Author

Brien Riley

Virginia Commonwealth 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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Chris ChatzinakosiD· 2 shared Stephen VienoiD· 2 shared Sydney KrameriD· 2 shared Amanda Elswick GentryiD· 1 shared Ananda B. AmstadteriD· 1 shared Bon Q. TrinhiD· 1 shared Bradley Todd WebbiD· 1 shared Christina M. SheeriniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chris ChatzinakosORCID

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2 papers

Recent·Most cited

Rare copy number variation in Post-traumatic stress disorder using whole genome sequencing and biobank data

Sydney Kramer, Saeed Farajzadeh Valilou, Madhur Singh, Stephen Vieno, Roseann E. Peterson, Chris Chatzinakos, Bradley Todd Webb, Jonathan R. I. Coleman, Ananda B. Amstadter, Amanda Elswick Gentry, Hermine H. Maes, Brien Riley, Kenneth S. Kendler, Christina M. Sheerin, Tan-Hoang Nguygen

This study investigates rare copy number variants in PTSD using whole-genome sequencing and biobank data, finding significant associations in specific ancestry groups and gene-sets.

medRxiv · Sep 17, 2026 · PreprintGenetic & Genomic Medicine

Prioritizing Genes and Rare Protein-Coding Variants in Acute Myeloid Leukemia via Whole Genome Sequencing Data

Stephen Vieno, Madhurbain Singh, Sydney Kramer, Chris Chatzinakos, Roseann Peterson, Brien Riley, Silviu‐Alin Bacanu, Thang N. Dinh, Bon Q. Trinh, Tan-Hoang Nguyen

The paper identifies rare and common genetic variants associated with acute myeloid leukemia using whole-genome sequencing data from the All of Us Research Program.

medRxiv · Aug 22, 2026 · PreprintGenetic & Genomic Medicine