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  1. Building Better Medicine: Translational Justice and the Quest for Equity in US Healthcare

    Article • The American Journal of Bioethics, February 2025, Taylor & Francis

    Dr. Marsha Michie

  2. Prenatal Care of Parents Who Continued Pregnancies With Down Syndrome, 2003–2022

    Article • American Journal of Medical Genetics Part A, January 2025, Wiley

    Dr. Marsha Michie

  3. “Down Syndrome is Not a Curse”: parent Perspectives on the Medicalization of Down Syndrome

    Article • AJOB Empirical Bioethics, August 2024, Taylor & Francis

    Dr. Marsha Michie

  4. Grounded in Reality: Integrating Community Values and Priorities of End Users in Human Gene Editing

    Article • The American Journal of Bioethics, August 2024, Taylor & Francis

    Dr. Marsha Michie

  5. Race-Based Screening under the Public Health Ethics Microscope — The Case of Prostate Cancer

    Article • The New England Journal of Medicine and Surgery and the Collateral Branches of Science, August 2024, New England Journal of Medicine (NEJM/MMS)

    Dr. Marsha Michie

  6. P813: Experiences of Black pregnant people offered prenatal diagnosis in the setting of fetal anomalies: A qualitative study

    Article • Genetics in Medicine Open, January 2024, Elsevier

    Dr. Marsha Michie

  7. Translational Justice in Human Gene Editing: Bringing End User Engagement and Policy Together

    Article • The American Journal of Bioethics, June 2023, Taylor & Francis

    Dr. Marsha Michie

  8. Views of parents of children with Down syndrome on Alzheimer’s disease vaccination

    Article • Journal of Intellectual Disabilities, May 2023, SAGE Publications

    Dr. Marsha Michie

  9. Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition

    Article • Journal of Community Genetics, April 2023, Springer Science + Business Media

    Dr. Marsha Michie

  10. Impact of Telehealth on the Delivery of Prenatal Care During the COVID-19 Pandemic: Mixed Methods Study of the Barriers and Opportunities to Improve Health Care Communication in Discussions About Pregnancy and Prenatal Genetic Testing

    Article • JMIR Formative Research, December 2022, JMIR Publications Inc.

    Dr. Marsha Michie

  11. Beyond Abortion Clinics: How Overturning Roe Will Obstruct Life-Saving Research and Fetal Therapy

    Article • The American Journal of Bioethics, August 2022, Taylor & Francis

    Dr. Marsha Michie

  12. Prenatal Care Healthcare Communication during the COVID-19 Pandemic: A Digital Divide Extending Beyond Technology Access (Preprint)

    Article • May 2022, JMIR Publications Inc.

    Dr. Marsha Michie

  13. What Really Matters Now in Prenatal Genetics

    Article • The American Journal of Bioethics, January 2022, Taylor & Francis

    Dr. Marsha Michie

  14. Is preparation a good reason for prenatal genetic testing? Ethical and critical questions

    Article • Birth Defects Research, March 2020, Wiley

    Dr. Marsha Michie

  15. Evaluating the Risks and Benefits of Genetic and Pharmacologic Interventions for Down Syndrome: Views of Parents

    Article • American Journal on Mental Retardation, January 2020, American Association on Intellectual and Developmental Disabilities (AAIDD)

    Dr. Marsha Michie

  16. Prioritizing Women's Health in Germline Editing Research

    Article • The AMA Journal of Ethic, December 2019, American Medical Association (AMA)

    Dr. Marsha Michie

  17. The personal utility of cfDNA screening: Pregnant patients' experiences with cfDNA screening and views on expanded cfDNA panels

