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T. Toda · SciRah

Researcher profile · Semantic Scholar

T. Toda

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T. Toda — researcher profile on SciRah

h-index: 65
Works: 412
Citations: 18K

Most-cited papers

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
H. Ishiura, S. Shibata, Jun Yoshimura, Yuta Suzuki +46 more
2019Nature Genetics402 citations
Semantic Scholar
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
J. Foo, E. Chew, Sun J. Chung, R. Peng +41 more
2020JAMA Neurology226 citations Open access
Semantic Scholar
Variants in saposin D domain of prosaposin gene linked to Parkinson's disease.
Yutaka Oji, T. Hatano, Shin-ichi Ueno, M. Funayama +28 more
2020Brain : a journal of neurology96 citations Open access
Semantic Scholar
Neurological and related adverse events in immune checkpoint inhibitors: a pharmacovigilance study from the Japanese Adverse Drug Event Report database
Kenichiro Sato, T. Mano, A. Iwata, T. Toda
2019Journal of Neuro-Oncology81 citations
Semantic Scholar
Quantifying normal and parkinsonian gait features from home movies: Practical application of a deep learning–based 2D pose estimator
Kenichiro Sato, Y. Nagashima, T. Mano, A. Iwata +1 more
2019bioRxiv78 citations Open access
Semantic Scholar
Wide distribution of alpha-synuclein oligomers in multiple system atrophy brain detected by proximity ligation
Hiroaki Sekiya, H. Kowa, H. Koga, M. Takata +10 more
2019Acta Neuropathologica76 citations Open access
Semantic Scholar
Facial nerve palsy following the administration of COVID-19 mRNA vaccines: analysis of a self-reporting database
Kenichiro Sato, T. Mano, Yoshiki Niimi, T. Toda +2 more
2021International Journal of Infectious Diseases58 citations Open access
Semantic Scholar
Discrepancy between distribution of alpha-synuclein oligomers and Lewy-related pathology in Parkinson’s disease
Hiroaki Sekiya, Asato Tsuji, Yukiko Hashimoto, M. Takata +8 more
2022Acta Neuropathologica Communications56 citations Open access
Semantic Scholar
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population
Ikuo Otsuka, M. Akiyama, O. Shirakawa, S. Okazaki +12 more
2019Neuropsychopharmacology46 citations Open access
Semantic Scholar
Effect of istradefylline on mood disorders in Parkinson's disease.
H. Nagayama, O. Kano, Hidetomo Murakami, K. Ono +5 more
2019Journal of Neurological Sciences46 citations
Semantic Scholar
Neuropsychiatric adverse events of chloroquine: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS) database.
Kenichiro Sato, T. Mano, A. Iwata, T. Toda
2020BioScience Trends42 citations Open access
Semantic Scholar
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy.
E. Bonora, Sanjiban Chakrabarty, Georgios Kellaris, M. Tsutsumi +63 more
2021Brain : a journal of neurology40 citations Open access
Semantic Scholar
Chronic cerebral hypoperfusion shifts the equilibrium of amyloid β oligomers to aggregation-prone species with higher molecular weight
Taro Bannai, T. Mano, Xi-Gu Chen, G. Ohtomo +9 more
2019Scientific Reports40 citations Open access
Semantic Scholar
Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients
D. Song, Yi Dai, Xiao-Yu Chen, Xiao-Na Fu +17 more
2020Clinical Genetics39 citations
Semantic Scholar
In vivo binding of a tau imaging probe, [11C]PBB3, in patients with progressive supranuclear palsy
H. Endo, H. Shimada, N. Sahara, M. Ono +13 more
2019Movement Disorders36 citations Open access
Semantic Scholar
Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy
N. Kuwabara, Rieko Imae, H. Manya, Tomohiro Tanaka +8 more
2020Nature Communications31 citations Open access
Semantic Scholar
Galectin 3–binding protein suppresses amyloid-β production by modulating β-cleavage of amyloid precursor protein
Tsuneyoshi Seki, M. Kanagawa, Kazuhiro Kobayashi, H. Kowa +5 more
