High-grade ER-negative tumour breast cancers are characteristic of both very young onset cases and patients with hereditary breast cancer

por Eccles, D, Gerty, S, Simmonds, P
Publicado 2006

TP53 intron 6 polymorphism and the risk of ovarian and breast cancer.

por Mavridou, D., Gornall, R., Campbell, I. G., Eccles, D. M.
Publicado 1998

BRCA1 polymorphisms.

por Campbell, I. G., Schroff, R., Englefield, P., Eccles, D. M.
Publicado 1997

No association of a 306-bp insertion polymorphism in the progesterone receptor gene with ovarian and breast cancer.

por Manolitsas, T. P., Englefield, P., Eccles, D. M., Campbell, I. G.
Publicado 1997

BRCA1 mutations in southern England.

por Eccles, D. M., Englefield, P., Soulby, M. A., Campbell, I. G.
Publicado 1998

Understanding of BRCA VUS genetic results by breast cancer specialists

por Eccles, B. K., Copson, E., Maishman, T., Abraham, J. E., Eccles, D. M.
Publicado 2015

Management of Hereditary Breast Cancer

por Eccles, D. M., Simmonds, P., Goddards, J., Coultas, M., Lalloo, F., Evans, G., Haites, N.
Publicado 1999

Overexpression of the p53 protein and allele loss at 17p13 in ovarian carcinoma.

por Eccles, D. M., Brett, L., Lessells, A., Gruber, L., Lane, D., Steel, C. M., Leonard, R. C.
Publicado 1992

Minisatellite instability is found in colorectal tumours with mismatch repair deficiency

por Coleman, M G, Gough, A C, Bunyan, D J, Braham, D, Eccles, D M, Primrose, J N
Publicado 2001

An evaluation of the prognostic model PREDICT using the POSH cohort of women aged ⩽40 years at breast cancer diagnosis

por Maishman, T, Copson, E, Stanton, L, Gerty, S, Dicks, E, Durcan, L, Wishart, G C, Pharoah, P, Eccles, D
Publicado 2015

Cervical intraepithelial neoplasia in lymphoma patients: a cytological and colposcopic study.

por Hughes, R. G., Colquhoun, M., Eccles, D. M., Alloub, M., Parker, A. C., Norval, M., Smart, G. E.
Publicado 1989

Chromosome 11 allele imbalance and clinicopathological correlates in ovarian tumours.

por Gabra, H., Taylor, L., Cohen, B. B., Lessels, A., Eccles, D. M., Leonard, R. C., Smyth, J. F., Steel, C. M.
Publicado 1995

Predictive genetic testing for BRCA1/2 in a UK clinical cohort: three-year follow-up

por Foster, C, Watson, M, Eeles, R, Eccles, D, Ashley, S, Davidson, R, Mackay, J, Morrison, P J, Hopwood, P, Evans, D G R
Publicado 2007

Predictive testing for BRCA1/2: attributes, risk perception and management in a multi-centre clinical cohort

por Foster, C, Evans, D G R, Eeles, R, Eccles, D, Ashley, S, Brooks, L, Davidson, R, Mackay, J, Morrison, P J, Watson, M
Publicado 2002

Psychosocial impact of breast/ovarian (BRCA1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort

por Watson, M, Foster, C, Eeles, R, Eccles, D, Ashley, S, Davidson, R, Mackay, J, Morrison, P J, Hopwood, P, Evans, D G R
Publicado 2004

A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes

por Hopwood, P, Wonderling, D, Watson, M, Cull, A, Douglas, F, Cole, T, Eccles, D, Gray, J, Murday, V, Steel, M, Burn, J, McPherson, K
Publicado 2004

Apoptosis, ageing and cancer susceptibility

por Camplejohn, R S, Gilchrist, R, Easton, D, McKenzie-Edwards, E, Barnes, D M, Eccles, D M, Ardern-Jones, A, Hodgson, S V, Duddy, P M, Eeles, R A
Publicado 2003

BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years

por Robertson, L, Hanson, H, Seal, S, Warren-Perry, M, Hughes, D, Howell, I, Turnbull, C, Houlston, R, Shanley, S, Butler, S, Evans, D G, Ross, G, Eccles, D, Tutt, A, Rahman, N
Publicado 2012

Cancer Genetics Services in Europe

por Hodgson, S., Milner, B., Brown, I., Bevilacqua, G., Chang-Claude, J., Eccles, D., Evans, G., Gregory, H., Møller, P., Morrison, P., Steel, M., Stoppa-Lyonnet, D., Vasen, H., Haites, N.
Publicado 1999

Utilisation of Prophylactic Mastectomy in 10 European Centres

por Evans, D. G. R., Anderson, E., Lalloo, F., Vasen, H., Beckmann, M., Eccles, D., Hodgson, S., Møller, P., Chang-Claude, J., Morrison, P., Stoppa-Lyonnet, D., Steel, M., Haites, N.
Publicado 1999