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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2008 1
2010 1
2011 1
2012 4
2013 3
2014 5
2015 4
2016 3
2017 4
2018 7
2019 1
2020 2
2021 2
2022 3
2023 2
2024 1

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40 results

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Page 1
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
Parsons MT, Tudini E, Li H, Hahnen E, Wappenschmidt B, Feliubadaló L, Aalfs CM, Agata S, Aittomäki K, Alducci E, Alonso-Cerezo MC, Arnold N, Auber B, Austin R, Azzollini J, Balmaña J, Barbieri E, Bartram CR, Blanco A, Blümcke B, Bonache S, Bonanni B, Borg Å, Bortesi B, Brunet J, Bruzzone C, Bucksch K, Cagnoli G, Caldés T, Caliebe A, Caligo MA, Calvello M, Capone GL, Caputo SM, Carnevali I, Carrasco E, Caux-Moncoutier V, Cavalli P, Cini G, Clarke EM, Concolino P, Cops EJ, Cortesi L, Couch FJ, Darder E, de la Hoya M, Dean M, Debatin I, Del Valle J, Delnatte C, Derive N, Diez O, Ditsch N, Domchek SM, Dutrannoy V, Eccles DM, Ehrencrona H, Enders U, Evans DG, Farra C, Faust U, Felbor U, Feroce I, Fine M, Foulkes WD, Galvao HCR, Gambino G, Gehrig A, Gensini F, Gerdes AM, Germani A, Giesecke J, Gismondi V, Gómez C, Gómez Garcia EB, González S, Grau E, Grill S, Gross E, Guerrieri-Gonzaga A, Guillaud-Bataille M, Gutiérrez-Enríquez S, Haaf T, Hackmann K, Hansen TVO, Harris M, Hauke J, Heinrich T, Hellebrand H, Herold KN, Honisch E, Horvath J, Houdayer C, Hübbel V, Iglesias S, Izquierdo A, James PA, Janssen LAM, Jeschke U, Kaulfuß S, Keupp K, Kiechle M, Kölbl A, Krieger S, Kruse TA, K… See abstract for full author list ➔ Parsons MT, et al. Among authors: feroce i. Hum Mutat. 2019 Sep;40(9):1557-1578. doi: 10.1002/humu.23818. Hum Mutat. 2019. PMID: 31131967 Free PMC article.
Metaplastic breast cancer: an all-round multidisciplinary consensus.
Corso G, Criscitiello C, Nicosia L, Pesapane F, Vicini E, Magnoni F, Sibilio A, Zanzottera C, De Scalzi AM, Mannucci S, Marabelli M, Calvello M, Feroce I, Zagami P, Porta FM, Toesca A, Tarantino P, Nicolò E, Mazzarol G, La Vecchia C, Bonanni B, Leonardi MC, Veronesi P, Fusco N. Corso G, et al. Among authors: feroce i. Eur J Cancer Prev. 2023 Jul 1;32(4):348-363. doi: 10.1097/CEJ.0000000000000794. Epub 2023 May 12. Eur J Cancer Prev. 2023. PMID: 37021548
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: feroce i. 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.
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: feroce i. 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: feroce i. 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: feroce i. Cancer Metastasis Rev. 2014 Dec;33(4):1081-94. doi: 10.1007/s10555-014-9528-y. Cancer Metastasis Rev. 2014. PMID: 25332147 Review.
The recognition of the profession of Genetic Counsellors in Europe.
Cordier C, McAllister M, Serra-Juhe C, Bengoa J, Pasalodos S, Bjornevoll I, Feroce I, Moldovan R, Paneque M, Lambert D; All are member of the Board of the Genetic Nurses and Genetic Counsellors Professional Branch of the European Board of Medical Genetics. Cordier C, et al. Among authors: feroce i. Eur J Hum Genet. 2018 Dec;26(12):1719-1720. doi: 10.1038/s41431-018-0260-x. Epub 2018 Sep 25. Eur J Hum Genet. 2018. PMID: 30254214 Free PMC article. No abstract available.
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: feroce i. Eur J Cancer Prev. 2018 May;27(3):279-286. doi: 10.1097/CEJ.0000000000000337. Eur J Cancer Prev. 2018. PMID: 28277317
40 results