• Jingwen & Luo

    Integration

    of quantitative genomics and neurobiology to understand Autism Spectrum Disorders

  • Family-Based Studies

    lead to better understanding of neurodiversity

  • Modeling Behavioral Traits

    in experimental organisms will lead to new therapies

  • Welcome to ASPE

    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.

    Latest News

    Want to know more about synapses?

    Want to know more about synapses? Quick summary! A neuron is a type of cell located in the brain that transmits information to other neurons through a junction called a synapse. The communication between neurons...

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    What is a neuron?

    What is a neuron? Quick summary! A neuron is a type of cell located in the brain that transmits information to other neurons through a junction called a synapse. The communication between neurons at synapses...

    Read More
    ASPE (Neurexin Nexus) blog introduction

    Quick Summary! Welcome to the Neurexin Nexus! Our hope is to use this platform to build a relationship between scientists and non-scientists and to make research findings accessible to the general public. This blog, written...

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    Events

    First Annual Braelyn Aubrey Foundation 5k – October 2, 2021

    “Our objective is to conduct a recurring 5K to raise awareness for our foundation, to be able to advocate for children with impairing conditions, and recruit sponsors to aid in furthering research as related to chromosomal deletions (including 2p16.3 deletions) and abnormalities which impair a child’s ability for self-independence.”

    https://braelynaubreyfoundation.squarespace.com/sponsors