Letter: Delayed drug-induced dystonias.

Por Simpson, M A
Publicado em 1973

Letter: An easy death--an uneasy argument.

Por Simpson, M A
Publicado em 1975

Future of British psychiatrists.

Por Simpson, M A
Publicado em 1971

Overseas students.

Por Simpson, M. A.
Publicado em 1967

Living with the dying.

Por Simpson, M. A.
Publicado em 1977

Female genital self-mutilation as a cause of vaginal bleeding

Por Simpson, M. A., Anstee, B. H.
Publicado em 1974

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

Por Simpson, M A, Squires, T J, Busuttil, A
Publicado em 2000

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

Por Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Publicado no Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

Por 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
Publicado no Mol Psychiatry (2018)

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

Por 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.
Publicado no J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

Por 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
Publicado em 2014

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

Por 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
Publicado no Mol Psychiatry (2016)

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

Por 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
Publicado no Mol Psychiatry (2015)

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

Por 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. 
Publicado em 2007