Author

Stephanie A. Morrison

Washington University in St. Louis

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:differential expression· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Claudia Soler‐AlfonsoiD· 1 shared Cole R. MicheliD· 1 shared Daniella Helena HockiD· 1 shared David A. StroudiD· 1 shared Dustin BaldridgeiD· 1 shared Eric TyckseniD· 1 shared Erin E. ConboyiD· 1 shared Farah A. LadhaiD· 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

Claudia Soler‐AlfonsoORCID

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1 paper

Recent·Most cited

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

Sara M. Fielder, Marisa W. Friederich, Daniella Helena Hock, Jessie R. Zhang, Liana Valin, Jill Anne Rosenfeld, Kevin T. A. Booth, Natasha J. Brown, Rocío Rius, Tanavi Sharma, Liana N. Semcesen, Kim C. Worley, Lindsay Catherine Burrage, Kayla M. Treat, Tara E. Samson, , Stephen C. Pak

This study identifies de novo ATP5F1A variants causing neurological disorders through dominant negative mechanisms, expanding the known phenotypic and genotypic spectrum of complex V deficiency.

EMBO Molecular Medicine · Aug 26, 2025Peer-reviewedGenetic & Genomic Medicine