Ryan Paquin

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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

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

Values clarification exercises improved parental decision making about newborn genomic sequencing

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?

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

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

Genetics blogs as a public health tool: Assessing credibility and influence

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

Parental decision making about genomic sequencing for their children: Ethical and practical considerations

Priorities when deciding on participation in early-phase gene therapy trials for Duchenne muscular dystrophy: A best–worst scaling experiment in caregivers and adult patients

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

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

Supporting parental decisions about genomic sequencing for newborn screening: The NC NEXUS decision aid

Correction of misleading information in prescription drug television advertising: The roles of advertisement similarity and time delay

Parental intentions to enroll children in a voluntary expanded newborn screening program

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

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