Author(s)
J. Hall, H. C. Whalley, D. E. Job, B. J. Baig, A. M. McIntosh, K. L. Evans, P. A. Thomson, D. J. Porteous, D. G. Cunningham-Owens, E. C. Johnstone, S. M. Lawrie
ISBN
1097-6256 (Print)
1097-6256 (Linking)
Publication year
2006
Periodical
Nat Neurosci
Periodical Number
12
Volume
9
Pages
1477-8
Author Address
Division of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Morningside Park, Edinburgh, EH10 5HF, UK. jhall5@staffmail.ed.ac.uk
NRG1, encoding neuregulin 1, is a susceptibility gene for schizophrenia, but no functional mutation causally related to the disorder has yet been identified. Here we investigate the effects of a variant in the human NRG1 promoter region in subjects at high risk of schizophrenia. We show that this variant is associated with (i) decreased activation of frontal and temporal lobe regions, (ii) increased development of psychotic symptoms and (iii) decreased premorbid IQ.