Author

Mainak Bardhan

Howard Hughes Medical InstituteORCID 0000-0002-4106-409XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:database / resource· 1 Organism:human· 1 Assay:protein structure· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Atchayaram NaliniiD· 1 shared Danny ReinbergiD· 1 shared Gary LeRoyiD· 1 shared Joseph M. SchulziD· 1 shared Moulinath AcharyaiD· 1 shared Robert C. ReynoldsiD· 1 shared Shamita SangaiD· 1 shared Stephan C. SchüreriD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 16 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Atchayaram NaliniORCID

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2 papers

Recent·Most cited

E3 Ligase Ligandalyzer: A Structure-First, Ligand-Centric Platform for E3 Ligase Recruiter Selection

Joseph M. Schulz, Mainak Bardhan, Robert C. Reynolds, Gary LeRoy, Danny Reinberg, Stephan C. Schürer

E3 Ligase Ligandalyzer provides a platform for exploring E3 ligase-recruiter complexes, enabling analysis of chemical and structural data to support degrader design.

bioRxiv · Oct 14, 2026 · PreprintBioinformatics

Identification of a shared, common haplotype cosegregating with an SGCB c.544A>C mutation in Indian patients affected with sarcoglycanopathy

Shamita Sanga, Sudipta Chakraborty, Mainak Bardhan, Atchayaram Nalini, Moulinath Acharya

The paper identifies a shared haplotype cosegregating with a c.544A>C mutation in SGCB in Indian sarcoglycanopathy patients, suggesting a founder effect and potential genetic marker for risk stratification.

medRxiv · Dec 3, 2021 · PreprintGenetic & Genomic Medicine