Members of the ELSI Scholar Directory are scholars and trainees with an interest in research on the ethical, legal, and social implications of genetics and genomics. You may contact members to organize collaborative projects or working groups, share speaking opportunities, solicit expert commentary, obtain advice on policy or legislation, network, and arrange mentor/mentee relationships.
1 - 5 of 5 Scholars
Join Directory-
Paul S. Appelbaum, M.D.
Elizabeth K. Dollard Professor of Psychiatry, Medicine and Law, and Director, Center for Law, Ethics and Psychiatry at Columbia
Institution: Columbia University
Contact: [email protected]
AREAS OF EXPERTISE
Show more- ELSI of neuropsychiatric genetics
- Return of genetic results
- Ethics of precision medicine
- Ethics of variant reinterpretation
- Consent for genetic testing
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Nanibaa' Garrison, Ph.D.
Associate Professor at the University of California, Los Angeles
Institution: University of California, Los Angeles
Contact: [email protected]
AREAS OF EXPERTISE
Show more- Indigenous Communities
- Community Engagement
- data sovereignty
- precision health
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Lucas J. Matthews, Ph.D.
Assistant Professor of Bioethics, Columbia University; Presidential Scholar, The Hastings Center; Research Scientist IV, Research Foundation for Mental Hygiene
Institution: Columbia University
Contact: [email protected]
AREAS OF EXPERTISE
Show more- Behavioral Genetics
- Doctor of Philosophy
- Philosophy
- Bioethics
- Behavioral and Social Science
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Will Schupmann, MA
PhD Student
Institution: UCLA
Contact: [email protected]
AREAS OF EXPERTISE
Show more- nondirective counseling
- Variants of Uncertain Significance
- Right Not To Know
- Return of results & incidental/secondary findings
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Richard R. Sharp, Ph.D.
Director of the Mayo Clinic Biomedical Ethics Program, the Center for Individualized Medicine Bioethics Program and the Clinical and Translational Research Ethics Program
Institution: Mayo Clinic
Contact: [email protected]
AREAS OF EXPERTISE
Show more- Patient and provider views of genomic medicin
- Biobanking
- Role of Disease-Advocacy Organizations
- Research Ethics
- Best practices for clinical and research ethics consultation