A biallelic variant in CLRN2 causes non-syndromic hearing loss in humansBarbara Vona, Hamid Galehdari, Abolfazl Rad et al.|Human Genetics|2021Cited by 28
Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneitySheng‐Jia Lin, Gaurav K. Varshney, Barbara Vona et al.|Genome Medicine|2023Cited by 14
MultiFRAGing: Rapid and Simultaneous Genotyping of Multiple Alleles in a Single ReactionCassidy Petree, Gaurav K. Varshney|Scientific Reports|2020Cited by 6
Rationally Designed TadA‐Derived Cytosine Editors Enable Context‐Independent Zebrafish Genome EditingWei Qin, Gaurav K. Varshney|Advanced Science|2025Cited by 2