Author

Gwendolyn Bennett

Quest Diagnostics (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 1

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Research Focus:benchmarking· 1 Approach:statistical model· 1

Frequent Co-Authors

Heidi L. RehmiD· 1 shared Izabela Karbassi· 1 shared Linyan MengiD· 1 shared Matthew S. LeboiD· 1 shared Narasimhan NaganiD· 1 shared Robert RigobelloiD· 1 shared Steven M. HarrisoniD· 1 shared Wenjie CheniD· 1 shared

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2025-2025 · peak 1/yr

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8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Heidi L. RehmORCID

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1 paper

Recent·Most cited

Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level

Gwendolyn Bennett, Izabela Karbassi, Wenjie Chen, Steven M. Harrison, Matthew S. Lebo, Linyan Meng, Narasimhan Nagan, Robert Rigobello, Heidi L. Rehm

The paper examines how variants of uncertain significance (VUS) are reclassified based on subclassification evidence levels across four clinical laboratories.

Genetics in Medicine · Feb 28, 2025Peer-reviewedGenetic & Genomic Medicine