7q11.23

Recent articles

Mother mouse with pups on white

Multiple genes may conspire to lead to autism traits

The many genes implicated in Williams syndrome, a condition related to autism, may all work together to exert their effects on behavior.

By Nicholette Zeliadt
23 December 2019 | 4 min read

Unusual gait marks mice with mutations related to autism

Mouse models of two genetic conditions related to autism show abnormalities in their movement patterns.

By Emily Anthes
20 October 2019 | 3 min read
child working on colorful puzzle on lightbox

Duplication of DNA on chromosome 7 increases risk of autism

Roughly one in five children who has an extra piece of chromosome 7 also meets the criteria for an autism diagnosis.

By Jessica Wright
1 February 2018 | 4 min read

Ratio reversal; gender bender; ad accusations and more

The male-dominated sex bias in autism is reversed in a related syndrome, a researcher’s gender could influence her study’s outcome, and an award-nominated ad featuring a young man with autism draws criticism.

By Emily Willingham
12 January 2018 | 4 min read

Tooth fairy delivers drug target for boosting social interest

Cells derived from the dental pulp of children with Williams syndrome hint at a treatment approach for autism.

By Ann Griswold
16 September 2016 | 4 min read
Spectrum from The Transmitter.

Sequencing studies sharpen focus on key autism genes

Two studies prioritize autism risk genes for further research and illuminate how different types of mutations may work together.

By Jessica Wright
1 October 2015 | 6 min read
Spectrum from The Transmitter.

Chromosome 7 flaws alter chemical tags throughout genome

Alterations to chromosome 7 lead to changes in the chemical marks that direct gene expression.

By Jessica Wright
21 August 2015 | 3 min read
Spectrum from The Transmitter.

Behavioral profile of DNA disorder reveals ties to autism

Children who carry an extra copy of part of chromosome 7 have symptoms ranging from social phobia to speech impediments. About one-third of them show signs of autism, according to the first systematic analysis of people with 7q11.23 duplication syndrome.

By Rachel Nuwer
26 May 2015 | 4 min read
Spectrum from The Transmitter.

Williams syndrome reverses patterns of neuronal branching

The branching patterns of excitatory neurons in people with Williams syndrome are roughly the opposite of the patterns seen normally, according to unpublished results from a small study presented Monday at the 2013 Society for Neuroscience annual meeting in San Diego.

By Jessa Netting
12 November 2013 | 3 min read
Spectrum from The Transmitter.

Genetics: Williams risk region linked to schizophrenia

The same genetic region that is missing in people with Williams syndrome is likely to be duplicated in some people with schizophrenia, according to a study published 17 July in Biological Psychiatry.

By Jessica Wright
17 September 2013 | 2 min read

Explore more from The Transmitter

Stack of papers.

Exclusive: The 23 studies the FDA based its expanded leucovorin label on

The studies include 46 people, mostly toddlers, who have cerebral folate deficiency due to variants in a folate transporter.

By Claudia López Lloreda
2 October 2025 | 6 min read
Hand holding a rubber stamp above a stack of papers.

Autism researchers ‘pleasantly surprised’ by list of NIH data project grantees, despite initial concerns

An atypical funding mechanism, truncated application timeline and opaque review process had generated concern over the quality of projects that would be selected for the Autism Data Science Initiative.

By Calli McMurray
2 October 2025 | 10 min read
Richard Frye.

Exclusive: Who is Richard Frye, the neurologist who researches and advocates for leucovorin as an autism treatment?

Frye has led two placebo-controlled trials of the folate supplement in autistic people; the first was suspended by regulators, and the other has yet to be published.

By Brendan Borrell
1 October 2025 | 11 min read

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