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Parkinsonism & Related Disorders|July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2026
Longitudinal Dynamics of Polyglutamine-Expanded ATXN3 in Biofluids of Spinocerebellar Ataxia Type 3Jordan Bartfield, Lukasz Milanowski, Karen R Jansen-West, et al.Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.Communications Biology|September 24, 2020
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosisRyoichi Nakamura, Kazuharu Misawa, Genki Tohnai, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 4, 2023
Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patientsRyoichi Nakamura, Genki Tohnai, Masahiro Nakatochi, et al.Neuroradiology|July 22, 2024
Conventional magnetic resonance imaging key features for distinguishing pathologically confirmed corticobasal degeneration from its mimics: a retrospective analysis of the J-VAC studyKeita Sakurai, Aya M Tokumaru, Mari Yoshida, et al.Communications Biology|December 5, 2025
A genome-wide association study identifies the GPM6A locus associated with age at onset in ALSRyoichi Nakamura, Genki Tohnai, Naoki Atsuta, et al.Brain Communications|December 13, 2023
Clinical course of pathologically confirmed corticobasal degeneration and corticobasal syndromeIkuko Aiba, Yuichi Hayashi, Takayoshi Shimohata, et al.Pageof 7