Associated Papers
EXPLORATORY ANALYSIS OF RARE AND NOVEL VARIANTS IN MEXICAN PATIENTS DIAGNOSED WITH SCHIZOPHRENIA AND DEMENTIA.
Martínez-Magaña JJ et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion, 2019
DISC1 causes associative memory and neurodevelopmental defects in fruit flies.
Furukubo-Tokunaga K et al.
Molecular Psychiatry, 2016
Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in mice.
Dachtler J et al.
Scientific Reports, 2016
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.
Thomson PA et al.
Molecular Psychiatry, 2014
DISC1-binding proteins in neural development, signalling and schizophrenia.
Bradshaw NJ et al.
Neuropharmacology, 2012
DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness.
Soares DC et al.
Acs Chemical Neuroscience, 2011
Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.
Osbun N et al.
American Journal of Medical Genetics. Part A, 2011
Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder.
Song W et al.
Neuroscience Letters, 2010
Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.
Song W et al.
Biochemical and Biophysical Research Communications, 2008
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