Tomoko Toyota

Kitakyushu, Japan

Last Updated: 09/26/2026

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Found 17 publications

Combination of CSF α-synuclein seed amplification assay and amyloid-β42 predicts cognitive decline in Parkinson's disease.

Combination of CSF α-synuclein seed amplification assay and amyloid-β42 predicts cognitive decline in Parkinson's disease.

Journal: Neurobiology of disease

Published: March 02, 2026

CSF α-synuclein aggregation is associated with APOE ε4 and progressive cognitive decline in Alzheimer's disease.

CSF α-synuclein aggregation is associated with APOE ε4 and progressive cognitive decline in Alzheimer's disease.

Journal: Neurobiology of aging

Published: October 28, 2024

Complete nanopore repeat sequencing of SCA27B (GAA-FGF14 ataxia) in Japanese.

Complete nanopore repeat sequencing of SCA27B (GAA-FGF14 ataxia) in Japanese.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: February 02, 2024

CSF 14-3-3β is associated with progressive cognitive decline in Alzheimer's disease.

CSF 14-3-3β is associated with progressive cognitive decline in Alzheimer's disease.

Journal: Brain communications

Published: July 12, 2023

CSF 14-3-3 zeta(ζ) isoform is associated with tau pathology and cognitive decline in Alzheimer's disease.

CSF 14-3-3 zeta(ζ) isoform is associated with tau pathology and cognitive decline in Alzheimer's disease.

Journal: Journal of the neurological sciences

Published: May 12, 2023

Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation.

Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation.

Journal: Journal of human genetics

Published: May 08, 2023

CSF GAP-43 as a biomarker of synaptic dysfunction is associated with tau pathology in Alzheimer's disease.

CSF GAP-43 as a biomarker of synaptic dysfunction is associated with tau pathology in Alzheimer's disease.

Journal: Scientific reports

Published: June 07, 2022

Erratum to: Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.

Erratum to: Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.

Journal: Brain : a journal of neurology

Published: May 04, 2021

Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.

Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.

Journal: Brain : a journal of neurology

Published: July 09, 2020

Hippocampal sclerosis without visually detectable hippocampal MRI abnormalities: automated subfield volumetric analysis.

Hippocampal sclerosis without visually detectable hippocampal MRI abnormalities: automated subfield volumetric analysis.

Journal: Japanese journal of radiology

Published: March 03, 2020

Detecting a long insertion variant in SAMD12 by SMRT sequencing: implications of long-read whole-genome sequencing for repeat expansion diseases.

Detecting a long insertion variant in SAMD12 by SMRT sequencing: implications of long-read whole-genome sequencing for repeat expansion diseases.

Journal: Journal of human genetics

Published: September 05, 2018

Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads.

Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads.

Journal: Genome biology

Published: August 14, 2018

Showing 1-12 of 17

Last Updated: 09/26/2026