Bingmei Li

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Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2020, Frontiers in Genetics.

BCOR variants are associated with X-linked recessive partial epilepsy

Xiao-Rong Liu, W. Liao, N. He, 2022, Epilepsy Research.

Cutaneous reactions induced by oxcarbazepine in Southern Han Chinese: Incidence, features, risk factors and relation to HLA-B alleles

Yi-wu Shi, Fu-Li Min, Xiao-Rong Liu, 2012, Seizure.

GRIN2A Variants Associated With Idiopathic Generalized Epilepsies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, Frontiers in Molecular Neuroscience.

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.

Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Journal of Neurodevelopmental Disorders.

An open-label study of topiramate as add-on therapy for epilepsy using slow titration

W. Liao, Yong-Hong Yi, Shuxiang Pu, 2005 .

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.

RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, Frontiers in Neuroscience.

ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2017, neurogenetics.

16p11.2 deletion in patients with paroxysmal kinesigenic dyskinesia but without intellectual disability

N. He, Weiping Liao, B. Tang, 2018, Brain and behavior.

Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation

Xiao-Rong Liu, W. Liao, T. Su, 2011, Epilepsy & Behavior.

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

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

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

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

Association of FAT1 with focal epilepsy and correlation between seizure relapse and gene expression stage

D. Zou, Xiao-Rong Liu, J. Liao, 2023, Seizure.

Association of the HLA‐B*15:02 allele with pure cervical lymphadenopathy induced by carbamazepine and oxcarbazepine: A case report and literature review

Hailing Liu, Yonghong Yi, De-Tian Liu, 2020, Basic & clinical pharmacology & toxicology.

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.

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.

HLA-A*24:02 as a common risk factor for antiepileptic drug–induced cutaneous adverse reactions

C. Ng, K. Lim, Jie Pan, 2017, Neurology.

HLA Risk Alleles in Aromatic Antiepileptic Drug-Induced Maculopapular Exanthema

P. Kwan, Yi-wu Shi, Fu-Li Min, 2021, Frontiers in Pharmacology.

Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Journal of neurodevelopmental disorders.

Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy

Xin Li, Xin Li, Xiao-Rong Liu, 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.

PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation

Yong-Hong Yi, Zhigang Liu, Bin Li, 2022, Frontiers in Neurology.

UNC13B variants associated with partial epilepsy with favourable outcome

Yanhui Chen, Yi-wu Shi, Xiao-Rong Liu, 2021, Brain : a journal of neurology.

Variants in BSN gene associated with epilepsy with favourable outcome

Xiao-Rong Liu, W. Liao, Tao Zeng, 2022, Journal of Medical Genetics.

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.

Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons

Yi-wu Shi, Mei-Mei Gao, W. Liao, 2020, Epilepsy Research.

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism

B. Tang, D. Zhou, Yi-wu Shi, 2023, Clinical and translational medicine.

Novel mutations and phenotypes of epilepsy‐associated genes in epileptic encephalopathies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Genes, brain, and behavior.

SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation

Y. Chen, Zhigang Liu, L. Gao, 2023, Frontiers in Molecular Neuroscience.

Variants in SBF1, CELSR2, and TENM1 are associated with childhood epileptic encephalopathies

Sheng, J. Chen, Yinwei Qu, 2023, medRxiv.

ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes

W. Liao, N. He, Yong-Hong Yi, 2024, Journal of Medical Genetics.

Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures

Mei-Mei Gao, Mei-juan Yu, W. Liao, 2012, Genes, brain, and behavior.

NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation.

W. Liao, N. He, Jie Wang, 2024, Molecular neurobiology.

Partial epilepsy with febrile seiure plus: A subtype of GFS+ or SM?

Mei-juan Yu, W. Liao, T. Su, 2007 .