Author

Haiyan Ma

Nanjing Brain Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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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 Jiajun GuoiD· 1 shared Jing‐Da QiaoiD· 1 shared Juan WangiD· 1 shared Lihong LiuiD· 1 shared Ming‐Feng HeiD· 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

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

Ming‐Feng He, Lihong Liu, Sheng Luo, Juan Wang, Jiajun Guo, Peng‐Yu Wang, Qiong‐Xiang Zhai, Su‐Li He, Dongfang Zou, Xiao‐Rong Liu, Bing-Mei Li, Haiyan Ma, Jing‐Da Qiao, Peng Zhou, Na He, , 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.

medRxiv · Jul 16, 2023 · PreprintGenetic & Genomic Medicine