Juli Bollinger

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy

Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing

Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study

Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies

Primary care patients’ views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study

The “All of Us” Research Program

Privacy in the age of medical big data

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study

A Survey of U.S Adults’ Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment

The impact of health information technology on patient safety

Clinical Trial Participants’ Views of the Risks and Benefits of Data Sharing

Safe Use of Health Information Technology

Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing

Preparing Health Professionals for Individualized Medicine

Public preferences for the return of research results in genetic research: a conjoint analysis

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

Sharing data under the 21st Century Cures Act

Risky Business: Risk Perception and the Use of Medical Services among Customers of DTC Personal Genetic Testing