Author

Arindam Chatterjee

University of CalcuttaORCID 0000-0001-8977-1669Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bidyut RoyiD· 1 shared Biswabandhu BankuraiD· 1 shared Debprasad ChattopadhyayiD· 1 shared Dhansagar U Wakle· 1 shared Dilip Kumar PaliD· 1 shared Kunal SarkariD· 1 shared Madhusudan DasiD· 1 shared Santanu ChakrabortyiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Bidyut RoyORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineFrontiers in Molecular BiosciencesPeer-reviewedDec 22, 2022

Whole Exome Sequencing (WES) identifies Homozygous mutation in g.37429732G>A in GRHPR gene is responsible for early onset of nephrolithiasis in the population of West Bengal, India

Arindam Chatterjee, Kunal Sarkar, Sarbashri Bank…·Madhusudan Das

7 citations

humanwhole-exome sequencing

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