Ryuki Hirano

911 total citations
12 papers, 673 citations indexed

About

Ryuki Hirano is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Immunology. According to data from OpenAlex, Ryuki Hirano has authored 12 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Immunology. Recurrent topics in Ryuki Hirano's work include Mitochondrial Function and Pathology (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Cancer therapeutics and mechanisms (2 papers). Ryuki Hirano is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Cancer therapeutics and mechanisms (2 papers). Ryuki Hirano collaborates with scholars based in Japan, Canada and Saudi Arabia. Ryuki Hirano's co-authors include Ikuko Kondo, Laila Begum, Jeffrey R. Lee, Lap‐Chee Tsui, David S. Sinasac, Keiko Kobayashi, Andrew P. Boright, Michael A. Crackower, Stephen W. Scherer and Sayaka Ikeda and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and The EMBO Journal.

In The Last Decade

Ryuki Hirano

12 papers receiving 664 citations

Peers

Ryuki Hirano

PPCH

SURGE

CMN

Bassam Abu‐Libdeh Israel

Hideo Sasai Japan

Giulia Polo Italy

Marjolein Turkenburg Netherlands

R. Gatti Italy

L. J. M. Spaapen Netherlands

Lorne E. Seargeant Canada

Christine Hendrickson United States

Célia Nogueira Portugal

Boris Gebhardt Germany

Bassam Abu‐Libdeh Israel

Ryuki Hirano

403 ×1.0

112 ×0.4

25 ×0.2

PPCH

61 ×0.6

SURGE

50 ×0.6

CMN

Citations per year, relative to Ryuki Hirano Ryuki Hirano (= 1×) peers Bassam Abu‐Libdeh

Countries citing papers authored by Ryuki Hirano

Since Specialization

Citations

This map shows the geographic impact of Ryuki Hirano'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 Ryuki Hirano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryuki Hirano more than expected).

Fields of papers citing papers by Ryuki Hirano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryuki Hirano. 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 Ryuki Hirano. The network helps show where Ryuki Hirano may publish in the future.

Co-authorship network of co-authors of Ryuki Hirano

This figure shows the co-authorship network connecting the top 25 collaborators of Ryuki Hirano. A scholar is included among the top collaborators of Ryuki Hirano 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 Ryuki Hirano. Ryuki Hirano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Walton, Cheryl, Heidrun Interthal, Ryuki Hirano, et al.. (2010). Spinocerebellar Ataxia with Axonal Neuropathy. Advances in experimental medicine and biology. 685. 75–83. 7 indexed citations

Hirano, Ryuki, Hiroshi Takashima, Yuji Okamoto, et al.. (2009). Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan. Journal of Human Genetics. 54(7). 377–381. 14 indexed citations

Hayashi, Daisuke, Ryuji Kubota, Norihiro Takenouchi, et al.. (2008). Reduced Foxp3 expression with increased cytomegalovirus-specific CTL in HTLV-I-associated myelopathy. Journal of Neuroimmunology. 200(1-2). 115–124. 16 indexed citations

Deguchi, Kimiko, Leah I. Elizondo, Ryuki Hirano, et al.. (2008). Neurologic Phenotype of Schimke Immuno-Osseous Dysplasia and Neurodevelopmental Expression of SMARCAL1. Journal of Neuropathology & Experimental Neurology. 67(6). 565–577. 22 indexed citations

Kajiya, Takashi, et al.. (2008). Pyogenic Liver Abscess Related to Dental Disease in an Immunocompetent Host. Internal Medicine. 47(7). 675–678. 31 indexed citations

Hirano, Ryuki, Heidrun Interthal, Cheng Huang, et al.. (2007). Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?. The EMBO Journal. 26(22). 4732–4743. 116 indexed citations

Okamoto, Yuji, Hiroshi Takashima, Itsuro Higuchi, et al.. (2006). Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene. Neurogenetics. 7(3). 175–183. 24 indexed citations

Takashima, Hiroshi, Ryuki Hirano, Hiroyuki Tomimitsu, et al.. (2006). Early clinical signs and imaging findings in Gerstmann–Straussler–Scheinker syndrome (Pro102Leu). Neurology. 66(11). 1672–1678. 50 indexed citations

Hirano, Ryuki, Hiroshi Takashima, Yuji Okamoto, et al.. (2004). Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families. Neurogenetics. 5(4). 215–221. 12 indexed citations

10.

Hirano, Ryuki, Hiroshi Takashima, Fujio Umehara, et al.. (2004). SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma. Neurology. 63(3). 577–580. 33 indexed citations

11.

Kobayashi, Keiko, David S. Sinasac, Mikio Iijima, et al.. (1999). The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Nature Genetics. 22(2). 159–163. 326 indexed citations

12.

Kitajima, Isao, Naohiro Hanyu, Yasuko Soejima, et al.. (1997). Efficient Transfer of Synthetic Ribozymes into Cells Using Hemagglutinating Virus of Japan (HVJ)-Cationic Liposomes. Journal of Biological Chemistry. 272(43). 27099–27106. 22 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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