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Patient Understanding of Oncology Clinical Trial Endpoints in Direct-to-Consumer Television Advertising

The oncologist (Dayton, Ohio), 2023-07, Vol.28 (7), p.e542-e553

2023

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Physician Perceptions of the FDA's Breakthrough Therapy Designation: An Update

The oncologist (Dayton, Ohio), 2022-02, Vol.27 (1), p.e85-e88

2022

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Shame-Free Guilt Appeals: Testing the Emotional and Cognitive Effects of Shame and Guilt Appeals

Psychology & marketing, 2013-09, Vol.30 (9), p.811-825

2013

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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

American journal of human genetics, 2020-10, Vol.107 (4), p.596-611

2020

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An Empirical Procedure to Evaluate Misinformation Rejection and Deception in Mediated Communication Contexts

Communication theory, 2022-02, Vol.32 (1), p.25-47

2022

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Fitting identity in the reasoned action framework: A meta-analysis and model comparison

The Journal of social psychology, 2017-01, Vol.157 (1), p.47-63

2017

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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

Orphanet journal of rare diseases, 2019-05, Vol.14 (1), p.102-102, Article 102

2019

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Physician Interpretation of Data of Uncertain Clinical Utility in Oncology Prescription Drug Promotion

The oncologist (Dayton, Ohio), 2021-12, Vol.26 (12), p.1071-1078

2021

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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

Health communication, 2022-11, Vol.37 (13), p.1609-1621

2022

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

Social science & medicine (1982), 2021-02, Vol.271, p.112037-112037, Article 112037

2021

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Implied Claims in Drug Advertising: A Review of Recent Literature and Regulatory Actions

Health communication, 2024-04, Vol.39 (4), p.652-665

2024

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Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid

Pediatrics (Evanston), 2016-01, Vol.137 Suppl 1, p.S16

2016

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Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

Trials, 2018-06, Vol.19 (1), p.344-344, Article 344

2018

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Values Clarification and Parental Decision Making About Newborn Genomic Sequencing

Health psychology, 2020-04, Vol.39 (4), p.335-344

2020

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

Research in social and administrative pharmacy, 2021-04, Vol.17 (4), p.733-743

2021

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Preferences for Accessing Electronic Health Records for Research Purposes: Views of Parents Who Have a Child With a Known or Suspected Genetic Condition

Value in health, 2020-12, Vol.23 (12), p.1639-1652

2020

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Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment

Genetics in medicine, 2018-02, Vol.20 (2), p.181-189

2018

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Using a Patient Portal to Increase Enrollment in a Newborn Screening Research Study: Observational Study

JMIR pediatrics and parenting, 2022-02, Vol.5 (1), p.e30941-e30941

2022

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

Clinical and translational science, 2021-05, Vol.14 (3), p.880-889

2021

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An Interrupted Time Series Evaluation of the Testing Makes Us Stronger HIV Campaign for Black Gay and Bisexual Men in the United States

Journal of health communication, 2018-11, Vol.23 (10-11), p.865-873

2018

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

Genetics in medicine, 2019-11, Vol.21 (11), p.2561-2568

2019

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Intentions and Beliefs About Getting Tested for STDs: Implications for Communication Interventions

Health communication, 2011-12, Vol.26 (8), p.701-711

2011

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

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1664-n/a

2021

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

Social science & medicine (1982), 2016-10, Vol.166, p.17-24

2016

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An Evidence-Based, Community-Engaged Approach to Develop an Interactive Deliberation Tool for Pediatric Neuromuscular Trials

Journal of genetic counseling, 2018-04, Vol.27 (2), p.416-425

2018

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Patient Understanding of Oncology Clinical Trial Endpoints in Direct-to-Consumer Television Advertising

Physician Perceptions of the FDA's Breakthrough Therapy Designation: An Update

Shame-Free Guilt Appeals: Testing the Emotional and Cognitive Effects of Shame and Guilt Appeals

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

An Empirical Procedure to Evaluate Misinformation Rejection and Deception in Mediated Communication Contexts

Fitting identity in the reasoned action framework: A meta-analysis and model comparison

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

Physician Interpretation of Data of Uncertain Clinical Utility in Oncology Prescription Drug Promotion

Detecting and Reporting Deceptive Prescription Drug Promotion: Differences Across Consumer and Physician Audiences and by Number and Type of Deceptive Claims and Tactics

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

Implied Claims in Drug Advertising: A Review of Recent Literature and Regulatory Actions

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid

Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol

Values Clarification and Parental Decision Making About Newborn Genomic Sequencing

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

Preferences for Accessing Electronic Health Records for Research Purposes: Views of Parents Who Have a Child With a Known or Suspected Genetic Condition

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment

Using a Patient Portal to Increase Enrollment in a Newborn Screening Research Study: Observational Study

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

An Interrupted Time Series Evaluation of the Testing Makes Us Stronger HIV Campaign for Black Gay and Bisexual Men in the United States

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

Intentions and Beliefs About Getting Tested for STDs: Implications for Communication Interventions

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

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

An Evidence-Based, Community-Engaged Approach to Develop an Interactive Deliberation Tool for Pediatric Neuromuscular Trials

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