Wei‐Ping Liao

机构：Second Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University · ORCID：0000-0001-9929-9185

发表论文 210 篇 · 总被引 4748 次 · h-index 37

代表论文

• Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders (2024 · The American Journal of Human Genetics · 被引 29)
• De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy (2025 · Epilepsia · 被引 19)
• Age at onset of genetic disease and genetic dependent stage: evidence from cases with SCN1A variants (2025 · Brain · 被引 18)
• CSMD1 as a causative gene of developmental and epileptic encephalopathy and generalized epilepsies (2024 · Genes & Diseases · 被引 16)
• Variants in CSMD2 and CSMD3 , genes involved in synaptogenesis, are associated with epilepsies (2025 · Epilepsia · 被引 8)
• Identification of MACF1 as a causative gene of generalised epilepsy (2025 · Journal of Medical Genetics · 被引 7)