Jiaoyang Chen
Beijing, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.
Journal: Frontiers in neurology
Published: September 11, 2022
Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing.
Journal: Journal of human genetics
Published: July 03, 2022
SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.
Journal: Frontiers in molecular neuroscience
Published: November 05, 2021
Phenotypes of GNAO1 Variants in a Chinese Cohort.
Journal: Frontiers in neurology
Published: January 31, 2021
Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABAA receptors.
Journal: Brain communications
Published: July 28, 2020
Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy.
Journal: Developmental medicine and child neurology
Published: May 26, 2020
CHD2-related epilepsy: novel mutations and new phenotypes.
Journal: Developmental medicine and child neurology
Published: August 21, 2019
The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet Syndrome.
Journal: Frontiers in neurology
Published: March 02, 2019
ATP1A3 mosaicism in families with alternating hemiplegia of childhood.
Journal: Clinical genetics
Published: December 22, 2018
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations.
Journal: Seizure
Published: November 01, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026