Author

Katarzyna D. Borys

University of Wisconsin–Madison

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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Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Bikash Ranjan PattnaikiD· 1 shared Dalton HermansiD· 1 shared David M. GammiD· 1 shared De‐Ann M. PillersiD· 1 shared Divya SinhaiD· 1 shared Elizabeth E. CapowskiiD· 1 shared Hannah M. MoultoniD· 1 shared Pawan Kumar ShahiiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Bikash Ranjan PattnaikORCID

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1 paper

Recent·Most cited

Gene augmentation and read-through rescue channelopathy in an iPSC-RPE model of congenital blindness

Pawan Kumar Shahi, Dalton Hermans, Divya Sinha, Simran Brar, Hannah M. Moulton, Sabrina Stulo, Katarzyna D. Borys, Elizabeth E. Capowski, De‐Ann M. Pillers, David M. Gamm, Bikash Ranjan Pattnaik

The paper tests read-through drugs and gene therapy in patient-derived iPSC-RPE cells with a KCNJ13 mutation to restore Kir7.1 channel function and rescue channelopathy in LCA16.

The American Journal of Human Genetics · Jan 24, 2019Peer-reviewedGenetics