Author

Sheng Luo

Second Affiliated Hospital of Guangzhou Medical UniversityORCID 0000-0002-7184-1267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Bing-Mei LiiD· 2 shared Dongfang ZouiD· 2 shared Jing‐Da QiaoiD· 2 shared Na HeiD· 2 shared Su‐Li HeiD· 2 shared Wei‐Ping LiaoiD· 2 shared Xiao‐Rong LiuiD· 2 shared Yong‐Hong YiiD· 2 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Bing-Mei LiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 25, 2023

Identification of novel causative genes of childhood epileptic encephalopathies

Yi‐Wu Shi, Jianguo Zhang, Zi-Long Ye…·Wei‐Ping Liao

The paper identifies three causative genes for childhood epileptic encephalopathies through trio-based whole-exome sequencing and individualized analysis of genetic variants.

8 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 16, 2023

ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favorable outcomes

Ming‐Feng He, Lihong Liu, Sheng Luo…·Wei‐Ping Liao

This study identifies ZFHX3 variants as a cause of childhood partial epilepsy and infantile spasms, with favorable treatment outcomes and insights into the developmental expression pattern of the gene.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky