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reproductive technologies
community engagement

641 - 650 of 683 Topics

  • Scholar

    Richard R. Sharp

    • Patient and provider views of genomic medicin
    • Biobanking
    • Role of Disease-Advocacy Organizations
    • Research Ethics
    • Best practices for clinical and research ethics consultation

  • Scholar

    Rachel A. Smith

    • Social influence
    • stigma
    • behavior change
    • Social networks
    • Social norms

  • Scholar

    Don Bailey

    • Newborn screening
    • Disability studies
    • Families

  • Scholar

    Katherine Hendy

    • Addiction
    • mental illness
    • Polygenic risk scores

  • Scholar

    Paul S. Appelbaum

    • ELSI of neuropsychiatric genetics
    • Return of genetic results
    • Ethics of precision medicine
    • Ethics of variant reinterpretation
    • Consent for genetic testing

  • Scholar

    Teri E. Klein

    • Pharmcogenomics
    • Pharmacogenetics
    • Biomedical informatics
    • Genomic medicine
    • Computational Biology

  • Scholar

    Gail E. Henderson

    • Decision-making processes for early phase clinical research participants
    • Genomic screening for healthy populations
    • Ethical and organizational issues in biobanking

  • Scholar

    Daniel Thiel

    • ELSI of gene-editing
    • Biobanking
    • Public attitudes towards genomics
    • Legacy and social media discourse on genomics
    • Socio-cultural meanings of genomics

  • Scholar

    Deborah J. Bowen

    • Behavioral Science

  • Scholar

    Jay Clayton

    • Literature and genetics
    • Film, television, and genetics
    • Medical humanities
    • genetic privacy