Tuesday, June 20, 2023
4:00pm ET - 5:00pm ET
Location: Zoom
Webinar Description
Equitable and just genetic research requires an examination of the ethical questions pertaining to marginalized communities. Many have expressed concerns over current practices of autism-related genetic research, urging the field to shift towards practices that ensure benefits and protect against harm. As an interdisciplinary working group of autistic and non-autistic individuals, we have developed guidelines for leveraging genetics to enhance the quality of life, health, and autonomy of autistic persons.
Presenters
Dr. Heini Natri is a computational scientist, functional genomicist, and advocate for socially responsible research. At The Translational Genomics Research Institute, my work involves integrating various types of genetic and molecular data to understand genetic variation and its functional consequences in the context of health and disease. In my bioethics-related work, I focus on questions at the intersection of genetics, bioethics, disability, and identity, and the ethical, legal, and societal implications of the implementation of genetic information in research and clinical decision-making. Supported by The Autism Intervention Research Network on Physical Health, I have lead a workgroup of geneticists, bioethicists, clinicians, and autism scholars in an effort to develop a framework for ethically responsible autism-related genomics research that respects stakeholders and has the potential to positively influence the well-being of autistic people.
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