A New Edition of Hastings Center Report Is Now Available

January 20, 2025

Hastings Center Report (vol. 54, Issue S2, 2024) is available online by subscription only.

Articles include:

  • “Expanding the Agenda for a More Just Genomics” by Deanne Dunbar Dolan, et al.
  • “Nothing about Us without Us in Precision Medicine: A Call to Reframe Disability Difference in Genetics and Genomics” by Kevin T. Mintz, Joseph A. Stramondo and Holly K. Tabor
  • “Where the Genetic Code Meets the Zip Code: Advancing Equity in Rare Disease Genomics” by Monica H. Wojcik, Hadley S. Smith and Yarden S. Fraiman
  • “The UN Declaration on the Rights of Indigenous Peoples and Genomics: Ethical Complementarity for Just Research” by Ibrahim Garba and Stephanie Russo Carroll

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Posted in Disability Ethics, Genetic Ethics, Journal Articles, Public Health, Research Ethics

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