Understanding of BRCA VUS genetic results by breast cancer specialists von Eccles, B K, Copson, E, Maishman, T, Abraham, J E, Eccles, D M

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Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies von Antoniou, A., Pharoah, P.D.P., Narod, S., Risch, H.A., Eyfjord, J.E., Hopper, J.L., Loman, N., Olsson, H., Johannsson, O., Borg, Å., Pasini, B., Radice, P., Manoukian, S., Eccles, D.M., Tang, N., Olah, E., Anton-Culver, H., Warner, E., Lubinski, J., Gronwald, J., Gorski, B., Tulinius, H., Thorlacius, S., Eerola, H., Nevanlinna, H., Syrjäkoski, K., Kallioniemi, O.-P., Thompson, D., Evans, C., Peto, J., Lalloo, F., Evans, D.G., Easton, D.F.

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A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations von Wilson, J R F, Bateman, A C, Hanson, H, An, Q, Evans, G, Rahman, N, Jones, J L, Eccles, D M

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Prevalence of BRCA1 and BRCA2 mutations in triple negative breast cancer von Evans, D G, Howell, A, Ward, D, Lalloo, F, Jones, J L, Eccles, D M

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Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification von BUNYAN, D. J, ECCLES, D. M, CROSS, N. C. P, SILLIBOURNE, J, WILKINS, E, THOMAS, N. Simon, SHEA-SIMONDS, J, DUNCAN, P. J, CURTIS, C. E, ROBINSON, D. O, HARVEY, J. F

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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance von Eccles, D.M., Mitchell, G., Monteiro, A.N.A., Schmutzler, R., Couch, F.J., Spurdle, A.B., Gómez-García, E.B., Driessen, R., Lindor, N.M., Blok, M.J., Moller, P., de la Hoya, M., Pal, T., Domchek, S., Nathanson, K., Van Asperen, C., Diez, O., Rheim, K., Stoppa-Lyonnet, D., Parsons, M., Goldgar, D.

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A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO von Evans, D G R, Eccles, D M, Rahman, N, Young, K, Bulman, M, Amir, E, Shenton, A, Howell, A, Lalloo, F

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Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies von Antoniou, A C, Pharoah, P D P, Narod, S, Risch, H A, Eyfjord, J E, Hopper, J L, Olsson, H, Johannsson, O, Borg, Å, Pasini, B, Radice, P, Manoukian, S, Eccles, D M, Tang, N, Olah, E, Anton-Culver, H, Warner, E, Lubinski, J, Gronwald, J, Gorski, B, Tulinius, H, Thorlacius, S, Eerola, H, Nevanlinna, H, Syrjäkoski, K, Kallioniemi, O-P, Thompson, D, Evans, C, Peto, J, Lalloo, F, Evans, D G, Easton, D F

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The presentation, management and outcome of inflammatory breast cancer cases in the UK: Data from a multi-centre retrospective review von Copson, E., Shaaban, A.M., Maishman, T., Moseley, P.M., McKenzie, H., Bradbury, J., Borley, A., Brzezinska, M., Chan, S.Y.T., Ching, J., Cutress, R.I., Danial, I., Dall, B., Kerin, M., Lowery, A.J., Macpherson, I.R., Romics, L., Sawyer, E., Sharmat, N., Sircar, T., Vidya, R., Pan, Y., Rea, D., Jones, L., Eccles, D.M., Berditchevski, F.

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Obesity and the outcome of young breast cancer patients in the UK: the POSH study von Copson, E.R., Cutress, R.I., Maishman, T., Eccles, B.K., Gerty, S., Stanton, L., Altman, D.G., Durcan, L., Wong, C., Simmonds, P.D., Jones, L., Eccles, D.M.

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Guidelines for a genetic risk based approach to advising women with a family history of breast cancer von Eccles, D M, Evans, D G R, Mackay, J

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Hereditary cancer: guidelines in clinical practice. Breast and ovarian cancer genetics von Eccles, D.M.

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Genetic testing in a cohort of young patients with HER2-amplified breast cancer von Eccles, D.M., Li, N., Handwerker, R., Maishman, T., Copson, E.R., Durcan, L.T., Gerty, S.M., Jones, L., Evans, D.G., Haywood, L., Campbell, I.

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Family history and outcome of young patients with breast cancer in the UK (POSH study) von Eccles, B. K., Copson, E. R., Cutress, R. I., Maishman, T., Altman, D. G., Simmonds, P., Gerty, S. M., Durcan, L., Stanton, L., Eccles, D. M.

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The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions von Antoniou, A C, Cunningham, A P, Peto, J, Evans, D G, Lalloo, F, Narod, S A, Risch, H A, Eyfjord, J E, Hopper, J L, Southey, M C, Olsson, H, Johannsson, O, Borg, A, Passini, B, Radice, P, Manoukian, S, Eccles, D M, Tang, N, Olah, E, Anton-Culver, H, Warner, E, Lubinski, J, Gronwald, J, Gorski, B, Tryggvadottir, L, Syrjakoski, K, Kallioniemi, O-P, Eerola, H, Nevanlinna, H, Pharoah, P D P, Easton, D F

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Polymorphic variation in CYP19 and the risk of breast cancer von Baxter, S.W., Choong, D.Y.H., Eccles, D.M., Campbell, I.G.

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Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene von ECCLES, D. M, VAN DER LUIJT, R, FODDE, R, BREUKEL, C, BULLMAN, H, BUNYAN, D, FISHER, A, BARBER, J, DU BOULAY, C, PRIMROSE, J, BURN, J

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Apoptosis, ageing and cancer susceptibility von CAMPLEJOHN, R. S, GILCHRIS, R, EASTON, D, MCKENZIE-EDWARDS, E, BARNES, D. M, ECCLES, D. M, ARDERN-JONES, A, HODGSON, S. V, DUDDY, P. M, EELES, R. A

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Final Results of the Prospective FH02 Mammographic Surveillance Study of Women Aged 35-39 at Increased Familial Risk of Breast Cancer von Evans, D G, Thomas, S, Caunt, J, Burch, A, Brentnall, A R, Roberts, L, Howell, A, Wilson, M, Fox, R, Hillier, S, Sibbering, D M, Moss, S, Wallis, M G, Eccles, D M, Duffy, S

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p53 mutation is a common genetic event in ovarian carcinoma von MILNER, B. J, ALLAN, L. A, ECCLES, D. M, KITCHENER, H. C, LEONARD, R. C. F, KELLY, K. F, PARKIN, D. E, HAITES, N. E

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