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Refining phenotype characterization in genetic linkage studies of schizophrenia.

Publication ,  Journal Article
Keefe, RS; Silverman, JM; Siever, LJ; Cornblatt, BA
Published in: Soc Biol
1991

A definitive replicable genetic linkage for a major locus underlying the susceptibility to schizophrenia has not been identified to date. Although there are several possible explanations for the failure to find linkage in schizophrenia, one major problem is that the range of phenotypic expressions of the genes for schizophrenia has not been clarified. A more refined understanding of the various phenotypic expressions of a gene related to schizophrenia would enhance the power of studies designed to detect a genetic linkage with a major chromosomal locus and would benefit other strategies for understanding the etiology of schizophrenia. The genes for schizophrenia may be frequently expressed in relatives of schizophrenic patients, although with less severe symptoms than those of chronic schizophrenia. Two series of findings support this notion. Nonschizophrenic relatives of schizophrenic patients demonstrate an increased incidence of nonpsychotic schizophrenia-like symptoms and traits, and they manifest deficit performances on several different laboratory tests of neurocognitive functioning. A more refined phenotypic expression of a schizophrenia-related gene may thus be indicated by personality traits and subclinical neurocognitive deficits. These personality traits and neurocognitive deficits are considered here as possible aids in the identification of affected cases in genetic linkage studies of schizophrenia. Terminology for different indicators of neurocognitive deficits is introduced, and the relative utility of personality traits and indicators of neurocognitive deficit for genetic linkage studies is discussed. As specific examples, schizophrenia-related personality traits that are unrelated to affective symptoms and performance deficits on tasks of eye tracking and continuous attention are considered for strategies for broadening phenotype characterization without reducing the specificity of affected case identification.

Duke Scholars

Published In

Soc Biol

DOI

ISSN

0037-766X

Publication Date

1991

Volume

38

Issue

3-4

Start / End Page

197 / 218

Location

United States

Related Subject Headings

  • Task Performance and Analysis
  • Schizophrenia
  • Phenotype
  • Personality Disorders
  • Humans
  • Genetic Linkage
  • Eye Movements
  • Demography
 

Citation

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Chicago
ICMJE
MLA
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Keefe, R. S., Silverman, J. M., Siever, L. J., & Cornblatt, B. A. (1991). Refining phenotype characterization in genetic linkage studies of schizophrenia. Soc Biol, 38(3–4), 197–218. https://doi.org/10.1080/19485565.1991.9988788
Keefe, R. S., J. M. Silverman, L. J. Siever, and B. A. Cornblatt. “Refining phenotype characterization in genetic linkage studies of schizophrenia.Soc Biol 38, no. 3–4 (1991): 197–218. https://doi.org/10.1080/19485565.1991.9988788.
Keefe RS, Silverman JM, Siever LJ, Cornblatt BA. Refining phenotype characterization in genetic linkage studies of schizophrenia. Soc Biol. 1991;38(3–4):197–218.
Keefe, R. S., et al. “Refining phenotype characterization in genetic linkage studies of schizophrenia.Soc Biol, vol. 38, no. 3–4, 1991, pp. 197–218. Pubmed, doi:10.1080/19485565.1991.9988788.
Keefe RS, Silverman JM, Siever LJ, Cornblatt BA. Refining phenotype characterization in genetic linkage studies of schizophrenia. Soc Biol. 1991;38(3–4):197–218.

Published In

Soc Biol

DOI

ISSN

0037-766X

Publication Date

1991

Volume

38

Issue

3-4

Start / End Page

197 / 218

Location

United States

Related Subject Headings

  • Task Performance and Analysis
  • Schizophrenia
  • Phenotype
  • Personality Disorders
  • Humans
  • Genetic Linkage
  • Eye Movements
  • Demography