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Spectrum: Autism Research News

Tag: sequencing

July 2017
Week of JulyJul
24th
2017

Edited human embryos; prenatal antidepressants; gut thinking and more

by  /  28 July 2017

Researchers in Oregon edit human embryos, prenatal antidepressants may play a role in autism risk, and gut microbiota are associated with early cognition.

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Large study shines spotlight on ‘mosaic’ mutations in autism

by  /  19 July 2017

About 8 percent of non-inherited mutations in people with autism occur in only some of the body’s cells, according to a study of 20,000 people.

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Massive collaboration unearths inherited risk factor for autism

by  /  17 July 2017

Autism runs in families, but the search for inherited risk factors has come up short — until now.

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June 2017
Week of JuneJun
26th
2017

Rogue poop; ancestral autism; travel limbo and more

by  /  30 June 2017

A Tampa clinic goes rogue with fecal transplants, autism’s genetic ancestry traces to our deep past, and the U.S. Supreme Court revives the travel ban.

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In race to crack autism’s code, two contenders shoot ahead

by  /  27 June 2017

Two candidate genes have risen to the top, and may help scientists understand what autism really is.

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May 2017

Complex gene interactions in autism offer avenues for treatment

by  /  23 May 2017

Teasing out how genes interact can offer clues to autism’s causes and point to treatment targets.

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Researchers correct statistical flaw in high-profile paper

by  /  3 May 2017

A February study that tied several new genes to autism contained a large statistical error, according to a report from 14 independent researchers; the original team is working on issuing a correction.

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April 2017

Molecular map outlines regulatory roles for RNA snippets

by  /  21 April 2017

A new atlas maps the locations of nearly 30,000 noncoding RNAs — genetic strips that may modify the expression of genes.

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Precocious baby teeth signal rare form of autism

by  /  20 April 2017

Most children with a rare autism-linked mutation develop baby teeth one to two years earlier than usual.

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March 2017

New method taps family trees for clues about conditions

by  /  10 March 2017

Asking participants in genetic databases about their family’s medical history can help researchers uncover genetic variants tied to conditions such as autism.

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