Author

Vinay More

Regional Centre for Biotechnology

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Research Focus:imputation· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Analabha BasuiD· 2 shared Punit PrasadiD· 2 shared Sunil K. RaghaviD· 2 shared Abdul JaleeliD· 1 shared Ankit Mukherjee· 1 shared Arghya Dey· 1 shared Arindam MaitraiD· 1 shared Arun KumariD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Analabha BasuORCID

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2 papers

Recent·Most cited

An Atlas of Indian Genetic Diversity

Krithika Subramanian, Chandrika Bhattacharyya, Pratheusa Machha, Ankit Mukherjee, Devashish Tripathi, Shreya Chakraborty, Sauma Suvra Majumdar, Shouvanik Sengupta, Priyanka Singh, Vinay More, Shreya Bari, Sreelekshmi MS, Eric Macwan, Debasrija Mondal, Arghya Dey, , Analabha Basu

The paper presents a comprehensive genomic atlas of Indian populations, identifying novel variants and highlighting genetic diversity and pharmacogenomic implications.

medRxiv · Mar 24, 2026 · PreprintGenetic & Genomic Medicine

Fine-scale genetic structure and population-specific clinically relevant variants in the indigenous tribal populations of India

Sudeshna Datta, Deepak Jena, Arup Ghosh, Viplov Kumar Biswas, Sudarshana Jena, Mamuni Swain, Vinay More, Soumendu Mahapatra, Rasmita Mishra, Bhawna Gupta, Analabha Basu, Punit Prasad, Sunil K. Raghav

The paper analyzes whole-exome sequencing data from 13 tribal groups in Odisha, India, identifying genetic structure, rare variants, and clinically relevant pathogenic variants.

medRxiv · Jan 13, 2026 · PreprintGenetic & Genomic Medicine