Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Contact information

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

Research groups

Institute of Developmental and Regenerative Medicine

Stephan Sanders

Professor of Neurogenetics

Recent publications

Author Correction: 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

Spatial transcriptomics implicates the thalamus and cortex in autism and schizophrenia.

Young DM. et al, (2026)

Spatiotemporal analysis of autism gene enrichment implicates cortex, thalamus, and hypothalamus.

Wang X. et al, (2026)

Molecular dynamics of Brodmann Area 22 in development and autism.

Suresh V. et al, (2026), bioRxiv

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, 58, 761 - 773

More publications