Author

Jillian N. Pearring

University of MichiganORCID 0000-0002-5352-2852Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Organism:mouse· 3 Assay:proteomics· 3 Approach:experimental assay· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1

Frequent Co-Authors

Jason R. WilleriD· 2 shared Jorge Y. Martínez-MárqueziD· 2 shared Alfredo Dueñas ReyiD· 1 shared Andreea M. Beu· 1 shared Anne HoorensiD· 1 shared Anne‐Françoise RouxiD· 1 shared Christopher B. Stein· 1 shared David G. Ball· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersCell Biology

Jason R. WillerORCID

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Author profile →

3 papers

Recent·Most cited

The tetraspanin disc proteins, peripherin-2 and ROM1, facilitate CNG channel localization to the rod outer segment

Molly T. Thorson, Stephanie E. Wei, Junseo Park, Jorge Y. Martínez-Márquez, David G. Ball, Jason R. Willer, William J. Spencer, Jillian N. Pearring

This study shows that peripherin-2's tetraspanin domain is essential for CNG channel localization to rod outer segments, and that ROM1 can compensate for its loss.

Molecular Biology of the Cell · Jul 1, 2026Peer-reviewedCell Biology

Targeted delivery of rhodopsin's assembled core is required for outer segment extension in mouse rod photoreceptors

Jorge Y. Martínez-Márquez, Sandy Hua, Andreea M. Beu, Christopher B. Stein, Jillian N. Pearring

This study identifies the minimal requirements for rhodopsin's targeted delivery to drive outer segment extension in mouse rod photoreceptors.

Journal of Biological Chemistry · Dec 24, 2025Peer-reviewedCell Biology

CEP162 deficiency causes human retinal degeneration and reveals a dual role inciliogenesis and neurogenesis

Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg, Melanie Jäger, Jason R. Willer, Jennifer Winter, Hanh M. Truong, Núria Gruartmoner Roura, Mattias Van Heetvelde, Joachim Wolf, Robert Merget, Sabine Grasshoff‐Derr, , Hanno J. Bolz

The paper shows that CEP162 deficiency causes retinal degeneration by impairing ciliary function, while retaining a role in neurogenesis.

Journal of Clinical Investigation · Mar 2, 2023Peer-reviewedGenetics