Misha Angrist
Associate Professor of the Practice in the Social Science Research Institute
Misha Angrist is Associate Professor of the Practice at SSRI, a Senior Fellow in Science & Society, and Visiting Associate Professor of the Practice in the Sanford School of Public Policy as part of the DeWitt Wallace Center for Media & Democracy. He directs the undergraduate Science & Society Certificate Program and the First-year FOCUS cluster on Science and the Public. He teaches and mentors students in the MA in Bioethics & Science Policy. He teaches science writing and scholarly writing to both undergraduate and graduate students. In his work, he explores the intersection of biology and society, especially as it relates to the governance of human participation in research and medicine. As the fourth participant in the Personal Genome Project, he was among the first to have his entire genome sequenced and made public. He chronicled this experience in his book, Here is a Human Being: At the Dawn of Personal Genomics. Angrist has an MFA from the Bennington Writing Seminars, an MS in genetic counseling from the University of Cincinnati, and a PhD in genetics from Case Western Reserve University.
Office Hours
Varies by semester or by appointment
Current Appointments & Affiliations
- Associate Professor of the Practice in the Social Science Research Institute, Social Science Research Institute, University Institutes and Centers 2014
- Senior Fellow in the Duke Initiative for Science & Society, Duke Science & Society, Initiatives 2014
Contact Information
- Box 90222, North Building Room 237, Durham, NC 27708-0222
- Box 90222, North Building Room 237, Durham, NC 27708-0222
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(919) 684-2872
- Background
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Education, Training, & Certifications
- M.F.A., Bennington College 2001
- Ph.D., Case Western Reserve University 1996
- M.S., University of Cincinnati 1990
- B.A., Indiana University at Bloomington 1985
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Duke Appointment History
- Visiting Associate Professor of the Practice in the Sanford School of Public Policy, Sanford School of Public Policy, Duke University 2015 - 2016
- Assistant Professor of the Practice in the Institute for Genome Sciences & Policy, University Institutes and Centers, Institutes and Provost's Academic Units 2012 - 2014
- Assistant Professor of the Practice in the Institute for Genome Sciences & Policy, Institutes and Centers, School of Medicine 2012
- Assistant Professor of the Practice in the Institute for Genome Sciences & Policy, University Institutes and Centers, Institutes and Provost's Academic Units 2010 - 2012
- Assistant Professor of the Practice in the Institute for Genome Sciences & Policy, Institutes and Centers, School of Medicine 2008 - 2010
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Leadership & Clinical Positions at Duke
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Director, Undergraduate Certificate In Science & Society
Director, First-Year Focus Cluster: Science and the Public
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Director, Undergraduate Certificate In Science & Society
- Recognition
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In the News
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Awards & Honors
- Publications & Artistic Works
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Selected Publications
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Academic Articles
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Hansen, Adam W., Mullai Murugan, He Li, Michael M. Khayat, Liwen Wang, Jill Rosenfeld, B Kim Andrews, et al. “A Genocentric Approach to Discovery of Mendelian Disorders.” Am J Hum Genet 105, no. 5 (November 7, 2019): 974–86. https://doi.org/10.1016/j.ajhg.2019.09.027.Full Text Link to Item
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Greshake Tzovaras, Bastian, Misha Angrist, Kevin Arvai, Mairi Dulaney, Vero Estrada-Galiñanes, Beau Gunderson, Tim Head, et al. “Open Humans: A platform for participant-centered research and personal data exploration.” Gigascience 8, no. 6 (June 2019). https://doi.org/10.1093/gigascience/giz076.Full Text
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Helbig, Katherine L., Robert J. Lauerer, Jacqueline C. Bahr, Ivana A. Souza, Candace T. Myers, Betül Uysal, Niklas Schwarz, et al. “De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.” Am J Hum Genet 104, no. 3 (March 7, 2019): 562. https://doi.org/10.1016/j.ajhg.2019.02.015.Full Text Link to Item
