Tatsushi Toda

发表

Autocorrelation-based method to identify disordered rhythm in Parkinson’s disease tasks: A novel approach applicable to multimodal devices

Kenichiro Sato, Tatsuo Mano, Atsushi Iwata, 2020, PloS one.

Autocorrelation-based method to identify disordered rhythm in Parkinson’s disease tasks: A novel approach applicable to multimodal devices

Kenichiro Sato, Tatsuo Mano, Atsushi Iwata, 2020, bioRxiv.

Quantifying normal and parkinsonian gait features from home movies: Practical application of a deep learning–based 2D pose estimator

Kenichiro Sato, Tatsuo Mano, Atsushi Iwata, 2019, PloS one.

Quantifying normal and parkinsonian gait features from home movies: Practical application of a deep learning–based 2D pose estimator

Atsushi Iwata, Tatsuo Mano, Tatsushi Toda, 2019, bioRxiv.

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Yusuke Nakamura, Takahisa Kawaguchi, Nobutaka Hattori, 2009, Nature Genetics.

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Takeshi Tsuchiya, Thomas Meitinger, Tatsuhiko Tsunoda, 2014, Circulation. Cardiovascular genetics.

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Aldo Quattrone, Nobutaka Hattori, Anthony E. Lang, 2011, Neurobiology of Aging.

Identification of a post‐translational modification with ribitol‐phosphate and its defect in muscular dystrophy: Roles of ISPD, fukutin, and FKRP in α‐dystroglycan glycosylation

Yoshiki Yamaguchi, Michiko Tajiri, Tatsushi Toda, 2016, Cell reports.

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.

Yuko Saito, Mari Yoshida, Fumitoshi Ishino, 2009, American journal of human genetics.

Modeling Alzheimer's disease with iPSCs reveals stress phenotypes associated with intracellular Aβ and differential drug responsiveness.

Katsuhiro Yoshikawa, Takashi Asada, Takashi Aoi, 2013, Cell stem cell.

Novel PINK1 mutations in early‐onset parkinsonism

Nobutaka Hattori, Yoshikuni Mizuno, Hiroyuki Tomiyama, 2004, Annals of neurology.

Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels

Jun Sese, Tatsushi Toda, Kazuya Iwamoto, 2012, PloS one.

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Yusuke Nakamura, Takahisa Kawaguchi, Nobutaka Hattori, 2009, Nature Genetics.

Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms

Ichiro Kanazawa, Tatsushi Toda, Miho Murata, 2002, Annals of neurology.

Disease-associated marked hyperalphalipoproteinemia

Tatsushi Toda, T. Toda, M. Doyu, 2014, Molecular genetics and metabolism reports.

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Shinichi Morishita, Yasuo Terao, Yuko Saito, 2019, Nature Genetics.

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Tatsushi Toda, Satoru Noguchi, Ichizo Nishino, 2003, Human molecular genetics.

Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity

Tatsushi Toda, Yoshitaka Nagai, Yasuo Nagaoka, 2006, Neuroscience Letters.

Protein transduction domain-mediated delivery of QBP1 suppresses polyglutamine-induced neurodegeneration in vivo.

Tatsushi Toda, Yoshitaka Nagai, T. Toda, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population

Nobutaka Hattori, Masahiko Watanabe, Saburo Sakoda, 2007, Neuroreport.

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation

Takashi Fujikado, Tomomitsu Miyoshi, Hajime Sawai, 2008, Nature Neuroscience.

Gait analysis of patients with Parkinson's disease using a portable triaxial accelerometer

Tatsushi Toda, Yasushi Chida, Shin Takano, 2016 .