Wen-hui Liu

613 West Huangpu Ave
Guangzhou, 510630, China

Last Updated: 09/26/2026

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Found 14 publications

Variants in KLHL15, encoding a regulator of protein ubiquitination, linked to focal epilepsy with neurodevelopmental disorders.

Variants in KLHL15, encoding a regulator of protein ubiquitination, linked to focal epilepsy with neurodevelopmental disorders.

Journal: Seizure

Published: March 17, 2026

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

Precision diagnosis of GABRA1-associated encephalopathies and epilepsy: optimizing variants classification and molecular subregional effects.

Precision diagnosis of GABRA1-associated encephalopathies and epilepsy: optimizing variants classification and molecular subregional effects.

Journal: Frontiers in genetics

Published: February 26, 2026

Correction: Exploring the landscape of developmental and epileptic encephalopathies and gene research global dynamics via bibliometric study 2001-2025.

Correction: Exploring the landscape of developmental and epileptic encephalopathies and gene research global dynamics via bibliometric study 2001-2025.

Journal: Frontiers in neurology

Published: January 05, 2026

Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: optimizing genetic diagnosis and molecular subregional effects.

Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: optimizing genetic diagnosis and molecular subregional effects.

Journal: Frontiers in neurology

Published: December 20, 2025

Biological Context-Informed and Population-Stratified Strategies Improve Genetic Diagnosis of CCDC22-Related Disorder.

Biological Context-Informed and Population-Stratified Strategies Improve Genetic Diagnosis of CCDC22-Related Disorder.

Journal: Genetics research

Published: December 10, 2025

Exploring the landscape of developmental and epileptic encephalopathies and gene research global dynamics via bibliometric study 2001-2025.

Exploring the landscape of developmental and epileptic encephalopathies and gene research global dynamics via bibliometric study 2001-2025.

Journal: Frontiers in neurology

Published: October 27, 2025

Genetic and expressional insights into the association of TRAPPC10 variants with neurodevelopmental disorders.

Genetic and expressional insights into the association of TRAPPC10 variants with neurodevelopmental disorders.

Journal: Neurogenetics

Published: December 23, 2024

Age at onset of genetic disease and genetic dependent stage: evidence from cases with SCN1A variants.

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.

De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy.

Journal: Epilepsia

Published: October 28, 2024

De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis.

De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis.

Journal: Frontiers in genetics

Published: September 21, 2024

De Novo ACTB Variant Associated With Juvenile-Onset Temporal Lobe Epilepsy With Favorable Outcomes.

De Novo ACTB Variant Associated With Juvenile-Onset Temporal Lobe Epilepsy With Favorable Outcomes.

Journal: Human mutation

Published: April 08, 2024

Showing 1-12 of 14

Last Updated: 09/26/2026