By mapping the brains of not 1 but 27 mouse models of autism, researchers are making sense of the widely divergent structural changes seen in autism brains, they reported Wednesday at the 2013 Society for Neuroscience annual meeting in San Diego.
The level of activity of a cellular signaling pathway correlates with the degree of social and cognitive impairments in children with an autism-linked genetic abnormality, according to unpublished research presented Sunday at the 2013 Society for Neuroscience annual meeting in San Diego.
A new test of mouse intelligence closely mimics the types of assays used with people and detects a subtle learning deficit reminiscent of one seen in teenagers with autism, according to findings presented Saturday at the 2013 Society for Neuroscience annual meeting in San Diego.
Researchers have found the first direct evidence that a hopscotching gene destabilizes the 15q13.3 chromosomal region, and may be to blame for the region’s role in autism and other brain disorders. They presented the unpublished results Wednesday at the American Society of Human Genetics Meeting in Boston, Massachusetts.
About one in four people diagnosed with a group of rare disorders have autism, according to a study published 7 October in the Journal of Medical Genetics. The disorders all affect a single cancer-related pathway, driven by a protein called RAS.
Elliott Sherr is unraveling the effects of genetics and brain structure in a handful of disparate disorders that each illuminates some aspect of autism.
The same genetic region that is missing in people with Williams syndrome is likely to be duplicated in some people with schizophrenia, according to a study published 17 July in Biological Psychiatry.
Duplications and deletions of large chromosomal regions are associated with intellectual disability, cognitive deficits and a low likelihood of having children, according to a population-wide study in Iceland. The results were presented Monday at a conference in Cambridge, Massachusetts.
A new clinical test for duplications or deletions of chromosomal regions is customized to detect more than 380 known changes, including many that are linked to autism. The method was published 24 June in the American Journal of Medical Genetics Part A.
Chromosomal abnormalities may be more prevalent in individuals with a rare form of childhood-onset schizophrenia than in those with the classic presentation of the disorder, according to a study published 21 May in Molecular Psychiatry.