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Mar 1, 2020

Personal genetic risk information is set to be become part of everyday healthcare. But is some unhelpful, even dangerous? What psychological impact does it have on patients? And do doctors know enough about genetics to effectively guide patients and inform treatment decisions?

Joining David to discussing what genetic risks should be communicated and how, we have:

With a special contribution from Jillian Hastings Ward, Chair of the participant panel for the 100,000 Genomes Project.

Views to share? Get in touch on Twitter @RiskyTalkPod or email

Risky Talk is produced by Ilan Goodman for the Winton Centre for Risk and Evidence Communication at the University of Cambridge.