| Genotype‐phenotype correlation of KATP channel gene defects causing permanent neonatal diabetes in Indian patients S Gopi, B Kavitha, S Kanthimathi, A Kannan, R Kumar, R Joshi, ... Pediatric Diabetes 22 (1), 82-92, 2021 | 16 | 2021 |
| Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children K Balamurugan, B Kavitha, Z Yang, V Mohan, V Radha, SL Shyng Pediatric diabetes 20 (4), 397-407, 2019 | 16 | 2019 |
| Successful transition to sulphonylurea therapy from insulin in a child with permanent neonatal diabetes due to a KCNJ11 gene mutation V Radha, B Ramya, S Gopi, B Kavitha, S Preetika, K Thai, R Unnikrishnan, ... Journal of Diabetology 9 (2), 65-67, 2018 | 9 | 2018 |
| Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins N DeForest, B Kavitha, S Hu, R Isaac, L Krohn, M Wang, X Du, ... Cell Genomics 3 (7), 2023 | 7 | 2023 |
| A novel stop-loss mutation in NKX2-2 gene as a cause of neonatal diabetes mellitus: molecular characterization and structural analysis B Kavitha, K Srikanth, D Singh, S Gopi, V Mohan, N Chandra, V Radha Acta Diabetologica 61 (2), 189-194, 2024 | 4 | 2024 |
| Molecular characterization and re-interpretation of HNF1A variants identified in Indian MODY subjects towards precision medicine B Kavitha, S Ranganathan, S Gopi, U Vetrivel, N Hemavathy, V Mohan, ... Frontiers in Endocrinology 14, 1177268, 2023 | 1 | 2023 |
| Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of multiple cardiovascular disease risk factors N DeForest, B Kavitha, S Hu, R Isaac, M Wang, X Du, ... medRxiv, 2022.03. 29.22273133, 2022 | | 2022 |
Amit R. MajithiaAssociate Professor of Medicine, UC San Diego School of MedicineVerified email at ucsd.edu