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Molecular Psychiatry|October 30, 2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delaySenwei Tan, Qiumeng Zhang, Rui Zhan, et al.
Molecular Psychiatry|June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autismBin Yu, Shimeng Zhu, Linhu Xiao, et al.
American Journal of Human Genetics|November 6, 2020
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of AutismHui Guo, Qiumeng Zhang, Rujia Dai, et al.
Science Advances|October 4, 2019
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionHui Guo, Ying Li, Lu Shen, et al.
The Journal of Clinical Investigation|March 28, 2023
CERT1 mutations perturb human development by disrupting sphingolipid homeostasisCharlotte Gehin, Museer A Lone, Winston Lee, et al.
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