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Spectrum: Autism Research News

Tag: intellectual disability

November 2013

Chemical messenger may drive maternal infection’s effects

by  /  13 November 2013

A mother’s exposure to infection can exacerbate the effects of a genetic mutation and contribute to autism or schizophrenia in her pups, suggests an unpublished mouse study presented Wednesday at the 2013 Society for Neuroscience annual meeting in San Diego.

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Results of 16p11.2 study show promise for autism biomarker

by  /  12 November 2013

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with the degree of social and cognitive impairments in children with an autism-linked genetic abnormality, according to unpublished research presented Sunday at the 2013 Society for Neuroscience annual meeting in San Diego.

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Gender affects nerve fiber integrity in tuberous sclerosis

by  /  11 November 2013

Boys with tuberous sclerosis complex, an autism-related disorder, have more disorganized nerve fibers in some regions of the brain than do girls with the disorder, according to unpublished work presented Sunday at the 2013 Society for Neuroscience annual meeting in San Diego.

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Genetic analysis links autism to missing brain structure

by  /  11 November 2013

The largest genetic analysis yet conducted of people lacking a brain structure called the corpus callosum shows that the condition shares many risk factors with autism. The study was published 3 October in PLoS Genetics. 

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‘Humanized’ mouse assays reveal subtle behaviors

by  /  10 November 2013

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.

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Medical record mining helps clarify complex diseases

by  /  6 November 2013

Researchers have mined the medical records of more than 100 million people and found close to 3,000 associations between single-gene diseases, such as cystic fibrosis, and complex genetic disorders such as autism. The results were published 26 September in Cell.

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SHANK mutations converge at neuronal junctions in autism

by ,  /  5 November 2013

SHANK3, one of the strongest candidate genes for autism, has the potential to be a molecular entry point into understanding the synaptic, developmental and circuit origins of the disorder.
 

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October 2013

Vision or hearing loss ups autism risk

by  /  31 October 2013

Children with poor vision or a hearing loss are more likely to be diagnosed with autism than are those in the general population, reports a large epidemiological study published in October.

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Adult focus

by  /  25 October 2013

Two new studies examine disruptive behavior and loneliness among adults with autism, generally a poorly studied group. 

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Best practices

by ,  /  22 October 2013

Guidelines for the use of electroencephalography in autism will ensure that researchers have a common set of standards, which will speed up discovery, say Sara Jane Webb and Raphael Bernier.

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