Author

Sudipta Chakraborty

National Institute of Biomedical GenomicsORCID 0000-0003-2277-9759Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Moulinath AcharyaiD· 2 shared Atchayaram NaliniiD· 1 shared Jyotishman Sarma· 1 shared Mahua MaulikiD· 1 shared Mainak BardhaniD· 1 shared Samsiddhi BhattacharjeeiD· 1 shared Sankhadip DasiD· 1 shared Sayani Bagchi· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Moulinath AcharyaORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintMar 14, 2024

Post-GWAS functional analyses of CNTNAP5 suggests its role in glaucomatous neurodegeneration

Sudipta Chakraborty, Jyotishman Sarma, Shantanu Saha Roy…·Moulinath Acharya

This study identifies CNTNAP5 as a candidate gene for glaucomatous neurodegeneration through zebrafish knockdown experiments showing retinal degeneration and behavioral changes.

5 citations

zebrafishexperimental assay

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Genetic & Genomic MedicinemedRxivPreprintDec 3, 2021

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…·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.

1 citation

humanwhole-exome sequencing

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