What is a disease?: Disease, disability and their definitions von Scully, Jackie Leach

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Disability, Disablism, and COVID-19 Pandemic Triage von Scully, JL

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Unveiling algorithmic power: exploring the impact of automated systems on disabled people’s engagement with social services von van Toorn, G, Scully, JL

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The responsibilities of the engaged bioethicist: Scholar, advocate, activist von Scully, JL

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Non-professionals’ evaluations of gene therapy ethics von Scully, Jackie Leach, Rippberger, Christine, Rehmann-Sutter, Christoph

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From "she would say that, wouldn't she?" to "does she take sugar?" epistemic injustice and disability von Scully, JL

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A mitochondrial story: Mitochondrial replacement, identity and narrative von Scully, JL

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Activism and Bioethics: Taking a Stand on Things That Matter von Rogers, WA, Scully, JL

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The Canadian environment for innovation and business development in the biotechnology industry: a firm-level analysis von Bagchi-Sen, Sharmistha, Scully, Jennifer L.

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Ethical Guidance for Hard Decisions: A Critical Review of Early International COVID-19 ICU Triage Guidelines von Aquino, YSJ, Rogers, WA, Scully, JL, Magrabi, F, Carter, SM

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The salience of genomic information to reproductive autonomy: Australian healthcare professionals’ views on a changing prenatal testing landscape von Drysdale, K, Scully, JL, Kint, L, Laginha, KJ, Hodgson, J, Holmes, I, MacKay, KL, Newson, AJ

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The opinions and experiences of people with intellectual disability regarding genetic testing and genetic medicine: A systematic review von Strnadová, I, Nevin, SM, Scully, JL, Palmer, EE

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When norms normalize : The case of genetic enhancement von SCULLY, Jackie Leach, REHMANN-SUTTER, Christoph

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The need for co-educators to drive a new model of inclusive, person-centred and respectful co-healthcare with people with intellectual disability von Molnar, C, Strnadová, I, Dunn, M, Loblinzk, J, Sarfaraz, S, Cathcart-King, Y, Tso, M, Danker, J, Hayes, S, Willow, SA, Hansen, J, Lim, TQ, Boyle, J, Terrill, B, Scully, JL, Palmer, EE

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Naming the dead: DNA-based identification of historical remains as an act of care von Scully, JL

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“I am not a number!” Opinions and preferences of people with intellectual disability about genetic healthcare von Strnadová, I, Loblinzk, J, Scully, JL, Danker, J, Tso, M, Jackaman, KM, Dunn, M, Willow, SA, Sarfaraz, S, Fitzgerald, V, Boyle, J, Palmer, EE

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Increased levels of NGF in sera of systemic lupus erythematosus patients von Bracci-Laudiero, L, Aloe, L, Levi-Montalcini, R, Galeazzi, M, Schilter, D, Scully, J L, Otten, U

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Experiences of faith group members using new reproductive and genetic technologies: A qualitative interview study von Scully, JL, Banks, S, Song, R, Haq, J

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Drawing a Line: Situating Moral Boundaries in Genetic Medicine von Scully, Jackie Leigh

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Disability Rights as a Necessary Framework for Crisis Standards of Care and the Future of Health Care von Guidry-Grimes, L, Savin, K, Stramondo, JA, Reynolds, JM, Tsaplina, M, Burke, TB, Ballantyne, A, Kittay, EF, Stahl, D, Scully, JL, Garland-Thomson, R, Tarzian, A, Dorfman, D, Fins, JJ

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