Author

Valérie Dufour

University of PennsylvaniaORCID 0000-0002-6465-1641Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Valérie Dufour1 paper · Université de Tours

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Ana Ripolles‐GarciaiD· 2 shared Gustavo David AguirreiD· 2 shared Simone IwabeiD· 2 shared William A. BeltraniD· 2 shared Alexa P. GrayiD· 1 shared Artur V. CideciyaniD· 1 shared Evelyn SantanaiD· 1 shared John G. FlanneryiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Ana Ripolles‐GarciaORCID

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2 papers

Recent·Most cited

Targeting ON-bipolar cells by AAV gene therapy stably reverses LRIT3-congenital stationary night blindness

Keiko Miyadera, Evelyn Santana, Karolina P. Roszak, Sommer Iffrig, Meike Visel, Simone Iwabe, Ryan F. Boyd, Joshua T. Bartoe, Yu Sato, Alexa P. Gray, Ana Ripolles‐Garcia, Valérie Dufour, Leah C. Byrne, John G. Flannery, William A. Beltran, Gustavo David Aguirre

This paper demonstrates that AAV gene therapy targeting ON-bipolar cells in a canine model of LRIT3-CSNB significantly improves night vision and restores LRIT3 function.

Proceedings of the National Academy of Sciences · Mar 22, 2022Peer-reviewedNeuroscience

Gene Therapy Reforms Photoreceptor Structure and Restores Vision in NPHP5-associated Leber Congenital Amaurosis

Gustavo David Aguirre, Artur V. Cideciyan, Valérie Dufour, Ana Ripolles‐Garcia, Raghavi Sudharsan, Małgorzata Świder, Roman Nikonov, Simone Iwabe, Sanford L. Boye, William W. Hauswirth, Samuel G. Jacobson, William A. Beltran

This paper demonstrates that gene therapy using AAV-mediated NPHP5 augmentation restores photoreceptor structure and function in a canine model of Leber congenital amaurosis.

Molecular Therapy · Mar 27, 2021Peer-reviewedNeuroscience