Skip to main content

Spectrum: Autism Research News

Tag: copy number variation

June 2017
Week of JuneJun
5th
2017

Injury risk; stem-cell start; food faces

by  /  9 June 2017

People with autism are at high risk of death from injury, China starts a clinical trial involving human embryonic stem cells, and individuals with autism have trouble seeing faces in food.

0 Comments
May 2017

Chromosome 16 mutations augur distinct developmental paths

by  /  25 May 2017

Children missing a stretch of DNA on chromosome 16 show worsening motor and social skills in the first eight years of life; those with an extra copy of the region do not show this decline.

0 Comments
April 2017

Rare mutation linked to autism affects language ability

by  /  24 April 2017

Mutations in a gene called TRIP12 — which is involved in tagging proteins for destruction — can lead to intellectual disability, language delay and autism.

0 Comments
March 2017

DNA deletion sparks separate outcomes of autism, schizophrenia

by  /  16 March 2017

In children with a deletion on chromosome 22, having autism does not boost the risk of developing schizophrenia later in life.

2 Comments

Sequencing thousands of whole genomes yields new autism genes

by  /  6 March 2017

An analysis of whole genomes from more than 5,000 people has unearthed 18 new candidate genes for autism.

0 Comments
February 2017

Many people with harmful genetic variants show no ill effects

by  /  22 February 2017

Most adults with genetic variants tied to certain conditions, such as heart disease or cancer, go undiagnosed.

0 Comments
October 2016

Many people harbor large mutations linked to autism

by  /  24 October 2016

DNA deletions and duplications tied to autism crop up in people without the condition, too.

0 Comments

Nature of risk mutations varies with families’ history of autism

by  /  10 October 2016

Large autism-linked mutations tend to be inherited in families with a history of the condition. By contrast, they often arise spontaneously in families with a single affected person.

1 Comment
A mutation in a human-specific DNA

Autism risk may originate in stretches of uniquely human DNA

by  /  6 October 2016

Mutations in certain newly evolved stretches of the genome may play a role in autism, although some experts are skeptical of this theory.

0 Comments
September 2016
Week of SeptemberSep
5th
2016

Sounding out ultrasounds; name game; geek gathering

by  /  9 September 2016

A tie between first-trimester ultrasounds and autism severity is tenuous at best, misnamed genes litter the literature, and neuroscientists enjoy their version of summer camp.

0 Comments