Bingmei Li

The clinical and genetic features of generalized epilepsy with febrile seizure plus (GEFS+) in Chinese families

Xiao-Rong Liu, W. Liao, Yuhong Deng, 2004 .

Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism

E. Delpire, Jing-Qiong Kang, Juexin Wang, 2020, Molecular Brain.

Altered Behaviour Associated With Autism in a Mouse Model of Fragile X Syndrome Treated With Bacteroides Fragilis BF839

Ting Zeng, Chu-Hui Lin, Bingmei Li, 2020 .

The anti-depression effect of Xylaria nigripes in patients with epilepsy: A multicenter randomized double-blind study

Z. Hong, Guo-xing Zhu, Li-Wen Wu, 2015, Seizure.

ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities

Xiaoyun Lei, N. He, Hankui Liu, 2022, Frontiers in Molecular Neuroscience.

CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications

Yi-wu Shi, N. He, Jie Wang, 2022, Frontiers in Molecular Neuroscience.

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2016, Neurology: Genetics.

SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges

N. He, Jie Wang, Yong-Hong Yi, 2022, Frontiers in Molecular Neuroscience.

CELSR1 variants are associated with partial epilepsy of childhood

Xiao-Rong Liu, W. Liao, Jie Wang, 2022, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, CNS neuroscience & therapeutics.