Author

Sherry Yang

Stanford UniversityORCID 0000-0002-6570-4864Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Assay:DNA methylation· 1 Assay:electronic health records· 1 Research Focus:eQTL / molecular QTL mapping· 1 Approach:experimental assay· 1

Frequent Co-Authors

Euan Angus AshleyiD· 2 shared Alexis Ferrasse· 1 shared Andrés Peña‐TauberiD· 1 shared Andrzej NowojewskiiD· 1 shared Anthony D. WagneriD· 1 shared Daniel C. NachuniD· 1 shared Elizabeth C. MorminoiD· 1 shared Ilaria StewartiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Euan Angus AshleyORCID

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2 papers

Recent·Most cited

An in silico framework for evaluating PRS-guided prognostic enrichment in clinical trial design

Ruoyi Cai, Joshua Gillard, Sherry Yang, Lindsay E. Clegg, Samvel B. Gasparyan, Ying Lü, Andrzej Nowojewski, Lü Tian, Ola Vedin, Euan Angus Ashley, Manuel A. Rivas, Jack William O’Sullivan

This paper develops an in silico framework to evaluate the impact of polygenic risk score (PRS)-guided prognostic enrichment on clinical trial design using genomic and electronic health record data.

medRxiv · Apr 21, 2026 · PreprintGenetic & Genomic Medicine

Long-read genome sequencing and multi-omics in aging and neurodegeneration

Tanner D. Jensen, Yann Le Guen, Lia Talozzi, Sherry Yang, John E. Gorzynski, Andrés Peña‐Tauber, Ilaria Stewart, Alexis Ferrasse, Daniel C. Nachun, Taylor M. Maurer, Justin Lee, Rafael Catoia Pulgrossi, Jun Young Park, Jingyu Zhang, Anthony D. Wagner, , Michael D. Greicius

The paper uses long-read genome sequencing and multi-omics data to identify structural variants associated with aging and neurodegenerative diseases, finding that SVs are more likely to be causal than SNVs.

medRxiv · Oct 10, 2025 · PreprintGenetic & Genomic Medicine