Linkage of eye movement dysfunction to chromosome 6p in schizophrenia: Additional evidence-Reference-Cited by-同舟云学术

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Linkage of eye movement dysfunction to chromosome 6p in schizophrenia: Additional evidence

Published:2004-05-20 Issue:1 Volume:128B Page:30-36
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Matthysse Steven,Holzman Philip S.,Gusella James F.,Levy Deborah L.,Harte Christopher B.,Jørgensen Åge,Møller Lise,Parnas Josef

Funder

NIH

Roy A. Hunt Foundation

NIH (to JFG)

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference46 articles.

1. Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease;Arolt;Am J Med Genet (Neuropsychiatr Genet),1996

2. Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosome 6, 8, 20, and 22 in families multiply affectd with schizophrenia;Arolt;Am J Med Genet (Neuropsychiatr Genet),1999

3. Eye tracking and optokinetic tests: Diagnostic significance in peripheral and central vestibular disorders;Benitez;Laryngoscope,1970

4. Motion perception in schizophrenia;Chen;Arch Gen Psychiatry,1999a

5. Dependence of impaired eye tracking on deficient velocity discrimination in schizophrenia;Chen;Arch Gen Psychiatry,1999b

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