Author

Wenyu Xiong

West China Hospital of Sichuan UniversityORCID 0000-0002-6317-0504Unclaimed 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-genome sequencing· 1

Frequent Co-Authors

Fengxiao BuiD· 1 shared Hua WaniD· 1 shared Huijun YuaniD· 1 shared Jing ChengiD· 1 shared Lanchen Wang· 1 shared Libo LiuiD· 1 shared Meilin CheniD· 1 shared Mingjun Zhong· 1 shared

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2024-2024 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Fengxiao BuORCID

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1 paper

Recent·Most cited

Frameshift variants in TBX2 underlie autosomal-dominant hearing loss with incomplete penetrance of nystagmus

Hua Wan, Yanfei Wang, Xiang Li, Lanchen Wang, Wenyu Xiong, Meilin Chen, Fengxiao Bu, Libo Liu, Mingjun Zhong, Yu Lu, Zhiyong Liu, Jing Cheng, Huijun Yuan

The paper identifies TBX2 frameshift variants as the cause of autosomal-dominant hearing loss with incomplete nystagmus penetrance, validated through linkage analysis, sequencing, and mouse models.

medRxiv · Jul 18, 2024 · PreprintGenetic & Genomic Medicine