Melissa Raspa

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Supporting informed clinical trial decisions: Results from a randomized controlled trial evaluating a digital decision support tool for those with intellectual disability

Making clinical trials more patient-centered using digital interactive e-consent tools

Early check: Translational science at the intersection of public health and newborn screening

Clinical models of telehealth in genetics: A regional telegenetics landscape

Health care for individuals with Fragile X Syndrome: Understanding access and quality

Early identification of fragile X syndrome through expanded newborn screening

A description of the educational setting among individuals with fragile x syndrome

A digital health app to assess decisional capacity to provide informed consent: Protocol for a randomized controlled trial

Mobile technology use and skills among individuals with fragile X syndrome: Implications for healthcare decision making

Sensory difficulties in children with an FMR1 premutation

A comparison of functional academic and daily living skills in males with fragile X syndrome with and without autism

A digital decision support tool to enhance decisional capacity for clinical trial consent: Design and development

Evaluating sensory processing in Fragile X Syndrome: Psychometric analysis of the Brain Body Center Sensory Scales (BBCSS)

Where do we go from here? The need for genetic referrals in patients who are deaf or hard of hearing: Findings from a regional survey

Early check: A voluntary newborn screening program and research registry to facilitate clinical trials in pre-symptomatic infants with rare diseases

A literature review of the economic burden of fragile X syndrome

Attendance at fragile X specialty clinics: Facilitators and barriers

Implications of the FMR1 premutation for children, adolescents, adults, and their families

Public health literature review of Fragile X syndrome

Promoting family outcomes in early intervention