    Article • Journal of Genetic Counseling, November 2019, Wiley

    Dr. Marsha Michie

  18. Attitudes Toward Hypothetical Uses of Gene-Editing Technologies in Parents of People with Autosomal Aneuploidies

    Article • The CRISPR Journal, October 2019, Mary Ann Liebert Inc

    Dr. Marsha Michie

  19. The clinical application of gene editing: ethical and social issues

    Article • Personalized Medicine, July 2019, Future Medicine

    Dr. Marsha Michie

  20. Response to Johansen Taber et al.

    Article • Genetics in Medicine, June 2019, Springer Science + Business Media

    Dr. Marsha Michie

  21. Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations

    Article • Genetics in Medicine, April 2019, Springer Science + Business Media

    Dr. Marsha Michie

  22. What do we do now?: Responding to claims of germline gene editing in humans

    Article • Genetics in Medicine, March 2019, Springer Science + Business Media

    Dr. Marsha Michie

  23. Weaponizing Hope: Sources of Hope, Unrealistic Optimism, and Denial

    Article • The American Journal of Bioethics, September 2018, Taylor & Francis

    Dr. Marsha Michie

  24. Gene modification therapies: views of parents of people with Down syndrome

    Article • Genetics in Medicine, June 2018, Springer Science + Business Media

    Dr. Marsha Michie

  25. Conflicts of interest in genetic counseling: persistent underlying questions

    Article • Genetics in Medicine, January 2018, Springer Science + Business Media

    Dr. Marsha Michie

  26. Toward an Ethically Sensitive Implementation of Noninvasive Prenatal Screening in the Global Context

    Article • The Hastings Center Report, March 2017, Wiley

    Dr. Marsha Michie

  27. Conflicts of interest in genetic counseling: acknowledging and accepting

    Article • Genetics in Medicine, January 2017, Springer Science + Business Media

    Dr. Marsha Michie

  28. Dr. Pangloss's Clinic: Prenatal Whole Genome Sequencing and a Return to Reality

    Article • The American Journal of Bioethics, December 2016, Taylor & Francis

    Dr. Marsha Michie

  29. Impact of the increased adoption of prenatal cfDNA screening on non-profit patient advocacy organizations in the United States

    Article • Prenatal Diagnosis, July 2016, Wiley

    Dr. Marsha Michie

  30. “I think we’ve got too many tests!”: Prenatal providers’ reflections on ethical and clinical challenges in the practice integration of cell-free DNA screening

    Article • Ethics Medicine and Public Health, July 2016, Elsevier

    Dr. Marsha Michie

  31. Informed decision-making about prenatal cfDNA screening: An assessment of written materials

    Article • Ethics Medicine and Public Health, July 2016, Elsevier

    Dr. Marsha Michie

  32. Spanish- and English-Speaking Pregnant Women’s Views on cfDNA and Other Prenatal Screening: Practical and Ethical Reflections

    Article • Journal of Genetic Counseling, January 2016, Wiley

    Dr. Marsha Michie

  33. Cherchez la Femme: Reproductive CRISPR and Women's Choices

    Article • The American Journal of Bioethics, December 2015, Taylor & Francis

    Dr. Marsha Michie

  34. “This lifetime commitment”: Public conceptions of disability and noninvasive prenatal genetic screening

    Article • American Journal of Medical Genetics Part A, November 2015, Wiley

    Dr. Marsha Michie

  35. Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues

    Article • Annual Review of Genomics and Human Genetics, August 2015, Annual Reviews

    Dr. Marsha Michie

  36. Flexible positions, managed hopes: The promissory bioeconomy of a whole genome sequencing cancer study

    Article • Social Science & Medicine, April 2015, Elsevier

    Dr. Marsha Michie

  37. Old Questions, New Paradigms: Ethical, Legal, and Social Complications of Noninvasive Prenatal Testing

    Article • AJOB Empirical Bioethics, January 2015, Taylor & Francis

    Dr. Marsha Michie

  38. “Don't Want No Risk and Don't Want No Problems”: Public Understandings of the Risks and Benefits of Noninvasive Prenatal Testing in the United States

    Article • AJOB Empirical Bioethics, January 2015, Taylor & Francis

    Dr. Marsha Michie

  39. Findings of Nonparentage: A Case for Autonomy

    Article • PEDIATRICS, January 2015, American Academy of Pediatrics (AAP)

    Dr. Marsha Michie

  40. Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing

    Article • Trends in Biotechnology, August 2013, Elsevier

    Dr. Marsha Michie

  41. What Research Ethics Should Learn from Genomics and Society Research: Lessons from the ELSI Congress of 2011

    Article • The Journal of Law Medicine & Ethics, December 2012, SAGE Publications

    Dr. Marsha Michie

  42. Am I a control?: Genotype-driven research recruitment and self-understandings of study participants

    Article • Genetics in Medicine, August 2012, Springer Science + Business Media

    Dr. Marsha Michie

  43. Research Participants' Perspectives on Genotype-Driven Research Recruitment

    Article • Journal of Empirical Research on Human Research Ethics, December 2011, SAGE Publications

    Dr. Marsha Michie

  44. The Meaning of Genetic Research Results: Reflections from Individuals with and without a Known Genetic Disorder

    Article • Journal of Empirical Research on Human Research Ethics, December 2011, SAGE Publications

    Dr. Marsha Michie

  45. “If I Could in a Small Way Help”: Motivations for and Beliefs About Sample Donation for Genetic Research

    Article • Journal of Empirical Research on Human Research Ethics, June 2011, SAGE Publications

    Dr. Marsha Michie

  46. Narrating Disability, Narrating Religious Practice: Reconciliation and Fragile X Syndrome

    Article • Intellectual and Developmental Disabilities, April 2010, American Association on Intellectual and Developmental Disabilities (AAIDD)

    Dr. Marsha Michie