2020Journal of Biological Chemistry31 citations Open access
Semantic Scholar
Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene
Natsuko Nakamura, K. Tsunoda, A. Mitsutake, S. Shibata +7 more
2020Investigative Ophthalmology and Visual Science29 citations Open access
Semantic Scholar
Arginine is a disease modifier for polyQ disease models that stabilizes polyQ protein conformation.
Eiko N. Minakawa, H. Popiel, M. Tada, Toshiaki Takahashi +23 more
2020Brain : a journal of neurology27 citations Open access
Semantic Scholar
Colocalization of BRCA1 with Tau Aggregates in Human Tauopathies
M. Kurihara, T. Mano, Yuko Saito, S. Murayama +2 more
2019Brain Science27 citations Open access
Semantic Scholar
TDP-43 regulates cholesterol biosynthesis by inhibiting sterol regulatory element-binding protein 2
Naohiro Egawa, Y. Izumi, Hidefumi Suzuki, I. Tsuge +16 more
2022Scientific Reports26 citations Open access
Semantic Scholar
Trans‐Ethnic Fine‐Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease
Tatsuhiko Naito, W. Satake, K. Ogawa, Ken Suzuki +5 more
2021Movement Disorders26 citations Open access
Semantic Scholar
Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis
H. Aizawa, H. Kato, K. Oba, Takuya Kawahara +27 more
2021Journal of Neurology23 citations Open access
Semantic Scholar
Clinical efficacy of haematopoietic stem cell transplantation for adult adrenoleukodystrophy
T. Matsukawa, Tomotaka Yamamoto, Akira Honda, T. Toya +44 more
2020Brain Communications23 citations Open access
Semantic Scholar
Aphasic status epilepticus preceding tumefactive left hemisphere lesion in anti-MOG antibody associated disease.
Kazuto Katsuse, M. Kurihara, Yusuke Sugiyama, S. Kodama +8 more
2019Multiple Sclerosis and Related Disorders23 citations Open access
Semantic Scholar
Predicting amyloid risk by machine learning algorithms based on the A4 screen data: Application to the Japanese Trial‐Ready Cohort study
Kenichiro Sato, R. Ihara, Kazushi Suzuki, Yoshiki Niimi +9 more
2021Alzheimer's & Dementia22 citations Open access
Semantic Scholar
Juvenile amyotrophic lateral sclerosis with complex phenotypes associated with novel SYNE1 mutations
H. Naruse, H. Ishiura, J. Mitsui, Yuji Takahashi +3 more
2020Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration20 citations
Semantic Scholar
A Novel de novo KIF1A Mutation in a Patient with Autism, Hyperactivity, Epilepsy, Sensory Disturbance, and Spastic Paraplegia
M. Kurihara, H. Ishiura, Taro Bannai, J. Mitsui +6 more
2019Internal medicine20 citations Open access
Semantic Scholar
Subtype‐Dependent Reporting of Stroke With SGLT2 Inhibitors: Implications From a Japanese Pharmacovigilance Study
Kenichiro Sato, T. Mano, A. Iwata, T. Toda
2019Journal of clinical pharmacology18 citations
Semantic Scholar
Lower Serum Calcium as a Potentially Associated Factor for Conversion of Mild Cognitive Impairment to Early Alzheimer’s Disease in the Japanese Alzheimer’s Disease Neuroimaging Initiative
Kenichiro Sato, T. Mano, R. Ihara, Kazushi Suzuki +11 more
2019Journal of Alzheimer's Disease18 citations
Semantic Scholar
Altered regulation of serum lysosomal acid hydrolase activities in Parkinson's disease: A potential peripheral biomarker?
Yoshiki Niimi, S. Ito, Y. Mizutani, Ken-ichiro Murate +6 more
2019Parkinsonism & Related Disorders17 citations
Semantic Scholar
Transcription Factor c-Maf Promotes Immunoregulation of Programmed Cell Death 1–Expressed CD8+ T Cells in Multiple Sclerosis
S. Koto, N. Chihara, R. Akatani, H. Nakano +4 more
2022Neurology: Neuroimmunology & Neuroinflammation16 citations Open access
Semantic Scholar
Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations
N. Seike, A. Yokoseki, R. Takeuchi, Kento Saito +15 more
2021Movement Disorders16 citations
Semantic Scholar
