Author

Jaya Narayanan

Seattle Children's 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 calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anita E. BeckiD· 1 shared Cate Randall PaschaliD· 1 shared Danny E. MilleriD· 1 shared Joy GoffenaiD· 1 shared Madelyn A. GillentineiD· 1 shared Miranda P.G. Zalusky· 1 shared Nikhita DamarajuiD· 1 shared Sophie H. R. StorziD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anita E. BeckORCID

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1 paper

Recent·Most cited

Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes

Cate Randall Paschal, Miranda P.G. Zalusky, Anita E. Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju, Joy Goffena, Sophie H. R. Storz, Danny E. Miller

This study evaluates whole-genome long-read sequencing for diagnosing Prader-Willi and Angelman syndromes, showing high accuracy in detecting genetic variants and methylation differences.

Journal of Molecular Diagnostics · Jan 5, 2025Peer-reviewedGenetic & Genomic Medicine