Ryan Paquin

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Implied claims in drug advertising: A review of recent literature and regulatory actions

Patient understanding of oncology clinical trial endpoints in direct-to-consumer television advertising

Detecting and reporting deceptive prescription drug promotion: Differences across consumer and physician audiences and by number and type of deceptive claims and tactics

Defining and measuring scientific misinformation

Using a patient portal to increase enrollment in a newborn screening research study: Observational study

Physician perceptions of the FDA’s Breakthrough Therapy designation: An update

An empirical procedure to evaluate misinformation rejection and deception in mediated communication contexts

Physician interpretation of data of uncertain clinical utility in oncology prescription drug promotion

Superimposed text size and contrast effects in direct-to-consumer television advertising: Which presentation format is best for Rx drug messaging to consumers?

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

Patients' and caregivers' maximum acceptable risk of death for non-curative gene therapy to treat Duchenne muscular dystrophy

Experimental evidence of consumer and physician detection and rejection of misleading prescription drug website content

A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newborns

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

Genomic sequencing for newborn screening: Results of the NC NEXUS Project

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

Using social media to conduct outreach and recruitment for expanded newborn screening

Values clarification and parental decision making about newborn genomic sequencing

Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders

North Carolina newborn exome sequencing for universal screening (NC nexus) detects molecular etiologies underlying inborn errors of metabolism and hearing loss