Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia (Q28265644)

Symptoms of schizophrenia. Methods, meanings, and mechanisms.

Europe PubMed Central

title

Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia (English)

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1

D H R Blackwood

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Walter J Muir

series ordinal

2

object named as

W J Muir

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language of work or name

English

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publication date

2004

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published in

Neurotoxicity Research

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volume

6

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issue

1

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page(s)

35-41

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cites work

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Manic-depression genes and the new millennium: poised for discovery

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Characterization of psychotic conditions. Use of the domains of psychopathology model.

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Association within a family of a balanced autosomal translocation with major mental illness

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DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

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Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q

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Correlation of auditory 'oddball' P300 with verbal memory deficits in schizophrenia

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Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

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Recent advances in the genetics of schizophrenia

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Information processing deficits in relatives of manic depressive patients

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Methodological considerations in measurement of the P300 component of the auditory oddball ERP in schizophrenia.

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Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

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Chromosome 1 loci in Finnish schizophrenia families

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