Author

Roxanne Diaz Caceres

Stanford Medicine

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 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Assay:ATAC-seq· 1 Assay:ChIP-seq· 1 Approach:contrastive learning· 1 Assay:CRISPR screen· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Organism:human· 1

Frequent Co-Authors

Anshul Bharat KundajeiD· 2 shared Chad S. WeldyiD· 2 shared Daniel Yuhang LiiD· 2 shared Markus O RamsteiD· 2 shared Quanyi ZhaoiD· 2 shared Soumya KunduiD· 2 shared Thomas QuertermousiD· 2 shared Trieu NguyeniD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenomics

Anshul Bharat KundajeORCID

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2 papers

Recent·Most cited

Vascular smooth muscle cell atherosclerosis trajectories characterized at single cell resolution identify causal transcriptomic and epigenomic mechanisms of disease risk

Daniel Yuhang Li, Soumya Kundu, Paul P. Cheng, Wenduo Gu, Matthew D. Worssam, William Jackson, Quanyi Zhao, Trieu Nguyen, A. Y-C. Yu, João P Monteiro, Roxanne Diaz Caceres, Stanley Dale, Brian T. Palmisano, Chad S. Weldy, Markus O Ramste, , Thomas Quertermous

The paper characterizes atherosclerosis trajectories in vascular smooth muscle cells using single-cell data and identifies causal transcriptomic and epigenomic mechanisms of CAD risk.

Nature Communications · Mar 17, 2026Peer-reviewedGenomics

Enhancer-targeting CRISPR screens at coronary artery disease loci suggest shared mechanisms of disease risk

Markus O Ramste, Chad S. Weldy, Soumya Kundu, Quanyi Zhao, Daniel Yuhang Li, Kayla Brand, Disha Sharma, Amanda Ramste, Evelyn Jagoda, Judhajeet Ray, Roxanne Diaz Caceres, James Galante, Andreas R. Gschwind, Nuutti Lahtinen, Trieu Nguyen, , Thomas Quertermous

The paper identifies causal genetic mechanisms at CAD GWAS loci using CRISPR screens and chromatin analysis, revealing enhancer-gene links and ancestry/sex-specific risk factors.

medRxiv · Aug 28, 2025 · PreprintGenetic & Genomic Medicine