Yi-wu L. Shi

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

Last Updated: 09/26/2026

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Found 44 publications

Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.

Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: April 03, 2026

STXBP1 Variants Associated With Epilepsy With Variable Severity.

STXBP1 Variants Associated With Epilepsy With Variable Severity.

Journal: CNS neuroscience & therapeutics

Published: October 29, 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

De novo heterozygous missense variants in ATP11A are associated with refractory focal epilepsy.

De novo heterozygous missense variants in ATP11A are associated with refractory focal epilepsy.

Journal: Journal of medical genetics

Published: November 25, 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

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

Heterozygous variants in USP25 cause genetic generalized epilepsy.

Heterozygous variants in USP25 cause genetic generalized epilepsy.

Journal: Brain : a journal of neurology

Published: January 24, 2024

De novo GABRA1 variants in childhood epilepsies and the molecular subregional effects.

De novo GABRA1 variants in childhood epilepsies and the molecular subregional effects.

Journal: Frontiers in molecular neuroscience

Published: October 13, 2023

NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation.

NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation.

Journal: Molecular neurobiology

Published: September 30, 2023

Effects of ppk1 deletion on the drug susceptibility of uropathogenic Escherichia coli producing ESBLs

Effects of ppk1 deletion on the drug susceptibility of uropathogenic Escherichia coli producing ESBLs

Journal: Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]

Published: August 13, 2023

NEXMIF variants are associated with epilepsy with or without intellectual disability.

NEXMIF variants are associated with epilepsy with or without intellectual disability.

Journal: Seizure

Published: May 09, 2023

HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism.

HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism.

Journal: Clinical and translational medicine

Published: December 20, 2022

Showing 1-12 of 44

Last Updated: 09/26/2026