| Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract V Nair, R Sankaranarayanan, AR Vasavada Indian Journal of Ophthalmology 69 (8), 2064-2070, 2021 | 19 | 2021 |
| Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida MER Paul Wolujewicz , Vanessa Aguiar-Pulido, Alice AbdelAleem, Vidya Nair ... Genetics in Medicine, 2021 | 13 | 2021 |
| Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia NG Vidya, S Rajkumar, AR Vasavada Ophthalmic Genetics 39 (3), 344-352, 2018 | 13 | 2018 |
| Trichostatin a restores expression of adherens and tight junction proteins during transforming growth factor β-mediated epithelial-to-mesenchymal transition DA Ganatra, AR Vasavada, NG Vidya, DU Gajjar, S Rajkumar Journal of ophthalmic & vision research 13 (3), 274, 2018 | 11 | 2018 |
| Iron-overload, oxidative DNA damage and differential transcript expression of iron homeostasis genes in human cortical cataracts S Rajkumar, NG Vidya, DA Ganatra, AR Vasavada Int J Ophthalmol Clin Res 5 (3), 091, 2018 | 4 | 2018 |
| Association of FOXE3-p. Ala170Ala and PITX3-p. Ile95Ile polymorphisms with congenital cataract and microphthalmia NG Vidya, D Ganatra, AR Vasavada, S Rajkumar Journal of Ophthalmic & Vision Research 13 (4), 397, 2018 | 3 | 2018 |
| Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population NG Vidya, AR Vasavada, S Rajkumar Journal of Postgraduate Medicine 64 (2), 86-91, 2018 | 3 | 2018 |
| Genetics of Microphthalmia: Global and Indian Perspectives S Rajkumar, VG Nair, AR Vasavada Advances in Vision Research, Volume III: Genetic Eye Research around the …, 2021 | | 2021 |
| A rare association of aniridia with conjunctival xerosis in two Indian siblings with PAX6 mutation NV Gopinathan, S Rajkumar, AR Vasavada Indian Journal of Ophthalmology 68 (11), 2635-2637, 2020 | | 2020 |
| COL6A Mutations in Patients with Congenital Muscular Dystrophy V Nair, M Elsaid, R Al Shami, N ElMudehki, K Mohamed, K Ibrahim, ... QScience Proceedings 2020 (2), 25, 2020 | | 2020 |
| Protective association of A-T-T haplotype of DMT1 gene against risk of human age-related nuclear cataract R Sankaranarayanan, NG Vidya, AR Vasavada Ophthalmic Genetics 40 (2), 99-109, 2019 | | 2019 |
Rajkumar SankaranarayananAGCT Genomics Pvt LtdVerified email at agctgenomics.in
