Author

Aziz El-Amraoui

InsermORCID 0000-0003-2692-4984Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:mouse· 2 Assay:CRISPR screen· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Abolfazl RadiD· 1 shared Alireza SedaghatiD· 1 shared Anne De CianiD· 1 shared Barbara VonaiD· 1 shared Ben Fowler· 1 shared Bruno SaubaméaiD· 1 shared Camille Robert· 1 shared Cassidy PetreeiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetics

Abolfazl RadORCID

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2 papers

Recent·Most cited

BioengineeringMolecular Therapy — Nucleic AcidsPeer-reviewedSep 30, 2024

Direct delivery of Cas9 or base editor protein and guide RNA complex enables genome editing in the retina

Juliette Pulman, Catherine Botto, Hugo Malki…·Deniz Dalkara

This study delivers Cas9 or base editor RNP complexes directly to retinal cells, achieving gene editing in photoreceptors and RPE, but with toxicity at high concentrations.

12 citations

mouseCRISPR screen

𝕏 PostBluesky

GeneticsHuman GeneticsPeer-reviewedJan 26, 2021

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

Barbara Vona, Neda Mazaheri, Sheng‐Jia Lin…·Hamid Galehdari

This study identifies biallelic mutations in CLRN2 as a cause of non-syndromic hearing loss through genetic analysis of a consanguineous family and functional validation in zebrafish and mouse models.

29 citations

humanzebrafish

𝕏 PostBluesky