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Spectrum: Autism Research News

Tag: Simons Simplex Collection

September 2013

Genetics: Recessive mutations may contribute to autism

by  /  3 September 2013

The genomes of people who have both autism and intellectual disability have more regions that may harbor recessive mutations than those of their unaffected siblings, according to a study published 11 July in the American Journal of Human Genetics.

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Study of nonverbal autism must go beyond words, experts say

by  /  2 September 2013

To better understand and treat nonverbal autism, the field must paradoxically move beyond focusing on speech production, say many researchers. Emerging research suggests that seemingly unrelated issues such as motor skills and joint attention may instead be key.

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August 2013

Large study links autism to autoimmune disease in mothers

by  /  22 August 2013

About one in ten women who have a child with autism have immune molecules in their bloodstream that react with proteins in the brain, according to a study published 20 August in Molecular Psychiatry.

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May 2013

Genetics: Common genomic duplications enriched in autism

by  /  28 May 2013

Children with autism have more copies of some chromosomal regions than controls do, according to a study published 19 April in Human Molecular Genetics. This is true even after excluding the regions that are the most likely to lead to autism.

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Clinical research: Quiet autism toddlers may learn to talk

by  /  10 May 2013

Most children with autism who have language delay at age 4 are able to speak later in childhood, according to a study published in the April issue of Pediatrics.

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Gender differences take center stage at autism conference

by  /  4 May 2013

Girls with autism carry more mutations than do boys with the disorder, and show greater differences in brain activity and response to social cues, according to several preliminary studies presented at the 2013 International Meeting for Autism Research in San Sebastián, Spain.

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April 2013

Genetics: Rare mutation linked to autism, psychosis

by  /  2 April 2013

A boy with a rare deletion in chromosome 3 was diagnosed with autism and psychotic symptoms by age 5, according to a case report published 26 February in the American Journal of Medical Genetics Part A. He is the second identified individual with this deletion who has these symptoms, which are exceedingly rare in combination.

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March 2013

Rho family of enzymes at crossroads of autism

by  /  12 March 2013

A number of autism risk factors converge on one cellular pathway: abnormal remodeling of the cell’s structural systems through the signaling protein Rho, says SFARI’s associate director for research, Alan Packer.

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Scientists hunt for ‘mini’ hotspots linked to autism

by  /  4 March 2013

Small regions of DNA that are structurally prone to deletions and duplications are unlikely to play a major role in autism, according to research published 7 February in the American Journal of Human Genetics.

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January 2013

Childhood-onset schizophrenia, autism share genetic links

by  /  23 January 2013

Individuals who have childhood-onset schizophrenia carry more DNA deletions and duplications associated with other disorders, such as autism, than their unaffected siblings do. The unpublished research was presented 16 January at the Salk Institute, Fondation IPSEN and Nature Symposium on Biological Complexity in La Jolla, California.

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