Genetics: Middle East study tags intellectual disability genes
By focusing on recessive mutations inherited from both parents, researchers have identified 50 new candidate genes for intellectual disability.
Charting the structure and function of the brain’s many circuits may unravel autism’s mysteries.
By focusing on recessive mutations inherited from both parents, researchers have identified 50 new candidate genes for intellectual disability.
Researchers can delay a monkey’s reaching movement by shining a beam of light into its brain, according to unpublished research presented at a poster session Sunday at the 2011 Society for Neuroscience annual meeting in Washington, D.C.
Mice lacking the autism risk gene SHANK2 show social deficits and are extremely hyperactive, according to unpublished research presented Saturday at the 2011 Society for Neuroscience annual meeting in Washington, D.C.
Deleting the Rett syndrome gene in a subset of neurons, instead of throughout the body, dramatically lowers the number of genes that are dysregulated in those neurons, according to results presented in a poster session Saturday at the 2011 Society for Neuroscience annual meeting in Washington, D.C.
Wenbao Gan describes the technique he has devised to track the development of neurons in live mouse brains.
A subset of people with autism have genetic and biochemical abnormalities in a sleep-related enzyme, according to research presented Friday at a satellite conference of the Society for Neuroscience annual meeting in Washington, D.C.
Non-verbal children with autism show structural differences in key language areas of the brain compared with controls, according to a poster presented Saturday at the Society for Neuroscience annual meeting in Washington, D.C.
In high-functioning adults with autism, the signal-to-noise ratio in the outer regions of the brain is significantly lower than in healthy controls, according to unpublished research presented Friday in Washington, D.C.
Individuals who have autism show distinct patterns of gene expression in neurological pathways compared with their unaffected siblings, according to unpublished work presented Saturday at the 2011 Society for Neuroscience annual meeting in Washington, D.C.
Mice missing the Rett syndrome gene MeCP2 show a gradual decline in vision, and too much inhibitory signaling in the visual cortex, according to unpublished research presented Thursday in Washington, D.C.