Yang Yang

13PUBLICATIONS
38CO-AUTHORS
Cellular nervous systemMedical infection agents (incl. prions)NanoelectronicsNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)
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Publications (13)

|Jul 30, 2026
Epilepsy-associated SCN2A-L1342P mutation drives network hyperexcitability and widespread transcriptomic changes in human cortical organoids.

|Feb 18, 2026
Human microglia in brain assembloids display region-specific diversity and respond to hyperexcitable neurons carrying SCN2A mutation.

Jiaxiang Wu, Xiaoling Chen, Jingliang Zhang

|Jan 19, 2026
An engineered UGA suppressor tRNA gene for disease-agnostic AAV delivery.

Mengyao Xu, Hao Liu, Jiaming Wang

|Sep 26, 2025
Single-nucleus transcriptomics reveal disrupted pathways in the prefrontal cortex of Scn2a -deficient mice.

Ye-Eun Yoo, Purba Mandal, Zhengkuan Tang

|Jun 12, 2025
Gene therapies alleviate absence epilepsy associated with Scn2a deficiency in DBA/2J mice.

Zaiyang Zhang, Jingliang Zhang, Xiaoling Chen

|Jun 12, 2025
Autism-associated SCN2A deficiency disrupts cortico-striatal circuitry in human brain assembloids.

Xiaoling Chen, Jingliang Zhang, Jiaxiang Wu

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Frequent Collaborators

6 joint publications

Jingliang Zhang

2 joint publications

Morgan Robinson

2 joint publications

Dan Wang

2 joint publications

Xiaoling Chen