Clinical AI Interest Group:Leveraging Large Language Models to generate accessible information guides for rare genetic neurodevelopmental disorders – November 2025

In this month’s Clinical AI Interest Group webinar, we heard from Pawan Prabhat of Short Hills AI; Dr Sid Banka, Professor of Genomic Medicine and Rare Diseases at the University of Manchester and co-lead for rare and inherited diseases within the NHS Genomic Networks of Excellence; and Dr Claire Andersen from Unique, a charity that supports families affected by rare genetic conditions.

The session focused on how large language models can help create clear, accessible information guides for people living with rare genetic neurodevelopmental disorders.

Catch up with the webinar by watching the recording below.