Author

Amy Snook

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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Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abbey A. ScottiD· 1 shared Alexandra KeefeiD· 1 shared Bethany Friedman· 1 shared Britt A. JohnsoniD· 1 shared Chayna J. Davis· 1 shared Colby T. MarviniD· 1 shared Dan DohertyiD· 1 shared Danny E. MilleriD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abbey A. ScottORCID

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1 paper

Recent·Most cited

SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns

Tara Lynn Wenger, Abbey A. Scott, Lukas Kruidenier, Megan C. Sikes, Alexandra Keefe, Kati J. Buckingham, Colby T. Marvin, Kathryn M. Shively, Tamara J. Bacus, Olivia M. Sommerland, Kailyn Anderson, Heidi I. S. Gildersleeve, Chayna J. Davis, Jamie A. Love-Nichols, Katherine E. MacDuffie, , Michael J. Bamshad

SeqFirst-neo uses a genotype-driven workflow with broad exclusion criteria to increase access to rapid whole genome sequencing in critically ill newborns, significantly improving the rate and equity of precise genetic diagnoses.

The American Journal of Human Genetics · Feb 24, 2025Peer-reviewedGenetic & Genomic Medicine