Publications
Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.
Journal article
De Jonghe J. et al, (2026), Nature
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Journal article
Rius R. et al, (2026), Nat Genet
Paediatric case of invasive group A streptococcal necrotising myositis: diagnostic challenges and lessons learned
Journal article
Yusuf S. et al, (2026), The Lancet Infectious Diseases, 26, e259 - e267
Ethics Review of AI research: An approach to reviewing and revising existing governance structures
Journal article
Kerasidou A. et al, (2026), Research Ethics, 22, 357 - 370
News
Dr Alexander Mentzer Named NIHR Oxford Senior Research Fellow
22 January 2026
Biomedical Research Career Week 13-17th July 2026
24 November 2025
Seminars
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration
Tuesday, 28 April 2026, 9.30am to 10.30am
