Author

A. J. Agopian

The University of Texas Health Science Center at HoustonORCID 0000-0002-5874-4155Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Archana RaiiD· 1 shared Bo YuaniD· 1 shared Bruce D. GelbiD· 1 shared Cecilia W. Y. LoiD· 1 shared Christine E. SeidmaniD· 1 shared Dennis KostkaiD· 1 shared Eric BoerwinkleiD· 1 shared Iman Egab· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Archana RaiORCID

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1 paper

Recent·Most cited

Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach

Archana Rai, Jonathan Klonowski, Bo Yuan, Karen J. Coveler, Zain Dardas, Iman Egab, Jiaoyang Xu, Philip J. Lupo, A. J. Agopian, Dennis Kostka, Cecilia W. Y. Lo, S. Stephen Yi, Bruce D. Gelb, Christine E. Seidman, Eric Boerwinkle, , Zeynep Coban‐Akdemir

The paper identifies trans-heterozygous digenic variants in laterality defect genes using exome/genome sequencing data from CHD cohorts, finding significant enrichment in laterality cases compared to controls.

The American Journal of Human Genetics · Jun 20, 2025Peer-reviewedGenetic & Genomic Medicine