Author

Katherine Hall

Children's Hospital of Orange County

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Virginia E. KimonisiD· 2 shared Angela M. Martin Rios· 1 shared Etta D'Orazio· 1 shared Fabiola Quintero‐RiveraiD· 1 shared Gisele Bentz PinoiD· 1 shared Kara MossleriD· 1 shared Karolina M. StępieńiD· 1 shared Kathryn OsanniD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Virginia E. KimonisORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Investigating Uptake and Impact of Genetic and Genomic Evaluation Following a Perinatal Demise

Kara Mossler, Etta D'Orazio, Katherine Hall, Kathryn Osann, Virginia E. Kimonis, Fabiola Quintero‐Rivera

This study evaluates the impact of geneticist involvement on genetic testing uptake, diagnostic yield, and patient education in perinatal demise cases.

medRxiv · Apr 23, 2026 · PreprintGenetic & Genomic Medicine

Expanding the phenotype spectrum of β-mannosidosis

Angela M. Martin Rios, Karolina M. Stępień, Liliane Gibbs, Katherine Hall, Patricia Hall, Gisele Bentz Pino, Raymond Wang, Nishitha R. Pillai, Troy C. Lund, Paul J. Orchard, Virginia E. Kimonis

The paper expands the clinical, biochemical, and brain imaging phenotype spectrum of β-mannosidosis by analyzing 44 patients and describing new features and genetic variants.

Neurology Genetics · Nov 7, 2025Peer-reviewedGenetic & Genomic Medicine