University of Zurich / Universität Zürich (UZH)

#EEGManyLabs: Investigating the replicability of influential EEG experiments (2021) Pavlov YG, Adamian N, Appelhoff S, Arvaneh M, Benwell CS, Beste C, Bland AR, et al. Journal article Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype (2021) Zanoni P, Steindl K, Sengupta D, Joset P, Bahr A, Sticht H, Lang-Muritano M, et al. Journal article Dynamic Effects and Hydrogen Bonding in Mixed-Halide Perovskite Solar Cell Absorbers (2021) Wilks RG, Erbing A, Sadoughi G, Starr DE, Handick E, Meyer F, Benkert A, et al. Journal article Medieval nanotechnology: Thickness determination of Zwischgold samples (2021) Wu Q, Watts B, Döbeli M, Müller J, Butz B, Lombardo T, Schmidt-Ott K, et al. Journal article Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior (2021) Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, Soucy A, et al. Journal article DLG4-related synaptopathy: a new rare brain disorder (2021) Rodriguez-Palmero A, Boerrigter MM, Gomez-Andres D, Aldinger KA, Marcos-Alcalde I, Popp B, Everman DB, et al. Journal article Cholesterol metabolites and plant sterols in cerebrospinal fluid are associated with Alzheimer's cerebral pathology and clinical disease progression (2021) Jahn T, Clark C, Kerksiek A, Lewczuk P, Lütjohann D, Popp J Journal article Updated insight into the mutational and phenotypic spectrum of MED13L-related intellectual disability (2020) Asadollahi R, Boonsawat P, Popp B, Torti E, Bader I, Vitobello A, Moutton S, et al. Conference contribution Expanding the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and functional proof of aberrant WRC-mediated actin dynamics (2020) Begemann A, Sticht H, Mcwalter K, Vitobello A, Faivre L, Alhaddad B, Banka S, et al. Conference contribution Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype (2020) Zanoni P, Steindl K, Sengupta D, Sticht H, Joset P, Baar A, Van Ravenswaaij-Arts CMA, et al. Conference contribution