Letter: Delayed drug-induced dystonias.

di Simpson, M A
Pubblicazione 1973

Letter: An easy death--an uneasy argument.

di Simpson, M A
Pubblicazione 1975

Future of British psychiatrists.

di Simpson, M A
Pubblicazione 1971

Overseas students.

di Simpson, M. A.
Pubblicazione 1967

Living with the dying.

di Simpson, M. A.
Pubblicazione 1977

Female genital self-mutilation as a cause of vaginal bleeding

di Simpson, M. A., Anstee, B. H.
Pubblicazione 1974

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

di Simpson, M A, Squires, T J, Busuttil, A
Pubblicazione 2000

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

di Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Pubblicato in Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

di 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
Pubblicato in Mol Psychiatry (2018)

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

di 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.
Pubblicato in J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

di 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
Pubblicazione 2014

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

di 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
Pubblicato in Mol Psychiatry (2016)

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

di 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
Pubblicato in Mol Psychiatry (2015)

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

di 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. 
Pubblicazione 2007