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Khan, Tahir N., Kamal Khan, Azita Sadeghpour, Hannah Reynolds, Yezmin Perilla, Marie T. McDonald, William B. Gallentine, et al. “Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.” Am J Hum Genet 104, no. 1 (January 3, 2019): 94–111. https://doi.org/10.1016/j.ajhg.2018.11.017.Full Text Link to Item
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Angrist, Misha. “A BRIEF HISTORY OF EVERYONE WHO EVER LIVED The Human Story Retold Through Our Genes.” New York Times Book Review 122, no. 47 (November 19, 2017): 29–29.Open Access Copy Link to Item
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Angrist, Misha. “MERCIES IN DISGUISE A Story of Hope, a Family's Genetic Destiny, and the Science That Rescued Them.” New York Times Book Review 122, no. 18 (April 30, 2017): 20–20.Open Access Copy Link to Item
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Angrist, Misha. “THE FAMILY GENE A Mission to Turn My Deadly Inheritance Into a Hopeful Future.” New York Times Book Review 122, no. 18 (April 30, 2017): 20–20.Link to Item
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Angrist, Misha. “Personal genomics: Where are we now?” Applied & Translational Genomics 8 (March 2016): 1–3. https://doi.org/10.1016/j.atg.2016.01.010.Full Text
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Angrist, Misha. “Start me up: ways to encourage sharing of genomic information with research participants.” Nature Reviews. Genetics 16, no. 8 (August 2015): 435–36. https://doi.org/10.1038/nrg3981.Full Text
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Angrist, M., and L. Jamal. “Living laboratory: whole-genome sequencing as a learning healthcare enterprise.” Clinical Genetics 87, no. 4 (April 2015): 311–18. https://doi.org/10.1111/cge.12461.Full Text
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Angrist, Misha, and Robert Cook-Deegan. “Distributing the future: The weak justifications for keeping human genomic databases secret and the challenges and opportunities in reverse engineering them.” Applied & Translational Genomics 3, no. 4 (December 2014): 124–27. https://doi.org/10.1016/j.atg.2014.09.005.Full Text
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Angrist, Misha. “The audacity of interpretation: Protecting patients or piling on?” Applied & Translational Genomics 3, no. 3 (September 2014): 68–69. https://doi.org/10.1016/j.atg.2014.06.003.Full Text
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Lu, Yi-Fan, David B. Goldstein, Misha Angrist, and Gianpiero Cavalleri. “Personalized medicine and human genetic diversity.” Cold Spring Harbor Perspectives in Medicine 4, no. 9 (September 2014): a008581. https://doi.org/10.1101/cshperspect.a008581.Full Text Open Access Copy
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Davis, E. E., J. H. Savage, J. R. Willer, Y. -. H. Jiang, M. Angrist, A. Androutsopoulos, and N. Katsanis. “Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.” Clin Genet 85, no. 4 (April 2014): 359–64. https://doi.org/10.1111/cge.12189.Full Text Link to Item
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Angrist, M., and R. Cook-Deegan. “Distributing the future: The weak justifications for keeping human genomic databases secret and the challenges and opportunities in reverse engineering them.” Applied and Translational Genomics 3, no. 4 (2014): 124–27. https://doi.org/10.1016/j.atg.2014.09.005.Full Text
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Angrist, Misha. “Open window: when easily identifiable genomes and traits are in the public domain.” Plos One 9, no. 3 (January 2014): e92060. https://doi.org/10.1371/journal.pone.0092060.Full Text
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Angrist, Misha. “Genetic privacy needs a more nuanced approach.” Nature 494, no. 7435 (February 2013): 7. https://doi.org/10.1038/494007a.Full Text
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Katsanis, N., M. Cotten, and M. Angrist. “Exome and genome sequencing of neonates with neurodevelopmental disorders.” Future Neurology 7, no. 6 (November 1, 2012): 655–58. https://doi.org/10.2217/fnl.12.74.Full Text
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Ball, Madeleine P., Joseph V. Thakuria, Alexander Wait Zaranek, Tom Clegg, Abraham M. Rosenbaum, Xiaodi Wu, Misha Angrist, et al. “A public resource facilitating clinical use of genomes.” Proceedings of the National Academy of Sciences of the United States of America 109, no. 30 (July 13, 2012): 11920–27. https://doi.org/10.1073/pnas.1201904109.Full Text
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Angrist, Misha. “You never call, you never write: why return of 'omic' results to research participants is both a good idea and a moral imperative.” Personalized Medicine 8, no. 6 (November 2011): 651–57. https://doi.org/10.2217/pme.11.62.Full Text
