D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 69 Citations 19,205 354 World Ranking 1617 National Ranking 64

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Mutation

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.

His most cited work include:

  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease (1232 citations)
  • Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease (1026 citations)
  • Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease (1026 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (32.05%)
  • Pathology (21.82%)
  • Muscular dystrophy (21.36%)

What were the highlights of his more recent work (between 2018-2021)?

  • Pathology (21.82%)
  • Genetics (32.05%)
  • Internal medicine (14.77%)

In recent papers he was focusing on the following fields of study:

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.

Between 2018 and 2021, his most popular works were:

  • Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease. (78 citations)
  • Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study (36 citations)
  • Neurological and related adverse events in immune checkpoint inhibitors: a pharmacovigilance study from the Japanese Adverse Drug Event Report database. (30 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Mutation

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.

Best Publications

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)

1845 Citations

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)

1403 Citations

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

Kazuhiro Kobayashi;Yutaka Nakahori;Masashi Miyake;Kiichiro Matsumura.
Nature (1998)

903 Citations

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.

Aruto Yoshida;Kazuhiro Kobayashi;Hiroshi Manya;Kiyomi Taniguchi.
Developmental Cell (2001)

810 Citations

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)

764 Citations

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)

560 Citations

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)

393 Citations

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)

372 Citations

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)

362 Citations

Novel PINK1 mutations in early-onset parkinsonism.

Yasuko Hatano;Yuanzhe Li;Kenichi Sato;Shuichi Asakawa.
Annals of Neurology (2004)

361 Citations

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