Qi Zeng

Shenzhen, China

Last Updated: 09/26/2026

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Found 23 publications

Beyond the genome: clinical challenges in diagnosing LONP1-related mitochondrial disorders.

Beyond the genome: clinical challenges in diagnosing LONP1-related mitochondrial disorders.

Journal: Frontiers in cell and developmental biology

Published: January 01, 2026

Genotypic spectrum in 1215 patients with Dravet syndrome or Dravet syndrome-like phenotype.

Genotypic spectrum in 1215 patients with Dravet syndrome or Dravet syndrome-like phenotype.

Journal: Pediatric research

Published: April 01, 2025

Unveiling β Subunit-Dependent Gating Defects in CaV2.1 Channelopathies: Investigation of a de novo CACNA1A Variant.

Unveiling β Subunit-Dependent Gating Defects in CaV2.1 Channelopathies: Investigation of a de novo CACNA1A Variant.

Journal: Neuroscience bulletin

Published: February 28, 2025

Magnetic/Acoustic Dual-Controlled Microrobot Overcoming Oto-Biological Barrier for On-Demand Multidrug Delivery against Hearing Loss.

Magnetic/Acoustic Dual-Controlled Microrobot Overcoming Oto-Biological Barrier for On-Demand Multidrug Delivery against Hearing Loss.

Journal: Small (Weinheim an der Bergstrasse, Germany)

Published: March 18, 2024

Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy.

Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy.

Journal: Frontiers in genetics

Published: May 18, 2023

Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing.

Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing.

Journal: Journal of human genetics

Published: July 03, 2022

Resective epilepsy surgery for West syndrome: The Hypsarrhythmic Asymmetric Scoring Scheme is a determining predictor of seizure outcome.

Resective epilepsy surgery for West syndrome: The Hypsarrhythmic Asymmetric Scoring Scheme is a determining predictor of seizure outcome.

Journal: Seizure

Published: June 17, 2022

Investigation of novel de novo KCNC2 variants causing severe developmental and early-onset epileptic encephalopathy.

Investigation of novel de novo KCNC2 variants causing severe developmental and early-onset epileptic encephalopathy.

Journal: Seizure

Published: May 19, 2022

Seizure course of PCDH19 clustering epilepsy in female children: A multicentre cohort study in China.

Seizure course of PCDH19 clustering epilepsy in female children: A multicentre cohort study in China.

Journal: Developmental medicine and child neurology

Published: April 06, 2022

Non-convulsive Status Epilepticus in SEMA6B-Related Progressive Myoclonic Epilepsy: A Case Report With Literature Review.

Non-convulsive Status Epilepticus in SEMA6B-Related Progressive Myoclonic Epilepsy: A Case Report With Literature Review.

Journal: Frontiers in pediatrics

Published: January 21, 2022

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.

Journal: Frontiers in molecular neuroscience

Published: November 05, 2021

Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants.

Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants.

Journal: Frontiers in molecular neuroscience

Published: November 04, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026