Author

Yu-Hsin Chao

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· 2

Signature Assays, Organisms & Methods

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Organism:Drosophila· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 1 Assay:metabolomics· 1

Frequent Co-Authors

Michael F. WangleriD· 2 shared Alfredo BruscoiD· 1 shared Amanda GerardiD· 1 shared Annalisa VetroiD· 1 shared Boris KereniD· 1 shared Brooke HulliD· 1 shared Catherine A. BrownsteiniD· 1 shared Chaya Nautiyal MuraliiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Michael F. WanglerORCID

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2 papers

Recent·Most cited

Drosophila Models Uncover Substrate Channeling Effects on Phospholipids and Sphingolipids in Peroxisomal Biogenesis Disorders

Michael F. Wangler, Yu-Hsin Chao, Mary R. Roth, Ruth Welti, James A. McNew

This study uses Drosophila models to identify phospholipid and sphingolipid abnormalities in peroxisomal biogenesis disorders, revealing substrate channeling effects on lipid acyl chain lengths.

PLoS ONE · Jun 11, 2025Peer-reviewedGenetics

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves, Sharayu V. Jangam, Xi Luo, Ning Liu, Danqing Bei, Yu-Hsin Chao, Brooke Hull, Pei-Tseng Lee, Hongling Pan, Pradnya Bhadane, , Shinya Yamamoto

The paper functionally tests ASD missense variants in Drosophila, finding 38% caused functional alterations and identifying GLRA2 as a cause of neurodevelopmental phenotypes.

Cell Reports · Mar 1, 2022Peer-reviewedGenetics