Dr Reham Nazzal

Reham is a clinical academic working in the field of rare disease genomic medicine. Along with colleagues in Exeter she established the Translational and Community Genomics Programme, “Stories of Hope, Stories from Palestine”, which aims to advance equitable access to genomic research and improve diagnostic and clinical care for underserved Palestinian communities.

Her research integrates neuroscience and genomic medicine to identify novel disease genes, uncover genetic mechanisms underlying rare conditions, and translate these discoveries into better healthcare outcomes. A key focus of her collaborative work with local clinicians and scientists is the development of a database of genomic variants identified to cause rare conditions in Palestine. This database is supporting development of a cost-effective genotyping platform for diagnostics, carrier testing and newborn screening. This approach is tailored for communities with limited access to genomic services and currently underrepresented in genomic research and healthcare.

Beyond research, Reham is deeply committed to healthcare engagement and genomic education. She works to equip healthcare professionals and early career medical scientists with the skills to interpret and apply genomic data in clinical practice. She is also working to develop community-informed resources and strengthening capacity within marginalized populations. Her efforts foster international collaboration and integrate research, clinical care, and patient experiences to improve outcomes for rare disease patients and their families worldwide.