Event Description
Genomics research and practice have complex ethical, legal, and social implications for diverse stakeholders – e.g., researchers, clinicians, persons living with or at risk for genetic disorders, family members, clergy, marginalized communities, the public. Widely differing perspectives both within and among stakeholder groups raise challenges for developing policy and practice recommendations. A variety of innovative methods seek to gather data on the views and values of members of diverse groups. This short course will provide an overview of approaches that can be used to encourage dialogue aimed at reaching broad understanding and elucidating areas of agreement and disagreement.
Event Speakers
Please visit the event webpage for speaker information.
Event Information:
Free and open to the public; registration required. For more information, please visit the event webpage.
Hosted by the Irving Institute for Clinical and Translational Research and Center for Research on Ethical, Legal and Social Implications of Psychiatric, Neurologic & Behavioral Genetics at Columbia University.
