Author

Keqing Wang

Baylor College of Medicine

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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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:metagenomics· 1

Frequent Co-Authors

Anna MatyniaiD· 1 shared Fengxia Yao· 1 shared Fernanda Belga Ottoni PortoiD· 1 shared Irma López· 1 shared Jongsu ChoiiD· 1 shared Junhong CheniD· 1 shared Kerry GoetziD· 1 shared Liang XiaoiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Anna MatyniaORCID

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2 papers

Recent·Most cited

Structural variants contribute to the gut microbiome, blood metabolic traits and their causal relationships

Qun Zhou, Keqing Wang, Junhong Chen, Xinjiang Tan, Xun Xu, Xin Jin, Shaoqiao Zhang, Liang Xiao, Tao Zhang, Xiaomin Liu

This study identifies 138,859 structural variants in 2,002 individuals, finding 30 associations with gut microbes and 48 with blood metabolites, including causal relationships between microbiome and metabolites.

bioRxiv · Mar 15, 2025 · PreprintGenomics

Systematic assessment of the contribution of structural variants to inherited retinal diseases

Shu Wen, Meng Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi, Mark Edward Pennesi, Paul G Yang, Molly H. Marra, Robert Karel Koenekoop, Irma López, Anna Matynia, Michael B. Gorin, Ruifang Sui, Fengxia Yao, , Rui Chen

This study identifies 16 pathogenic structural variants in 16 IRD families using whole-genome sequencing, finding SVs contribute 2.1% to unresolved IRD cases but less than SNVs and indels.

Human Molecular Genetics · Feb 22, 2023Peer-reviewedGenetics