Author

Merry Mclaird

Children's Mercy 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· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jasmine A. McQuerryiD· 1 shared Jeffrey J. JohnstoniD· 1 shared John C. Means· 1 shared Samantha N. Hartin· 1 shared Scott T. YoungeriD· 1 shared Tomi PastineniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Jasmine A. McQuerryORCID

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1 paper

Recent·Most cited

Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients

Jasmine A. McQuerry, Merry Mclaird, Samantha N. Hartin, John C. Means, Jeffrey J. Johnston, Tomi Pastinen, Scott T. Younger

The paper identifies functionally consequential noncoding variants in undiagnosed rare disease patients using a massively parallel reporter assay and integrative analysis.

Scientific Reports · May 9, 2022Peer-reviewedGenetic & Genomic Medicine