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

Click to filter author papers

Genetics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Eric A. PierceORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

Priya R Gupta, Nachiket D. Pendse, Scott H. Greenwald, Mihoko Leon, Qin Liu, Eric A. Pierce, 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.

Human Molecular Genetics · Apr 4, 2018Peer-reviewedGenetics

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, Michelle S. Prew, Daniel Navarro-Gomez, Scott H. Greenwald, Eric A. Pierce, J. Keith Joung, 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.

The CRISPR Journal · Feb 1, 2018Peer-reviewedGenetics