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Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease.

Abstract:
Intermediate phenotypes are traits positioned somewhere between genetic variation and disease. They represent a target for attempts to find disease-associated genetic variants and elucidation of mechanisms. Psychiatry has been particularly enamoured with intermediate phenotypes, due to uncertainty about disease aetiology, inconclusive results in early psychiatric genetic studies, and their appeal relative to traditional diagnostic categories. In this review, we argue that new genetic findings are relevant to the question of the utility of these constructs. In particular, results from genome-wide association studies of psychiatric disorders now allow an assessment of the potential role of particular intermediate phenotypes. Based on such an analysis, as well as other recent results, we conclude that intermediate phenotypes are likely to be most valuable in understanding mechanism.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.tins.2014.08.007

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author


Publisher:
Elsevier
Journal:
Trends in Neurosciences More from this journal
Volume:
37
Issue:
12
Pages:
733-741
Publication date:
2014-12-01
DOI:
EISSN:
1878-108X
ISSN:
0166-2236


Language:
English
Pubs id:
pubs:485033
UUID:
uuid:f67c77ea-f89e-4c90-ab02-394f1f3d295f
Local pid:
pubs:485033
Source identifiers:
485033
Deposit date:
2014-09-23
ARK identifier:

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