Dup15q 2012

Recent articles

Spectrum from The Transmitter.

Chromosome 15 duplications common in autism

About 1 in 500 children referred to genetic testing for undefined developmental delay, intellectual disability, or autism have duplications of the 15q11-13 chromosomal region, according to a new analysis. That makes the region the second most common large genetic alteration linked to autism.

By Emily Singer
30 August 2012 | 4 min read
Spectrum from The Transmitter.

Researchers eye pigs for modeling autism-related disorder

Researchers plan to develop pig models of Prader-Willi syndrome, an inherited disorder caused by the deletion of an autism-linked region of chromosome 15.

By Emily Singer
13 August 2012 | 2 min read
Spectrum from The Transmitter.

Researchers home in on dosage effects of 15q11-13 region

Researchers are beginning to tease apart how dosage of genes within the 15q11-13 chromosomal region contributes to autism symptoms.

By Emily Singer
13 August 2012 | 5 min read

Explore more from The Transmitter

Illustration of a leaking pipe.

Securing the academic pipeline amid uncertain U.S. funding climate

Finding creative ways to keep early-career researchers in academia—for example, through part-time roles—can help the field weather the storm.

By Lucina Q. Uddin
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Illustration of a sheet of paper with many holes punched out of it.

Let’s teach neuroscientists how to be thoughtful and fair reviewers

Blanco-Suárez revamped the traditional journal club by developing a course in which students peer review preprints alongside the published papers that evolved from them.

By Elena Blanco-Suárez
6 March 2026 | 6 min read
Megaphone with many different shapes and textures emanating from it.

New autism committee positions itself as science-backed alternative to government group

The Independent Autism Coordinating Committee plans to meet at the same time as the U.S. federal Interagency Autism Coordinating Committee later this month—and offer its own research agenda.

By Angie Voyles Askham
5 March 2026 | 5 min read

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