Author

Rajni Rani

National Institute of ImmunologyORCID 0000-0002-4767-5879Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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

Aayush GuptaiD· 1 shared Archana Kumari SinghiD· 1 shared Arijit MukhopadhyayiD· 1 shared Debasis DashiD· 1 shared Hemanta Kumar KariD· 1 shared Iti GuptaiD· 1 shared Kiran NartaiD· 1 shared Madeeha GhaziiD· 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 paperGenomics

Aayush GuptaORCID

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Author profile →

1 paper

Recent·Most cited

Whole exome-sequencing of vitiligo lesions indicate lower burden of somatic variations: implications in risk for non-melanoma skin cancers

Iti Gupta, Shambhavi Shankrit, Kiran Narta, Madeeha Ghazi, Ritika Grover, Rajesh Pandey, Hemanta Kumar Kar, Shruti M. Menon, Aayush Gupta, Vamsi Krishna Yenamandra, Archana Kumari Singh, Mitali Mukerji, Arijit Mukhopadhyay, Rajni Rani, Rajesh S. Gokhale, , Vivek T. Natarajan

The paper uses whole exome sequencing to show lower somatic mutation burden in vitiligo lesions, linked to reduced non-melanoma skin cancer risk through enhanced DNA repair.

Journal of Investigative Dermatology · Dec 16, 2022Peer-reviewedGenomics