Author

Stephen Vieno

Virginia Commonwealth UniversityORCID 0009-0004-4328-0011Unclaimed ORCID profile · follow to get notified of new preprints

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

Brien Riley· 2 shared Chris ChatzinakosiD· 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

Brien Riley

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 17, 2026

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

Sydney Kramer, Saeed Farajzadeh Valilou, Madhur Singh…·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.

DOI 10.64898/2026.09.11.26362867

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 22, 2026

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

Stephen Vieno, Madhurbain Singh, Sydney Kramer…·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.

DOI 10.64898/2026.08.19.26360760

humanwhole-genome sequencing

𝕏 PostBluesky