Author

Pratishtha Varshney

Oklahoma Medical Research FoundationORCID 0000-0002-2619-7775Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:zebrafish· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Cassidy PetreeiD· 2 shared Gaurav K. VarshneyiD· 2 shared Sheng‐Jia LiniD· 2 shared Abolfazl RadiD· 1 shared Alireza SedaghatiD· 1 shared Aziz El-AmraouiiD· 1 shared Barbara VonaiD· 1 shared Ben Fowler· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Cassidy PetreeORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJan 28, 2025

TadA-Derived Cytosine Base Editor for Precise Genome Editing in Zebrafish

Wei Qin, Sheng‐Jia Lin, Cassidy Petree…·Gaurav K. Varshney

The paper introduces zTadCBE, a TadA-derived cytosine base editor for precise genome editing in zebrafish, showing high efficiency, reduced off-target effects, and expanded targeting range.

DOI 10.1101/2025.01.28.635338

zebrafishwhole-genome sequencing

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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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