Jianda Wang - Publications

An EEG-based patient-independent epileptic seizure detection method based on domain generative adversarial network.

Journal: Health information science and systems

Published: March 03, 2025

Real-Time Epileptic Seizure Detection Based on Deep Learning.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 12, 2023

Giant axonal neuropathy (GAN) in an 8-year-old girl caused by a homozygous pathogenic splicing variant in GAN gene.

Journal: American journal of medical genetics. Part A

Published: February 24, 2021

Differential Functional Changes of Nav1.2 Channel Causing SCN2A-Related Epilepsy and Status Epilepticus During Slow Sleep.

Journal: Frontiers in neurology

Published: January 14, 2021

Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation.

Journal: Stem cell research

Published: September 22, 2020

Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1.

Journal: Neurogenetics

Published: February 10, 2020

Electrophysiological features: The next precise step for SCN2A developmental epileptic encephalopathy.

Journal: Molecular genetics & genomic medicine

Published: October 12, 2019

Correlation of phosphorylated S6 protein expression in blood and brain tissue in mice and rats with kainic acid-induced seizure

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: September 10, 2019

Effects of Honokiol on cognitive function in mice with kainic acid-induced epilepsy

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: January 30, 2019

Genotype and phenotype analysis using an epilepsy-associated gene panel in Chinese pediatric epilepsy patients.

Journal: Clinical genetics

Published: May 31, 2018

Q10R mutation in SCN9A gene is associated with generalized epilepsy with febrile seizures plus.

Journal: Seizure

Published: January 02, 2017

De novo mutation in DEPDC5 associated with unilateral pachygyria and intractable epilepsy.

Journal: Seizure

Published: December 03, 2016