Author

Andrew K. Solomon

University of Washington

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 Research Focus:variant effect prediction· 2 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Andrew B. StergachisiD· 2 shared Danny E. MilleriD· 2 shared Elisabeth A. RosenthaliD· 2 shared Elizabeth BlueiD· 2 shared Elsa V. BaltoniD· 2 shared Ian A. GlassiD· 2 shared Jane E. RanchalisiD· 2 shared Kathleen A. LeppigiD· 2 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew B. StergachisORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Phenotype-Specific Recalibration of MAVE Data Enables Repurposing of BAP1 Functional Assays for Kury-Isidor Syndrome

Pankhuri Gupta, Elsa V. Balton, Malvika Tejura, Runjun D. Kumar, Matthew W. Snyder, Jeremy Stone, Rehan Marie Villani, Peter H. Byers, Chanprasert Sirisak, Ian A. Glass, Martha J. Horike-Pyne, Danny E. Miller, Jane E. Ranchalis, Elisabeth A. Rosenthal, Andrew K. Solomon, , Andrew B. Stergachis

The paper recalibrates BAP1 MAVE data for different disease phenotypes to enable accurate variant classification across related disorders.

medRxiv · May 21, 2026 · PreprintGenetic & Genomic Medicine

Genome-wide detection and clinical prioritization of tandem repeat outliers using long-read sequencing

Sophia B Gibson, Nikhita Damaraju, J. (Gus) Gustafson, Elsa V. Balton, Sirisak Chanprasert, Ian A. Glass, Martha J. Horike-Pyne, Runjun D. Kumar, Kathleen A. Leppig, Chris Lundberg, Jane E. Ranchalis, Elisabeth A. Rosenthal, Andrew K. Solomon, Andrew B. Stergachis, Mark Wener, , Danny E. Miller

The paper develops TRoLR, a pipeline using long-read sequencing to detect and prioritize pathogenic tandem repeat expansions in diverse populations, identifying known and novel expansions with clinical relevance.

medRxiv · May 1, 2026 · PreprintGenetic & Genomic Medicine