Author

Margie Glissmeyer

Seattle Children's Hospital

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 Organism:Drosophila· 1 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alexander G. IoannidisiD· 1 shared Amanda Peterson· 1 shared Anne GregoriD· 1 shared Antonio NovelliiD· 1 shared Benjamin CognéiD· 1 shared Boris KereniD· 1 shared Can Luo· 1 shared Catherine Ward Melver· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander G. IoannidisORCID

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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

De novo variants in LDB1 are linked to distinct neurodevelopmental phenotypes determined by variant location and differing pathomechanisms

Rebecca Fluri, Mireia Coll-Tané, Theresa Brunet, Benjamin Cogné, Solène Conrad, Mathilde Nizon, Francesco Nicita, Lorena Travaglini, Antonio Novelli, Margie Glissmeyer, Amanda Peterson, Jillian G. Buchan, Dan Serber, Kolja Meier, Jutta Gärtner, , Anne Gregor

The paper identifies de novo LDB1 variants linked to distinct neurodevelopmental phenotypes based on variant location and pathomechanisms, confirmed through in vitro and in vivo studies.

The American Journal of Human Genetics · Jun 19, 2026Peer-reviewedGenetic & Genomic Medicine