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Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 15, 2019
Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal developmentWenjing Zhao, Jieqiong Tan, Tengfei Zhu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2024
KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13Jianbo Cheng, Zhen Wang, Manpei Tang, et al.
Neuroscience Bulletin|June 24, 2025
Csde1 Mediates Neurogenesis via Post-transcriptional Regulation of the Cell CycleXiangbin Jia, Wenqi Xie, Bing Du, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 30, 2026
X-linked SYTL4 missense variant disrupts RAB27A-dependent vesicle trafficking and synaptic transmission in autismYang Liao, Shuju Zhang, Xiaolei Zhang, et al.
Molecular Psychiatry|July 16, 2026
Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genesSenwei Tan, Yongqing Lyu, Xiaoyue Sun, et al.
The Journal of Clinical Investigation|August 2, 2022
GIGYF1 disruption associates with autism and impaired IGF-1R signalingGuodong Chen, Bin Yu, Senwei Tan, 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.
The Journal of Clinical Investigation|September 18, 2025
Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse developmentXiaoxia Peng, Xiangbin Jia, Hanying Wang, et al.
Science Advances|August 17, 2022
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disordersXiangbin Jia, Shujie Zhang, Senwei Tan, et al.
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