Author

Kimberly A. Kripps

Oregon Health & Science UniversityORCID 0000-0002-1343-9974Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Austin A LarsoniD· 2 shared Jill Anne RosenfeldiD· 2 shared Adeline L. VanderveriD· 1 shared Amy C. GoldsteiniD· 1 shared Aneal KhaniD· 1 shared April N. LehmaniD· 1 shared Arnaud Vincent VanlanderiD· 1 shared Brendan LeeiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Austin A LarsonORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 15, 2026

The clinical utility of functional testing in fibroblasts to diagnose primary mitochondrial disease

Johan L.K. Van Hove, Marisa W. Friederich, Roxanne A. Van Hove…·Jennifer H. Yang

Four mitochondrial functional tests in fibroblasts show good sensitivity and excellent specificity for diagnosing primary mitochondrial disease.

1 citation

humanproteomics

𝕏 PostBluesky

GeneticsGenetics in MedicinePeer-reviewedDec 18, 2018

Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy and hypermobility syndrome: Further delineation of the 17p13.3 microdeletion spectrum

Lisa Emrick, Jill Anne Rosenfeld, Seema R. Lalani…·Brendan Lee

The paper investigates 17p13.3 deletions between YWHAE/CRK and PAFAH1B1, identifying white matter lesions and hypermobility, and narrows the critical region to 345 kb with RTN4RL1 as a candidate gene.

15 citations

humanstatistical model

𝕏 PostBluesky