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Author Details

Mildred K Cho
Center for Biomedical Ethics, Stanford University School of Medicine
1985
174
44
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36301246Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review.J Genet Couns2023
37703349Stronger regulation of AI in biomedicine.Sci Transl Med2023
37971798Developer Perspectives on Potential Harms of Machine Learning Predictive Analytics in Health Care: Qualitative Analysis.J Med Internet Res2023
37353052Innovating for a Just and Equitable Future in Genomic and Precision Medicine Research.Am J Bioeth2023
37092651To Understand Inequity, Bioethics Needs to Sort Things Out.Hastings Cent Rep2023
36724788Trustworthiness matters: Building equitable and ethical science.Cell2023
36541003Not in my AI: Moral engagement and disengagement in health care AI development.Pac Symp Biocomput2023
36507873Epistemic Rights and Responsibilities of Digital Simulacra for Biomedicine.Am J Bioeth2023
36535703Paging the Clinical Informatics Community: Respond STAT to Dobbs v. Jackson's Women's Health Organization.Appl Clin Inform2023
36524987Words matter: The language of difference in human genetics.Genet Med2023
36227983Data sharing and community-engaged research.Science2022
35475967Bridging the AI Chasm: Can EBM Address Representation and Fairness in Clinical Machine Learning?Am J Bioeth2022
36533507Values and Practices to Strengthen Genetic Research Partnerships with Indigenous Communities.Prog Community Health Partnersh2022
36313457A mixed-methods protocol to develop and validate a stewardship maturity matrix for human genomic data in the cloud.Front Genet2022
35935917Three decades of ethical, legal, and social implications research: Looking back to chart a path forward.Cell Genom2022
33358138Ethical issues in using ambient intelligence in health-care settings.Lancet Digit Health2021
33649579Taking an antiracist posture in scientific publications in human genetics and genomics.Genet Med2021
33616487The Invisibility of Asian Americans in COVID-19 Data, Reporting, and Relief.Am J Bioeth2021
33582752Use of Korean dramas to facilitate precision mental health understanding and discussion for Asian Americans.Health Promot Int2021
34893774Rising to the challenge of bias in health care AI.Nat Med2021
34156338A Typology of Existing Machine Learning-Based Predictive Analytic Tools Focused on Reducing Costs and Improving Quality in Health Care: Systematic Search and Content Analysis.J Med Internet Res2021
34321310Diverse experts' perspectives on ethical issues of using machine learning to predict HIV/AIDS risk in sub-Saharan Africa: a modified Delphi study.BMJ Open2021
34319252Ethical Development of Digital Phenotyping Tools for Mental Health Applications: Delphi Study.JMIR Mhealth Uhealth2021
33972720Genetic counseling and testing for Asian Americans: a systematic review.Genet Med2021
31570382Informed Consent in the Genomics Era.Cold Spring Harb Perspect Med2020
31896335Partial Entrustment in Pragmatic Clinical Trials.Am J Bioeth2020
32716767Resource Allocation in COVID-19 Research: Which Trials? Which Patients?Am J Bioeth2020
32596893Digital Contact Tracing, Privacy, and Public Health.Hastings Cent Rep2020
32269455Perspectives on Precision Health Among Racial/Ethnic Minority Communities and the Physicians That Serve Them.Ethn Dis2020
31160819In support of mitochondrial replacement therapy.Nat Med2019
29887604"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.Genet Med2019
29976988Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background.Genet Med2019
31216626Using Korean Dramas as a Precision Mental Health Education Tool for Asian Americans: A Pilot Study.Int J Environ Res Public Health2019
30975992Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study.Sci Data2019
30938756Disposition toward privacy and information disclosure in the context of emerging health technologies.J Am Med Inform Assoc2019
31048483Consent insufficient for data release.Science2019
29313771The Emergence of Clinical Research Ethics Consultation: Insights From a National Collaborative.Am J Bioeth2018
31211249Data mining for health: staking out the ethical territory of digital phenotyping.NPJ Digit Med2018
30361364Protect NIH's DNA advisory committee.Science2018
29697352Trustworthiness in Untrustworthy Times: Response to Open Peer Commentaries on Beyond Consent.Am J Bioeth2018
29493583Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease.Genet Med2018
29621457Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.Am J Bioeth2018
29393779Defining the Scope and Improving the Quality of Clinical Research Ethics Consultation: Response to Open Peer Commentaries About the National Collaborative.Am J Bioeth2018
29267267Metaphors matter: from biobank to a library of medical information.Genet Med2018
27625314A randomized study of multimedia informational aids for research on medical practices: Implications for informed consent.Clin Trials2017
30146866Research on Medical Practices (ROMP): Attitudes of IRB Personnel about Randomization and Informed Consent.IRB2017
30387977Research on Medical Practices: Why Patients Consider Participating and the Investigational Misconception.IRB2017
29020542Fairness and Transparency in an Expanded Access Program: Allocation of the Only Treatment for SMA1.Am J Bioeth2017
28700542Consent and engagement, security, and authentic living using wearable and mobile health technology.Nat Biotechnol2017
27973671Feasibility of Obtaining Measures of Lifestyle From a Smartphone App: The MyHeart Counts Cardiovascular Health Study.JAMA Cardiol2017
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Collaborators

Stanford Center for Biomedical Ethics, Stanford University
Co-authored papers 32
University of Washington School of Medicine.
Co-authored papers 20
Division of Ethics, Department of Medical Humanities and Ethics, Columbia University
Co-authored papers 17
University of Pennsylvania, Department of Medical Ethics and Health Policy
Co-authored papers 15
Mayo Clinic
Co-authored papers 13
Stanford University School of Medicine
Co-authored papers 13
University of Washington School of Medicine
Co-authored papers 12
The Center for Law and the Biosciences, Stanford University
Co-authored papers 12
Gould School of Law & Keck School of Medicine, University of Southern California
Co-authored papers 8
Google
Co-authored papers 6
Stanford Center for Biomedical Ethics.
Co-authored papers 6
Penn State College of Medicine
Co-authored papers 6
Seattle Children's Hospital
Co-authored papers 6
Berman Institute of Bioethics, Johns Hopkins University
Co-authored papers 6
Seattle Children's Hospital, University of Washington School of Medicine
Co-authored papers 6
University of British Columbia.
Co-authored papers 5
University of California-San Francisco.
Co-authored papers 5
Institute for Society and Genetics, University of California los angeles
Co-authored papers 5
Clinical Center, National Institutes of Health
Co-authored papers 5
Faculty of Law and School of Public Health, University of Alberta
Co-authored papers 5
Division of Medical Ethics, New York University Grossman School of Medicine
Co-authored papers 4
Stanford University
Co-authored papers 4
Law School and Medical School, University of Minnesota
Co-authored papers 4
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 4
Medical Ethics and Health Policy, University of Pennsylvania
Co-authored papers 4
Baylor College of Medicine.
Co-authored papers 4
National Institutes of Health Clinical Center
Co-authored papers 4
Arizona State University.
Co-authored papers 4
Stanford Center for Biomedical Ethics (SCBE), Stanford University
Co-authored papers 4
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 3