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Marsha Michie, PhD

TitleAssistant Professor
InstitutionUniversity of California San Francisco
DepartmentInstitute for Health Aging
Address3333 California Street
San Francisco CA 94118
Phone415-502-6491
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    Collapse Biography 
    Collapse Education and Training
    University of North Carolina - Chapel HillPhD2010Anthropology
    Agnes Scott CollegeBA1990Mathematics/Music

    Collapse Overview 
    Collapse Overview
    Marsha Michie is an anthropologist and empirical bioethicist who studies social and ethical issues in genetics, including moral and religious perspectives. Dr. Michie has conducted qualitative research on families of children with genetic disorders, on the understandings and self-perceptions of genetic research participants, and on individual and community religious identities. Her dissertation was a long-term ethnography of an independent Pentecostal church community in North Carolina.

    Dr. Michie's current research examines social and ethical issues in the translation of non-invasive prenatal genetic screening from laboratory innovation to a recommended component of prenatal care, through interviews and mixed-method research with patients, obstetricians, and other stakeholders in this technology.


    Collapse Research 
    Collapse Research Activities and Funding
    Mapping an ELSI-integrated translational pathway with cell-free fetal DNA testing
    NIH/NHGRI R00HG006452Aug 19, 2014 - May 31, 2017
    Role: Principal Investigator
    Mapping an ELSI-integrated translational pathway with cell-free fetal DNA testing
    NIH/NHGRI K99HG006452Jun 1, 2012 - May 31, 2014
    Role: Principal Investigator

