@inbook{d16d7c437d5a40f3b4eb39f5c9514a92,
title = "Characterizing social behavior in genetically targeted mouse models of brain disorders",
abstract = "Fragile X syndrome, the leading inherited cause of mental retardation and autism spectrum disorders worldwide, is caused by a tandem repeat expansion in the FMR1 (fragile X mental retardation 1) gene. It presents with a distinct behavioral phenotype which overlaps significantly with that of autism. Emerging evidence suggests that tandem repeat polymorphisms (TRPs) might also play a key role in modulating disease susceptibility for a range of common polygenic disorders, including the broader autism spectrum of disorders (ASD) and other forms of psychiatric illness such as schizophrenia, depression, and bipolar disorder [1]. In order to understand how TRPs and associated gene mutations mediate pathogenesis, various mouse models have been generated. A crucial step in such functional genomics is high-quality behavioral and cognitive phenotyping. This chapter presents a basic behavioral battery for standardized tests for assaying social phenotypes in mouse models of brain disorders, with a focus on aggression.",
keywords = "aggression, autism, fragile X syndrome, mouse model",
author = "Burrows, {Emma L.} and Hannan, {Anthony J.}",
year = "2013",
doi = "10.1007/978-1-62703-438-8_7",
language = "English",
isbn = "9781627034371",
series = "Methods in Molecular Biology",
publisher = "Humana Press Inc.",
pages = "95--104",
editor = "Hatters, {Danny M.} and Hannan, {Anthony J.}",
booktitle = "Tandem repeats in genes, proteins, and disease",
}