Letter: Delayed drug-induced dystonias.

od Simpson, M A
Izdano 1973

Letter: An easy death--an uneasy argument.

od Simpson, M A
Izdano 1975

Future of British psychiatrists.

od Simpson, M A
Izdano 1971

Overseas students.

od Simpson, M. A.
Izdano 1967

Living with the dying.

od Simpson, M. A.
Izdano 1977

Female genital self-mutilation as a cause of vaginal bleeding

od Simpson, M. A., Anstee, B. H.
Izdano 1974

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

od Simpson, M A, Squires, T J, Busuttil, A
Izdano 2000

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

od Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Izdano u Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

od 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
Izdano u Mol Psychiatry (2018)

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

od 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.
Izdano u J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

od 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
Izdano 2014

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

od 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
Izdano u Mol Psychiatry (2016)

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

od 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
Izdano u Mol Psychiatry (2015)

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

od 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. 
Izdano 2007