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Predictive testing for BRCA1 and 2 mutations: a male contribution.
Daly PA, Nolan C, Green A, Ormiston W, Cody N, McDevitt T, O'hIci B, Byrne D, McDermott E, Carney DN, O'Higgins N, Barton DE. Daly PA, et al. Among authors: mcdevitt t. Ann Oncol. 2003 Apr;14(4):549-53. doi: 10.1093/annonc/mdg164. Ann Oncol. 2003. PMID: 12649099 Free article.
Familial breast cancer genetic testing in the West of Ireland.
McVeigh TP, Irwin R, Cody N, Miller N, McDevitt T, Sweeney KJ, Green A, Kerin MJ. McVeigh TP, et al. Among authors: mcdevitt t. Ir J Med Sci. 2014 Jun;183(2):199-206. doi: 10.1007/s11845-013-0990-2. Epub 2013 Jul 26. Ir J Med Sci. 2014. PMID: 23884708
Detection of novel germline mutations for breast cancer in non-BRCA1/2 families.
Aloraifi F, McDevitt T, Martiniano R, McGreevy J, McLaughlin R, Egan CM, Cody N, Meany M, Kenny E, Green AJ, Bradley DG, Geraghty JG, Bracken AP. Aloraifi F, et al. Among authors: mcdevitt t. FEBS J. 2015 Sep;282(17):3424-37. doi: 10.1111/febs.13352. Epub 2015 Jul 14. FEBS J. 2015. PMID: 26094658 Free article.
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.
Farrell MP, Hughes DJ, Berry IR, Gallagher DJ, Glogowski EA, Payne SJ, Kennedy MJ, Clarke RM, White SA, Muldoon CB, Macdonald F, Rehal P, Crompton D, Roring S, Duke ST, McDevitt T, Barton DE, Hodgson SV, Green AJ, Daly PA. Farrell MP, et al. Among authors: mcdevitt t. Fam Cancer. 2012 Sep;11(3):509-18. doi: 10.1007/s10689-012-9544-4. Fam Cancer. 2012. PMID: 22773173 Review.
When good CF tests go bad.
McDevitt T, Barton D. McDevitt T, et al. Eur J Hum Genet. 2009 Apr;17(4):403-5. doi: 10.1038/ejhg.2008.229. Epub 2008 Dec 3. Eur J Hum Genet. 2009. PMID: 19050722 Free PMC article. No abstract available.
199 results