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Methodology of genetic research in psychiatry

Published online by Cambridge University Press:  18 September 2015

Extract

Most forms of behaviour whether normal or abnormal, show a tendency to run in families. However, these can range from symptoms of dementia and movement disorder caused by the comparatively rare autosomal dominant Huntington's disease to common everyday aspects of behaviour such as religious persuasion or career choice. Normal behaviours and most common disorders do not show simple mendelian inheritance but instead have more complex patterns of transmission involving either major genes with incomplete penetrance, multiple genes of small effect, or a combination of the two. In addition, common complex phenotypes usually involve the combination of genetic and environmental factors. Therefore once family studies have shown that a disorder or trait is familial the next stage is to perform twin studies and, if possible adoption studies to investigate whether this results from shared genes, shared environment or a combination of the two.

Type
Research Article
Copyright
Copyright © Scandinavian College of Neuropsychopharmacology 1999

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References

Literature

1.McGuffin, P, Owen, MJ, O'Donovan, MC, et al.Sem psychiat Gen Roy Coll Psychiat, 1994.Google Scholar
2Plomin, R., Owen, MJ, McGuffin, P. The genetic basis of complex human behaviours. Science 1994; 264: 1733–9.CrossRefGoogle Scholar
3.Gottesman, II, Shields, J. A polygenic theory of schizophrenia. Proc nat Acad Sci USA 1967; 1: 199205.CrossRefGoogle Scholar
4.Neale, MC, Cardon, LR. Methodology of Genetic Studies of Twins and Families. Dordrecht: Kluwer, 1991.Google Scholar
5.Thapar, AG, Harold, G, McGuffin, P. Life events and depressive symptoms-shared genes or shared adversity? A research Note. J Child Psychol Psychiat 1998; 39: 1153–8.CrossRefGoogle ScholarPubMed
6.Kendler, KS, Heath, A, Martin, N, Eaves, LJ. Symptoms of anxiety and depression in a volunteer twin population. The etiologic role of genetic and environmental factors. Arch gen Psychiatry 1986; 43: 213–21.CrossRefGoogle Scholar
7.Risch, N, Botstein, D. A manic depressive history. Nat Gen 1996; 12: 351–3.CrossRefGoogle ScholarPubMed
8.Moldin, SO. The maddening hunt for madness genes. Nat Gen 1997; 17: 127–9.CrossRefGoogle ScholarPubMed
9.Spielman, RS, McGinnis, RE, Ewens, WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J hum Gen 1993; 52: 506–16.Google ScholarPubMed
10.Asherson, P, Curan, S, McGuffin, P. Approaches to gene mapping. CNS 1998; 4: 1822.Google Scholar