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Genome-wide association study with memory measures as a quantitative trait locus for schizophrenia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 255-259, 2012.
Artículo en Chino | WPRIM | ID: wpr-295499
ABSTRACT
<p><b>OBJECTIVE</b>To assess the association between gene polymorphisms and memory function through a genome-wide association study (GWAS) of schizophrenia and control group. Memory cognition was used as a quantitative trait (QT).</p><p><b>METHODS</b>Ninty-eight subjects with chronic schizophrenia and 60 matched controls were genotyped with HumanHap660 Bead Array. The results were correlated with quantitative traits including memory and memory delay.</p><p><b>RESULTS</b>Five candidate genes, including RASGRF2 (rs401758, P = 8.03×10(-5)), PLCG2 (rs7185362, P= 4.54×10(-5)), LMO1 (rs484161, P=9.80×10(-7), CSMD1 (rs2469383, P= 2.77×10(-6)) and PRKG1 (rs7898516, P=6.94×10(-5)) were associated with memory cognition deficits.</p><p><b>CONCLUSION</b>Using memory cognition as a quantitative trait, this Genome- wide association study has identified 5 susceptibility loci. With their association with nervous system development, neuronal growth, axon guidance and plasticity, brain development, above loci may play a role in the development of memory dysfunction in schizophrenia.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fisiología / Esquizofrenia / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo / Genética / Memoria / Métodos Límite: Adulto / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2012 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fisiología / Esquizofrenia / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Sitios de Carácter Cuantitativo / Estudio de Asociación del Genoma Completo / Genética / Memoria / Métodos Límite: Adulto / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2012 Tipo del documento: Artículo