Author

Lingji Chen

Fujian Medical University

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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Genetics· 1

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Hailong HuangiD· 1 shared Haiwei WangiD· 1 shared Hua CaoiD· 1 shared Jia LiiD· 1 shared Liangpu XuiD· 1 shared Meihua Tan· 1 shared Meihuan CheniD· 1 shared Na LiniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Hailong HuangORCID

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1 paper

Recent·Most cited

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family via up-regulation of the PI3K-Akt signaling pathway

Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Wei Li, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, , Hua Cao

The paper identifies a novel PLS1 variant causing autosomal-dominant hearing loss by inducing exon8 skipping and upregulating the PI3K-Akt pathway in zebrafish.

bioRxiv · Mar 17, 2022 · PreprintGenetics