open. 2024 Apr 1;7(4):e247862. doi: 10.1001/jamanetworkopen.2024.7862. JAMA Netw Open. 2024. PMID: 38652475 Free PMC article.
Hereditary lobular breast cancer with an emphasis on E-cadherin genetic defect.
Corso G, Figueiredo J, La Vecchia C, Veronesi P, Pravettoni G, Macis D, Karam R, Lo Gullo R, Provenzano E, Toesca A, Mazzocco K, Carneiro F, Seruca R, Melo S, Schmitt F, Roviello F, De Scalzi AM, Intra M, Feroce I, De Camilli E, Villardita MG, Trentin C, De Lorenzi F, Bonanni B, Galimberti V. Corso G, et al. Among authors: bonanni b. J Med Genet. 2018 Jul;55(7):431-441. doi: 10.1136/jmedgenet-2018-105337. Epub 2018 Jun 21. J Med Genet. 2018. PMID: 29929997 Review.
Germline pathogenic variants in metaplastic breast cancer patients and the emerging role of the BRCA1 gene.
Corso G, Marabelli M, Calvello M, Gandini S, Risti M, Feroce I, Mannucci S, Girardi A, De Scalzi AM, Magnoni F, Marino E, Bernard L, Veronesi P, Guerini-Rocco E, Barberis M, Guerrieri-Gonzaga A, Bonanni B. Corso G, et al. Among authors: bonanni b. Eur J Hum Genet. 2023 Nov;31(11):1275-1282. doi: 10.1038/s41431-023-01429-2. Epub 2023 Jul 18. Eur J Hum Genet. 2023. PMID: 37460658
E-cadherin germline mutation carriers: clinical management and genetic implications.
Corso G, Figueiredo J, Biffi R, Trentin C, Bonanni B, Feroce I, Serrano D, Cassano E, Annibale B, Melo S, Seruca R, De Lorenzi F, Ferrara F, Piagnerelli R, Roviello F, Galimberti V. Corso G, et al. Among authors: bonanni b. Cancer Metastasis Rev. 2014 Dec;33(4):1081-94. doi: 10.1007/s10555-014-9528-y. Cancer Metastasis Rev. 2014. PMID: 25332147 Review.
BRCA1/2 germline missense mutations: a systematic review.
Corso G, Feroce I, Intra M, Toesca A, Magnoni F, Sargenti M, Naninato P, Caldarella P, Pagani G, Vento A, Veronesi P, Bonanni B, Galimberti V. Corso G, et al. Among authors: bonanni b. Eur J Cancer Prev. 2018 May;27(3):279-286. doi: 10.1097/CEJ.0000000000000337. Eur J Cancer Prev. 2018. PMID: 28277317
Prognostic impact of germline mutations in inherited cancer syndromes.
Corso G, Feroce I, Intra M, Veronesi P, Sacchini V, Bonanni B, Galimberti V. Corso G, et al. Among authors: bonanni b. Future Oncol. 2017 Oct;13(24):2125-2127. doi: 10.2217/fon-2017-0296. Epub 2017 Oct 6. Future Oncol. 2017. PMID: 28984488 No abstract available.
309 results