Sheng Luo

7PUBLICATIONS
22CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cellular nervous systemNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (7)

|Jun 24, 2026
Biological Context-Informed and Population-Stratified Strategies Improve Genetic Diagnosis of CCDC22-Related Disorder.

|Oct 27, 2025
De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

Xiao-Yu Liang, Xiang-Hong Meng, Wu-Chen Wu

|Jul 18, 2025
De Novo ACTB Variant Associated With Juvenile-Onset Temporal Lobe Epilepsy With Favorable Outcomes.

Hong-Jun Yan, Peng-Yu Wang, Wen-Hui Liu

|Jul 09, 2025
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.

Xiang Li, Lin Wang, Xiao-Yu Liang

|May 11, 2025
Identification of MACF1 as a causative gene of generalised epilepsy.

Xiao-Yun Lei, Meng-Wen Zhang, Hui Sun

|Mar 20, 2025
De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy.

Sheng Luo, Wen-Jun Zhang, Mi Jiang

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Frequent Collaborators

5 joint publications

Wei-Ping Liao

3 joint publications

Na He

3 joint publications

Peng-Yu Wang

2 joint publications

Yong-Hong Yi