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Scientific Reports|February 7, 2015
Association of genetic variants of GRIN2B with autismYongcheng Pan, Jingjing Chen, Hui Guo, et al.European Archives of Psychiatry and Clinical Neuroscience|August 27, 2014
AMPD1 functional variants associated with autism in Han Chinese populationLusi Zhang, Jianjun Ou, Xiaojuan Xu, et al.Iscience|August 27, 2024
Deep learning-enhanced R-loop prediction provides mechanistic implications for repeat expansion diseasesJiyun Hu, Zetong Xing, Hongbing Yang, et al.Nature Communications|January 12, 2026
Precise excision of expanded GGC repeats in NOTCH2NLC via CRISPR/Cas9 for treating neuronal intranuclear inclusion diseaseNina Xie, Yongcheng Pan, Huichun Tong, et al.European Journal of Neurology|November 17, 2023
GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degenerationQiong Liu, Juan Chen, Jin Xue, et al.Science Advances|November 23, 2022
Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion diseaseQiong Liu, Kailin Zhang, Yunhee Kang, et al.Journal of Medical Genetics|June 4, 2014
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopiaHui Guo, Xuemin Jin, Tengfei Zhu, et al.Ebiomedicine|January 15, 2026
Plasma p-tau species are elevated in presymptomatic and symptomatic neuronal intranuclear inclusion diseaseSizhe Zhang, Bin Jiao, Yan Zeng, et al.Pageof 3