Author

Wei‐Ping Liao

Second Affiliated Hospital of Guangzhou Medical UniversityORCID 0000-0001-9929-9185Unclaimed 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

Na HeiD· 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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3 shared papersGenetic & Genomic Medicine

Na HeORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintAug 2, 2023

Genetic Dependence and Genetic Diseases

Bin Li, Wen‐Jun Bian, Peng Zhou…·Wei‐Ping Liao

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

25 citations

𝕏 PostBluesky

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