Author

Mei Wu

University of WashingtonPrimary ORCID profile (0000-0002-2467-1402 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Mei WuiD1 paper · Leibniz-Forschungsinstitut für Molekulare Pharmakologie

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:ATAC-seq· 1 Assay:CUT&Tag· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam FrankishiD· 1 shared Alawi A.A. Alsheikh-AliiD· 1 shared Andrea GuarracinoiD· 1 shared Andrew P. BlairiD· 1 shared Andrew W. CarrolliD· 1 shared Ann M. Mc CartneyiD· 1 shared Anna-Sophie Fiston-LavieriD· 1 shared Bernhard SuteriD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam FrankishORCID

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1 paper

Recent·Most cited

Pangenome discovery of missing autism variants

Yang Sui, Jiadong Lin, Michelle D. Noyes, Youngjun Kwon, Isaac Wong, Nidhi Koundinya, William T. Harvey, Mei Wu, Kendra Hoekzema, Katherine M. Munson, Gage H. Garcia, Jordan Knuth, Julie Wertz, Tianyun Wang, Kelsey M. Hennick, , Glenn Hickey

The paper uses long-read sequencing to identify pathogenic variants in autism cases, finding three pathogenic mutations and nine candidate structural variants missed by short-read sequencing.

Nature Communications · Jan 23, 2026Peer-reviewedGenetic & Genomic Medicine