His primary scientific interests are in Genetics, Muscular dystrophy, Fukutin, Congenital muscular dystrophy and Mutation. As part of his studies on Genetics, he frequently links adjacent subjects like Parkinsonism. His biological study spans a wide range of topics, including Laminin and Dystroglycan.
His Fukutin research is multidisciplinary, incorporating elements of Fukuyama congenital muscular dystrophy and Exon. The concepts of his Congenital muscular dystrophy study are interwoven with issues in Fukutin-related protein and Anatomy. His Genome-wide association study study integrates concerns from other disciplines, such as MEDLINE, LRRK2, Locus, Genetic heterogeneity and Genetic variation.
Tatsushi Toda spends much of his time researching Genetics, Pathology, Muscular dystrophy, Fukutin and Congenital muscular dystrophy. His work in Gene, Locus, Haplotype, Allele and Mutation is related to Genetics. His Pathology research focuses on Internal medicine and how it connects with Cardiology.
His research integrates issues of Molecular biology and Fukutin-related protein in his study of Muscular dystrophy. As part of the same scientific family, he usually focuses on Fukutin, concentrating on Cell biology and intersecting with Neurodegeneration. His Congenital muscular dystrophy research includes elements of Laminin and Endocrinology.
The scientist’s investigation covers issues in Pathology, Genetics, Internal medicine, Gene and Disease. His Pathology research includes themes of Muscular dystrophy, Epilepsy and Skeletal muscle. He interconnects Transferase, Protein domain, Glycan, Protein structure and Fukutin-related protein in the investigation of issues within Muscular dystrophy.
His study connects Amyotrophic lateral sclerosis and Genetics. The concepts of his Internal medicine study are interwoven with issues in Oncology and Cardiology. His Disease study deals with Cohort intersecting with Cohort study.
Tatsushi Toda mainly focuses on Pathology, Disease, Gene, Neurodegeneration and Genetics. His studies deal with areas such as Neocortex, Proximity ligation assay, Purkinje cell and Ligation as well as Pathology. He focuses mostly in the field of Disease, narrowing it down to matters related to Cohort and, in some cases, Genetic heterogeneity, Genotype, Confounding, Vitamin D and neurology and Alzheimer's Disease Neuroimaging Initiative.
His studies in Genetic heterogeneity integrate themes in fields like Odds ratio and Genome-wide association study. His study in Gene is interdisciplinary in nature, drawing from both Hierarchical clustering, Pathological, Neuroscience and Temporal lobe. His Genetics research incorporates themes from Amyotrophic lateral sclerosis, Case-control study and Age of onset.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz.
The New England Journal of Medicine (2009)
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Wataru Satake;Yuko Nakabayashi;Yuko Nakabayashi;Ikuko Mizuta;Ikuko Mizuta;Yushi Hirota;Yushi Hirota.
Nature Genetics (2009)
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
Kazuhiro Kobayashi;Yutaka Nakahori;Masashi Miyake;Kiichiro Matsumura.
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
Aruto Yoshida;Kazuhiro Kobayashi;Hiroshi Manya;Kiyomi Taniguchi.
Developmental Cell (2001)
Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness
Takayuki Kondo;Masashi Asai;Masashi Asai;Kayoko Tsukita;Yumiko Kutoku.
Cell Stem Cell (2013)
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.
Christina M. Lill;Johannes T. Roehr;Johannes T. Roehr;Matthew B. McQueen;Fotini K. Kavvoura;Fotini K. Kavvoura;Fotini K. Kavvoura.
PLOS Genetics (2012)
Interleukin 6 signaling promotes anti-aquaporin 4 autoantibody production from plasmablasts in neuromyelitis optica
Norio Chihara;Toshimasa Aranami;Wakiro Sato;Yusei Miyazaki.
Proceedings of the National Academy of Sciences of the United States of America (2011)
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease
Kenya Nishioka;Shin Hayashi;Matthew J. Farrer;Andrew B. Singleton.
Annals of Neurology (2006)
A toxic monomeric conformer of the polyglutamine protein.
Yoshitaka Nagai;Takashi Inui;Takashi Inui;Takashi Inui;H Akiko Popiel;Nobuhiro Fujikake.
Nature Structural & Molecular Biology (2007)
Novel PINK1 mutations in early-onset parkinsonism.
Yasuko Hatano;Yuanzhe Li;Kenichi Sato;Shuichi Asakawa.
Annals of Neurology (2004)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: