Letter: Delayed drug-induced dystonias.

od Simpson, M A
Wydane 1973

Letter: An easy death--an uneasy argument.

od Simpson, M A
Wydane 1975

Future of British psychiatrists.

od Simpson, M A
Wydane 1971

Overseas students.

od Simpson, M. A.
Wydane 1967

Living with the dying.

od Simpson, M. A.
Wydane 1977

Female genital self-mutilation as a cause of vaginal bleeding

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

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

od Simpson, M A, Squires, T J, Busuttil, A
Wydane 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.
Wydane w 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.
Wydane 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
Wydane w 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.
Wydane w 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
Wydane 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
Wydane w 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
Wydane w 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. 
Wydane 2007