Penn Study Points to High Priority Genes as Potential Research Targets in Autistic Spectrum Disorder
The Perelman School of Medicine at the University of Pennsylvania established ASPE, the Autism Spectrum Program of Excellence, in 2017 to significantly improve the understanding of the genetic causes of Autism Spectrum Disorder (ASD) in order to energize the research and clinical community across the globe. The ASPE program was made possible by a generous donation from an anonymous philanthropist.
Genetic studies of ASD will give us greater insight into the genetic roots of the entire autism spectrum. A major focus of ASPE will be on the NRXN1 gene, which codes for the protein neurexin 1 and has been associated with autism spectrum disorder and other psychiatric and neurodevelopmental disorders.
Penn Study Points to High Priority Genes as Potential Research Targets in Autistic Spectrum Disorder
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Penn will host a mini-symposium for ASPE on October 22, 2018 to review early findings and stimulate new research avenues.
Title: Exploring the phenotypic, genetic, and biologic diversity of the autism spectrum
Time: Monday, October 22, 2018 3:00-5:00pm
Place: Jordan Medical Education Center Law Auditorium
Contact us for info regarding the symposium.