Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromes.
Jannis Buecking, Baran E. Güler, Michael Eibl, Azmal Syed Ali, Tobias Walczuch, Tobias Beschauner, Susanne Theiß, Melanie Spanjaard, Katrin Hinderhofer, Freya Herrmann-Sim, Celine E. de Esch, Derek J.C. Tai, Michael E. Talkowski, Jeroen Krijgsveld, Christian P. Schaaf, Magdalena Laugsch
This study identifies MAGEL2-driven defects in human corticogenesis shared between Prader-Willi and Schaaf-Yang syndromes using multi-omics profiling of induced neurons.
bioRxiv · May 5, 2026 · PreprintNeuroscience