Gaurav K. Varshney

ORCID: 0000-0002-0429-1904

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 21 papers. Top paper: “Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder”.

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.015

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0.312DataRank · unranked

7 citations

Cailyn P Leo, Chenghong Deng, Sheng‐Jia Lin, Reza Maroofian, Reneé C. Lin +95 more

MultiFRAGing: Rapid and Simultaneous Genotyping of Multiple Alleles in a Single Reaction

Scientific Reports(2020)10.1038/s41598-020-59986-1

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0DataRank · unranked

6 citations

Gaurav K. Varshney, Cassidy Petree

Expression patterns of activating transcription factor 5 (atf5a and atf5b) in zebrafish

Gene Expression Patterns(2020)10.1016/j.gep.2020.119126

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0DataRank · unranked

3 citations

Viveca Vélez-Negrón, Aranza Torrado-Tapias, Gaurav K. Varshney, Martine Behra, Roberto Rodríguez‐Morales

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

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.29.222828

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0DataRank · unranked

3 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +19 more

High-throughput generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.04.325621

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0DataRank · unranked

0 citations

Khriezhanuo Nakhro, Chang-Kyu Oh, Blake Carrington, Hayne Song, Gaurav K. Varshney +15 more

Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes

DNA repair(2021)10.1016/j.dnarep.2021.103173

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0DataRank · unranked

31 citations

Khriezhanuo Nakhro, Chang‐Kyu Oh, Blake Carrington, HeaIn Song, Gaurav K. Varshney +14 more

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Human Genetics(2021)10.1007/s00439-020-02254-z

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0DataRank · unranked

28 citations

Neda Mazaheri, Sheng‐Jia Lin, Lucy A Dunbar, Reza Maroofian, Héla Azaiez +21 more

Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors

Frontiers in Molecular Neuroscience(2021)10.3389/fnmol.2021.624265

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0DataRank · unranked

4 citations

Roberto Rodríguez‐Morales, Alexis Santana-Cruz, Juan A. Cantres-Velez, Aranza Torrado-Tapias, Sheng‐Jia Lin +8 more

Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

Human Mutation(2022)10.1002/humu.24435

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0DataRank · unranked

29 citations

Barbara Vona, Hillary M. Porter, Mahmoud Izadi, Kevin Huang, Yves Lacassie +20 more

Chondroitin/dermatan sulfate glycosyltransferase genes are essential for craniofacial development

PLoS Genetics(2022)10.1371/journal.pgen.1010067

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0DataRank · unranked

6 citations

Gaurav K. Varshney, Laura Waldmann, Daniel Snitting, Amin Allalou, Hanqing Zhang +7 more

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain(2023)10.1093/brain/awad380

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0DataRank · unranked

19 citations

Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin +84 more

ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish

Nature Communications(2024)10.1038/s41467-024-49943-1

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0DataRank · unranked

29 citations

Fang Ting Liang, Sheng‐Jia Lin, Cassidy Petree, Kevin Huang, Yu Zhang +6 more

Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy

Nature Communications(2024)10.1038/s41467-024-51310-z

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0DataRank · unranked

5 citations

Vincent Francis, Sheng‐Jia Lin, Fares Kharfallah, Vladimir S. Fonov, Maxime Lévesque +80 more

Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.002

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0DataRank · unranked

2 citations

Sheng‐Jia Lin, Reza Maroofian, Alper Gezdirici, Hamoud Alhebby, Aurélien Trimouille +30 more

Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a syndromic neurodevelopmental disorder

medRxiv(2024)10.1101/2024.07.18.24310581

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0DataRank · unranked

1 citations

Cailyn P Leo, Chenghong Deng, Kejia Zhang, Sheng‐Jia Lin, Reza Maroofian +75 more

Naa80 is required for actin N-terminal acetylation and normal hearing in zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.17.585386

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0DataRank · unranked

0 citations

Sheng‐Jia Lin, Lars Ole Sti Dahl, Kevin Huang, Cassidy Petree, Gaurav K. Varshney +2 more

Optimizing gRNA selection for high-penetrance F0 CRISPR screening for interrogating disease gene function

Nucleic Acids Research(2025)10.1093/nar/gkaf180

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0DataRank · unranked

11 citations

Kevin Huang, Cassidy Petree, Wei Qin, Pratishtha Varshney, Gaurav K. Varshney +1 more

CRISPR-based functional genomics tools in vertebrate models

Experimental & Molecular Medicine(2025)10.1038/s12276-025-01514-0

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0DataRank · unranked

9 citations

Shawn M. Burgess, Gaurav K. Varshney

Rationally Designed TadA‐Derived Cytosine Editors Enable Context‐Independent Zebrafish Genome Editing

Advanced Science(2025)10.1002/advs.202509800

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0DataRank · unranked

3 citations

Sheng‐Jia Lin, Yu Zhang, Kevin Huang, Cassidy Petree, Kevin Boyd +3 more

Building the vertebrate codex using the gene breaking protein trap library

eLife(2020)10.7554/elife.54572

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0DataRank · unranked

16 citations

MaKayla R. Serres, Rhianna Urban, Mark D. Urban, Anthony J. Treichel, Kyle Schaefbauer +26 more

Uncovering dual molecular diagnoses in families with complex phenotypes through structural and clinical studies of novel COL4A6 variants

QJM(2025)10.1093/qjmed/hcaf246

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0DataRank · unranked

2 citations

Abolfazl Rad, Constantin Cretu, Sheng‐Jia Lin, Hafiz Saad Bin Mustafa, Kevin Huang +8 more