Author

Mingjun Zhong

West China Hospital of Sichuan University

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

Biology Disciplines

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Genetic & Genomic Medicine· 2 Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:database / resource· 1

Frequent Co-Authors

Jing ChengiD· 4 shared Fengxiao BuiD· 3 shared Huijun YuaniD· 2 shared Yu LuiD· 2 shared Dong LiuiD· 1 shared Fandi Ai· 1 shared Fuping QianiD· 1 shared Hua WaniD· 1 shared

Activity by Year

2024-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Jing ChengORCID

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4 papers

Recent·Most cited

HSD17B7 is required for the function of sensory hair cells by regulating cholesterol synthesis

Yuqian Shen, Ziyang Wang, Xun Wang, Fuping Qian, Mingjun Zhong, Xin Wang, Jing Cheng, Dong Liu

This study identifies HSD17B7 as critical for sensory hair cell function by regulating cholesterol synthesis, showing its role in auditory physiology and hearing loss.

eLife · Jun 3, 2026Peer-reviewedDevelopmental Biology

RGnet: Recessive Genotype Network in a Large Mendelian Disease Cohort

Fandi Ai, Lu Kang, Jiayi Zeng, Mingmin He, Mingjun Zhong, Jing Cheng, Yu Lu, Huijun Yuan, Fengxiao Bu

RGnet identifies pathogenic variants in recessive disorders by analyzing genotype networks in a large cohort of hearing loss cases.

medRxiv · Dec 2, 2024 · PreprintGenetic & Genomic Medicine

GDC: An Integrated Resource to Explore the Pathogenesis of Hearing Loss through Genetics and Genomics

Hui Cheng, Xuegang Wang, Mingjun Zhong, Jia Geng, Wenjian Li, Kanglu Pei, Yu Lu, Jing Cheng, Fengxiao Bu, Huijun Yuan

The paper introduces GDC, a database integrating genetic and genomic data to study hearing loss, identifying novel mutational hotspots and candidate genes.

bioRxiv · Aug 19, 2024 · PreprintGenetics

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