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International Journal of Geriatric Psychiatry|November 1, 2023
Developing a predictive model for mortality in patients with cognitive impairmentTaiki Sugimoto, Takashi Sakurai, Taiji Noguchi, et al.
Investigative Ophthalmology & Visual Science|April 17, 2025
Application of Metagenomic Long-Read Sequencing for the Diagnosis of Herpetic UveitisYoshito Koyanagi, Ai Fujita Sajiki, Kenya Yuki, et al.
JAR Life|June 23, 2025
Multidomain interventions for preventing cognitive decline in older adults with type 2 diabetes and mild cognitive impairment: Secondary analysis of the J-MINT: Multidomain intervention in type 2 diabetesTaiki Sugimoto, Paul K Crane, Seo-Eun Choi, et al.
Diabetes, Obesity & Metabolism|July 14, 2025
Differential effects of a multidomain intervention on cognitive decline in older adults with type 2 diabetes according to white matter hyperintensity status: A secondary analysis of the J-MIND-DiabetesTaiki Sugimoto, Takuya Omura, Atsushi Araki, et al.
Ophthalmology|July 2, 2019
Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up StudyKoji M Nishiguchi, Yasuhiro Ikeda, Kosuke Fujita, et al.
Plos One|December 21, 2017
Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7Yukihiro Shiga, Koji M Nishiguchi, Yosuke Kawai, et al.
Frontiers in Neuroscience|July 19, 2019
STEFTR: A Hybrid Versatile Method for State Estimation and Feature Extraction From the Trajectory of Animal BehaviorShuhei J Yamazaki, Kazuya Ohara, Kentaro Ito, et al.
JACC. Asia|October 7, 2024
Transcatheter Aortic Valve Implantation in Japanese Patients With Large Annulus: The OCEAN-TAVI RegistryKyohei Onishi, Kazuki Mizutani, Kosuke Fujita, et al.
Communications Biology|January 30, 2021
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosaKoji M Nishiguchi, Fuyuki Miya, Yuka Mori, et al.
Translational Psychiatry|May 28, 2024
Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperatureDaisuke Mori, Chihiro Inami, Ryosuke Ikeda, et al.
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