Elementary phenotypes in the neurobiological and genetic study of schizophrenia.

Abstract:

:This review describes the strategy of using elementary phenotypes for neurobiological and genetic linkage studies of schizophrenia. The review concentrates on practical aspects of selecting the phenotype and then understanding the confounds in its measurement and interpretation. Examples from the authors' studies of deficits in P50 inhibition and smooth pursuit eye movement dysfunction are presented. These two phenotypes share considerable similarity in their neurobiology, including a similar response to nicotine. They also appear to co-segregate with the genetic risk for schizophrenia as autosomal co-dominant phenotypes. Although most schizophrenic patients inherit these abnormalities unilinealy, i.e., from one parent, apparent bilineal inheritance produces a more severe illness, observed clinically as childhood-onset schizophrenia. The initial study showing linkage of the P50 deficit to the chromosome 15q14 locus of the alpha 7-nicotinic acetylcholine receptor is an example of the potential usefulness of these phenotypes for combined genetic and neurobiological study of schizophrenia.

journal_name

Biol Psychiatry

journal_title

Biological psychiatry

authors

Adler LE,Freedman R,Ross RG,Olincy A,Waldo MC

doi

10.1016/s0006-3223(99)00085-2

subject

Has Abstract

pub_date

1999-07-01 00:00:00

pages

8-18

issue

1

eissn

0006-3223

issn

1873-2402

pii

S0006-3223(99)00085-2

journal_volume

46

pub_type

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