Reproductive Autonomy in Light of Expanded Prenatal Genomic Testing: the Use of Polygenic Risk Score for Embryo Selection

Reproductive Autonomy in an Expanding Genomic Landscape: For Whom, and Under What Context?

Public Value and Industry Partnerships in Data-Intensive Health Innovation

When 'More Isn't More': The Normative and Practical Case for Improving Genetic Data Infrastructure

Expanding Access to Genomic Sequencing in the Neonatal Intensive Care Unit: A Roadmap to Discharge and Beyond

The Stories We Tell About Genetics: Freedom, Disability, and Determinism

Beyond Roadmaps: Contractual Governance in Genomic Diagnosis

Genomic Medicine and Equity in Relation to Health Systems

Reframing the Ethics of Prenatal Testing: From Autonomy to Social and Societal Implications

David's Sling: Bioethics Empiricism as Big Tech Goliaths Enter Genomics

The European Health Data Space as a Compass for Academic/Industry Collaborations

Genetic Testing in Autism Spectrum Disorder: Searching for a Ticket or Roadmap

Reproductive Autonomy in Prenatal Genomics: embedding Legal Safeguards for Life-Affirming Choices and the Value of Prenatal Life

Governing Academic-Industry Genomic Partnerships for the Public Interest in a Corporatized Academy

The Power of Meso-Level Levers for Enhancing Genomics Research Partnerships

The Challenges of Reproductive Autonomy in an Unjust System

Impact of the U.S. Department of Justice Data Security Program on Genomic Data Sharing

Ticket, Roadmap, or Road Not Taken?

Expanded Prenatal Genomic Testing: Reproductive Autonomy Can Go in More than One Way

Digital Life Models and the Genomic Knowledge Paradox: A Proposal for AI-Assisted Reflection in Genetic Decision-Making

The Value of Genomic Information: Quality Over Quantity