| Haplotype-based genomic analysis reveals novel association of CNTNAP5 genic region with primary angle closure glaucoma Sudipta Chakraborty, Anshul Sharma, Arundhati Sharma, Ramanjit Sihota ... Journal of Biosciences 46 ((2021) 15), 2021 | 6 | 2021 |
| A genomewide association study on individuals with occludable angles identifies potential risk loci for intraocular pressure Sudipta Chakraborty, Anshul Sharma, Indranil Bagchi, Soumen Pal, Chandrika ... Journal of Genetics 100 (69 (2021)), 2021 | 3 | 2021 |
| A quantitative trait GWAS on lens thickness identifies novel risk loci on PTPRM in the narrow angle individuals susceptible to PACG S Chakraborty, A Sharma, S Pal, A Sharma, R Sihota, S Bhattacharjee, ... European Journal of Ophthalmology 33 (5), 1922-1930, 2023 | 1 | 2023 |
| Post-GWAS functional analyses of CNTNAP5 suggests its role in glaucomatous neurodegeneration S Chakraborty, J Sarma, SS Roy, S Mitra, S Bagchi, S Das, S Saha, ... bioRxiv, 2024.03. 14.583830, 2024 | | 2024 |
| Identifcation of a shared, common haplotype segregating with an SGCB c.544T>G mutation in Indian patients afected with sarcoglycanopathy Sanga S, Chakraborty S, Bardhan M, Polavarapu K, Kumar VP, Bhattacharya C ... Scientific Reports 13 (1), 15095, 2023 | | 2023 |
| Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy S Sanga, S Chakraborty, M Bardhan, K Polavarapu, VP Kumar, ... Scientific Reports 13 (1), 15095, 2023 | | 2023 |
| A whole-exome analysis of non-syndromic hearing loss patients from India reveals a wide spectrum of known and novel mutations S Chakraborty, S Mitra, A Ghosh, K Kumar, S Sanga, AK Dutta, ... | | 2023 |
| An integeative GWAS followed by functional investigation reveals possible involvement of CNTNAP5 in glaucomatous neurodegeneration Chakraborty Sudipta, Saha Roy Shantanu , Sarma Jyotishman , Das Sankhadip ... J Neurochem 166 (doi.org/10.1111/jnc.15896), 30, 2023 | | 2023 |
| P142: Whole-exome analyses of non-syndromic hearing loss patients from India reveal a wide spectrum of known and novel mutations S Chakraborty, S Mitra, S Sanga, A Ghosh, S Mukherjee, N Biswas, ... Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| Investigating the Genetic Architecture of Human Disease using Genome Wide Association Studies: Benefits and Challenges S Chakraborty, M Acharya ISBN: 978-81-959389-7-1; The Registrar (officiating), West Bengal State …, 2023 | | 2023 |
| A genome wide copy number variation analysis reveals NLGN1 is overrepresented in primary angle closure glaucoma patients S Chakraborty, C Das, R Kaur, P Das, N Biswas, M Acharya Investigative Ophthalmology & Visual Science 63 (7), 4394–A0437-4394–A0437, 2022 | | 2022 |
| eP327: A quantitative trait GWAS on lens thickness identifies risk loci on PTPRM in the narrow-angle individuals anatomically susceptible to PACG, Genetics in Medicine, Sudipta Chakraborty, Samsiddhi Bhattacharjee, Moulinath Acharya Genetics in Medicine 24 (3), S204-S205, 2022 | | 2022 |
| Peeping into Breast Cancer in the Human Epigenome and Analysis of the Treatment Associated Degradation of Cognitive Functions A Samanta, S Chakraborty, R Roy Recent Development of Chemical Research being Implemented in Biology and …, 2022 | | 2022 |
| Identification of a shared, common haplotype cosegregating with an SGCB c.544A>C mutation in Indian patients affected with sarcoglycanopathy S Sanga, S Chakraborty, M Bardhan, A Nalini, M Acharya medRxiv, 2021.12. 03.21266857, 2021 | | 2021 |
| A “CRISPR” OVERVIEW OF GENOME EDITING: POTENTIALS AND CHALLENGES S CHAKRABORTY, M ACHARYA SCIENCE AND CULTURE, 2017 | | 2017 |
Moulinath AcharyaNational Institute of Biomedical Genomics, IndiaVerified email at nibmg.ac.in
