Warren symposium follows legacy of geneticist giant

If we want to understand how the brain creates memories, and how genetic disorders distort the brain’s machinery, then the fragile X gene is an ideal place to start. That’s why the Stephen T. Warren Memorial Symposium, taking place November 28-29 at Emory, will be a significant event for those interested in neuroscience and genetics.

Stephen T. Warren, 1953-2021

Warren, the founding chair of Emory’s Department of Human Genetics, led an international team that discovered the gene responsible for fragile X syndrome in the 1990s. Please check out this mini-biography of Warren, who died in 2021. Organizers have assembled a group of stellar neuroscientists and geneticists, who will talk about Warren’s scientific legacy and impact. 

Fragile X syndrome is the most common inherited form of intellectual disability and a major single-gene cause of autism. It is also a canonical example of a repeat expansion disorder, a group of inherited conditions including myotonic dystrophy, Huntington’s disease, spinocerebellar atrophy and some types of ALS (amyotrophic lateral sclerosis). Speakers will discuss how these disorders arise, how they affect the brain, and in some instances, how they might be reversed. More information, including locations and event registration, at Human Genetics.

Posted on by Quinn Eastman in Neuro Leave a comment

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Quinn Eastman

Science Writer, Research Communications qeastma@emory.edu 404-727-7829 Office

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