Danya F. Vears

Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation

Australian public perspectives on genomic newborn screening: which conditions should be included?

Ethics of artificial intelligence in prenatal and pediatric genomic medicine

Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations

Return of individual research results from genomic research: A systematic review of stakeholder perspectives

Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

Attitudes of publics who are unwilling to donate DNA data for research

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

Key Implications of Data Sharing in Pediatric Genomics

Genomic newborn screening: public health policy considerations and recommendations

Expanded carrier screening for monogenic disorders: where are we now?

Reporting practices for variants of uncertain significance from next generation sequencing technologies

Points to consider for laboratories reporting results from diagnostic genomic sequencing

The challenges of the expanded availability of genomic information: an agenda-setting paper

Ethical sharing of health data in online platforms – which values should be considered?

Public Views on Genetics and Genetic Testing: A Survey of the General Public in Belgium

Participation of Children in Medical Decision-Making: Challenges and Potential Solutions

Parents’ experiences with requesting carrier testing for their unaffected children