Letter: Delayed drug-induced dystonias.

av Simpson, M A
Publicerad 1973

Letter: An easy death--an uneasy argument.

av Simpson, M A
Publicerad 1975

Future of British psychiatrists.

av Simpson, M A
Publicerad 1971

Overseas students.

av Simpson, M. A.
Publicerad 1967

Living with the dying.

av Simpson, M. A.
Publicerad 1977

Female genital self-mutilation as a cause of vaginal bleeding

av Simpson, M. A., Anstee, B. H.
Publicerad 1974

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

av Simpson, M A, Squires, T J, Busuttil, A
Publicerad 2000

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

av Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
I publikationen Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

av 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
I publikationen Mol Psychiatry (2018)

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

av 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.
I publikationen J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

av 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
Publicerad 2014

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

av 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
I publikationen Mol Psychiatry (2016)

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

av 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
I publikationen Mol Psychiatry (2015)

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

av 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. 
Publicerad 2007