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

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

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

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

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neurons in people with Williams syndrome are roughly the opposite of the patterns seen normally, according to unpublished results from a small study presented Monday at the 2013 Society for Neuroscience annual meeting in San Diego.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

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

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Rajesh Rao reflects on predictive brains, neural interfaces and the future of human intelligence

Twenty-five years ago, Rajesh Rao proposed a seminal theory of how brains could implement predictive coding for perception. His modern version zeroes in on actions.

By Paul Middlebrooks
18 December 2024 | 97 min listen

In memoriam: Yves Frégnac, influential and visionary French neuroscientist

Frégnac, who died on 18 October at the age of 73, built his career by meeting neuroscience’s complexity straight on.

By Bahar Gholipour
18 December 2024 | 9 min read
Illustration shows a solitary figure moving through a green and blue field of dots moving at different rates.

Explaining ‘the largest unexplained number in brain science’: Q&A with Markus Meister and Jieyu Zheng

The human brain takes in sensory information roughly 100 million times faster than it can respond. Neuroscientists need to explore this perceptual paradox to better understand the limits of the brain, Meister and Zheng say.

By Claudia López Lloreda
17 December 2024 | 8 min read