Author

Jeremy Wegner

University of Oregon

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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Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:zebrafish· 3 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Jennifer B. PhillipsiD· 3 shared David P. CoreyiD· 2 shared Maryna V. IvanchenkoiD· 2 shared Monte WesterfieldiD· 2 shared Abbey A. ScottiD· 1 shared Alex J. KleiniD· 1 shared Alistair Duncan CalderiD· 1 shared Alyssa A. Tran· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersNeuroscience

Jennifer B. PhillipsORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Mini-Pcdh15b Gene Therapy Rescues Visual Deficits in a Zebrafish Model of Usher Syndrome Type 1F

Xinlan Chen, Daniel M. Hathaway, Alex J. Klein, Jennifer B. Phillips, Kevin T. A. Booth, Muriel Heitsch, Anton Lytvyn, Bruce H. Derfler, Jeremy Wegner, Corey Goldstein, Andrew Murphy, Sean G. Megason, Monte Westerfield, David P. Corey, Maryna V. Ivanchenko

This paper shows that a gene therapy using a shortened PCDH15 variant rescues vision in a zebrafish model of Usher Syndrome Type 1F.

bioRxiv · Nov 5, 2025 · PreprintNeuroscience

Hexafluoro slows retinal degeneration and improves visual function in zebrafish models of Usher syndrome 1F

Jennifer B. Phillips, Siena Kulis, Sara H. Buchner, Eric J. Fox, Jeremy Wegner, Judy Peirce, Maryna V. Ivanchenko, David P. Corey, Jack L. Arbiser, Monte Westerfield

Hexafluoro improves visual function and reduces retinal degeneration in zebrafish models of Usher syndrome 1F by protecting photoreceptors from light-induced damage.

bioRxiv · Dec 29, 2023 · PreprintNeuroscience

COPB2 haploinsufficiency causes a coatopathy with osteoporosis and developmental delay

Ronit Marom, Lindsay Catherine Burrage, Aurélie Clément, Bernardo Blanco‐Sánchez, Rossella Venditti, Mahim Jain, Ingo Grafe, Daryl A. Scott, Jill Anne Rosenfeld, Vernon Reid Sutton, Marwan S. Shinawi, Ghayda Mirzaa, Catherine J DeVile, Rowenna Roberts, Alistair Duncan Calder, , Brendan Lee

This study identifies COPB2 haploinsufficiency as a cause of a coatopathy with osteoporosis and developmental delay, showing disrupted collagen trafficking and potential treatment with ascorbic acid.

bioRxiv · Sep 14, 2020 · PreprintGenetics