Author

Huijun Yuan

West China Hospital of Sichuan UniversityORCID 0000-0002-2523-9611Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:gene regulatory network inference· 3 Research Focus:database / resource· 2 Research Focus:differential expression· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2 Research Focus:clustering· 1

Frequent Co-Authors

Fengxiao BuiD· 3 shared Yu LuiD· 3 shared Jing ChengiD· 2 shared Mingjun Zhong· 2 shared Ahmad N. Abou TayouniD· 1 shared Alex Chapin· 1 shared Amy Hernandez· 1 shared Andrea M. OzaiD· 1 shared

Activity by Year

2019-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Fengxiao BuORCID

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4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 26, 2025

Whole-Genome Sequencing Pilot Study of the Central Asian Genetic Diversity Project Reveals Distinct Genetic Histories, Adaptive Processes, and Introgression Events

Guanglin He, Huang Su, Qiuxia Sun…·Mengge Wang

This study uses whole-genome sequencing of Central Asians to reveal genetic diversity, admixture events, and adaptive processes shaping their demographic history and medical relevance.

1 citation

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintDec 2, 2024

RGnet: Recessive Genotype Network in a Large Mendelian Disease Cohort

Fandi Ai, Lu Kang, Jiayi Zeng…·Fengxiao Bu

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

1 citation

humanwhole-exome sequencing

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GeneticsbioRxivPreprintAug 19, 2024

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

Hui Cheng, Xuegang Wang, Mingjun Zhong…·Huijun Yuan

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

1 citation

humanmouse

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GenomicsGenetics in MedicinePeer-reviewedMar 20, 2019

ClinGen Expert Clinical Validity Curation of 164 Hearing Loss Gene-Disease Pairs

Marina T. DiStefano, Sarah E. Hemphill, Andrea M. Oza…·Keijan Zhang

The paper curates 164 gene-disease pairs for hearing loss, classifying their clinical validity to improve genetic testing accuracy.

88 citationstop 2%

humanGWAS summary statistics

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