Yi-Wu Shi

发表

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

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

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.

Distinct placental molecular processes associated with early-onset and late-onset preeclampsia

Zhonglu Ren, Yi-wu Shi, Xiaoxue Yang, 2021, Theranostics.

Landscape of Dysregulated Placental RNA Editing Associated With Preeclampsia

Zhonglu Ren, Yi-wu Shi, Sheng Li, 2020, Hypertension.

Distinct Molecular Processes in Placentae Involved in Two Major Subtypes of Preeclampsia

Zhonglu Ren, Yi-wu Shi, Xiaoxue Yang, 2019, bioRxiv.

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

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

HLA Risk Alleles in Aromatic Antiepileptic Drug-Induced Maculopapular Exanthema

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

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.

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.

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.

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

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

Epilepsy-associated genes

Yi-wu Shi, W. Liao, Liu Liu, 2017, Seizure.

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene

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

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.

Hla-B alleles and lamotrigine-induced cutaneous adverse drug reactions in the Han Chinese population.

Yi-wu Shi, Fu-Li Min, Xiao-Rong Liu, 2011, Basic & clinical pharmacology & toxicology.

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

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

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.

Transcriptomics of Gabra4 knockout mice reveals common NMDAR pathways underlying autism, memory, and epilepsy

U. Dräger, Yi-wu Shi, Xiaoxue Yang, 2020, Molecular Autism.

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.

Association between HLA and Stevens–Johnson Syndrome Induced by Carbamazepine in Southern Han Chinese: Genetic Markers besides B*1502?

Q. Wang, Yi-wu Shi, Fu-Li Min, 2012, Basic & clinical pharmacology & toxicology.

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

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

Milder phenotype with SCN1A truncation mutation other than SMEI

Yi-wu Shi, Xiao-Rong Liu, Mei-Mei Gao, 2010, Seizure.

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

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

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy

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

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

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

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.

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

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

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.

Genetic Dependence and Genetic Diseases

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

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

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

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.

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

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