
Dr Katie Hasson
Associate Director of the Center for Genetics and Society, a nonprofit public affairs organization that advocates for responsible use of genetic technology.
Top 3 podcasts with Dr Katie Hasson
Ranked by the Snipd community

13 snips
May 28, 2025 • 23min
Can doctors test embryos for autism? And should they?
In this engaging discussion, Vardit Ravitsky, a bioethicist at Harvard Medical School, and Katie Hasson of the Center for Genetics and Society, dissect the complex world of polygenic embryo screening. They delve into the ethical dilemmas surrounding the genetic selection of embryos for conditions like autism. The conversation highlights societal pressures, stigma, and ableism, revealing how these factors intertwine with parental choices. The duo also critiques the potential normalization of such practices and the implications for social inequality.

Dec 3, 2025 • 55min
Bay Area Startups Want to Make Genetically Engineered Babies. What Could Go Wrong?
Join Dr. Fyodor Urnov, a gene-editing expert, Catherine Long, a Wall Street Journal investigative reporter, and Katie Hasson, an advocate for genetic ethics, as they delve into the controversial world of genetically engineered babies. They discuss Bay Area startups pushing boundaries in embryo editing, the ethical implications of such technologies, and the troubling echoes of eugenics. Through scientific insights and real-life experiences, the conversation raises critical questions about who gets to decide the future of genetics.

Oct 9, 2024 • 22min
To spit or not to spit - when handing your DNA over might harm you
Dr. Katie Hasson, an expert from the Centre for Genetics and Society, dives into the risks associated with at-home DNA testing. She highlights how easily genetic information can fall into the wrong hands, causing potential harm to individuals. The discussion touches on the dark web market for stolen genetic data and the lack of robust protections in place. Hasson also addresses the dual nature of genetic testing—while it offers benefits in understanding ancestry and health, it poses significant privacy risks that users must consider.


