Turning genomic data into hope for those with epilepsy

By Alexandra Michaelidou on 23 Mar 2026

In this series, we explore the impact of data from the National Genomic Research Library and highlight opportunities for researchers. In this blog, we focus on rare epilepsies.

Research

Genomics 101: How can genomics help us understand rare conditions?

By Eleanor Roshier on 11 Mar 2026

In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we explain the vital role of genomics in helping us to better understand and treat rare conditions.

Progress in treating rare conditions: hype and hope?

By Ana Lisa Taylor Tavares on 24 Feb 2026

Ana Lisa Tavares, Clinical Lead for Rare Disease Research at Genomics England, shares her thoughts on the 'hype and hope' around progress in treating rare conditions.

Rare disease

How can we work towards equity in rare conditions?

By Natalie Banner on 5 Feb 2026

Natalie Banner, Chief Ethics and Engagement Officer for Genomics England, shares how we can help to address the inequities in rare conditions surrounding accessible information, disparities in data, and access to innovation.

Rare disease

Genomics 101: How can genomics help us understand cancer?

By Florence Cornish on 21 Jan 2026

In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we explain why genomics is vital to help us understand cancer.

What does a User Researcher do?

By Adrian Bussone on 12 Jan 2026

User research means studying users to understand their specific needs, motivations and behaviours, so that services and products can be designed to meet them. In this blog, Adrian Bussone, Principal User Researcher for Genomics England, shares more about her role and how it impacts patients.