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Journal of Genetics and Genomics = Yi Chuan Xue Bao|March 25, 2022
Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesisGuodong Chen, Lin Han, Senwei Tan, et al.European Journal of Medical Genetics|March 26, 2021
Mutation pattern and genotype-phenotype correlations of SETD2 in neurodevelopmental disordersMeilin Chen, Yingting Quan, Guiqin Duan, et al.Molecular Genetics & Genomic Medicine|June 15, 2019
Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disordersLin Han, Meilin Chen, Yazhe Wang, et al.Journal of Molecular Neuroscience : MN|June 12, 2020
Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental DisordersYingting Quan, Qiumeng Zhang, Meilin Chen, et al.Molecular Genetics & Genomic Medicine|November 12, 2022
Nance-Horan syndrome pedigree due to a novel microdeletion and skewed X chromosome inactivationYazhou Huang, Linya Ma, Zhaoxia Zhang, et al.Molecular Genetics & Genomic Medicine|July 27, 2019
POGZ de novo missense variants in neuropsychiatric disordersWenjing Zhao, Yingting Quan, Huidan Wu, et al.European Journal of Medical Genetics|August 28, 2020
Excess of RALGAPB de novo variants in neurodevelopmental disordersAbid Ali Shah, Ge Zhang, Kuokuo Li, 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.Nature Communications|July 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Christine L Dixon, Hui Guo, et al.Pageof 1