Author

Amrita Mukhopadhyay

Banaras Hindu UniversityORCID 0009-0005-9158-1633Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Amrita Mukhopadhyay1 paper · Banaras Hindu University

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:whole-exome sequencing· 3 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:variant effect prediction· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:simulation· 1

Frequent Co-Authors

Bhagyalaxmi MohapatraiD· 3 shared Dharmendra JainiD· 2 shared Anurag T. K. BaidyaiD· 1 shared Ashok KumariD· 1 shared Ashok KumariD· 1 shared Bharti DeviiD· 1 shared Manohar Lal YadaviD· 1 shared Prerna GiriiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

9 top collaborators · 18 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Bhagyalaxmi MohapatraORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 4, 2025

Whole exome sequencing reveals UNC45B as a novel candidate gene functionally associated with Dilated Cardiomyopathy

Amrita Mukhopadhyay, Dharmendra Jain, Ashok Kumar, Bhagyalaxmi Mohapatra

The paper identifies UNC45B variants in DCM patients and shows they cause structural and functional defects leading to cardiac dysfunction.

DOI 10.64898/2025.11.28.25340252

humanwhole-exome sequencing

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GeneticsbioRxivPreprintOct 21, 2025

Identification and functional characterization of LDB3 gene variants in DCM patients from Indian Population

Bhagyalaxmi Mohapatra, Amrita Mukhopadhyay, Prerna Giri…·Ashok Kumar

This study identifies and functionally characterizes LDB3 gene variants in Indian DCM patients, finding six novel missense variants that affect protein structure, expression, and Z-disc integrity.

DOI 10.1101/2025.10.21.683814

humanDNA methylation

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BioinformaticsbioRxivPreprintNov 10, 2024

Implication of TITIN Variations in Dilated Cardiomyopathy: Integrating Whole Exome Sequencing With Molecular Dynamics Simulation Study

Amrita Mukhopadhyay, Bharti Devi, Anurag T. K. Baidya…·Bhagyalaxmi Mohapatra

The paper identifies TITIN variants in DCM patients and uses molecular dynamics to show how these variants affect protein structure and function.

2 citations

humanwhole-exome sequencing

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