Letter: Delayed drug-induced dystonias.

по Simpson, M A
Опубликовано 1973

Letter: An easy death--an uneasy argument.

по Simpson, M A
Опубликовано 1975

Future of British psychiatrists.

по Simpson, M A
Опубликовано 1971

Overseas students.

по Simpson, M. A.
Опубликовано 1967

Living with the dying.

по Simpson, M. A.
Опубликовано 1977

Female genital self-mutilation as a cause of vaginal bleeding

по Simpson, M. A., Anstee, B. H.
Опубликовано 1974

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

по Simpson, M A, Squires, T J, Busuttil, A
Опубликовано 2000

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

по Tang, S., Hughes, E., Lascelles, K., Simpson, M. A., Pal, D. K.
Опубликовано в: Am J Med Genet A (2016)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis

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

A genome-wide association study for extremely high intelligence

по 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
Опубликовано в: Mol Psychiatry (2018)

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

по 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.
Опубликовано в: J Thromb Haemost (2015)

Germline CDH1 mutations in bilateral lobular carcinoma in situ

по 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
Опубликовано 2014

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

по 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
Опубликовано в: Mol Psychiatry (2016)

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

по 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
Опубликовано в: Mol Psychiatry (2015)

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

по 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. 
Опубликовано 2007