Author

Wan-Ping Lee

The Jackson Laboratory for Genomic 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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Genomics· 2 Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 3 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:multiple species· 1

Frequent Co-Authors

Charles LeeiD· 3 shared Evan E. EichleriD· 3 shared Jan O. KorbeliD· 3 shared Mark ChaissoniD· 3 shared Mark GersteiniD· 3 shared Michael E. TalkowskiiD· 3 shared Peter A. AudanoiD· 3 shared Ryan E. MillsiD· 3 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Charles LeeORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohort

Brenna Cholerton, Dana Godrich, Jeremy Pasteris, Joe Rivero, Eden R. Martin, Brian W. Kunkle, Adam Christian Naj, Kara L. Hamilton‐Nelson, Hui Wang, Wan-Ping Lee, Logan C. Dumitrescu, Timothy J. Hohman, Richard P Mayeux, Eric Berg Larson, Paul K. Crane, , Thomas Jude Montine

This paper performs a large-scale GWAS meta-analysis of neuropathologic lesions in Alzheimer's disease and related dementias, identifying both known and novel genetic associations.

PLoS Genetics · Jun 29, 2026Peer-reviewedGenetic & Genomic Medicine

Impact and characterization of serial structural variations across humans and great apes

Wolfram Höps, Tobias Rausch, Michael Jendrusch, Hufsah Ashraf, Peter A. Audano, Ola Austine, Anna O. Basile, Christine R. Beck, Marc Jan Bonder, Marta Byrska-Bishop, Mark Chaisson, Zechen Chong, André Corvelo, Scott E. Devine, Peter Ebert, , Fritz J. Sedlazeck

The paper introduces NAHRwhals, a method to detect serial structural variations in long-read genomes, identifies 37 sSV loci in humans, and shows their relevance to disease.

Nature Communications · Sep 12, 2024Peer-reviewedBioinformatics

Expectations and blind spots for structural variation detection from short-read alignment and long-read assembly

Xuefang Zhao, Ryan L. Collins, Wan-Ping Lee, Alexandra M. Weber, Yukyung Jun, Qihui Zhu, Ben Weisburd, Yongqing Huang, Peter A. Audano, Harold Wang, Mark Walker, Chelsea Lowther, Jack M. Fu, Mark Gerstein, Scott E. Devine, , Michael E. Talkowski

The paper compares structural variant detection using short-read and long-read sequencing in three trios, showing lrWGS finds more SVs but srWGS has high concordance in non-repetitive regions.

bioRxiv · Jul 3, 2020 · PreprintGenomics

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Ankit Malhotra, David Porubskỳ, Tobias Rausch, Eugene J. Gardner, Oscar L. Rodriguez, Li Guo, Ryan L. Collins, Xian Fan, Jia Wen, Robert E. Handsaker, Susan Fairley, Zev N. Kronenberg, , Charles Lee

This study identifies a large number of structural variants in human genomes using multiple sequencing technologies and presents them as a gold standard for future studies.

Nature Communications · Apr 16, 2019Peer-reviewedGenomics