Letter: Delayed drug-induced dystonias.

由 Simpson, M A
出版 1973

Letter: An easy death--an uneasy argument.

由 Simpson, M A
出版 1975

Future of British psychiatrists.

由 Simpson, M A
出版 1971

Overseas students.

由 Simpson, M. A.
出版 1967

Living with the dying.

由 Simpson, M. A.
出版 1977

Female genital self-mutilation as a cause of vaginal bleeding

由 Simpson, M. A., Anstee, B. H.
出版 1974

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

由 Simpson, M A, Squires, T J, Busuttil, A
出版 2000

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

由 Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
發表在 Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

由 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
發表在 Mol Psychiatry (2018)

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

由 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.
發表在 J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

由 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
出版 2014

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

由 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
發表在 Mol Psychiatry (2016)

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

由 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
發表在 Mol Psychiatry (2015)

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

由 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. 
出版 2007