Junji Nishimoto

810 total citations
22 papers, 485 citations indexed

About

Junji Nishimoto is a scholar working on Physiology, Molecular Biology and Surgery. According to data from OpenAlex, Junji Nishimoto has authored 22 papers receiving a total of 485 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Physiology, 9 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Junji Nishimoto's work include Lysosomal Storage Disorders Research (10 papers), Glycogen Storage Diseases and Myoclonus (3 papers) and Musculoskeletal pain and rehabilitation (3 papers). Junji Nishimoto is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Glycogen Storage Diseases and Myoclonus (3 papers) and Musculoskeletal pain and rehabilitation (3 papers). Junji Nishimoto collaborates with scholars based in Japan, United States and Netherlands. Junji Nishimoto's co-authors include Koji Inui, Shintaro Okada, Norio Sakai, Itaru Yanagihara, Hiroko Tsukamoto, Masako Taniike, Toshinori Nishigaki, Keiichi Ozono, N Tatsumi and Hisao Fukushima and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Annals of Neurology.

In The Last Decade

Junji Nishimoto

20 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Junji Nishimoto Japan 10 293 226 105 90 64 22 485
Céline Cluzeau United States 12 250 0.9× 274 1.2× 61 0.6× 57 0.6× 57 0.9× 15 529
Martina Cesani Italy 12 220 0.8× 290 1.3× 52 0.5× 107 1.2× 169 2.6× 12 540
Advait Limaye United States 7 175 0.6× 231 1.0× 69 0.7× 75 0.8× 117 1.8× 10 424
Han Zhi Rao United States 8 251 0.9× 172 0.8× 92 0.9× 90 1.0× 79 1.2× 8 357
S. Treiber-Held Germany 10 187 0.6× 184 0.8× 196 1.9× 26 0.3× 38 0.6× 11 502
Marina Stroppiano Italy 17 634 2.2× 271 1.2× 223 2.1× 210 2.3× 58 0.9× 34 822
Denia Ramirez‐Montealegre United States 13 561 1.9× 285 1.3× 279 2.7× 88 1.0× 62 1.0× 18 707
Aiyin Liao United Kingdom 8 270 0.9× 149 0.7× 119 1.1× 80 0.9× 63 1.0× 14 376
Anton Emelyanov Russia 11 233 0.8× 224 1.0× 114 1.1× 55 0.6× 12 0.2× 39 482
Nima Moaven United States 6 461 1.6× 152 0.7× 301 2.9× 125 1.4× 16 0.3× 8 643

Countries citing papers authored by Junji Nishimoto

Since Specialization
Citations

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

Fields of papers citing papers by Junji Nishimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Junji Nishimoto

This figure shows the co-authorship network connecting the top 25 collaborators of Junji Nishimoto. A scholar is included among the top collaborators of Junji Nishimoto 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 Junji Nishimoto. Junji Nishimoto 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
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Ogihara, Satoshi, Takashi Yamazaki, Hirotaka Chikuda, et al.. (2021). Risk factors for deep surgical site infection after posterior cervical spine surgery in adults: a multicentre observational cohort study. Scientific Reports. 11(1). 7519–7519. 12 indexed citations
5.
Kurotaki, Naohiro, Joseph Shen, Tatsuro Kondoh, et al.. (2005). Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency. Genetics in Medicine. 7(7). 479–483. 33 indexed citations
6.
Itoh, Kohji, Michie Shimmoto, Junji Nishimoto, et al.. (1997). Molecular form and subcellular distribution of acid β-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosis. Brain and Development. 19(2). 126–130. 6 indexed citations
7.
Sakai, Norio, Koji Inui, N Tatsumi, et al.. (1996). Molecular Cloning and Expression of cDNA for Murine Galactocerebrosidase and Mutation Analysis of the Twitcher Mouse, a Model of Krabbe's Disease. Journal of Neurochemistry. 66(3). 1118–1124. 166 indexed citations
8.
Sakai, Norio, Koji Inui, Noriko Fujii, et al.. (1994). Krabbe Disease: Isolation and Characterization of a Full-Length cDNA for Human Galactocerebrosidase. Biochemical and Biophysical Research Communications. 198(2). 485–491. 76 indexed citations
9.
Nishimoto, Junji, et al.. (1994). Effects of double amino-acid substitution polymorphism in acid β-galactosidase gene in two inbred strains of mice. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1217(1). 41–48. 29 indexed citations
10.
Tsukamoto, Hiroko, Koji Inui, Masako Taniike, et al.. (1992). A case of Hallervorden-Spatz disease: Progressive and intractable dystonia controlled by bilateral thalamotomy. Brain and Development. 14(4). 269–272. 29 indexed citations
11.
Taniike, Masako, Harutoshi Fujimura, Shigetoyo Kogaki, et al.. (1992). A case of pigmentary type of orthochromatic leukodystrophy with early onset and globoid cells. Acta Neuropathologica. 83(4). 427–433. 4 indexed citations
12.
Boustany, Rose‐Mary, et al.. (1991). Genetic cause of a juvenile form of tay‐sachs disease in a lebanese child. Annals of Neurology. 29(1). 104–107. 11 indexed citations
13.
Nishimoto, Junji, Eiji Nanba, Koji Inui, Seigo Okada, & Kotaro Suzuki. (1991). GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients.. PubMed. 49(3). 566–74. 52 indexed citations
14.
Nishimoto, Junji, Akemi Tanaka, Eiji Nanba, & Kotaro Suzuki. (1991). Expression of the beta-hexosaminidase alpha subunit gene with the four-base insertion of infantile Jewish Tay-Sachs disease. Journal of Biological Chemistry. 266(22). 14306–14309. 10 indexed citations
15.
Inui, Koji, et al.. (1990). Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease. Journal of the Neurological Sciences. 100(1-2). 124–130. 6 indexed citations
16.
Nishimoto, Junji, et al.. (1990). Corneal arcus as an indicator of hypercholesterolemia.. PubMed. 61(1). 44–9. 8 indexed citations
17.
Fukushima, H., Junji Nishimoto, & Shintaro Okada. (1990). Sequencing and expression of a full‐length cDNA for humanα‐L‐fucosidase. Journal of Inherited Metabolic Disease. 13(5). 761–765. 6 indexed citations
18.
Taniike, Masako, Koji Inui, Yoshio Hirabayashi, et al.. (1989). Immunohistochemical Demonstration of GM2‐Ganglioside in the Central Nervous System of a 19‐week‐old Fetus of Tay‐Sachs Disease. Journal of Inherited Metabolic Disease. 12(S2). 372–374. 1 indexed citations
19.
Nishimoto, Junji, et al.. (1988). A family with pseudodeficiency of acid α‐glucosidase. Clinical Genetics. 33(4). 254–261. 9 indexed citations
20.

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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