Jie Wang

Key Laboratory Of Neurogenetics And Channelopathies Of Guangdong Province And The Ministry Of Education Of China
Guangzhou, China

Last Updated: 09/26/2026

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Found 56 publications

RLIM variant associated with X-linked epilepsy with neurodevelopmental disorders and the molecular sub-regional effects.

RLIM variant associated with X-linked epilepsy with neurodevelopmental disorders and the molecular sub-regional effects.

Journal: Seizure

Published: February 28, 2026

Explainable End-to-End Seizure Prediction via Stationary Wavelet Transform-Driven Dynamic Multiscale Fuzzy Clustering.

Explainable End-to-End Seizure Prediction via Stationary Wavelet Transform-Driven Dynamic Multiscale Fuzzy Clustering.

Journal: IEEE journal of biomedical and health informatics

Published: November 19, 2025

Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.

Reply: USP25 in genetic generalized epilepsy: a gene under scrutiny.

Journal: Brain : a journal of neurology

Published: August 15, 2025

ATP2B1 variants associated with generalized epilepsy without neurodevelopmental disorders and the underlying mechanism.

ATP2B1 variants associated with generalized epilepsy without neurodevelopmental disorders and the underlying mechanism.

Journal: Seizure

Published: July 27, 2025

De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

Journal: Epilepsia

Published: June 26, 2025

Identification of CDK5RAP2 as a causative gene of focal epilepsy without microcephaly.

Identification of CDK5RAP2 as a causative gene of focal epilepsy without microcephaly.

Journal: Seizure

Published: June 09, 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

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

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.

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.

Identification of MACF1 as a causative gene of generalised epilepsy.

Journal: Journal of medical genetics

Published: February 09, 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

Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.

Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.

Journal: Pediatric research

Published: October 21, 2024

Showing 1-12 of 56

Last Updated: 09/26/2026