- 2023 - 2026 Investigation of genetic variants and clinical risk factors associated with the progression rate of visual field defect in glaucoma
- 2022 - 2025 The impacts of providing learning environments based on visual function on low-vision children enrolled in regular classes
- 2021 - 2024 Establishing a Risk Prediction Method for Primary Open Angle Glaucoma Using Next Generation Sequencer and Analysis on Non-synonymous Valiant
- 2020 - 2023 Identification and kinetic analysis of glaucoma resistance gene with primary open angle glaucoma
- 2020 - 2023 遺伝解析の統計的検出力を高めるための緑内障臨床情報クラスタリング手法の開発
- 2017 - 2021 Evaluation of genetic factors for deterioration of primary open angle glaucoma
- 2017 - 2020 Identification of variants associated with intraocular pressure lowering efficacy of glaucoma eye drops by genome-wide association study
- 2017 - 2020 Identification of responsible genomic region of Primary Open Angle Glaucoma with International Consortium
- 2014 - 2017 Revealing pathogenesis of Fuchs endothelial corneal dystrophy in Japanese by means of exome array
- 2014 - 2017 Genome wide association study by visual field defect pattern in primary open angle glaucoma
- 2012 - 2015 Candidate gene analysis of well-known genes in primary open-angle glaucoma patients utilizing custom-made gene chip
- 2011 - 2013 Identification of Japanese-specific SNP in exfoliation glaucoma patients with genome-wide association analysis of 1000K microarray
- 2009 - 2011 Evaluation of oxidative stress on trabecular meshwork cells and lens or iris epithelial cells in pseudoexfoliation glaucoma patients
- 2009 - 2011 Investigation of epigenetic factors in the pathogenesis of glucocorticoid-induced glaucoma
- 2006 - 2008 オプチニューリン遺伝子発現調節と緑内障発症における機能的役割の解析
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