The Effect of the Neurogranin Schizophrenia Risk Variant rs12807809 on Brain Structure and Function

A single nucleotide polymorphism rs12807809 located upstream of the neurogranin (NRGN) gene has been identified as a risk variant for schizophrenia in recent genome-wide association studies. To date, there has been little investigation of the endophenotypic consequences of this variant, and our own...

Full description

Saved in:
Bibliographic Details
Published in:Twin research and human genetics 2012-06, Vol.15 (3), p.296-303
Main Authors: Rose, Emma J., Morris, Derek W., Fahey, Ciara, Robertson, Ian H., Greene, Ciara, O'Doherty, John, Newell, Fiona N., Garavan, Hugh, McGrath, Jane, Bokde, Arun, Tropea, Daniela, Gill, Michael, Corvin, Aiden P., Donohoe, Gary
Format: Article
Language:English
Subjects:
Adult
Alleles
Brain
Brain - pathology
Brain - physiopathology
Female
Genetic Predisposition to Disease
Genotype
Humans
Imaging
Localization of functions
Magnetic Resonance Imaging
Male
Memory, Short-Term
Neurogranin - genetics
Polymorphism, Single Nucleotide
Risk factors
Schizophrenia
Schizophrenia - genetics
Schizophrenia - pathology
Schizophrenia - physiopathology
Young Adult
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!