Contact information
Research groups
Stephan Sanders
Professor of Neurogenetics
Recent publications
-
Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry.
Gui A. et al, (2025), Nat Hum Behav
-
Systematic identification of disease-causing promoter and untranslated region variants in 8040 undiagnosed individuals with rare disease.
Martin-Geary AC. et al, (2025), Genome Med, 17
-
Consensus guidelines for assessing eligibility of pathogenic DNA variants for antisense oligonucleotide treatments.
Cheerie D. et al, (2025), Am J Hum Genet
-
Targeted BDNF upregulation via upstream open reading frame disruption
Feng N. et al, (2025)
-
Contribution of autosomal rare and de novo variants to sex differences in autism
Koko M. et al, (2025), American Journal of Human Genetics, 112, 599 - 614