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Cook-Deegan, R., S. Chandrasekharan, B. Sampat, E. R. Gold, J. Carbone, and L. Knowles. “Letter to editor.” Nature Biotechnology 28, no. 12 (December 1, 2010): 1243. https://doi.org/10.1038/nbt1210-1243a.Full Text
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Angrist, Misha. “Urge overkill: protecting deidentified human subjects at what price?” The American Journal of Bioethics : Ajob 10, no. 9 (September 2010): 17–18. https://doi.org/10.1080/15265161.2010.494217.Full Text
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Carbone, Julia, E Richard Gold, Bhaven Sampat, Subhashini Chandrasekharan, Lori Knowles, Misha Angrist, and Robert Cook-Deegan. “DNA patents and diagnostics: not a pretty picture.” Nature Biotechnology 28, no. 8 (August 2010): 784–91. https://doi.org/10.1038/nbt0810-784.Full Text
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Angrist, M. “Orchid agonistes.” Nature 465, no. 7297 (May 27, 2010): 518. https://doi.org/10.1038/465518a.Full Text
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Angrist, Misha, Subhashini Chandrasekharan, Christopher Heaney, and Robert Cook-Deegan. “Impact of gene patents and licensing practices on access to genetic testing for long QT syndrome.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 12, no. 4 Suppl (April 2010): S111–54. https://doi.org/10.1097/gim.0b013e3181d68293.Full Text
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Angrist, Misha. “Only connect: personal genomics and the future of American medicine.” Molecular Diagnosis & Therapy 14, no. 2 (April 2010): 67–72. https://doi.org/10.2165/11534710-000000000-00000.Full Text
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Lunshof, J. E., J. Bobe, J. Aach, M. Angrist, J. V. Thakuria, D. B. Vorhaus, M. R. Hoehe, and G. M. Church. “Personal genomes in progress: From the human genome project to the Personal Genome Project.” Dialogues in Clinical Neuroscience 12, no. 1 (2010): 44–57.
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Lunshof, J. E., J. Bobe, J. Aach, M. Angrist, J. V. Thakuria, D. B. Vorhaus, M. R. Hoehe, and G. M. Church. “Personal genomes in progress: From the human genome project to the Personal Genome Project.” Dialogues in Clinical Neuroscience 12, no. 1 (January 1, 2010): 44–57.
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Lunshof, Jeantine E., Jason Bobe, John Aach, Misha Angrist, Joseph V. Thakuria, Daniel B. Vorhaus, Margret R. Hoehe, and George M. Church. “Personal genomes in progress: from the human genome project to the personal genome project.” Dialogues in Clinical Neuroscience 12, no. 1 (January 2010): 47–60.
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Angrist, Misha. “Eyes wide open: the personal genome project, citizen science and veracity in informed consent.” Personalized Medicine 6, no. 6 (November 2009): 691–99. https://doi.org/10.2217/pme.09.48.Full Text
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Cook-Deegan, Robert, Subhashini Chandrasekharan, and Misha Angrist. “The dangers of diagnostic monopolies.” Nature 458, no. 7237 (March 2009): 405–6. https://doi.org/10.1038/458405a.Full Text
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Angrist, Misha. “We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.” The American Journal of Bioethics : Ajob 9, no. 6–7 (January 2009): 30–31. https://doi.org/10.1080/15265160902893999.Full Text
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Angrist, M. “Personal genomics: Access denied? : Consumers have a right to their genomes.” Technology Review 111, no. 5 (September 1, 2008).
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Angrist, M. “Paper boy.” Literary Review 49, no. 4 (December 1, 2006).
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Ginsburg, Geoffrey S., Misha Angrist, and Robert Cook-Deegan. “Public health. Genomics and medicine at a crossroads in Chernobyl.” Science 314, no. 5796 (October 6, 2006): 62–63. https://doi.org/10.1126/science.1130274.Full Text Link to Item
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Ginsburg, Geoffrey S., and Misha Angrist. “The future may be closer than you think: a response from the Personalized Medicine Coalition to the Royal Society's report on personalized medicine.” Per Med 3, no. 2 (May 2006): 119–23. https://doi.org/10.2217/17410541.3.2.119.Full Text Link to Item
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Angrist, Misha, and Robert M. Cook-Deegan. “Who owns the genome?” New Atlantis (Washington, D.C.) 11 (January 2006): 87–96.
