Carl von Ossietzky Universität Oldenburg

DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects (2026) Dombrowsky G, van der Laan L, Silva A, Breckpot J, Audain E, Wilsdon A, Levy MA, et al. Journal article Lower butyrylcholinesterase is associated with postoperative delirium in adult cardiac surgery patients: a secondary analysis of two prospective studies (2026) Beyer LP, von zur Gathen L, El-Rayah B, Wolke M, Dewald O, Schaefer ST, Guenther U Journal article Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia (2026) Menden B, Incebacak Eltemur RD, Demidov G, Sturm M, Park J, Huridou C, Fath F, et al. Journal article Effects of Square-Stepping Exercise on cognitive function in early geriatric rehabilitation: A randomized controlled explorative study (2026) Fränzel K, Koschate-Storm J, Freiberger E, Shigematsu R, Zieschang T, Tietgen S Journal article Structural control and depth clustering of extensive hydrothermal venting on the shelf of Milos Island (2025) Nomikou P, Bejelou K, Koschinsky A, dos Santos Ferreira C, Papanikolaou D, Lampridou D, Kilias SP, et al. Journal article Hierarchical Event Descriptor library schema for EEG data annotation (2025) Hermes D, Pal Attia T, Beniczky S, Bosch-Bayard J, Delorme A, Lundstrom BN, Rogers C, et al. Journal article Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types (2025) Disse S, Ramantani G, Küpper H, Bock A, Korenke GC, Weidner B, Preisel M, et al. Journal article Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor (2025) Wegert J, Appenzeller S, Treger TD, Streitenberger H, Ziegler B, Bausenwein S, Vokuhl C, et al. Journal article Combinatorial ab initio calculations and core spectroscopy unravel the electronic structure of nickel cobalt manganese oxide (2025) Reents T, Kataev E, Duarte-Ruiz D, Wilks RG, Garcia-Diez R, Bär M, Cocchi C Journal article Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function (2025) Asadollahi R, Ahmad A, Boonsawat P, Shahanoor Hinzen J, Lohse M, Bouazza-Arostegui B, Sun S, et al. Journal article