W. Liao

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.

Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation

D. Zou, W. Liao, N. He, 2022, Frontiers in Molecular Neuroscience.

ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus

Zhen Shi, W. Liao, Xiao-jing Li, 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.

The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

B. Li, Yi-wu Shi, Xiao-Rong Liu, 2015, Human mutation.

Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures

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

A Point Mutation in SCN1A 5′ Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug

Yi-wu Shi, W. Liao, N. He, 2017, Molecular Neurobiology.

Identification of the promoter region and the 5′‐untranslated exons of the human voltage‐gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5′‐untranslated exons

Yi-wu Shi, W. Liao, T. Su, 2008, Journal of neuroscience research.

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.

Characterization of The Promoter Region and Upstream Regulation Region of Human and Mouse SCN3A Gene*: Characterization of The Promoter Region and Upstream Regulation Region of Human and Mouse SCN3A Gene*

W. Liao, Tao Zeng, Wei-Wen Sun, 2009 .

HLA-B*1502 screening and toxic effects of carbamazepine.

Yi-wu Shi, Fu-Li Min, W. Liao, 2011, The New England journal of medicine.

Association of HLA‐B*1502 allele with lamotrigine‐induced Stevens–Johnson syndrome and toxic epidermal necrolysis in Han Chinese subjects: a meta‐analysis

Yi-wu Shi, Fu-Li Min, W. Liao, 2015, International journal of dermatology.

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.

[Efficacy and safety of cyclophosphamide as a sequential immunotherapy drug for anti-N-methyl-D-aspartate receptor encephalitis in children].

W. Liao, Yong-Hong Yi, Wei-wen Zhu, 2017, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Human transcription factor genes involved in neuronal development tend to have high GC content and CpG elements in the proximal promoter region.

W. Liao, T. Su, Y. Long, 2011, Journal of genetics and genomics = Yi chuan xue bao.

Antiepileptic drug trials with greater attention to daily clinical practice and special epilepsy syndromes

W. Liao, 2007 .

Evaluation of cell damage in organotypic hippocampal slice culture from adult mouse: A potential model system to study neuroprotection

B. Paradiso, W. Liao, M. Simonato, 2011, Brain Research.

Functional Differences Between Two Kv1.1 RNA Editing Isoforms: a Comparative Study on Neuronal Overexpression in Mouse Prefrontal Cortex

P. Zhu, W. Liao, T. Su, 2021, Molecular Neurobiology.

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene

Zhixian Yang, K. Xia, B. Tang, 2018, Human molecular genetics.

P. Zhu, W. Liao, T. Su, 2018, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Alteration of Scn3a expression is mediated via CpG methylation and MBD2 in mouse hippocampus during postnatal development and seizure condition.

Lingjia Tang, Mei-Mei Gao, W. Liao, 2015, Biochimica et biophysica acta.

Laminar Distribution of Neurochemically-Identified Interneurons and Cellular Co-expression of Molecular Markers in Epileptic Human Cortex

Yousheng Shu, G. Luan, W. Liao, 2018, Neuroscience Bulletin.

GRIN2A Variants Associated With Idiopathic Generalized Epilepsies

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

Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification

Na He, Bin Li, Xiao-Rong Liu, 2020, Briefings Bioinform..

Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy

Yi-wu Shi, W. Liao, N. He, 2017, Neuroscience Bulletin.

Seizure control and treatment in pregnancy

S. Kochen, M. Bacher, B. Steinhoff, 2006, Neurology.

Identification of the transcriptional promoters in the proximal regions of human microRNA genes

Yue-Sheng Long, Yong-Hong Yi, Tao Su, 2011, Molecular Biology Reports.

Involvement of FMRP in Primary MicroRNA Processing via Enhancing Drosha Translation

Mei-Mei Gao, W. Liao, Y. Long, 2016, Molecular Neurobiology.

A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X Syndrome

Lingjia Tang, W. Liao, Y. Long, 2014, Molecular Neurobiology.

A microRNA profile in Fmr 1 knockout mice reveals microRNA expression alterations with possible roles in fragile X syndrome

Lingjia Tang, W. Liao, Y. Long, 2014 .

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Neuroscience Bulletin.

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.

Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1

Lingjia Tang, W. Liao, Tao Zeng, 2014, Molecular Neurobiology.

Experimental identification of microRNA targets on the 3′ untranslated region of human FMR1 gene

W. Liao, Y. Long, Yong-Hong Yi, 2010, Journal of Neuroscience Methods.

Conservation-based prediction of the transcription regulatory region of the SCN1A gene

Yi-wu Shi, W. Liao, Y. Long, 2009 .

Epigenetic Downregulation of Scn3a Expression by Valproate: a Possible Role in Its Anticonvulsant Activity

Mei-Mei Gao, W. Liao, Hui-Ling Tang, 2017, Molecular Neurobiology.

A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

Lingjia Tang, Yi-wu Shi, W. Liao, 2014, Human Genetics.

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

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

A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

Lingjia Tang, Yi-wu Shi, W. Liao, 2014, Human Genetics.