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Willard, Huntington F., Misha Angrist, and Geoffrey S. Ginsburg. “Genomic medicine: genetic variation and its impact on the future of health care.” Philos Trans R Soc Lond B Biol Sci 360, no. 1460 (August 29, 2005): 1543–50. https://doi.org/10.1098/rstb.2005.1683.Full Text Link to Item
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Angrist, Misha. “Breast cancer: integrating the patient with her genome.” Trends in Biotechnology 23, no. 1 (January 2005): 3–5. https://doi.org/10.1016/j.tibtech.2004.11.007.Full Text
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Angrist, M. “Swedish bricks and minerals.” Michigan Quarterly Review 42, no. 1 (December 1, 2003).
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Gabriel, Stacey B., Rémi Salomon, Anna Pelet, Misha Angrist, Jeanne Amiel, Myriam Fornage, Tania Attié-Bitach, et al. “Segregation at three loci explains familial and population risk in Hirschsprung disease.” Nature Genetics 31, no. 1 (May 2002): 89–93. https://doi.org/10.1038/ng868.Full Text
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Blagoev, Blagoy, Mogens M. Nielsen, Misha Angrist, Aravinda Chakravarti, and Akhilesh Pandey. “Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.” Gene 284, no. 1–2 (February 2002): 161–68. https://doi.org/10.1016/s0378-1119(02)00380-3.Full Text
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Bolk, S., A. Pelet, R. M. Hofstra, M. Angrist, R. Salomon, D. Croaker, C. H. Buys, S. Lyonnet, and A. Chakravarti. “A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.” Proceedings of the National Academy of Sciences of the United States of America 97, no. 1 (January 2000): 268–73. https://doi.org/10.1073/pnas.97.1.268.Full Text
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Southard-Smith, E. M., M. Angrist, J. S. Ellison, R. Agarwala, A. D. Baxevanis, A. Chakravarti, and W. J. Pavan. “The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.” Genome Research 9, no. 3 (March 1999): 215–25.
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Angrist, M., S. Bolk, K. Bentley, S. Nallasamy, M. K. Halushka, and A. Chakravarti. “Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.” Oncogene 17, no. 23 (December 1998): 3065–70. https://doi.org/10.1038/sj.onc.1202226.Full Text
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Angrist, M. “Less is more: compact genomes pay dividends.” Genome Research 8, no. 7 (July 1998): 683–85. https://doi.org/10.1101/gr.8.7.683.Full Text
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Angrist, M., S. Jing, S. Bolk, K. Bentley, S. Nallasamy, M. Halushka, G. M. Fox, and A. Chakravarti. “Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.” Genomics 48, no. 3 (March 1998): 354–62. https://doi.org/10.1006/geno.1997.5191.Full Text
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Chadwick, B. P., L. A. Helbling, M. Angrist, A. Chakravarti, J. F. Gusella, and S. A. Slaugenhaupt. “Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.” Cytogenetics and Cell Genetics 83, no. 3–4 (January 1998): 236–37. https://doi.org/10.1159/000015189.Full Text
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Angrist, M. “Does phaster mean better?” Clinical Chemistry 43, no. 3 (March 1997): 424–26.
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Angrist, M., S. Bolk, M. Halushka, P. A. Lapchak, and A. Chakravarti. “Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.” Nature Genetics 14, no. 3 (November 1996): 341–44. https://doi.org/10.1038/ng1196-341.Full Text
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Bolk, S., M. Angrist, J. Xie, M. Yanagisawa, J. M. Silvestri, D. E. Weese-Mayer, and A. Chakravarti. “Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.” Nature Genetics 13, no. 4 (August 1996): 395–96. https://doi.org/10.1038/ng0896-395.Full Text
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Bolk, S., M. Angrist, S. Schwartz, J. M. Silvestri, D. E. Weese-Mayer, and A. Chakravarti. “Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.” American Journal of Medical Genetics 63, no. 4 (June 1996): 603–9. https://doi.org/10.1002/(sici)1096-8628(19960628)63:4<603::aid-ajmg14>3.0.co;2-m.Full Text
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Hofstra, R. M., J. Osinga, G. Tan-Sindhunata, Y. Wu, E. J. Kamsteeg, R. P. Stulp, C. van Ravenswaaij-Arts, et al. “A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).” Nature Genetics 12, no. 4 (April 1996): 445–47. https://doi.org/10.1038/ng0496-445.Full Text
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ANGRIST, M. “Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.” Nature Genet 14 (1996): 341–44.