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    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Stoll KA, Mackison A, Allyse MA, Michie M. Conflicts of interest in genetic counseling: persistent underlying questions. Genet Med. 2018 Jan 04. PMID: 29300378.
      View in: PubMed
    2. Allyse M, Aypar U, Bonhomme N, Darilek S, Dougherty M, Farrell R, Grody W, Highsmith WE, Michie M, Nunes M, Otto L, Pabst R, Palomaki G, Runke C, Sharp RR, Skotko B, Stoll K, Wick M. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 Jul; 26(7):755-761. PMID: 28388340.
      View in: PubMed
    3. Mozersky J, Ravitsky V, Rapp R, Michie M, Chandrasekharan S, Allyse M. Toward an Ethically Sensitive Implementation of Noninvasive Prenatal Screening in the Global Context. Hastings Cent Rep. 2017 Mar; 47(2):41-49. PMID: 28301696.
      View in: PubMed
    4. Stoll KA, Mackison A, Allyse MA, Michie M. Conflicts of interest in genetic counseling: acknowledging and accepting. Genet Med. 2017 08; 19(8):864-866. PMID: 28125084.
      View in: PubMed
    5. Allyse M, Evans JP, Michie M. Dr. Pangloss's Clinic: Prenatal Whole Genome Sequencing and a Return to Reality. Am J Bioeth. 2017 Jan; 17(1):21-23. PMID: 27996895.
      View in: PubMed
    6. Michie M, Kraft SA, Minear MA, Ryan RR, Allyse MA. Informed decision-making about prenatal cfDNA screening: An assessment of written materials. Ethics Med Public Health. 2016 Jul-Sep; 2(3):362-371. PMID: 27699200.
      View in: PubMed
    7. Meredith S, Kaposy C, Miller VJ, Allyse M, Chandrasekharan S, Michie M. Impact of the increased adoption of prenatal cfDNA screening on non-profit patient advocacy organizations in the United States. Prenat Diagn. 2016 Aug; 36(8):714-9. PMID: 27244688; PMCID: PMC4974118 [Available on 08/01/17].
      View in: PubMed, PubMed Central
    8. Floyd E, Allyse MA, Michie M. Spanish- and English-Speaking Pregnant Women's Views on cfDNA and Other Prenatal Screening: Practical and Ethical Reflections. J Genet Couns. 2016 Oct; 25(5):965-77. PMID: 26739840; PMCID: PMC4936962 [Available on 07/07/17].
      View in: PubMed, PubMed Central
    9. Steinbach RJ, Allyse M, Michie M, Liu EY, Cho MK. "This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening. Am J Med Genet A. 2016 Feb; 170A(2):363-74. PMID: 26566970; PMCID: PMC4948186 [Available on 02/01/17].
      View in: PubMed, PubMed Central
    10. Haase R, Michie M, Skinner D. Flexible positions, managed hopes: the promissory bioeconomy of a whole genome sequencing cancer study. Soc Sci Med. 2015 Apr; 130:146-53. PMID: 25697637; PMCID: PMC4363274.
      View in: PubMed, PubMed Central
    11. Minear MA, Alessi S, Allyse M, Michie M, Chandrasekharan S. Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues. Annu Rev Genomics Hum Genet. 2015; 16:369-98. PMID: 26322648.
      View in: PubMed
    12. Allyse M, Michie M, Mozersky J, Rapp R. Cherchez la Femme: Reproductive CRISPR and Women's Choices. Am J Bioeth. 2015; 15(12):47-9. PMID: 26632363.
      View in: PubMed
    13. Allyse M, Sayres LC, Goodspeed T, Michie M, Cho MK. "Don't Want No Risk and Don't Want No Problems": Public Understandings of the Risks and Benefits of Non-Invasive Prenatal Testing in the United States. AJOB Empir Bioeth. 2015; 6(1):5-20. PMID: 25932463.
      View in: PubMed
    14. Michie M, Allyse M. Old Questions, New Paradigms: Ethical, Legal, and Social Complications of Noninvasive Prenatal Testing. AJOB Empir Bioeth. 2015 Jan 01; 6(1):1-4. PMID: 26185771.
      View in: PubMed
    15. Michie M, Allyse M. Findings of nonparentage: a case for autonomy. Pediatrics. 2015 Jan; 135(1):e284-5. PMID: 25554818.
      View in: PubMed
    16. Allyse M, Michie M. Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing. Trends Biotechnol. 2013 Aug; 31(8):439-41. PMID: 23664778; PMCID: PMC4086155.
      View in: PubMed, PubMed Central
    17. Michie M, Cadigan RJ, Henderson G, Beskow LM. Am I a control?: Genotype-driven research recruitment and self-understandings of study participants. Genet Med. 2012 Dec; 14(12):983-9. PMID: 22935717; PMCID: PMC3578310.
      View in: PubMed, PubMed Central
    18. Henderson GE, Juengst ET, King NM, Kuczynski K, Michie M. What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011. J Law Med Ethics. 2012; 40(4):1008-24. PMID: 23289702; PMCID: PMC4103651.
      View in: PubMed, PubMed Central
    19. Cadigan RJ, Michie M, Henderson G, Davis AM, Beskow LM. The meaning of genetic research results: reflections from individuals with and without a known genetic disorder. J Empir Res Hum Res Ethics. 2011 Dec; 6(4):30-40. PMID: 22228058; PMCID: PMC3386306.
      View in: PubMed, PubMed Central
    20. Beskow LM, Namey EE, Cadigan RJ, Brazg T, Crouch J, Henderson GE, Michie M, Nelson DK, Tabor HK, Wilfond BS. Research participants' perspectives on genotype-driven research recruitment. J Empir Res Hum Res Ethics. 2011 Dec; 6(4):3-20. PMID: 22228056; PMCID: PMC3395316.
      View in: PubMed, PubMed Central
    21. Michie M, Henderson G, Garrett J, Corbie-Smith G. "If I could in a small way help": motivations for and beliefs about sample donation for genetic research. J Empir Res Hum Res Ethics. 2011 Jun; 6(2):57-70. PMID: 21680977; PMCID: PMC3313647.
      View in: PubMed, PubMed Central
    22. Michie M, Skinner D. Narrating disability, narrating religious practice: reconciliation and fragile X syndrome. Intellect Dev Disabil. 2010 Apr; 48(2):99-111. PMID: 20597744; PMCID: PMC3129695.
      View in: PubMed, PubMed Central
    23. Michie M, Kraft S, Minear MA, Ryan R, Allyse MA.Informed decision-making about prenatal cfDNA screening: An assessment of written materials. Ethics, Medicine, and Public Health. In press.
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