Author

Na He

Second Affiliated Hospital of Guangzhou Medical UniversityORCID 0000-0002-9712-7782Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Wei‐Ping LiaoiD· 3 shared Yong‐Hong YiiD· 3 shared Bing-Mei LiiD· 2 shared Cui-Xia Fan· 2 shared Dongfang ZouiD· 2 shared Haiqing Xu· 2 shared Jing‐Da QiaoiD· 2 shared Peng ZhouiD· 2 shared

Activity by Year

2023-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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

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3 shared papersGenetic & Genomic Medicine

Wei‐Ping LiaoORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic Dependence and Genetic Diseases

Bin Li, Wen‐Jun Bian, Peng Zhou, Jie Wang, Cui-Xia Fan, Haiqing Xu, Lu Yu, Na He, Yi‐Wu Shi, Tao Su, Yong‐Hong Yi, Wei‐Ping Liao

The paper examines genetic dependence features of genes and their role in determining pathogenicity and clinical features of genetic diseases.

bioRxiv · Aug 2, 2023 · PreprintGenetics

Identification of novel causative genes of childhood epileptic encephalopathies

Yi‐Wu Shi, Jianguo Zhang, Zi-Long Ye, Na He, Wenbin Li, Hankui Liu, Zhi-Gang Liu, Nan-Xiang Shen, Xiao-Chong Qu, Cui-Xia Fan, Jie Wang, Sheng Luo, Yudan Lv, Li Gao, Jing Chen, , 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.

medRxiv · Jul 25, 2023 · PreprintGenetic & Genomic Medicine

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