List of works - Wei-Ping Liao

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 ⬇️

scientific article published on May 23, 2013

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

scientific article published on 13 November 2017

Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic-clonic seizures: A double-blind, randomized, placebo-controlled trial

scientific article published on 29 September 2018

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

scientific article published on March 17, 2012

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

scientific article published on May 26, 2011

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

scientific article published on 23 December 2021

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

scientific article published on 09 June 2021

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

scientific article published on 20 March 2018

HLA-B Alleles and Lamotrigine-Induced Cutaneous Adverse Drug Reactions in the Han Chinese Population ⬇️

scientific article published on March 16, 2011

HLA-B*1502 Screening and Toxic Effects of Carbamazepine ⬇️

scientific article published on August 18, 2011

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

scientific article published on January 7, 2011

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

scientific article published on April 8, 2011

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

scientific article published on November 24, 2010

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

scientific article published on 31 August 2018

Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons ⬇️

scientific article published on June 16, 2013

Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures ⬇️

scientific article published on December 14, 2011

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

scientific article published on July 26, 2013

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

scientific article published on December 21, 2012

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

scientific article published on 4 January 2018

UNC13B variants associated with partial epilepsy with favourable outcome

scientific article published on 01 November 2021

List of works by Wei-Ping Liao