Ryuichiro Atarashi

10.3k total citations · 1 hit paper
63 papers, 2.9k citations indexed

About

Ryuichiro Atarashi is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Ryuichiro Atarashi has authored 63 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 24 papers in Neurology and 20 papers in Nutrition and Dietetics. Recurrent topics in Ryuichiro Atarashi's work include Prion Diseases and Protein Misfolding (61 papers), Neurological diseases and metabolism (24 papers) and Trace Elements in Health (20 papers). Ryuichiro Atarashi is often cited by papers focused on Prion Diseases and Protein Misfolding (61 papers), Neurological diseases and metabolism (24 papers) and Trace Elements in Health (20 papers). Ryuichiro Atarashi collaborates with scholars based in Japan, United States and Slovakia. Ryuichiro Atarashi's co-authors include Noriyuki Nishida, Kazunori Sano, Katsuya Satoh, Byron Caughey, Takehiro Nakagaki, Daisuke Ishibashi, Brent Race, Takayuki Fuse, Shigeru Katamine and Kazuto Shigematsu and has published in prestigious journals such as Journal of Biological Chemistry, Nature Medicine and The Journal of Immunology.

In The Last Decade

Ryuichiro Atarashi

61 papers receiving 2.9k citations

Hit Papers

Ultrasensitive human prion detection in cerebrospinal flu... 2011 2026 2016 2021 2011 100 200 300 400

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ryuichiro Atarashi Japan 26 2.5k 1.2k 733 496 436 63 2.9k
Diane Ritchie United Kingdom 27 2.7k 1.1× 1.2k 1.0× 643 0.9× 323 0.7× 303 0.7× 61 3.0k
Noriyuki Nishida Japan 33 3.4k 1.3× 1.6k 1.3× 1.1k 1.5× 588 1.2× 464 1.1× 105 4.1k
Corinne Ida Lasmézas France 33 2.8k 1.1× 1.3k 1.1× 969 1.3× 463 0.9× 307 0.7× 48 3.3k
Jonathan D. F. Wadsworth United Kingdom 36 4.0k 1.6× 2.1k 1.7× 1.3k 1.8× 564 1.1× 563 1.3× 85 4.5k
Richard J. Kascsak United States 29 2.4k 0.9× 1.1k 0.9× 911 1.2× 601 1.2× 159 0.4× 56 2.8k
Regina Kascsak United States 27 2.5k 1.0× 1.1k 0.9× 1.0k 1.4× 351 0.7× 247 0.6× 40 2.8k
Vincent Béringue France 31 3.7k 1.5× 1.7k 1.4× 1.2k 1.6× 357 0.7× 176 0.4× 113 4.0k
Lynne D. Raymond United States 23 1.9k 0.8× 1.0k 0.8× 690 0.9× 475 1.0× 352 0.8× 26 2.3k
Ruth Gabizon Israel 35 4.4k 1.7× 2.3k 1.9× 1.9k 2.7× 479 1.0× 301 0.7× 91 4.8k
Michael Baier Germany 27 1.8k 0.7× 630 0.5× 438 0.6× 441 0.9× 220 0.5× 57 2.5k

Countries citing papers authored by Ryuichiro Atarashi

Since Specialization
Citations

This map shows the geographic impact of Ryuichiro Atarashi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ryuichiro Atarashi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryuichiro Atarashi more than expected).

Fields of papers citing papers by Ryuichiro Atarashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryuichiro Atarashi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ryuichiro Atarashi. The network helps show where Ryuichiro Atarashi may publish in the future.

