Thank you for your interest in our study!
  • The overarching goal of the study is to understand normal variation in language and cognitive features across carriers of the fragile X premutation and mothers who have a child with fragile X syndrome or the FMR1 premutation.
  • You will be asked to complete questionnaires and interviews related to your thoughts and experiences, and participate in assessments of language and cognition.
  • In addition, you would be asked to provide a cheek swab in order to index the FMR1 gene (FMR1 is a gene that is highly implicated in autism and other developmental disorders). For this study we are focused on normal variation on the gene and how it may relate to normal variation in language and cognition).
  • Participation would take 3-4 hours and the compensation is $80.
  • In-person and virtual participation options are offered!
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