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Angrist, M., D. E. Wells, A. Chakravarti, and A. Pandey. “Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.” Genomics 30, no. 3 (December 1995): 623–25. https://doi.org/10.1006/geno.1995.1289.Full Text
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Angrist, M., S. Bolk, B. Thiel, E. G. Puffenberger, R. M. Hofstra, C. H. Buys, D. T. Cass, and A. Chakravarti. “Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.” Human Molecular Genetics 4, no. 5 (May 1995): 821–30. https://doi.org/10.1093/hmg/4.5.821.Full Text
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Hentati, A., M. A. Pericak-Vance, F. Lennon, B. Wasserman, F. Hentati, T. Juneja, M. H. Angrist, W. Y. Hung, R. M. Boustany, and S. Bohlega. “Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.” Hum Mol Genet 3, no. 10 (October 1994): 1867–71. https://doi.org/10.1093/hmg/3.10.1867.Full Text Link to Item
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Puffenberger, E. G., E. R. Kauffman, S. Bolk, T. C. Matise, S. S. Washington, M. Angrist, J. Weissenbach, K. L. Garver, M. Mascari, and R. Ladda. “Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.” Human Molecular Genetics 3, no. 8 (August 1994): 1217–25. https://doi.org/10.1093/hmg/3.8.1217.Full Text
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Angrist, M., E. Kauffman, S. A. Slaugenhaupt, T. C. Matise, E. G. Puffenberger, S. S. Washington, A. Lipson, D. T. Cass, T. Reyna, and D. E. Weeks. “A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.” Nature Genetics 4, no. 4 (August 1993): 351–56. https://doi.org/10.1038/ng0893-351.Full Text
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Dalrymple, N. J., and M. H. Angrist. “Autism resources at the higher education level in Indiana.” Journal of Autism and Developmental Disorders 19, no. 1 (March 1989): 173–75. https://doi.org/10.1007/bf02212729.Full Text
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Dalrymple, N. J., and M. H. Angrist. “Toilet training a sixteen year old with autism in a natural setting.” British Journal of Mental Subnormality 34, no. 67 (January 1, 1988): 117–30. https://doi.org/10.1179/bjms.1988.016.Full Text
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Katsanis, Sara Huston, Mollie A. Minear, Azita Sadeghpour, Heidi Cope, Yezmin Perilla, Robert Cook-Deegan, Nicholas Katsanis, Erica E. Davis, and Misha Angrist. “Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions.” Journal of Participatory Medicine 10, no. 1 (n.d.): e2–e2. https://doi.org/10.2196/jopm.8958.Full Text Open Access Copy
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Murray, Michael F., James P. Evans, Misha Angrist, Wendy R. Uhlmann, Debra Lochner Doyle, Stephanie M. Fullerton, Theodore G. Ganiats, et al. “A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults.” Nam Perspectives, n.d. https://doi.org/10.31478/201812a.Full Text Open Access Copy
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Conference Papers
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Angrist, M., S. Jing, M. Halushka, K. Bentley, S. Bolk, S. Nallasamy, G. M. Fox, and A. Chakravarti. “Genomic organization of RET-signaling pathway genes and mutation analysis in Hirschsprung disease patients.” In American Journal of Human Genetics, 61:A303–A303. CELL PRESS, 1997.Link to Item
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Bolk, S., A. Pelet, R. M. W. Hofstra, B. Salomon, M. Angrist, C. H. C. M. Buys, S. Lyonnet, and A. Chakravarti. “Multigenic inheritance of Hirschsprung disease.” In American Journal of Human Genetics, 61:A41–A41. CELL PRESS, 1997.Link to Item
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HOFSTRA, R. M. W., M. ANGRIST, J. OSINGA, R. P. STULP, G. TAN, E. J. KAMSTEEG, H. SCHEFFER, A. CHAKRAVARTI, and C. H. C. M. BUYS. “MUTATION SCREENING OF THE RET, EDNRB AND ET3 GENES IN HIRSCHSPRUNG PATIENTS.” In American Journal of Human Genetics, 57:1110–1110. UNIV CHICAGO PRESS, 1995.Link to Item
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HENTATI, A., M. A. PERICAKVANCE, F. LENNON, B. WASSERMAN, F. HENTATI, T. JUNEJA, M. H. ANGRIST, et al. “LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME 2P MARKERS.” In Cytogenetics and Cell Genetics, 67:244–244. KARGER, 1994.Link to Item
