Letter: Delayed drug-induced dystonias.

par Simpson, M A
Publié 1973

Letter: An easy death--an uneasy argument.

par Simpson, M A
Publié 1975

Future of British psychiatrists.

par Simpson, M A
Publié 1971

Overseas students.

par Simpson, M. A.
Publié 1967

Living with the dying.

par Simpson, M. A.
Publié 1977

Female genital self-mutilation as a cause of vaginal bleeding

par Simpson, M. A., Anstee, B. H.
Publié 1974

The case of Jane Anderson, Portobello, 1889-1914.

par Simpson, M A, Squires, T J, Busuttil, A
Publié 2000

New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy

par Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Publié dans Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

par Walsh, D. M., Shah, S. H., Simpson, M. A., Morgan, N. V., Khaliq, S., Trembath, R. C., Mehdi, S. Q., Maher, E. R.
Publié 2012

A genome-wide association study for extremely high intelligence

par Zabaneh, D, Krapohl, E, Gaspar, H A, Curtis, C, Lee, S H, Patel, H, Newhouse, S, Wu, H M, Simpson, M A, Putallaz, M, Lubinski, D, Plomin, R, Breen, G
Publié dans Mol Psychiatry (2018)

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

par Leo, V. C., Morgan, N. V., Bem, D., Jones, M. L., Lowe, G. C., Lordkipanidzé, M., Drake, S., Simpson, M. A., Gissen, P., Mumford, A., Watson, S. P., Daly, M. E.
Publié dans J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

par Petridis, C, Shinomiya, I, Kohut, K, Gorman, P, Caneppele, M, Shah, V, Troy, M, Pinder, S E, Hanby, A, Tomlinson, I, Trembath, R C, Roylance, R, Simpson, M A, Sawyer, E J
Publié 2014

A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

par Spain, S L, Pedroso, I, Kadeva, N, Miller, M B, Iacono, W G, McGue, M, Stergiakouli, E, Smith, G D, Putallaz, M, Lubinski, D, Meaburn, E L, Plomin, R, Simpson, M A
Publié dans Mol Psychiatry (2016)

Erratum: A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence

par Spain, S L, Pedroso, I, Kadeva, N, Miller, M B, Iacono, W G, McGue, M, Stergiakouli, E, Smith, G D, Putallaz, M, Lubinski, D, Meaburn, E L, Plomin, R, Simpson, M A
Publié dans Mol Psychiatry (2015)

Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development

par Simpson, M. A. , Hsu, R. , Keir, L. S. , Hao, J. , Sivapalan, G. , Ernst, L. M. , Zackai, E. H. , Al-Gazali, L. I. , Hulskamp, G. , Kingston, H. M. , Prescott, T. E. , Ion, A. , Patton, M. A. , Murday, V. , George, A. , Crosby, A. H. 
Publié 2007