Author

Benyam Kinde

Massachusetts Eye and Ear InfirmaryORCID 0000-0003-0867-1282Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Caitlin Finn· 1 shared Dana Schlegel· 1 shared Daniel Navarro-Gomez· 1 shared Emily PlaceiD· 1 shared Eric A. PierceiD· 1 shared Erin ZampaglioneiD· 1 shared Farzad JamshidiiD· 1 shared J. Alex Mazzone· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Caitlin Finn

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1 paper

Recent·Most cited

GenomicsGenetics in MedicinePeer-reviewedFeb 9, 2020

Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations

Erin Zampaglione, Benyam Kinde, Emily Place…·Kinga M. Bujakowska

The paper identifies copy-number variations (CNVs) as a significant contributor to unsolved inherited retinal degeneration (IRD) cases, increasing the genetic diagnostic rate through NGS-based CNV detection.

110 citationstop 3%

humanwhole-exome sequencing

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