Testing for the breast cancer predisposition gene, BRCA1.

per Eeles, R.
Publicat 1996

BRCA1, BRCA2 and their possible function in DNA damage response

per Kote-Jarai, Z, Eeles, R A
Publicat 1999

Management of Breast Cancer in BRCA1/2 Mutation Carriers

per Eeles, R. A., Camplejohn, R., Peacock, J., McMillan, T.
Publicat 1999

Non-Hodgkin's lymphoma presenting with extradural spinal cord compression: functional outcome and survival.

per Eeles, R. A., O'Brien, P., Horwich, A., Brada, M.
Publicat 1991

Familial breast cancer: a controlled study of risk perception, psychological morbidity and health beliefs in women attending for genetic counselling.

per Lloyd, S., Watson, M., Waites, B., Meyer, L., Eeles, R., Ebbs, S., Tylee, A.
Publicat 1996

The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer

per Watson, M, Lloyd, S, Davidson, J, Meyer, L, Eeles, R, Ebbs, S, Murday, V
Publicat 1999

SNPs in the kallikrein gene region associated with prostate cancer risk: true cause or association by design?

per Eeles, R, Giles, G, Neal, D, Hamdy, F, Donovan, J, Muir, K, Easton, D
Publicat 2008

Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer

per Hodgson, S., Heap, E., Cameron, J., Ellis, D., Mathew, C., Eeles, R., Solomon, E., Lewis, C.
Publicat 1999

No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours

per Jefferies, S, Edwards, S M, Hamoudi, R A, A'Hern, R, Foulkes, W, Goldgar, D, Eeles, R
Publicat 2001

Construction of tissue microarrays from prostate needle biopsy specimens

per Jhavar, S, Corbishley, C M, Dearnaley, D, Fisher, C, Falconer, A, Parker, C, Eeles, R, Cooper, C S
Publicat 2005

Glutathione-S-transferase M1, T1 and P1 polymorphisms, and breast cancer risk, in BRCA1/2 mutation carriers

per Kadouri, L, Kote-Jarai, Z, Hubert, A, Baras, M, Abeliovich, D, Hamburger, T, Peretz, T, Eeles, R A
Publicat 2008

Family history of breast cancer: what do women understand and recall about their genetic risk?

per Watson, M, Duvivier, V, Wade Walsh, M, Ashley, S, Davidson, J, Papaikonomou, M, Murday, V, Sacks, N, Eeles, R
Publicat 1998

A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers

per Kadouri, L, Kote-Jarai, Z, Hubert, A, Durocher, F, Abeliovich, D, Glaser, B, Hamburger, T, Eeles, R A, Peretz, T
Publicat 2004

Polygenic susceptibility to prostate and breast cancer: implications for personalised screening

per Pashayan, N, Duffy, S W, Chowdhury, S, Dent, T, Burton, H, Neal, D E, Easton, D F, Eeles, R, Pharoah, P
Publicat 2011

Ambiguity in a masculine world: Being a BRCA1/2 mutation carrier and a man with prostate cancer

per Moynihan, C., Bancroft, E.K., Mitra, A., Ardern‐Jones, A., Castro, E., Page, E.C., Eeles, R.A.
Publicat a Psychooncology (2017)

Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

per Eng, C, Murday, V, Seal, S, Mohammed, S, Hodgson, S V, Chaudary, M A, Fentiman, I S, Ponder, B A, Eeles, R A
Publicat 1994

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information

per Hallowell, N, Foster, C, Eeles, R, Ardern-Jones, A, Murday, V, Watson, M, Clarke, A, Hallowell, N, Watson, M
Publicat 2003

Feasibility of familial PSA screening: psychosocial issues and screening adherence

per Sweetman, J, Watson, M, Norman, A, Bunstead, Z, Hopwood, P, Melia, J, Moss, S, Eeles, R, Dearnaley, D, Moynihan, C
Publicat 2006

Short report. The AIDIT and IMPACT conference 2006: Outcomes and future directions

per Doherty, R, Lubinski, J, Manguoglu, E, Luleci, G, Christie, M, Craven, P, Bancroft, E, Mitra, A, Morgan, S, Eeles, R
Publicat 2007

The feasibility and results of a population-based approach to evaluating prostate-specific antigen screening for prostate cancer in men with a raised familial risk

per Melia, J, Dearnaley, D, Moss, S, Johns, L, Coulson, P, Moynihan, C, Sweetman, J, Parkinson, M C, Eeles, R, Watson, M
Publicat 2006