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McNeill, E., Cunningham, H., & Sabatello, M. (2025). Transitional Justice — A Politico-Legal Approach to Health Equity. New England Journal of Medicine, 392(1), 85–89. https://doi.org/10.1056/nejmms2408222

Karabin, J., Adsit-Morris, C., Lee, S. S.-J., Fullerton, S. M., Cho, M. K., & Reardon, J. (2024). A conjunctural analysis of the origins of ‘embedded ELSI’ in U.S. genomic medicine. Journal of Responsible Innovation, 11(1). https://doi.org/10.1080/23299460.2024.2413698

Weiss, R., Milo Rasouly, H., Marasa, M., Fernandez, H., Lin, F., & Sabatello, M. (2024). Nephrologists’ Views on a Workflow for Returning Genetic Results to Research Participants. Kidney International Reports, 9(11), 3278–3289. https://doi.org/10.1016/j.ekir.2024.08.026

Matthews, L. J. (2024). The Geneticization of Education and Its Bioethical Implications. Cambridge Quarterly of Healthcare Ethics, 1–17. https://doi.org/10.1017/s096318012400046x

Fernandez, H. E., Lipton, M., Balderes, O., Lin, F., Marasa, M., Milo Rasouly, H., & Sabatello, M. (2024). Pediatric nephrologists’ perspectives and clinical practices related to genetic testing and education. Pediatric Nephrology. https://doi.org/10.1007/s00467-024-06539-7

Jeske, M., Saperstein, A., Lee, S. S.-J., & Shim, J. K. (2024). Marginalized measures: The harmonization of diversity in precision medicine research. Social Studies of Science. https://doi.org/10.1177/03063127241288498

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Lewis, A. C. F., Chisholm, R. L., Connolly, J. J., Esplin, E. D., Glessner, J., Gordon, A., Green, R. C., Hakonarson, H., Harr, M., Holm, I. A., Jarvik, G. P., Karlson, E., Kenny, E. E., Kottyan, L., Lennon, N., Linder, J. E., Luo, Y., Martin, L. J., Perez, E., … Fullerton, S. M. (2024). Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network. The American Journal of Human Genetics, 111(6), 999–1005. https://doi.org/10.1016/j.ajhg.2024.04.005

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Hu, N. Y. (2024). Storytelling and the Electronic Health Record. Pediatrics, 153(3). https://doi.org/10.1542/peds.2022-060880

Sabatello, M., Bakken, S., Chung, W. K., Cohn, E., Crew, K. D., Kiryluk, K., Kukafka, R., Weng, C., & Appelbaum, P. S. (2024). Return of polygenic risk scores in research: Stakeholders’ views on the eMERGE-IV study. Human Genetics and Genomics Advances, 5(2), 100281. https://doi.org/10.1016/j.xhgg.2024.100281

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Badger, K., Baez Caraballo, P., Gibbs, A., Messina, L., Halpern, M., & Amesty, S. (2024). Thoughts of self-harm in adolescents: Relationship with violence in the Dominican Republic. PLOS Global Public Health, 4(1), e0002711. https://doi.org/10.1371/journal.pgph.0002711

Vasquez, E. E., Foti, N., McMahon, C. E., Jeske, M., Bentz, M., Fullerton, S., Shim, J. K., & Lee, S. S.-J. (2023). Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research. Public Health Genomics, 103–112. Portico. https://doi.org/10.1159/000531656

Green, S., Prainsack, B., & Sabatello, M. (2023). The Roots of (in)Equity in Precision Medicine: Gaps in the Discourse. Personalized Medicine, 21(1), 5–9. https://doi.org/10.2217/pme-2023-0097

Lewis, H., Biesecker, B., Lee, S. S.-J., Anderson, K., Joseph, G., Jenkins, C. L., Bulkley, J. E., Leo, M. C., Goddard, K. A. B., & Wilfond, B. S. (2023). Promoting equity, inclusion, and efficiency: A team science approach to the development of authorship guidelines for a multi-disciplinary research team. Journal of Clinical and Translational Science, 7(1). https://doi.org/10.1017/cts.2023.685

McMahon, C. E., Foti, N., Jeske, M., Britton, W. R., Fullerton, S. M., Shim, J. K., & Lee, S. S.-J. (2023). Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers. AJOB Empirical Bioethics, 15(2), 108–119. https://doi.org/10.1080/23294515.2023.2279965

Moorthy, T., Nguyen, H., Chen, Y., Austin, J., Smoller, J. W., Hercher, L., & Sabatello, M. (2023). How do experts in psychiatric genetics view the clinical utility of polygenic risk scores for schizophrenia? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 192(7–8), 161–170. Portico. https://doi.org/10.1002/ajmg.b.32939

Shim, J. K., Foti, N., Vasquez, E., Fullerton, S. M., Bentz, M., Jeske, M., & Lee, S. S.-J. (2023). Community Engagement in Precision Medicine Research: Organizational Practices and Their Impacts for Equity. AJOB Empirical Bioethics, 14(4), 185–196. https://doi.org/10.1080/23294515.2023.2201478

Heinonen, G., Spiegel, M., & Blinderman, C. D. (2023). Conducting a narrative medicine workshop in ambulatory palliative care: A feasibility and exploratory study. Palliative and Supportive Care, 1–6. https://doi.org/10.1017/s1478951523001499

Lewis V, C., Huebner, J., Hripcsak, G., & Sabatello, M. (2023). Underrepresentation of blind and deaf participants in the All of Us Research Program. Nature Medicine, 29(11), 2742–2747. https://doi.org/10.1038/s41591-023-02607-x

