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Our Latest Publication: Autism Traits Are Predictive of Specific Gene Networks in Intellectual Disab

Last week our team published its newest work in the realm of autism genetics in Frontiers in Psychiatry titled, “Widespread Genotype-Phenotype Correlations in Intellectual Disability.” For those of you who don’t follow genetics closely, that title probably means little to you. So I’m going to try to explain what we found and why we think it’s so interesting.

This work was performed in conjunction with one of my primary collaborators, Dr. Alex Feltus at Clemson University and one of his students, Zach Gerstner. We took a large group of genes associated with intellectual disability (mental retardation) and divided them into subgroups based on whether the conditions had the following clinical features:

  1. high co-occurring rates of autism

  2. high co-occurring rates of epilepsy

  3. association with different types of facial malformations

  4. association with neurodegeneration or other neurodegenerative features like brain atrophy and certain movements disorders

CFD = complex (multiple) facial malformations; SFD = simple (single) facial malformations; NLF = neurodegenerative and neurodegenerative-like features; None = no features of interest.

This breakdown led to 18 different subgroups of genes to which we added other interacting and co-expressed genes to expand the overall network. When we looked at this larger network of genes, we found that our different subgroups fell very predictably into clusters that for the most part only connected to other genes within that same cluster. You can see the main results in the image below in frame A. The side panels show closeups of some of the interconnecting nodes between clusters and panel F is the SFARI-based autism-associated gene clusters alone. (Sorry for the large image but there’s a lot of detail.)

Complicated pictures aside, what does it all mean??

So here’s the gist. These results suggest there is a strong relationship between the presence of features like autism in intellectual disability and the gene networks that are affected due to gene mutations. If looked at in reverse: mutations that target key gene networks significantly increase the likelihood an individual with intellectual disability will also develop autism. This also indicates that even though different individuals with intellectual disability + autism may have different genetic syndromes (e.g., Fragile X Syndrome vs. CHARGE Syndrome), on the whole they do share some biologic commonalities at the gene network level that may be the reason for their common traits of autism.

We also discovered that conditions with a high association with autism were much more likely to have facial malformations, for reasons not well understood. Undoubtedly, some of these same gene networks are involved in facial development as well as that of the brain. This association may give us some clues as to what these genes are doing in the brain and whether they’re key in specific stages of development.

Illustration of a baby with CHARGE Syndrome and facial malformation.

There are many other findings, both clinical and genetic, in this paper and for anyone interested in further reading please access the original article, which is available open access. Feel free to email me with questions. However, since most of my readers here have a personal and/or professional interest in autism, I’ve kept this summary more focused.

Although this work centered on intellectual disability (for geneticists this is called “taking the easy way out” 😉 ), we suspect that many of these same autism-related gene networks are involved in the entirety of the autism spectrum, although we’ll need to test that hypothesis with further research. However, despite the obvious heterogeneity of the autism spectrum, we do nevertheless feel that it is a spectrum and shares some common biology. This paper suggests at least within rare forms of intellectual disability, that’s the case.

#autismgenetics #autismspectrumdisorder #rarediseases #epilepsygenetics #ASD #learningdisability #autism #neurodegeneration #intellectualdisability #mentalretardation


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