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Nobuo FUSE, Tohoku University - Department of Integrative Genomics | Cited by 4,068 | of Tohoku University, Sendai (Tohokudai) | Read 198 publications | Contact Nobuo FUSE
Jan 12, 2023 · Nobuo Fuse (0000-0003-0237-4746) - ORCID. Activities. Collapse all. expand_more. Works (7) sort Sort. Exome sequencing reveals that the CYP1B1 and FOXC1 genes are mainly responsible for childhood glaucoma in Japanese patients. 2023-01-12 | Preprint. DOI: 10.21203/rs.3.rs-2445970/v1.
Miki Atsuya, Fuse Nobuo, Fujimoto Satoko, et al. Prevalence, Associated Factors, and Inter-Eye Differences of Refractive Errors in a Population-Based Japanese Cohort: The Tohoku Medical Megabank Eye Study.
The databases will be shared with the research community as a basis for advancing medical innovation. By collaborating with other research institutes inside and outside of Japan, we would like to investigate how genomic diversity is related to the cause of diseases. Professor. Seizo Koshiba.
Mar 1, 2022 · Ophthalmology Science. Volume 2, Issue 1, March 2022, 100113. Original Article. Genome-wide Association Study of Axial Length in Population-based Cohorts in Japan: The Tohoku Medical Megabank Organization Eye Study. Author links open overlay panel. Nobuo Fuse MD, PhD 1. , Miyuki Sakurai PhD 1. , Ikuko N. Motoike PhD 1. , Kaname Kojima PhD 1. ,
Dec 19, 2021 · Genetic Risk of Cardiovascular Disease Is Associated with Macular Ganglion Cell–Inner Plexiform Layer Thinning in an Early Glaucoma Cohort.
NC measurement is a simple and non-invasive way to assess the risk of DR and its severity and combining the systemic characteristics of age, sex, systolic blood pressure, estimated glomerular filtration rate, hemoglobin A1c level, and history of hypertension and dyslipidemia could indicate the presence of DR and PDR. Expand. 1. PDF. Cite.
