Ryuji Kaji

2.0k total citations
52 papers, 1.4k citations indexed

About

Ryuji Kaji is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ryuji Kaji has authored 52 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Ryuji Kaji's work include Neurological diseases and metabolism (7 papers), Hereditary Neurological Disorders (7 papers) and Genetic Neurodegenerative Diseases (5 papers). Ryuji Kaji is often cited by papers focused on Neurological diseases and metabolism (7 papers), Hereditary Neurological Disorders (7 papers) and Genetic Neurodegenerative Diseases (5 papers). Ryuji Kaji collaborates with scholars based in Japan, Italy and United States. Ryuji Kaji's co-authors include Hiroyuki Nodera, Masataka Nishimura, Jun Kimura, Hugh Bostock, Edward C. Cooper, G. Glassmeier, Jürgen R. Schwarz, Takahiro Mezaki, Nobuyuki Oka and Takeshi Nishio and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Neurology.

In The Last Decade

Ryuji Kaji

46 papers receiving 1.4k citations

Peers

Countries citing papers authored by Ryuji Kaji

Since Specialization

Citations

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

Fields of papers citing papers by Ryuji Kaji

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryuji Kaji

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Pathological and bacteriological investigations of Pasteurella multocida-induced epididymitis in calves 2025 ·Veterinary Microbiology ·(unknown), Akira Terao, Yuichi Ueno, (unknown), (unknown), Ryuji Kaji, (unknown), (unknown), (unknown), (unknown), Shogo Tanaka, Kumiko KIMURA	0
2	Peripheral nerve excitability abnormalities in Neuronal Intranuclear Inclusion Disease: Assessment with histopathological analysis 2024 ·Clinical Neurophysiology ·Yusuke Osaki, Hiroyuki Nodera, (unknown), (unknown), Koji Fujita, Ryosuke Miyamoto, (unknown), Hiroki Yamazaki, Hiroyuki Morino, Takashi Kanda, Shigeo Murayama, Ryuji Kaji, Yuishin Izumi	0
3	A look at the future—new BoNTs and delivery systems in development: What it could mean in the clinic 2023 ·Toxicon ·Ryuji Kaji	5
4	PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability 2019 ·Neuromuscular Disorders ·Toshitaka Kawarai, Hiroki Yamazaki, Ryosuke Miyamoto, Naoko Takamatsu, Atsuko Mori, Yusuke Osaki, Antonio Orlacchio, Hiroyuki Nodera, Akihiro Hashiguchi, Yujiro Higuchi, Akiko Yoshimura, Hiroshi Takashima, Ryuji Kaji	5
5	Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability 2017 ·Parkinsonism & Related Disorders ·Masaki Kamada, Toshitaka Kawarai, Ryosuke Miyamoto, (unknown), (unknown), (unknown), (unknown), Carlo Caltagirone, Antonio Orlacchio, Ryuji Kaji	8
6	A homozygous mutation ofVWA3Bcauses cerebellar ataxia with intellectual disability 2015 ·Journal of Neurology Neurosurgery & Psychiatry ·Toshitaka Kawarai, Atsushi Tajima, Yukiko Kuroda, Naoki Saji, Antonio Orlacchio, (unknown), Hirotaka Shimizu, Yasushi Kita, Yuishin Izumi, Takao Mitsui, Issei Imoto, Ryuji Kaji	14
7	Development of a highly sensitive immunohistochemical method to detect neurochemical molecules in formalin-fixed and paraffin-embedded tissues from autopsied human brains 2015 ·Frontiers in Neuroanatomy ·Satoshi Goto, Ryoma Morigaki, Shinya Okita, Shinji Nagahiro, Ryuji Kaji	21
8	Exome sequencing identifies a novel intronic mutation in ENG that causes recurrence of pulmonary arteriovenous malformations 2015 ·Journal of the Neurological Sciences ·Naoki Saji, Toshitaka Kawarai, Ryosuke Miyamoto, (unknown), Hiroyuki Morino, Antonio Orlacchio, Ryosuke Oki, Kazumi Kimura, Ryuji Kaji	2
