Weiping Liao

Guangzhou, China

Last Updated: 09/26/2026

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Found 50 publications

Clinical practice guidelines for the diagnosis and treatment of diffuse glioma-related epilepsy: 2025 update.

Clinical practice guidelines for the diagnosis and treatment of diffuse glioma-related epilepsy: 2025 update.

Journal: Cancer letters

Published: December 04, 2025

Precision gene diagnosis and treatment of epilepsy: a new frontier in medical care.

Precision gene diagnosis and treatment of epilepsy: a new frontier in medical care.

Journal: Acta epileptologica

Published: October 01, 2025

Efficacy and Safety of Adjunctive Cenobamate in Chinese Participants with Focal Seizure.

Efficacy and Safety of Adjunctive Cenobamate in Chinese Participants with Focal Seizure.

Journal: Advances in therapy

Published: September 12, 2025

Variants in ARHGAP21, encoding a Rho GTPase-activating protein, are associated with focal epilepsy and neurodevelopmental disorders.

Variants in ARHGAP21, encoding a Rho GTPase-activating protein, are associated with focal epilepsy and neurodevelopmental disorders.

Journal: Genes & diseases

Published: June 02, 2025

Sodium channel blockers for the treatment of focal epilepsy: A Chinese expert consensus.

Sodium channel blockers for the treatment of focal epilepsy: A Chinese expert consensus.

Journal: Seizure

Published: January 03, 2025

MDN1 variants cause susceptibility to epilepsy : For the China Epilepsy Gene 1.0 Project.

MDN1 variants cause susceptibility to epilepsy : For the China Epilepsy Gene 1.0 Project.

Journal: Acta epileptologica

Published: December 17, 2024

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Journal: The Journal of clinical investigation

Published: August 20, 2024

CSMD1 as a causative gene of developmental and epileptic encephalopathy and generalized epilepsies.

CSMD1 as a causative gene of developmental and epileptic encephalopathy and generalized epilepsies.

Journal: Genes & diseases

Published: July 09, 2024

Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.

Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.

Journal: American journal of human genetics

Published: June 18, 2024

SLC2A1 variants cause late-onset epilepsy and the genetic-dependent stage feature : For the China Epilepsy Gene 1.0 Project.

SLC2A1 variants cause late-onset epilepsy and the genetic-dependent stage feature : For the China Epilepsy Gene 1.0 Project.

Journal: Acta epileptologica

Published: June 13, 2024

Variants of TSC1 are associated with developmental and epileptic encephalopathy and focal epilepsy without tuberous sclerosis : For the China Epilepsy Gene 1.0 Project.

Variants of TSC1 are associated with developmental and epileptic encephalopathy and focal epilepsy without tuberous sclerosis : For the China Epilepsy Gene 1.0 Project.

Journal: Acta epileptologica

Published: May 07, 2024

Characteristic spatial and frequency distribution of mutations in SCN1A.

Characteristic spatial and frequency distribution of mutations in SCN1A.

Journal: Acta epileptologica

Published: April 08, 2024

Showing 1-12 of 50

Last Updated: 09/26/2026