Rebecca R. Moultrie

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Parents' opinions about using their children's EMR for research: A continuum of perspectives across three genetic groups

APHA Annual Meeting 2018

Education and consent for population-based DNA screening: A mixed-methods evaluation of the Early Check Newborn Screening Pilot Study

Perceived healthcare provider reactions to patient and caregiver use of online health communities

Misunderstood terms and concepts identified through user testing of educational materials for fragile X premutation: "Not weak or fragile?"

Visual presentations of efficacy data in direct-to-consumer prescription drug print and television advertisements: A randomized study

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

A review on spinal muscular atrophy: Awareness, knowledge, and attitudes

Science Literacy and Health Literacy Rationales, Definitions, and Measurement: Commissioned supplementary paper in support of the National Academies of Sciences, Engineering, and Medicine report "Science literacy: Concepts, contexts, and consequences"

Program Implementation Approaches to Build and Sustain Health Care Coordination for Type 2 Diabetes

Improving the implementation of diabetes self-management: Findings from the Alliance to Reduce Disparities in Diabetes.

Outreach to new mothers through direct mail and email: Recruitment in the Early Check research study

Improving the implementation of diabetes self-management: Findings from the Alliance to Reduce Disparities in Diabetes

Formative research to develop a clinical trial decision aid that integrates quantitative patient preference data

Presenting efficacy information in direct-to-consumer prescription drug advertisements

Assessing patient-provider communication barriers to implementing new expert panel risk reduction guidelines

Peer-generated health information: The role of online communities in patient and caregiver health decisions

Barriers and facilitators to genetic service delivery models: Scoping review

Ethical, legal, and social issues related to the inclusion of individuals with intellectual disabilities in electronic health record research: Scoping review

Preferences for accessing electronic health records for research purposes: Views of parents who have a child with a known or suspected genetic condition