Xiao-Rong Liu

发表

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.

Milder phenotype with SCN1A truncation mutation other than SMEI

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

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

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

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

Huidong Tang, S. Chen, Wotu Tian, 2020, Movement disorders : official journal of the Movement Disorder Society.

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.

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

B. Tang, Huidong Tang, S. Chen, 2018, Movement disorders : official journal of the Movement Disorder Society.

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene

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

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.

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.

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.

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.

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..

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.

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.

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.

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.

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

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

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.

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.

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.

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.

Editorial: Sub-molecular mechanism of genetic epilepsy

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

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.

ATP6V1A variants are associated with childhood epilepsy with favorable outcome

Jie Xu, Zhen Shi, Xiao-Rong Liu, 2023, Seizure: European Journal of Epilepsy.

NEXMIF variants are associated with epilepsy with or without intellectual disability

Yunqing Ma, Yi-wu Shi, Xiao-Rong Liu, 2023, Seizure: European Journal of Epilepsy.

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

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