Stephanie A Kraft
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Clement A. Adebamowo, Sc.D., B.M., Ch.B.
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Sandra Soo-Jin Lee, Ph.D.
Chief of the Division of Ethics, Columbia University; Professor of Medical Humanities and Ethics, Columbia University; Co-Director, Center for ELSI Resources and Analysis (CERA), NIH/National Human Genome Research Institute; Co-Director, ELSI Congress, NIH/National Human Genome Research Institute
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David Magnus, Ph.D.
Thomas A. Raffin Professor of Medicine and Biomedical Ethics, Professor of Pediatrics and Medicine at Stanford University
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genetic testing, Stem Cell Research, Organ transplantation, End of Life Issues, Ethical considerations for machine learning/artificial intelligence in research/healthcare -
Carole A. Federico, Ph.D.
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Stephanie M. Fullerton, DPhil
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Health Equity, precision medicine, Data Governance, Biobanking, Stakeholder Engagement -
Laura M. Beskow, M.P.H, Ph.D.
Ann Geddes Stahlman Chair in Medical Ethics, Professor of Health Policy
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Human Research Protections, Informed Consent, Research Recruitment, Biobanking, Pragmatic Trials -
Maxwell J. Mehlman, J.D.
Distinguished University Professor, Arthur E. Petersilge Professor of Law and Co-Director of the Law-Medicine Center, Case Western Reserve University School of Law, and Professor of Biomedical Ethics, Case Western Reserve University School of Medicine
Institution: Case Western Reserve University
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Genetics and the Law, The patient-physician relationship, Biomedical enhancement, Military bioethics, Research Ethics -
Susan M. Wolf, J.D.
McKnight Presidential Professor of Law, Medicine & Public Policy; Faegre Baker Daniels Professor of Law; Professor of Medicine
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Return of results & incidental/secondary findings, Law of genomics, Governance of emerging genomic technologies, Research Ethics, ELSI Issues in Large-scale Population Cohort Studies -
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
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Patient and provider views of genomic medicin, Biobanking, Role of Disease-Advocacy Organizations, Research Ethics, Best practices for clinical and research ethics consultation -
Nanibaa' Garrison, Ph.D.
Associate Professor at the University of California, Los Angeles
Institution: University of California, Los Angeles
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Elisa J. Gordon, Ph.D., M.P.H.
Professor at Vanderbilt University Medical Center
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Christi J. Guerrini, J.D., M.P.H.
Assistant Professor
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Intellectual property and health innovation|Investigative genetic genealogy, Ethical, legal, and social implications of genomic technologies, Citizen science/DIY biology/biohacking, Research Ethics -
Kayte Spector-Bagdady, J.D., MBe
Assistant Professor, Department of Obstetrics and Gynecology; Chief, Research Ethics Service, Center for Bioethics & Social Sciences in Medicine
Institution: University of Michigan Medical School
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Research Ethics, Human subjects research regulations, Data science, Secondary research use of data and biospecimens, Health Policy -
Mildred K. Cho, Ph.D.
SCBE Associate Director, Professor (Research) of Medicine and Pediatrics
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Ellen W. Clayton, M.D., J.D.
Craig-Weaver Professor of Pediatrics, Professor of Health Policy, Center for Biomedical Ethics and Society, Vanderbilt University Medical Center, Professor of Law, Vanderbilt University School of Law
Institution: Vanderbilt University Medical Center and Vanderbilt University
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Research Ethics, clinical translation, law, Pediatrics, reproductive rights -
Kate Saylor, M.S.
Doctoral student in Public Policy
Institution: University of North Carolina
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Priority setting, Cost-Effectiveness, Research Ethics, public health genomics, Quantitative data analysis -
Subhashini Chandrasekharan, Ph.D.
Health Scientist Administrator
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Jeffrey Kahn, Ph.D., M.P.H.
Andreas C. Dracopoulos Director
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genetic technologies, Public Health, Research Ethics -
Eric M. Meslin, PhD, FRSC, FCAHS
President and CEO Council of Canadian Academies
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Research Ethics, Evidence for policy, Disuruptive technology ethics, Governance -
Steven Joffe, M.D., M.P.H
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Research Ethics, Pediatric bioethics, ELSI Genomics, Science Policy -
Camille Nebeker, EdD, M.S.
Associate Professor
Institution: University of California, San Diego
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Ilaria Galasso
Postdoctoral Researcher
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Health Equity, bounded justice, Bioethics, social determinants of health, Ethics of precision medicine -
Maya Sabatello, LLB, Ph.D.
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Mark A. Rothstein, J.D.
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genetic nondiscrimination law, genetic privacy, public health ethics, Research Ethics -
Liza-Marie Johnson, MD, MPH, MSB
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Informed Consent, Pediatric bioethics, Consent for Genomic Testing, Pediatric Research, Best practices for clinical and research ethics consultation -
Alison Bateman-House, PhD, MPH, MA
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Jessica Mozersky, MBE, PhD
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Qualitative Methods, ELSI Genomics, Bioethical Issues, Alzheimer's disease risk, Research Ethics -
Marianna J. Bledsoe, M.A.
Independent Consultant; Deputy Editor
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Biobanking, Research Ethics, Science Policy, Secondary research use of data and biospecimens, genomic data sharing -
Catherine Hammack-Aviran, MA, JD
Core Faculty, Center for Biomedical Ethics & Society
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Bioethics, Death, Medical law, Research Ethics, Ethical Legal and Social Implications (ELSI) -
James M. DuBois, DSc, PhD
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Bioethics, data sharing policy, Informed Consent, Research integrity, ELSI