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ANGRIST, M., E. KAUFFMAN, T. C. MATISE, S. A. SLAUGENHAUPT, S. BOLK, E. G. PUFFENBERGER, A. LIPSON, et al. “A GENETIC-LOCUS FOR HIRSCHSPRUNG DISEASE IN THE PERICENTROMERIC REGION OF CHROMOSOME-10.” In American Journal of Human Genetics, 53:134–134. UNIV CHICAGO PRESS, 1993.Link to Item
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PUFFENBERGER, E. G., E. R. KAUFFMAN, S. BOLK, M. ANGRIST, T. C. MATISE, and A. CHAKRAVARTI. “IDENTITY-BY-DESCENT MAPPING OF HIRSCHSPRUNG DISEASE IN A LARGE MENNONITE KINDRED.” In American Journal of Human Genetics, 53:1062–1062. UNIV CHICAGO PRESS, 1993.Link to Item
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SLAUGENHAUPT, S. A., M. ANGRIST, R. D. LEARISH, D. H. LESH, S. S. WASHINGTON, and A. CHAKRAVARTI. “HIRSCHSPRUNG DISEASE - LINKAGE ANALYSIS OF CANDIDATE REGIONS ON HUMAN-CHROMOSOME, CHROMOSOME-13 AND CHROMOSOME-21.” In American Journal of Human Genetics, 49:359–359, 1991.Link to Item
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- Teaching & Mentoring
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Recent Courses
- AAAS 196FS: Patient and Research Participant Activism and Advocacy 2020
- BIOETHIC 510S: Science and the Media: Narrative Writing about Science, Health and Policy 2020
- BIOETHIC 605S: Contemporary Issues in Bioethics and Science Policy 2020
- BIOETHIC 700: Research Independent Study in Bioethics and Science Policy 2020
- CULANTH 196FS: Patient and Research Participant Activism and Advocacy 2020
- GLHLTH 196FS: Patient and Research Participant Activism and Advocacy 2020
- PJMS 510S: Science and the Media: Narrative Writing about Science, Health and Policy 2020
- POE 105: Spring Breakthrough 2020
- PSY 196FS: Patient and Research Participant Activism and Advocacy 2020
- PUBPOL 196FS: Patient and Research Participant Activism and Advocacy 2020
- PUBPOL 510S: Science and the Media: Narrative Writing about Science, Health and Policy 2020
- SCISOC 196FS: Patient and Research Participant Activism and Advocacy 2020
- SCISOC 256: Science and Society 2020
- SCISOC 293: Research Independent Study in Science & Society 2020
- SCISOC 498S: Science & Society Capstone 2020
- SOCIOL 196FS: Patient and Research Participant Activism and Advocacy 2020
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Advising & Mentoring
- Misha Angrist has lectured in Duke undergraduate and graduate courses since 2006 and taught courses in genome sciences and policy, science writing, patient advocacy, and human genetics as a Duke faculty member since 2008. He has served on many undergraduate thesis committees and overseen numerous independent study students. This work involves regular meetings and provision of feedback on and oversight of multiple revisions. Currently he is Associate Director of the Genome Sciences & Policy Certificate program and a core faculty member in the Master of Arts in Bioethics & Science Policy program. In the latter role he serves as a faculty advisor to current MA students and serves on their exam committees. He has also served as a thesis advisor to students in Public Policy and International Comparative Studies.
- Scholarly, Clinical, & Service Activities
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Outreach & Engaged Scholarship
- Bass Connections Team Leader. Gene Therapy for Alzheimer's Disease and Ethical Aspects of Genome Editing. 2020 - 2021 2020 - 2021
- Bass Connections Team Leader. Gene Therapy in Alzheimer's Disease: Novel Therapies and Ethical Aspects of Somatic Gene Editing. 2019 - 2020 2019 - 2020
- Associate Editor. Applied & Translational Genomics. 2014 - 2016 2014 - 2016
- Organizer, Duke SciComm Fellowship Program. 2014 - 2015 2014 - 2015
- Co-convener. Duke Genomes Family Forum. 2013 - 2015 2013 - 2015
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Service to the Profession
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Service to Duke
Some information on this profile has been compiled automatically from Duke databases and external sources. (Our About page explains how this works.) If you see a problem with the information, please write to Scholars@Duke and let us know. We will reply promptly.