Neuron-specific analysis of histone modifications with post-mortem brains
Kagari Koshi-Mano, T. Mano, M. Morishima, S. Murayama +4 more
2020Scientific Reports16 citations Open access
Semantic Scholar
CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model
Hideki Tokuoka, Rieko Imae, H. Nakashima, H. Manya +9 more
2022Nature Communications15 citations Open access
Semantic Scholar
Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients
Pei-Chieng Cha, W. Satake, Yuko Ando-Kanagawa, Ken Yamamoto +2 more
2020Journal of Human Genetics15 citations Open access
Semantic Scholar
Characterization of dystroglycan binding in adhesion of human induced pluripotent stem cells to laminin-511 E8 fragment
Yumika Sugawara, K. Hamada, Y. Yamada, Ku-Mai Jun +8 more
2019Scientific Reports15 citations Open access
Semantic Scholar
Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis
H. Naruse, H. Ishiura, J. Mitsui, Yuji Takahashi +11 more
2020Neurogenetics14 citations
Semantic Scholar
The impact of COVID-19 pandemic on the utilization of ambulatory care for patients with chronic neurological diseases in Japan: Evaluation of an administrative claims database.
Kenichiro Sato, T. Mano, Yoshiki Niimi, A. Iwata +2 more
2021BioScience Trends13 citations Open access
Semantic Scholar
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population
H. Naruse, H. Ishiura, J. Mitsui, Yuji Takahashi +7 more
2020Journal of Human Genetics13 citations
Semantic Scholar
Variable Cardiac Responses to Immunosuppressive Therapy in Anti-Mitochondrial Antibody-Positive Myositis.
S. Bujo, E. Amiya, Toshiya Kojima, S. Yamada +8 more
2019Canadian Journal of Cardiology13 citations
Semantic Scholar
Safety of Memantine in Combination with Potentially Interactive Drugs in the Real World: A Pharmacovigilance Study Using the Japanese Adverse Drug Event Report (JADER) Database
Kenichiro Sato, T. Mano, A. Iwata, T. Toda
2021Journal of Alzheimer's Disease12 citations Open access
Semantic Scholar
Isolated seizure as initial presentation of GABAA receptor antibody-associated encephalitis.
M. Kurihara, T. Sasaki, K. Sakuishi, Y. Terao +5 more
2020Journal of Neurological Sciences12 citations
Semantic Scholar
Visualizing modules of coordinated structural brain atrophy during the course of conversion to Alzheimer's disease by applying methodology from gene co-expression analysis
Kenichiro Sato, T. Mano, H. Matsuda, M. Senda +10 more
2019NeuroImage: Clinical12 citations Open access
Semantic Scholar
Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy
Shigefumi Morioka, Hirofumi Sakaguchi, Hiroaki Mohri, M. Taniguchi-Ikeda +6 more
2020PLoS Genetics11 citations Open access
Semantic Scholar
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populations
H. Naruse, T. Matsukawa, H. Ishiura, J. Mitsui +5 more
2019Neurogenetics11 citations
Semantic Scholar
Bardet–Biedl syndrome and related disorders in Japan
M. Hirano, W. Satake, N. Moriyama, Ken Saida +5 more
2020Journal of Human Genetics10 citations
Semantic Scholar
Assessment of the upper limb muscles in patients with Fukuyama muscular dystrophy: Noninvasive assessment using visual ultrasound muscle analysis and shear wave elastography.
Risa Harada, M. Taniguchi-Ikeda, Miwako Nagasaka, Tatsuya Nishii +8 more
2022Neuromuscular Disorders9 citations Open access
Semantic Scholar
Anti-Ku Antibody-Positive Myositis Presenting as a Wide Range of Axial Myopathies and Myocarditis: A Case Report and Review of the Literature.
M. Kono, T. Komai, Hayato Yuki, N. Hanata +6 more
2021Modern Rheumatology Case Reports8 citations
Semantic Scholar
Familial dementia with Lewy bodies with VPS13C mutations.
R. Kobayashi, H. Naruse, Shingo Koyama, S. Kawakatsu +7 more
2020Parkinsonism & Related Disorders8 citations
Semantic Scholar

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