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)

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|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 <i>ACTB</i> 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 <i>MACF1</i> 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

Wei-Ping Liao

Na He

Peng-Yu Wang

Yong-Hong Yi

Jie Wang

Xiao-Rong Liu

Dong-Fang Zou

Wen-Hui Liu

Xiao-Yu Liang

Xiang-Hong Meng

Frequent Collaborators

Wei-Ping Liao

Na He

Peng-Yu Wang

Yong-Hong Yi