Author

Pin Huang

University of Southern California

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· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:GWAS summary statistics· 1 Organism:mouse· 1

Frequent Co-Authors

Calvin PaniD· 2 shared Hooman AllayeeiD· 2 shared Jaana HartialaiD· 2 shared Janet Gukasyan· 2 shared Nicholas C. Woodward· 2 shared Yi Ying HaniD· 2 shared Aldons Jake LusisiD· 1 shared Benjamin P. HurrelliD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Calvin PanORCID

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2 papers

Recent·Most cited

Effect of Genetic and Dietary Perturbation of Glycine Metabolism on Atherosclerosis in Humans and Mice

Subarna Biswas, James R. Hilser, Nicholas C. Woodward, Zeneng Wang, Janet Gukasyan, Ina Nemet, William S. Schwartzman, Pin Huang, Yi Ying Han, Zachary Fouladian, Sarada Charugundla, Neal J. Spencer, Calvin Pan, W.H. Wilson Tang, Aldons Jake Lusis, , Hooman Allayee

This study investigates the causal relationship between circulating glycine levels and atherosclerosis using genetic analyses in humans and dietary experiments in mice, finding no strong causal evidence despite observational associations.

medRxiv · Dec 8, 2023 · PreprintGenetic & Genomic Medicine

Large-scale Genetic Analysis Identifies 66 Novel Loci for Asthma

Yi Ying Han, Qiong Jia, Pedram Shafiei-Jahani, Benjamin P. Hurrell, Calvin Pan, Pin Huang, Janet Gukasyan, Nicholas C. Woodward, Eleazar Eskin, Frank D. Gilliland, Omid Akbari, Jaana Hartiala, Hooman Allayee

This study identifies 66 novel asthma susceptibility loci through GWAS and finds gene-sex interactions and immune-related candidate genes, suggesting CD52 as a potential therapeutic target.

bioRxiv · Aug 29, 2019 · PreprintGenetics