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| Inherited retinal diseases: linking genes, disease-causing variants, and relevant therapeutic modalities N Schneider, Y Sundaresan, P Gopalakrishnan, A Beryozkin, M Hanany, ... Progress in retinal and eye research 89, 101029, 2022 | 78 | 2022 |
| Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily T Millo, A Rivera, A Obolensky, D Marks-Ohana, M Xu, Y Li, E Wilhelm, ... Genetics in Medicine 24 (7), 1523-1535, 2022 | 7 | 2022 |
| The fission yeast MAPK Spc1 senses perturbations in Cdc25 and Wee1 activities and targets Rad24 to restore this balance M Paul, A Ghosal, S Bandyopadhyay, U Selvam, N Rai, G Sundaram Yeast 35 (3), 261-271, 2018 | 7 | 2018 |
| Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature … A Beryozkin, A Samanta, P Gopalakrishnan, S Khateb, E Banin, D Sharon, ... International journal of molecular sciences 23 (7), 3541, 2022 | 6 | 2022 |
| Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p. Arg523∗ Human Nonsense Pathogenic Variant C Matsevich, P Gopalakrishnan, A Obolensky, E Banin, D Sharon, ... Ophthalmology Science 3 (1), 100229, 2023 | 5 | 2023 |
| MTHFR and MTHFD1 gene polymorphisms are not associated with pseudoexfoliation syndrome in South Indian population P Gopalakrishnan, A Haripriya, P Sundaresan International Ophthalmology 38, 599-606, 2018 | 3 | 2018 |
| Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa C Matsevich, P Gopalakrishnan, N Chang, A Obolensky, A Beryozkin, ... Molecular Therapy 31 (10), 2948-2961, 2023 | 2 | 2023 |
| Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice A Abu-Diab, P Gopalakrishnan, C Matsevich, M de Jong, A Obolensky, ... Translational Vision Science & Technology 12 (3), 3-3, 2023 | 2 | 2023 |
| Morphological and Functional Comparison of Mice Models for Retinitis Pigmentosa P Gopalakrishnan, A Beryozkin, E Banin, D Sharon Retinal Degenerative Diseases XIX: Mechanisms and Experimental Therapy, 365-370, 2023 | 1 | 2023 |
| Relatively Slow Retinal Degeneration Process in a Fam161a Knock-in (KI) Mouse Model for the Human Nonsense Mutation p. Arg 523 P Gopalakrishnan, C Matsevich, E Banin, D Sharon, A Beryozkin, ... Investigative Ophthalmology & Visual Science 63 (7), 2588–F0471-2588–F0471, 2022 | | 2022 |
| Genetics of Exfoliation Syndrome in Asians P Gopalakrishnan, A Haripriya, B Ratukondla, P Sundaresan Advances in Vision Research, Volume II: Genetic Eye Research in Asia and the …, 2019 | | 2019 |
| Decoding of tyrosinase leads to albinism in a nonidentical twin RK Raj, P Gopalakrishnan, V Perumalsamy, P Sundaresan Journal of Clinical Neonatology 7 (1), 59-62, 2018 | | 2018 |
| Molecular analyses of various risk factors involved in pseudoexfoliation syndrome G Prakadeeswari Madurai, 0 | | |
