Author

L Weaver

University of Utah

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:benchmarking· 2 Organism:human· 2 Approach:statistical model· 2 Assay:electronic health records· 1

Frequent Co-Authors

Chelsea M. Solorzano· 2 shared Jorie ButleriD· 2 shared Kelsey A. SimekiD· 2 shared Martin Tristani‐FirouziiD· 2 shared Mickey L BolyardiD· 2 shared Paul Estabrooks· 2 shared Peter A. TaberiD· 2 shared Sabrina Malone JenkinsiD· 2 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chelsea M. Solorzano

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2 papers

Recent·Most cited

Evolving clinical roles in the era of genomic medicine: Insights from rapid genome sequencing in the neonatal intensive care unit

Peter A. Taber, Chelsea M. Solorzano, L Weaver, Kelsey A. Simek, Rachel N. Palmquist, Jorie Butler, Tanner Ellsworth, Mickey L Bolyard, Martin Tristani‐Firouzi, Paul Estabrooks, Sabrina Malone Jenkins

The paper examines challenges in clinical roles during rapid genome sequencing in NICUs, identifying ambiguities in subspecialist consultations and responsibilities.

medRxiv · Sep 29, 2026 · PreprintGenetic & Genomic Medicine

Usability and workflow implications of an electronic health record-integrated tool for automated phenotyping: Formative evaluation of Pheno+

Peter A. Taber, L Weaver, Tony Di Sera, Chelsea M. Solorzano, Emerson Lebleu, Mickey L Bolyard, Jorie Butler, Tanner Ellsworth, Isabelle B. Cooperstein, Paul Estabrooks, Kensaku Kawamoto, Phillip B. Warner, Kelsey A. Simek, Martin Tristani‐Firouzi, Alistair Ward, , Sabrina Malone Jenkins

The paper evaluates Pheno+, an EHR-integrated tool for automated phenotyping, finding it has good usability but requires curation to reduce errors and reshape clinical workflows.

medRxiv · Sep 23, 2026 · PreprintGenetic & Genomic Medicine