Jungels, A., Demers, L., Ford, E., Stevens, B. K., Sabatello, M., & Dasgupta, S. (2023). Project Inclusive Genetics: Protecting reproductive autonomy from bias via prenatal patient-centered counseling. Human Genetics and Genomics Advances, 4(4), 100228. https://doi.org/10.1016/j.xhgg.2023.100228

Sanabria, G., Stonbraker, S., Bateman, M., Halpern, M., & Amesty, S. (2023). Impact of an STI Diagnosis on People Living With HIV in La Romana, Dominican Republic: A Cross-Sectional, Qualitative, Descriptive Study. Journal of the Association of Nurses in AIDS Care, 34(6), 582–589. https://doi.org/10.1097/jnc.0000000000000431

Bentz, M., Saperstein, A., Fullerton, S. M., Shim, J. K., & Lee, S. S.-J. (2024). Conflating race and ancestry: Tracing decision points about population descriptors over the precision medicine research life course. Human Genetics and Genomics Advances, 5(1), 100243. https://doi.org/10.1016/j.xhgg.2023.100243

Martschenko, D. O., Matthews, L. J., & Sabatello, M. (2024). Social and Behavioral Genomics: What Does It Mean for Pediatrics? The Journal of Pediatrics, 264, 113735. https://doi.org/10.1016/j.jpeds.2023.113735

Green, S., Prainsack, B., & Sabatello, M. (2023). Precision medicine and the problem of structural injustice. Medicine, Health Care and Philosophy, 26(3), 433–450. https://doi.org/10.1007/s11019-023-10158-8

Connolly, J. J., Berner, E. S., Smith, M., Levy, S., Terek, S., Harr, M., Karavite, D., Suckiel, S., Holm, I. A., Dufendach, K., Nelson, C., Khan, A., Chisholm, R. L., Allworth, A., Wei, W.-Q., Bland, H. T., Clayton, E. W., Soper, E. R., Linder, J. E., … Sabatello, M. (2023). Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores. Genetics in Medicine, 25(9), 100906. https://doi.org/10.1016/j.gim.2023.100906

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Esmonde, K., Roth, S., & Walker, A. (2023). A social and ethical framework for providing health information obtained from combining genetics and fitness tracking data. Technology in Society, 74, 102297. https://doi.org/10.1016/j.techsoc.2023.102297

Joseph, G., Lindberg, N. M., Guerra, C., Hernandez, C., Karliner, L. S., Gilmore, M. J., Zepp, J., Rolf, B. A., Caruncho, M., Riddle, L., Kauffman, T. L., Leo, M. C., & Wilfond, B. S. (2023). Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome. Journal of Genetic Counseling, 32(4), 870–886. Portico. https://doi.org/10.1002/jgc4.1695

Clayton, E. W., Smith, M. E., Anderson, K. C., Chung, W. K., Connolly, J. J., Fullerton, S. M., McGowan, M. L., Peterson, J. F., Prows, C. A., Sabatello, M., & Holm, I. A. (2023). Studying the impact of translational genomic research: Lessons from eMERGE. The American Journal of Human Genetics, 110(7), 1021–1033. https://doi.org/10.1016/j.ajhg.2023.05.011

Coffelt, A., & Djandji, A. (2022). Mutant metaphors:Frankensteinin the era of COVID-19. Medical Humanities, 49(2), 272–277. https://doi.org/10.1136/medhum-2022-012405

Lee, S. S.-J., Caruncho, M., Chung, W. K., Johnston, J., Tabb, K., & Appelbaum, P. S. (2023). Individualized interventions for rare genetic conditions and the research-treatment spectrum: Stakeholder perspectives. Genetics in Medicine, 25(6), 100832. https://doi.org/10.1016/j.gim.2023.100832

Kapur, S. L., & Sabatello, M. (2023). People with disability and privacy in precision medicine research: what’s at stake? Trends in Genetics, 39(5), 335–337. https://doi.org/10.1016/j.tig.2023.01.001

Rasouly, H. M., Balderes, O., Marasa, M., Fernandez, H., Lipton, M., Lin, F., Gharavi, A. G., & Sabatello, M. (2023). The effect of genetic education on the referral of patients to genetic evaluation: Findings from a national survey of nephrologists. Genetics in Medicine, 25(5), 100814. https://doi.org/10.1016/j.gim.2023.100814

Linder, J. E., Allworth, A., Bland, H. T., Caraballo, P. J., Chisholm, R. L., Clayton, E. W., Crosslin, D. R., Dikilitas, O., DiVietro, A., Esplin, E. D., Forman, S., Freimuth, R. R., Gordon, A. S., Green, R., Harden, M. V., Holm, I. A., Jarvik, G. P., Karlson, E. W., Labrecque, S., … Peterson, J. F. (2023). Returning integrated genomic risk and clinical recommendations: The eMERGE study. Genetics in Medicine, 25(4), 100006. https://doi.org/10.1016/j.gim.2023.100006

Reardon, J., Lee, S. S.-J., Goering, S., Fullerton, S. M., Cho, M. K., Panofsky, A., & Hammonds, E. M. (2023). Trustworthiness matters: Building equitable and ethical science. Cell, 186(5), 894–898. https://doi.org/10.1016/j.cell.2023.01.008

Bergen, S., Murimi, D., Gruer, C., Munene, G., Nyachieo, A., Owiti, M., & Sommer, M. (2023). Living with Endometriosis: A Narrative Analysis of the Experiences of Kenyan Women. International Journal of Environmental Research and Public Health, 20(5), 4125. https://doi.org/10.3390/ijerph20054125