Author

Laura Godfrey Hendon

University of Mississippi Medical CenterORCID 0000-0003-0645-1315Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Candice R. FinnilaiD· 2 shared Donald R. LatneriD· 2 shared Gregory M. CooperiD· 2 shared James M.J. LawloriD· 2 shared Kevin M. BowlingiD· 2 shared Michelle L. ThompsoniD· 2 shared Stephanie A. FelkeriD· 2 shared Susan M. HiattiD· 2 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Candice R. FinnilaORCID

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2 papers

Recent·Most cited

GeneticsGenetics in MedicinePeer-reviewedMay 6, 2023

Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing

Stephanie A. Felker, James M.J. Lawlor, Susan M. Hiatt…·Gregory M. Cooper

The paper identifies clinically relevant variants in poison exons (PEs) that improve diagnostic yield for neurodevelopmental disorders by uncovering variants previously overlooked in standard analyses.

19 citations

mousehuman

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Genetic & Genomic MedicinemedRxivPreprintAug 31, 2021

Genome sequencing as a first-line diagnostic test for hospitalized newborns

Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila…·Gregory M. Cooper

This study evaluates genome sequencing in hospitalized newborns, finding it more effective than standard care in identifying genetic diagnoses, especially in those with specific phenotypes.

1 citation

humanwhole-genome sequencing

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