Author

Se Jun Park

Emory 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· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Behrang MahjaniiD· 1 shared Bernie DevliniD· 1 shared Catalina BetancuriD· 1 shared David J. CutleriD· 1 shared Emilie M. WigdoriD· 1 shared F. Kyle SatterstromiD· 1 shared Gad HatemiD· 1 shared Jack M. FuiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Behrang MahjaniORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 7, 2026

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder

F. Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani…·David J. Cutler

The paper develops a model to analyze X-linked rare variation in ASD, identifying 9 genes associated with ASD and explaining how X-linked variation could contribute to sex-differential prevalence.

1 citation

humanwhole-exome sequencing

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