Sonika Rathi

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Publications (13)

• CTx001 for Geographic Atrophy: A Gene Therapy Expressing Soluble, Truncated Complement Receptor 1 (Mini-CR1)
  Ophthalmology Science 2026 DOI: 10.1016/j.xops.2025.100980
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• Multimodal Imaging of the Corneal Endothelial Transition Zone Reveals Progenitor Cell Population.
  Cells 2025 DOI: 10.3390/cells14231851
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• Potential Involvements of Cilia-Centrosomal Genes in Primary Congenital Glaucoma.
  International journal of molecular sciences 2024 DOI: 10.3390/ijms251810028
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• A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.
  Cell 2024 DOI: 10.1016/j.cell.2023.12.006
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• Therapeutic targeting of the complement system in ocular disease.
  Drug discovery today 2023 DOI: 10.1016/j.drudis.2023.103757
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• Molecular Genetics and Functional Analysis Implicate CDKN2BAS1-CDKN2B Involvement in POAG Pathogenesis.
  Cells 2020 DOI: 10.3390/cells9091934
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• Dual SMAD inhibition and Wnt inhibition enable efficient and reproducible differentiations of induced pluripotent stem cells into retinal ganglion cells.
  Scientific reports 2020 DOI: 10.1038/s41598-020-68811-8
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• SNP located in an AluJb repeat downstream of TMCO1, rs4657473, is protective for POAG in African Americans.
  The British journal of ophthalmology 2019 DOI: 10.1136/bjophthalmol-2018-313086
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• Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes.
  Clinical epigenetics 2019 DOI: 10.1186/s13148-019-0608-2
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• Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity.
  Frontiers in immunology 2017 DOI: 10.3389/fimmu.2017.01868
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