Author

Ming‐Feng He

Second Affiliated Hospital of Guangzhou Medical UniversityORCID 0000-0003-0748-5306Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Bing-Mei LiiD· 1 shared Dongfang ZouiD· 1 shared Haiyan Ma· 1 shared Jiajun GuoiD· 1 shared Jing‐Da QiaoiD· 1 shared Juan WangiD· 1 shared Lihong LiuiD· 1 shared Na HeiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Bing-Mei LiORCID

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1 paper

Recent·Most cited

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

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