How to get involved

If you choose to participate in this research study, we will ask you to complete an online questionnaire administered via secure, HIPAA-compliant servers. Additionally, if you’re chosen to participate, we will ask you to complete additional questionnaires and provide a saliva sample for genetic testing.

Thank you for your interest in the ASPE Study. Currently, we are only enrolling those with a deletion or duplication in the NEUREXIN 1 gene (NRXN1) which is in the Chromosome 2p16.3 region.

All other enrollment is on pause and we are uncertain at this time when it will start back up. If you have a NRXN1 variant or would like to join our waitlist, please click the link below associated with the age of the person wanting to participate and provide your contact information.

Adult: https://redcap.link/aspe

Adolescent (16-17): https://redcap.link/aspe_adolescent

Child (3-15): https://redcap.link/aspe_child

Thank you,

THE ASPE Study Team

Interested in enrolling someone under 18?

If you would like to enroll an adolescent (age 16-17 years) with a NRXN1 gene variant or deletion, click here.

If you would like to enroll a child (age 3-15 years) with a NRXN1 gene variant or deletion, click here.

For more information, leave a message for our study team. You can also email aspe@pennmedicine.upenn.edu.

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