Author

Kiana Jodeiry

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

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, Gad Hatem, Se Jun Park, Lambertus Klei, Jack M. Fu, Emilie M. Wigdor, Catalina Betancur, Mark J. Daly, Kathryn Roeder, Bernie Devlin, Joseph D. Buxbaum, 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.

medRxiv · May 7, 2026 · PreprintGenetic & Genomic Medicine