Institutional members access full text with Ovid®

Share this article on:

Consideration of plausible genetic architectures for schizophrenia and implications for analytic approaches in the era of next generation sequencing

Curtis, David

doi: 10.1097/YPG.0b013e32835d7e5a
Commentary

The results of linkage and association studies imply that there are no common, dominantly active variants which have a substantial effect on the risk of schizophrenia. However, there are rare structural variants with a major effect and it is argued that results to date are not incompatible with the existence of large numbers of individually rare sequence variants with major effect, since these would not have been detected by the methods used to date. It is also argued that the epidemiology is consistent with a contribution from recessively acting variants and that likewise these might have gone undetected. It is shown that methods of analysis specifically designed to detect recessive variants through testing departure from Hardy–Weinberg equilibrium offer substantial increases of power over conventional methods. It is recommended that analytic approaches aim to detect very rare variants with major effect and that specific attempts are made to detect recessively acting loci.

Centre for Psychiatry, Barts and the London School of Medicine and Dentistry, London, UK

Correspondence to David Curtis, MD, PhD, Centre for Psychiatry, Barts and the London School of Medicine and Dentistry, London E1 1BB, UK Tel: +44 20 7377 7729; fax: +44 20 7377 7316; e-mail: david.curtis@qmul.ac.uk

Received July 27, 2012

Accepted November 18, 2012

© 2013 Lippincott Williams & Wilkins, Inc.