TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencingJunling Wang, Bei Tang, Qian Pan et al.|Brain|2010Cited by 277
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Alison M. Muir, Christine L. Dixon et al.|Nature Communications|2019Cited by 249
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQiying Sun, Beisha Tang, Qian Xu et al.|Brain|2019Cited by 189
BAG5 Protects against Mitochondrial Oxidative Damage through Regulating PINK1 DegradationXuejing Wang, Beisha Tang, Jifeng Guo et al.|PLoS ONE|2014Cited by 59
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of AutismHui Guo, Kun Xia|The American Journal of Human Genetics|2020Cited by 41