Rare Disease Gene Association Discovery in The 100,000 Genomes Project

29 Jan 2026
Precision Medicine & Patient Stratification Stage
  • Present findings from the 100,000 Genomes Project on novel gene associations linked to rare diseases. 

  • Demonstrate how large-scale genomic sequencing and data integration enable the identification of previously unknown disease-causing variants. 

  • Highlight clinical and research implications for diagnosis, treatment, and future genetic studies in rare diseases. 

Speakers
Hannah Mitchison
Hannah Mitchison, Professor of Molecular Medicine - University College London