Wei-ping Liao
Guangzhou, China
Last Updated: 09/26/2026
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Found 73 publications
Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.
Journal: Brain : a journal of neurology
Published: August 15, 2025
CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.
Journal: Journal of medical genetics
Published: May 20, 2025
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.
Journal: Epilepsia
Published: March 17, 2025
Identification of MACF1 as a causative gene of generalised epilepsy.
Journal: Journal of medical genetics
Published: February 09, 2025
Age at onset of genetic disease and genetic dependent stage: evidence from cases with SCN1A variants.
Journal: Brain : a journal of neurology
Published: December 17, 2024
De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy.
Journal: Epilepsia
Published: October 28, 2024
Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.
Journal: Pediatric research
Published: October 21, 2024
Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.
Journal: Orphanet journal of rare diseases
Published: May 10, 2024
Association of LONP1 gene with epilepsy and the sub-regional effect.
Journal: Scientific reports
Published: April 25, 2024
Last Updated: 09/26/2026