Yong-Hong Yi

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.

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.

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.

GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions

Mei-Mei Gao, T. Zeng, Hui-Ling Tang, 2017, Neuropharmacology.

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.

Early continuous inhibition of group 1 mGlu signaling partially rescues dendritic spine abnormalities in the Fmr1 knockout mouse model for fragile X syndrome

Mei-Mei Gao, Wei-Wen Sun, T. Su, 2011, Psychopharmacology.

[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.

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.

Alpha-asarone improves striatal cholinergic function and locomotor hyperactivity in Fmr1 knockout mice

Jialing Guo, Jie Wu, Yong-Hong Yi, 2016, Behavioural Brain Research.

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.

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 .

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.

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.

Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation

Xiao-Rong Liu, Liu Liu, T. Su, 2019, Seizure.

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.

MDH2 is an RNA binding protein involved in downregulation of sodium channel Scn1a expression under seizure condition.

Mei-Mei Gao, Tao Zeng, Hui-Ling Tang, 2017, Biochimica et biophysica acta. Molecular basis of disease.

A novel role of fragile X mental retardation protein in pre-mRNA alternative splicing through RNA-binding protein 14

Mei-Mei Gao, Wei-Wen Sun, Y. Long, 2017, Neuroscience.

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.

Yousheng Shu, Mei-Mei Gao, Wei-Wen Sun, 2019, Neuroscience.

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.

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.

FMRP-absence-induced up-regulation of hypothalamic MAP1B expression decreases AgRP level linking with reduces in food intake and body weight

Mei-Mei Gao, P. Lu, Wei-Wen Sun, 2020, Neurochemistry International.

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

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

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.

UNC13B variants associated with partial epilepsy with favourable outcome

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

Genetic Dependence and Genetic Diseases

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

Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome

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

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.

Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders

Yun Li, N. He, Jianhang Guo, 2023, Seizure: European Journal of Epilepsy.

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

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

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.

Epilepsy-associated genes: an update

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

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

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