Author

Chris Lundberg

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

Frequent Co-Authors

Danny E. MilleriD· 2 shared Elisabeth A. RosenthaliD· 2 shared Elizabeth BlueiD· 2 shared Elsa V. BaltoniD· 2 shared Gail Pairitz JarvikiD· 2 shared Ian A. GlassiD· 2 shared Kathleen A. LeppigiD· 2 shared Katrina M. DippleiD· 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

Danny E. MillerORCID

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2 papers

Recent·Most cited

A high-resolution human pangenome structural variant resource for improved disease association

Jiadong Lin, Jonas A. Gustafson, Julie Wertz, Yang Sui, DongAhn Yoo, David Porubskỳ, Can Luo, Isaac Wong, Kiran V. Garimella, Quihui Li, Luyao Ren, Nidhi Koundinya, Nikhita Damaraju, Lingbin Ni, Chenlu Di, , Evan E. Eichler

The paper constructs a high-resolution human pangenome structural variant resource, identifies disease-associated SVs, and demonstrates its utility in filtering variants from probands and associating SVs with traits in a large cohort.

medRxiv · Aug 25, 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