Author

Scott H. Greenwald

Massachusetts Eye and Ear Infirmary

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· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2

Frequent Co-Authors

Eric A. PierceiD· 2 shared Mihoko Leon· 2 shared Qin LiuiD· 2 shared Benjamin P. KleinstiveriD· 1 shared Daniel Navarro-Gomez· 1 shared J. Keith JoungiD· 1 shared Kinga M. BujakowskaiD· 1 shared Michelle S. PrewiD· 1 shared

Activity by Year

2018-2018 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetics

Eric A. PierceORCID

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2 papers

Recent·Most cited

GeneticsHuman Molecular GeneticsPeer-reviewedApr 4, 2018

Ift172 conditional knockout mice exhibit rapid retinal degeneration and protein trafficking defects

Priya R Gupta, Nachiket D. Pendse, Scott H. Greenwald…·Kinga M. Bujakowska

This study creates a mouse model of IFT172-associated retinal degeneration and shows that IFT172 depletion causes rapid retinal degeneration and protein trafficking defects.

27 citations

mouseexperimental assay

𝕏 PostBluesky

GeneticsThe CRISPR JournalPeer-reviewedFeb 1, 2018

Allele-specific CRISPR/Cas9 genome editing of the single-base P23H mutation for rhodopsin associated dominant retinitis pigmentosa

Pingjuan Li, Benjamin P. Kleinstiver, Mihoko Leon…·Qin Liu

This study demonstrates allele-specific CRISPR/Cas9 editing of the P23H mutation in Rho-P23H mice, reducing mutant allele expression and delaying photoreceptor degeneration.

116 citationstop 2%

mouseexperimental assay

𝕏 PostBluesky