9	Cyclin-dependent kinase 5 with phosphorylation of tyrosine 15 residue is enriched in striatal matrix compartment in adult mice 2011 ·Neuroscience ·Ryoma Morigaki, Wataru Sako, Shinya Okita, Jiro Kasahara, Hironori Yokoyama, S. Nagahiro, Ryuji Kaji, Satoshi Goto	9
10	Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy 2011 ·Nature ·Mariko Taniguchi‐Ikeda, Kazuhiro Kobayashi, Motoi Kanagawa, Chih‐Chieh Yu, (unknown), Tetsuya Oda, Atsushi Kuga, Hiroki Kurahashi, Hasan O. Akman, Salvatore DiMauro, Ryuji Kaji, Toshifumi Yokota, Shin’ichi Takeda, Tatsushi Toda	132
11	Effects of a Brain-Engraftable Microglial Cell Line Expressing Anti-Prion scFv Antibodies on Survival Times of Mice Infected with Scrapie Prions 2011 ·Cellular and Molecular Neurobiology ·Koji Fujita, Yoshitaka Yamaguchi, Tsuyoshi Mori, (unknown), (unknown), Masashi Yano, Hironori Miyata, Akira Ootsuyama, Makoto Sawada, Haruo Matsuda, Ryuji Kaji, Suehiro Sakaguchi	18
12	Nucling interacts with nuclear factor‐κB, regulating its cellular distribution 2009 ·FEBS Journal ·Li Liu, Takashi Sakai, (unknown), (unknown), Ryuji Kaji, Kiyoshi Fukui	11
13	Neurological deterioration in small vessel disease may be associated with increase of infarct volume 2008 ·Journal of the Neurological Sciences ·Yuka Terasawa, Yasuyuki Iguchi, Kazumi Kimura, Kazuto Kobayashi, Junya Aoki, Noriko Matsumoto, Kensaku Shibazaki, Takeshi Inoue, Ryuji Kaji	45
14	Reduced Neuron-Specific Expression of the TAF1 Gene Is Associated with X-Linked Dystonia-Parkinsonism 2007 ·The American Journal of Human Genetics ·Satoshi Makino, Ryuji Kaji, Satoshi Ando, M. Tomizawa, Katsuhito Yasuno, Satoshi Goto, (unknown), (unknown), (unknown), (unknown), Lillian V. Lee, Kazumasa Ogasawara, Ikuo Tooyama, Hiroyasu Akatsu, Masataka Nishimura, Gen Tamiya	173
15	KCNQ channels mediate I_Ks, a slow K⁺ current regulating excitability in the rat node of Ranvier 2006 ·The Journal of Physiology ·Jürgen R. Schwarz, G. Glassmeier, Edward C. Cooper, (unknown), Hiroyuki Nodera, (unknown), Ryuji Kaji, Hugh Bostock	183
16	Glutathione‐S‐transferase‐1 and interleukin‐1β gene polymorphisms in Japanese patients with Parkinson's disease 2005 ·Movement Disorders ·Masataka Nishimura, Sadako Kuno, Ryuji Kaji, Katsuhito Yasuno, Hideshi Kawakami	30
17	Influence of polymorphisms in the genes for cytokines and glutathione S-transferase omega on sporadic Alzheimer’s disease 2004 ·Neuroscience Letters ·Masataka Nishimura, (unknown), Ryuji Kaji, Hideshi Kawakami	47
18	Nucling Recruits Apaf-1/Pro-caspase-9 Complex for the Induction of Stress-induced Apoptosis 2004 ·Journal of Biological Chemistry ·Takashi Sakai, Li Liu, (unknown), (unknown), Hidenori Shimada, Ryuji Kaji, Tasuku Mitani, Mitsuru Matsumoto, Kazunori Toida, Kazunori Ishimura, Yuji Shishido, Tak W. Mak, Kiyoshi Fukui	47
19	[Treatment of spasticity with botulinum toxin and muscle afferent block]. 1996 ·PubMed ·Ryuji Kaji, Takahiro Mezaki, Tamotsu Kubori, Nagako Murase, Junko Kimura	1
20	A Novel Point Mutation in the Mitochondrial tRNASer(UCN) Gene Detected in a Family with MERRF/MELAS Overlap Syndrome 1995 ·Biochemical and Biophysical Research Communications ·Masaichi Nakamura, S Nakano, Yu‐ichi Goto, (unknown), Yasuhiro Nagahama, Hidenao Fukuyama, (unknown), Ryuji Kaji, Jun Kimura	84

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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