| Detection of pregnancy and fertility status in big cats using an enzyme immunoassay based on 5α-pregnan-3α-ol-20-one G Umapathy, V Kumar, M Kabra, S Shivaji General and Comparative Endocrinology 180, 33-38, 2013 | 55 | 2013 |
| Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma M Kabra, W Zhang, S Rathi, AK Mandal, S Senthil, G Pyatla, M Ramappa, ... Human genetics 136 (8), 941-949, 2017 | 46 | 2017 |
| Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathy M Kabra, PK Shahi, Y Wang, D Sinha, A Spillane, GA Newby, S Saxena, ... The Journal of Clinical Investigation 133 (19), 2023 | 34 | 2023 |
| Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil MB de Melo, AK Mandal, IM Tavares, MH Ali, M Kabra, ... PLoS One 10 (5), e0127147, 2015 | 27 | 2015 |
| Sensing through non-sensing ocular ion channels M Kabra, BR Pattnaik International Journal of Molecular Sciences 21 (18), 6925, 2020 | 20 | 2020 |
| Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure C Labelle-Dumais, G Pyatla, S Paylakhi, NG Tolman, S Hameed, ... Disease models & mechanisms 13 (5), dmm042853, 2020 | 20 | 2020 |
| Kir7.1 disease mutant T153I within the inner pore affects K+ conduction KM Beverley, PK Shahi, M Kabra, Q Zhao, J Heyrman, J Steffen, ... American Journal of Physiology-Cell Physiology 323 (1), C56-C68, 2022 | 16 | 2022 |
| Comprehensive analysis of CRISPR base editing outcomes for multimeric protein M Kabra, M Moosajee, GA Newby, K Molugu, K Saha, DR Liu, ... bioRxiv, 2022.06. 20.496792, 2022 | 3 | 2022 |
| Preventing vision loss in a mouse model of Leber Congenital Amaurosis by engineered tRNA E Akyuz, PK Shahi, L Gissot, A Al Saneh, D Sinha, GM Hanstad, M Kabra, ... bioRxiv, 2025 | 2 | 2025 |
| Peters anomaly in Nail-Patella syndrome: a case report and clinico-genetic correlation M Ramappa, U Gandhi, S Chaurasia, M Kabra, I Kaur, R Mittal, DK Mishra, ... Cornea 40 (11), 1487-1490, 2021 | 2 | 2021 |
| Genetic interactions of crystallins with known primary congenital glaucoma genes S Chakrabarti, M Kabra, G Pyatla, S Rathi, AK Mandal, S Senthil, I Kaur, ... Investigative Ophthalmology & Visual Science 59 (9), 5148-5148, 2018 | 2 | 2018 |
| The transcription factors PBX1 and GATA1 are regulated by the mutation profiles of CYP1B1 in primary congenital glaucoma S Chakrabarti, M Kabra, AK Mandal, S Senthil, I Kaur Investigative Ophthalmology & Visual Science 57 (12), 803-803, 2016 | 2 | 2016 |
| Transplacental Transfer of Oxytocin and Its Impact on Neonatal Cord Blood and In Vitro Retinal Cell Activity CO Adegboro, W Luo, M Kabra, RM McAdams, NW York, RI Wijenayake, ... Cells 13 (20), 1735, 2024 | 1 | 2024 |
| Strategies for Readthrough of Premature Termination Codons to Restore Ion Channel Function S Fulbright, M Kabra, PK Shahi, A Spillane, C Ahern, BR Pattnaik Investigative Ophthalmology & Visual Science 64 (8), 414-414, 2023 | 1 | 2023 |
| Nonviral base editing of KCNJ13 mutation preserves vision in an inherited retinal channelopathy M Kabra, PK Shahi, Y Wang, D Sinha, A Spillane, GA Newby, S Saxena, ... bioRxiv, 2022.07. 12.499808, 2022 | 1 | 2022 |
| CRISPR base editing as a potential therapeutic approach for Kir7. 1 channelopathy M Kabra, PK Shahi, A Spillane, Y Wang, D Sinha, GA Newby, S Saxena, ... Investigative Ophthalmology & Visual Science 62 (8), 1483-1483, 2021 | 1 | 2021 |
| Complex Molecular Mechanisms Underlie Primary Congenital Glaucoma Due to the Involvement of Multiple Biochemical Pathways S Chakrabarti, G Pyatla, W Zhang, R Dixit, LM Leon, AK Mandal, S Senthil, ... Investigative Ophthalmology & Visual Science 61 (7), 3516-3516, 2020 | 1 | 2020 |
| Runs of homozygosity across the whole genome suggests two novel genes in primary congenital glaucoma S Chakrabarti, S Ganguly, M Kabra, A Mandal, S Senthil, I Kaur, ... Investigative Ophthalmology & Visual Science 54 (15), 4499-4499, 2013 | 1 | 2013 |
| Precision therapeutic tRNA rescue of nonsense mutation R166X in KCNJ13 to restore K+ channel function A Spillane, E Akyuz, M Kabra, D Sinha, C Soref, L Gissot, A Al Saneh, ... The Journal of Precision Medicine: Health and Disease 4, 100019, 2025 | | 2025 |
| WT1-MMP9 regulatory axis and its modulation by TNF-α in early and late onset glaucoma phenotypes T Ahmed, J Sarma, M Kabra, SS Roy, S Bera, AK Mishra, D Roy, S Bagchi, ... | | 2025 |
