Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
Simons Searchlight
Summary
Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.
Description
Simons Searchlight has expanded over the last several years to include additional gene changes and participation through remote formats, either online or by phone. This allows English and Spanish-speaking families from across the world to participate at times that are convenient to their schedule. Participants can donate blood, saliva, or both. These samples are then linked to medical, behavioral, learning, and developmental data in order to understand the effects of specific gene changes. Information provided by participants will be stripped of any personal identifying information and made a…
Eligibility
- Age range
- Not specified
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Subjects of any age with a genetic condition on our eligible list along with their biological family members. Current list can be found at: https://www.simonssearchlight.org/research/what-we-study/ * Must be fluent in English or a supported language. Current supported languages are Spanish, French, and Dutch, with more to come. * Able to register and participate through our online platform, which can be accessed through any device able to connect to the internet. * Able and willing to provide consent. Exclusion Criteria: -Some genetic changes that we study have regions…
Locations (2)
- Boston Children's HospitalBoston, Massachusetts
- Geisinger Health SystemLewisburg, Pennsylvania