Author

Chayna J. Davis

University of Washington

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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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Colby T. MarviniD· 2 shared Jessica X. ChongiD· 2 shared Kathryn M. Shively· 2 shared Kati J. BuckinghamiD· 2 shared Michael J. BamshadiD· 2 shared Tamara J. Bacus· 2 shared Abbey A. ScottiD· 1 shared Aishwarya RamamurthyiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Colby T. MarvinORCID

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2 papers

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

Precision medicine for developmental and epileptic encephalopathies in Africa: strategies for a resource-limited setting.

Alina Izabela Esterhuizen, Nicki Tiffin, Gillian Tracy Riordan, Marie Wessels, Richard Joseph Burman, Miriam C. Aziz, Jeffrey Dennis Calhoun, Jonathan Gunti, Ezra E. Amiri, Aishwarya Ramamurthy, Michael J. Bamshad, Suzanne M. Leal, Deborah A. Nickerson, Peter Anderson, Tamara J. Bacus, , Gemma L. Carvill

The paper identifies genetic variants in South African children with developmental and epileptic encephalopathies and proposes a 'Think-Genetics' strategy for early genetic diagnosis in resource-limited settings.

Genetics in Medicine · Dec 8, 2022Peer-reviewedGenetic & Genomic Medicine