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Contact information

Email
stephan.sanders@paediatrics.ox.ac.uk

Research groups

Institute of Developmental and Regenerative Medicine

Stephan Sanders

Professor of Neurogenetics

Recent publications

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rius R. et al, (2026), Nat Genet

Human-specific features of the cerebellum and ZP2-regulated synapse development.

Kim S-K. et al, (2026), Cell, 189, 1802 - 1819.e28

Targeted BDNF upregulation via upstream open reading frame disruption.

Feng N. et al, (2026), Mol Ther, 34, 1652 - 1671

Association of Carboxypeptidase B2 Gene Polymorphisms With Graft Loss in Kidney Transplantation.

Poppelaars F. et al, (2026), Transplant Direct, 12

Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: A retrospective cohort study.

Cheerie D. et al, (2026), Genet Med, 28

More publications