Shujie Yu

Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome

Yuehua Zhang, X. Bao, Qingping Zhang, 2019, Seizure.

Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene

X. Bao, Qingping Zhang, Yan Chen, 2019, Molecular genetics & genomic medicine.

Novel SLC16A2 mutations in Chinese patients with Allan-Herndon-Dudley Syndrome

X. Bao, Qingping Zhang, Jiaping Wang, 2018, Translational Science of Rare Diseases.

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Liping Wei, X. Bao, Jiarui Li, 2017, BMC Medical Genetics.

Germline de novo variants in CSNK2B in Chinese patients with epilepsy

Y. Liu, Zhixian Yang, Yuwu Jiang, 2019, Scientific Reports.

Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

X. Bao, Qingping Zhang, Y. Wen, 2018, BMC medical genetics.