The Troubled Helix: Social and Psychological Implications of the New Human Genetics

Por Lucassen, A.
Publicado em 2000

Concern for families and individuals in clinical genetics

Por Parker, M, Lucassen, A
Publicado em 2003

Clinical geneticists' attitudes and practice towards testing for breast cancer susceptibility genes

Por LUCASSEN, A., HOULSTON, R.
Publicado em 2000

Genetic testing without consent: the implications of the new Human Tissue Act 2004

Por Lucassen, A, Kaye, J
Publicado em 2006

Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome represent one condition with variable expression and age‐related penetrance: results of a clinical study of PTEN mutation carr...

Por Lachlan, K L, Lucassen, A M, Bunyan, D, Temple, I K
Publicado em 2007

Education improves general practitioner (GP) management of familial breast/ovarian cancer: findings from a cluster randomised controlled trial

Por Watson, E, Clements, A, Lucassen, A, Yudkin, P, Mackay, J, Austoker, J
Publicado em 2002

Evaluation of the impact of two educational interventions on GP management of familial breast/ovarian cancer cases: a cluster randomised controlled trial.

Por Watson, E, Clements, A, Yudkin, P, Rose, P, Bukach, C, Mackay, J, Lucassen, A, Austoker, J
Publicado em 2001

Multiple DNA Variant Association Analysis: Application to the Insulin Gene Region in Type 1 Diabetes

Por Julier, C., Lucassen, A., Villedieu, P., Delepine, M., Levy-Marchal, C., Danzé, P. M., Bianchi, F., Boitard, C., Froguel, P., Bell, J., Lathrop, G. M.
Publicado em 1994

Exonic STK11 deletions are not a rare cause of Peutz‐Jeghers syndrome

Por Hearle, N C M, Rudd, M F, Lim, W, Murday, V, Lim, A G, Phillips, R K, Lee, P W, O'Donohue, J, Morrison, P J, Norman, A, Hodgson, S V, Lucassen, A, Houlston, R S
Publicado em 2006

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

Por Beysen, D., Raes, J., Leroy, B. P., Lucassen, A., Yates, J. R. W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J. P., Kim, J. R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L. M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R. A., De Paepe, A., De Baere, E.
Publicado em 2005

Further observations on LKB1/STK11 status and cancer risk in Peutz–Jeghers syndrome

Por Lim, W, Hearle, N, Shah, B, Murday, V, Hodgson, S V, Lucassen, A, Eccles, D, Talbot, I, Neale, K, Lim, A G, O'Donohue, J, Donaldson, A, Macdonald, R C, Young, I D, Robinson, M H, Lee, P W R, Stoodley, B J, Tomlinson, I, Alderson, D, Holbrook, A G, Vyas, S, Swarbrick, E T, Lewis, A A M, Phillips, R K S, Houlston, R S
Publicado em 2003