Biography and Research Interest

Publications

Non-Zebrafish Publications

Chakraborty, S., Mitra, S., Ghosh, A., Kumar, K., Sanga, S., Dutta, A.K., Mukherjee, S., Biswas, N.K., Chakrabarti, S. and Acharya, M., 2025. Whole exome sequencing reveals novel and rare variants in non-syndromic hearing loss-related genes: A focus on GPSM2 compound heterozygosity. Journal of Biosciences, 50(2), p.35.

Sanga, S., Chakraborty, S*., Bardhan, M., Polavarapu, K., Kumar, V.P., Bhattacharya, C., Nashi, S., Vengalil, S., Geetha, T.S., Ramprasad, V. and Nalini, A., 2023. Identification of a shared, common haplotype segregating with an SGCB c. 544 T> G mutation in Indian patients affected with sarcoglycanopathy. Scientific Reports, 13(1), p.15095.

Chakraborty, S., Das, C., Kaur, R., Das, P., Biswas, N. and Acharya, M., 2022. A genome wide copy number variation analysis reveals NLGN1 is overrepresented in primary angle closure glaucoma patients. Investigative Ophthalmology & Visual Science, 63(7), pp.4394-A0437.

Chakraborty, S., Sharma, A., Pal, S., Sharma, A., Sihota, R., Bhattacharjee, S. and Acharya, M., 2023. A quantitative trait GWAS on lens thickness identifies novel risk loci on PTPRM in the narrow angle individuals susceptible to PACG. European Journal of Ophthalmology, 33(5), pp.1922-1930.

Chakraborty, S., Sharma, A., Bagchi, I., Pal, S., Bhattacharyya, C., Gupta, V., Maitra, A., Bhattacharjee, S., Sharma, A., Sihota, R. and Acharya, M., 2021. A genomewide association study on individuals with occludable angles identifies potential risk loci for intraocular pressure. Journal of genetics, 100(2), p.69.

Chakraborty, S., Sharma, A., Sharma, A., Sihota, R., Bhattacharjee, S. and Acharya, M., 2021. Haplotype-based genomic analysis reveals novel association of CNTNAP5 genic region with primary angle closure glaucoma. J Biosci, 46(1), pp.1-9.

Chakraborty, S. and Acharya, M., 2017. A “Crispr” Overview of Genome Editing: Potentials and Challenges. Science and Culture.