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BMC Psychiatry|July 7, 2022
Single-case experimental designs for bumetanide across neurodevelopmental disorders: BUDDI protocolLisa Geertjens, Gianina Cristian, Eva Haspels, et al.Genes|February 25, 2022
Following Excitation/Inhibition Ratio Homeostasis from Synapse to EEG in Monogenetic Neurodevelopmental DisordersLisa Geertjens, Torben W van Voorst, Arianne Bouman, et al.Contemporary Clinical Trials Communications|March 27, 2024
Corrigendum to "Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trials" [Contemp. Clin. Trials Commun. 36 (2023)/ DOI: 10.1016/j.conctc.2023.101233]Bibiche den Hollander, Marieke Rothuizen-Lindenschot, Lisa Geertjens, et al.Contemporary Clinical Trials Communications|December 25, 2023
Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trialsBibiche den Hollander, Marieke Rothuizen-Lindenschot, Lisa Geertjens, et al.Molecular Genetics and Metabolism|November 20, 2025
Potential benefits of l-serine in children with GRIN2B loss-of-function variants: Randomized n-of-1 trialsBibiche den Hollander, Marieke Rothuizen-Lindenschot, Hoang Lan Le, et al.Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.Pageof 1