Rebecca R. Moultrie

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Preconception health social marketing plan

Managing uncertainty and responding to difficult emotions: Cancer patients’ perspectives on clinician response during the COVID-19 pandemic

Use of a web-based portal to return normal individual research results in Early Check: Exploring user behaviors and attitudes

Parental views on newborn next generation sequencing: Implications for decision support

Women's knowledge, attitudes, and beliefs about Down syndrome: A qualitative research study

Preferences for the research use of electronic health records among young adults with fragile X syndrome or autism spectrum disorder

Factors affecting the communication experiences of newly diagnosed colorectal cancer patients

Benefit-risk preferences of patients for the use of artificial intelligence and ultrasound imaging in different settings in echocardiography

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

Patients' experiences with cancer care: Impact of the COVID-19 pandemic

Design and development of a perinatal safety intervention program: Background interview report

Psychometric evaluation and design of patient-centered communication measures for cancer care settings

Virtual versus in-person focus groups: Comparison of costs, recruitment, and participant logistics

An evidence-based, community-engaged approach to develop an interactive deliberation tool for pediatric neuromuscular trials

Oncology patients' communication experiences during COVID-19: Comparing telehealth consultations to in-person visits

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

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

Engaging patient advocates and other stakeholders to design measures of patient-centered communication in cancer care

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

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