Contact information
Research groups
Stephan Sanders
Professor of Neurogenetics
Recent publications
Molecular dynamics of Brodmann Area 22 in development and autism.
Journal article
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.
Journal article
Rius R. et al, (2026), Nat Genet, 58, 761 - 773
Deleterious coding variation associated with autism is shared across ancestries.
Journal article
Natividad Avila M. et al, (2026), Nat Med
Human-specific features of the cerebellum and ZP2-regulated synapse development.
Journal article
Kim S-K. et al, (2026), Cell, 189, 1802 - 1819.e28
Crossing the finish line towards a disease-modifying treatment for Angelman syndrome.
Journal article
Judson MC. et al, (2026), J Neurodev Disord, 18