Author

Sandrine Vitry

InsermORCID 0000-0003-4693-7694Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Abolfazl RadiD· 1 shared Alireza SedaghatiD· 1 shared Aziz El-AmraouiiD· 1 shared Barbara VonaiD· 1 shared Ben Fowler· 1 shared Cassidy PetreeiD· 1 shared Christian BeetziD· 1 shared David P. MurphyiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Abolfazl RadORCID

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1 paper

Recent·Most cited

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

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