D-Index & Metrics Best Publications

Osamu Onodera

Niigata University
Japan

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 Citations Publications World Ranking National Ranking

Biology and Biochemistry D-index 69 Citations 14,754 362 World Ranking 4737 National Ranking 315

Overview

What is he best known for?

The fields of study Osamu Onodera is best known for:

Gene
Alzheimer's disease
Parkinson's disease

His Allele research is covered under the topics of Trinucleotide repeat expansion and Haplotype. The study of Trinucleotide repeat expansion is intertwined with the study of Gene in a number of ways. Osamu Onodera undertakes multidisciplinary investigations into Gene and Penetrance in his work. He carries out multidisciplinary research, doing studies in Haplotype and Allele. His Phenotype study is within the categories of Penetrance and Clinical phenotype. Clinical phenotype is closely attributed to Phenotype in his study. Osamu Onodera connects Genetics with Molecular biology in his study. His work blends Molecular biology and Genetics studies together. His study on Disease is mostly dedicated to connecting different topics, such as Dementia.

His most cited work include:

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) (1059 citations)
Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy (180 citations)
-Synuclein gene alterations in dementia with Lewy bodies (154 citations)

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

Frameshift mutation and Missense mutation are the areas that his Mutation study falls under. Osamu Onodera performs multidisciplinary studies into Missense mutation and Mutation in his work. Osamu Onodera performs multidisciplinary study in Internal medicine and Endocrinology in his work. He combines Endocrinology and Internal medicine in his research. He performs integrative Gene and Phenotype research in his work. He integrates many fields in his works, including Phenotype and Gene. Osamu Onodera performs multidisciplinary study in Genetics and Frameshift mutation in his work. His research ties Spinocerebellar ataxia and Disease together. His study in Disease extends to Spinocerebellar ataxia with its themes.

Osamu Onodera most often published in these fields:

Internal medicine (50.00%)
Gene (47.06%)
Genetics (44.12%)

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

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

R. Koide;T. Ikeuchi;O. Onodera;H. Tanaka.
Nature Genetics (1994)

1362 Citations

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease

Shoji Tsuji;Osamu Onodera.
The New England Journal of Medicine (2010)

487 Citations

Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription.

Takayoshi Shimohata;Toshihiro Nakajima;Mitsunori Yamada;Chiharu Uchida.
Nature Genetics (2000)

485 Citations

TDP-43 mutation in familial amyotrophic lateral sclerosis

Akio Yokoseki;Atsushi Shiga;Chun-Feng Tan;Asako Tagawa.
Annals of Neurology (2008)

444 Citations

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

Hidetoshi Date;Osamu Onodera;Hajime Tanaka;Kiyoshi Iwabuchi.
Nature Genetics (2001)

413 Citations

Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration

Jun Mitsui;Takashi Matsukawa;Hiroyuki Ishiura;Yoko Fukuda;Yoko Fukuda.
The New England Journal of Medicine (2013)

361 Citations

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

Chun-Feng Tan;Hiroto Eguchi;Asako Tagawa;Osamu Onodera.
Acta Neuropathologica (2007)

334 Citations

Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Naoki Hattori;Masahiko Yamamoto;Tsuyoshi Yoshihara;Haruki Koike.
Brain (2003)

271 Citations

Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic.

Toshiaki Takahashi;Shinya Kikuchi;Shinichi Katada;Yoshitaka Nagai.
Human Molecular Genetics (2008)

257 Citations

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.

Kaoru Okuizumi;Osamu Onodera;Yoshio Namba;Kazuhiko Ikeda.
Nature Genetics (1995)

229 Citations

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Frequent Co-Authors

External Links

Personal Website for Osamu Onodera