Co-authorship network of co-authors of Ryuichiro Atarashi

This figure shows the co-authorship network connecting the top 25 collaborators of Ryuichiro Atarashi. A scholar is included among the top collaborators of Ryuichiro Atarashi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ryuichiro Atarashi. Ryuichiro Atarashi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Miyata, Hironori, Junji Chida, Hideyuki Hara, et al.. (2022). Central residues in prion protein PrPC are crucial for its conversion into the pathogenic isoform. Journal of Biological Chemistry. 298(9). 102381–102381. 1 indexed citations
3.
Uchiyama, Keiji, Hideyuki Hara, Junji Chida, et al.. (2021). Ethanolamine Is a New Anti-Prion Compound. International Journal of Molecular Sciences. 22(21). 11742–11742. 6 indexed citations
4.
Fuse, Takayuki, Takehiro Nakagaki, Takujiro Homma, et al.. (2021). Dextran sulphate inhibits an association of prions with plasma membrane at the early phase of infection. Neuroscience Research. 171. 34–40. 2 indexed citations
5.
Matsubara, Takehiro, Katsuya Satoh, Takujiro Homma, et al.. (2020). Prion protein interacts with the metabotropic glutamate receptor 1 and regulates the organization of Ca2+ signaling. Biochemical and Biophysical Research Communications. 525(2). 447–454. 9 indexed citations
6.
Kishimoto, Yasushi, Moritoshi Hirono, Ryuichiro Atarashi, et al.. (2020). Impairment of cerebellar long-term depression and GABAergic transmission in prion protein deficient mice ectopically expressing PrPLP/Dpl. Scientific Reports. 10(1). 15900–15900. 4 indexed citations
7.
Fuchigami, Takeshi, Takehiro Nakagaki, Kazunori Sano, et al.. (2019). Development of Radioiodinated Benzofuran Derivatives for in Vivo Imaging of Prion Deposits in the Brain. ACS Infectious Diseases. 5(12). 2003–2013. 6 indexed citations
8.
Agbemabiese, Chantal Ama, Toyoko Nakagomi, Sher Bahadur Pun, et al.. (2019). Whole genome characterisation of G11P[25] and G9P[19] rotavirus A strains from adult patients with diarrhoea in Nepal. Infection Genetics and Evolution. 69. 246–254. 7 indexed citations
9.
Satoh, Katsuya, Ryuichiro Atarashi, & Noriyuki Nishida. (2017). Real-Time Quaking-Induced Conversion for Diagnosis of Prion Disease. Methods in molecular biology. 1658. 305–310. 10 indexed citations
10.
Mori, Tsuyoshi, Ryuichiro Atarashi, Katsuya Satoh, et al.. (2016). A direct assessment of human prion adhered to steel wire using real-time quaking-induced conversion. Scientific Reports. 6(1). 24993–24993. 22 indexed citations
11.
Sano, Kazunori, Ryuichiro Atarashi, & Noriyuki Nishida. (2015). Structural conservation of prion strain specificities in recombinant prion protein fibrils in real-time quaking-induced conversion. Prion. 9(4). 237–243. 9 indexed citations
12.
Homma, Takujiro, Daisuke Ishibashi, Takehiro Nakagaki, et al.. (2015). Ubiquitin-specific protease 14 modulates degradation of cellular prion protein. Scientific Reports. 5(1). 11028–11028. 44 indexed citations
13.
Sanjo, Nobuo, Makoto Tomita, Ryuichiro Atarashi, et al.. (2014). Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. BMJ Open. 4(5). e004968–e004968. 37 indexed citations
14.
Homma, Takujiro, Daisuke Ishibashi, Takehiro Nakagaki, et al.. (2014). Persistent prion infection disturbs the function of Oct-1, resulting in the down-regulation of murine interferon regulatory factor-3. Scientific Reports. 4(1). 6006–6006. 5 indexed citations
15.
Nakagaki, Takehiro, Katsuya Satoh, Daisuke Ishibashi, et al.. (2013). FK506 reduces abnormal prion protein through the activation of autolysosomal degradation and prolongs survival in prion-infected mice. Autophagy. 9(9). 1386–1394. 78 indexed citations
16.
Sano, Kazunori, Katsuya Satoh, Ryuichiro Atarashi, et al.. (2013). Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay. PLoS ONE. 8(1). e54915–e54915. 103 indexed citations
17.
Atarashi, Ryuichiro, Kazunori Sano, Katsuya Satoh, & Noriyuki Nishida. (2011). Real-time quaking-induced conversion. Prion. 5(3). 150–153. 123 indexed citations
18.
Matsui, Yuki, Katsuya Satoh, Toshiaki Miyazaki, et al.. (2011). High sensitivity of an ELISA kit for detection of the gamma-isoform of 14-3-3 proteins: usefulness in laboratory diagnosis of human prion disease. BMC Neurology. 11(1). 120–120. 33 indexed citations
19.
Atarashi, Ryuichiro, Noriyuki Nishida, Kazuto Shigematsu, et al.. (2003). Deletion of N-terminal Residues 23–88 from Prion Protein (PrP) Abrogates the Potential to Rescue PrP-deficient Mice from PrP-like Protein/Doppel-induced Neurodegeneration. Journal of Biological Chemistry. 278(31). 28944–28949. 40 indexed citations
20.
Sakaguchi, Suehiro, Kazuto Shigematsu, Ryuichiro Atarashi, et al.. (2000). Physiological Expression of the Gene for PrP-Like Protein, PrPLP/Dpl, by Brain Endothelial Cells and its Ectopic Expression in Neurons of PrP-Deficient Mice Ataxic Due to Purkinje Cell Degeneration. American Journal Of Pathology. 157(5). 1447–1452. 75 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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