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Nav1.1

S. Duan, Yi-wu Shi, Xiao-Rong Liu, 2010, Epilepsia.

Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy

Yi-wu Shi, W. Liao, N. He, 2017, Neuroscience Bulletin.

A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis

Yi-wu Shi, Mei-Mei Gao, W. Liao, 2011, neurogenetics.

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect

Xiao-Rong Liu, W. Liao, N. He, 2020, Frontiers in Neuroscience.

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.

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.

CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures

Jing Zhu, Yi-wu Shi, Xiao-Rong Liu, 2021, CNS neuroscience & therapeutics.

Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability

Xiao-Rong Liu, W. Liao, N. He, 2022, CNS neuroscience & therapeutics.

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

Michael R. Johnson, Josemir W Sander, A. Ingason, 2017, Neurology.

Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes.

R. Macdonald, Yi-wu Shi, W. Liao, 2019, Brain : a journal of neurology.

ABCB1 G2677T/A polymorphism is associated with the risk of drug-resistant epilepsy in Asians

W. Liao, Yong-Hong Yi, Guozhen Qiu, 2015, Epilepsy Research.

Promoter Analysis of Mouse Scn3a Gene and Regulation of the Promoter Activity by GC Box and CpG Methylation

Yi-wu Shi, Xiao-Rong Liu, Mei-juan Yu, 2011, Journal of Molecular Neuroscience.

Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti‐seizure medications

P. Sham, P. Kwan, S. Cherny, 2022, Epilepsia.

A conserved region in the 3′ untranslated region of the human LIMK1 gene is critical for proper expression of LIMK1 at the post-transcriptional level

W. Liao, Wei-Wen Sun, Y. Long, 2013, Neuroscience Bulletin.

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.

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

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

Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes

W. Liao, N. He, T. Su, 2013, Genes, brain, and behavior.

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.

Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy

B. Tang, Mugen Liu, Ji-feng Guo, 2023, Science China Life Sciences.

Aetiology of epilepsy in surgically treated patients in China

Dong Zhou, Ning Zhang, B. Xiao, 2004, Seizure.

Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases

K. Xia, B. Tang, Zhengmao Hu, 2013, Neuroscience Letters.

Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Genetics in Medicine.

Common genetic epilepsies, pathogenicity of genes/variants, and genetic dependence

W. Liao, N. He, T. Su, 2023, Seizure: European Journal of Epilepsy.

Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration

Xiao-Rong Liu, W. Liao, T. Su, 2022, Frontiers in Molecular Neuroscience.

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.

Genetic Dependence and Genetic Diseases

Yi-wu Shi, W. Liao, N. He, 2023, bioRxiv.

Editorial: Sub-molecular mechanism of genetic epilepsy

Xiao-Rong Liu, W. Liao, Yu-wu Jiang, 2022, Frontiers in Molecular Neuroscience.

Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome

Z. Xiong, W. Liao, Yong-Hong Yi, 2008, Cerebral cortex.

Roadmap for a competency-based educational curriculum in epileptology : report of the Epilepsy Education Task Force of the International League Against Epilepsy

J. Gotman, I. Rektor, J. Wilmshurst, 2019 .

Electrophysiological Differences between the Same Pore Region Mutation in SCN1A and SCN3A

Y. Zeng, Mei-Mei Gao, W. Liao, 2014, Molecular Neurobiology.

Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons

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

Expression changes of microtubule associated protein 1B in the brain of Fmr1 knockout mice

W. Liao, Yong-jie Bai, Rong Wang, 2007, Neuroscience bulletin.

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.

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

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

[Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome].

Yi-wu Shi, W. Liao, Yong-Hong Yi, 2009, Zhonghua yi xue za zhi.

Altered intrinsic properties and bursting activities of neurons in layer IV of somatosensory cortex from Fmr-1 knockout mice

Meng Li, P. Zhu, W. Liao, 2016, Experimental Neurology.

Transcription of the Human Sodium Channel SCN1A Gene Is Repressed by a Scaffolding Protein RACK1

Lingjia Tang, W. Liao, Tao Zeng, 2014, Molecular Neurobiology.

DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders

W. Liao, N. He, Zhigang Liu, 2023, Seizure: European Journal of Epilepsy.

ABCB1 G2677T/A polymorphism is associated with the risk of drug-resistant epilepsy in Asians

W. Liao, Yong-Hong Yi, Guozhen Qiu, 2015, Epilepsy Research.

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

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

DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders

W. Liao, N. He, Zhigang Liu, 2023, Seizure: European Journal of Epilepsy.

Epilepsy-associated genes: an update

W. Liao, N. He, Jie Wang, 2023, Seizure: European Journal of Epilepsy.

HLA-B*1502 genotyping in two Chinese patients with phenytoin-induced Stevens–Johnson syndrome

W. Liao, Fuli Min, Yi-Wu Shi, 2011, Epilepsy & Behavior.

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

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

Electrophysiological Differences between the Same Pore Region Mutation in SCN1A and SCN3A

Mei-Mei Gao, W. Liao, Yang Zeng, 2014, Molecular Neurobiology.

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

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

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Zhixian Yang, K. Xia, B. Tang, 2018, Human molecular genetics.