Yuzo Tanabe

1.8k total citations
40 papers, 1.3k citations indexed

About

Yuzo Tanabe is a scholar working on Molecular Biology, Clinical Biochemistry and Infectious Diseases. According to data from OpenAlex, Yuzo Tanabe has authored 40 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 7 papers in Infectious Diseases. Recurrent topics in Yuzo Tanabe's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (8 papers) and Muscle Physiology and Disorders (6 papers). Yuzo Tanabe is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (8 papers) and Muscle Physiology and Disorders (6 papers). Yuzo Tanabe collaborates with scholars based in Japan, United States and United Kingdom. Yuzo Tanabe's co-authors include Junko Arii, Ken Inoue, James R. Lupski, Ikuya Nonaka, Jun‐ichi Takanashi, Yoichi Kohno, Yu‐ichi Goto, Yasuo Akanuma, Ryoichi Sakuta and Yoshio Yazaki and has published in prestigious journals such as New England Journal of Medicine, Annals of Neurology and The Journal of Pediatrics.

In The Last Decade

Yuzo Tanabe

37 papers receiving 1.3k citations

Peers

Yuzo Tanabe
Yong Seung Hwang South Korea
Yuzo Tanabe
Citations per year, relative to Yuzo Tanabe Yuzo Tanabe (= 1×) peers Yong Seung Hwang

Countries citing papers authored by Yuzo Tanabe

Since Specialization
Citations

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

Fields of papers citing papers by Yuzo Tanabe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuzo Tanabe

This figure shows the co-authorship network connecting the top 25 collaborators of Yuzo Tanabe. A scholar is included among the top collaborators of Yuzo Tanabe 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 Yuzo Tanabe. Yuzo Tanabe 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.
Arai, Hidee, Makiko Hayashi, Kiyoshi Hayasaka, Takashi Kanda, & Yuzo Tanabe. (2013). The first Japanese case of Charcot–Marie–Tooth disease type 4H with a novel FGD4 c.837-1G>A mutation. Neuromuscular Disorders. 23(8). 652–655. 4 indexed citations
2.
Fujii, Katsunori, et al.. (2012). 14-3-3 Proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in children. Brain and Development. 35(6). 555–560. 2 indexed citations
3.
Fujii, Katsunori, Narihiro Minami, Yukiko Hayashi, et al.. (2009). Homozygous female Becker muscular dystrophy. American Journal of Medical Genetics Part A. 149A(5). 1052–1055. 26 indexed citations
4.
Itoh, Masayuki, Sachio Takashima, Shinichi Kudo, et al.. (2007). Methyl CpG-Binding Protein 2 (a Mutation of Which Causes Rett Syndrome) Directly Regulates Insulin-Like Growth Factor Binding Protein 3 in Mouse and Human Brains. Journal of Neuropathology & Experimental Neurology. 66(2). 117–123. 68 indexed citations
5.
Kuwabara, Satoshi, Sonoko Misawa, Katsunori Fujii, et al.. (2006). Electrophysiological subtypes and prognosis of childhood Guillain–Barré syndrome in Japan. Muscle & Nerve. 33(6). 766–770. 54 indexed citations
6.
Fujii, Katsunori, et al.. (2005). Detection of 14-3-3 protein in the cerebrospinal fluid in mitochondrial encephalopathy with lactic acidosis and stroke-like episodes. Journal of the Neurological Sciences. 239(1). 115–118. 12 indexed citations
7.
Kubota, Hiroaki, Takashi Kanbayashi, Yuzo Tanabe, et al.. (2003). Decreased Cerebrospinal Fluid Hypocretin-1 Levels Near the Onset of Narcolepsy in 2 Prepubertal Children. SLEEP. 26(5). 555–557. 26 indexed citations
8.
Suzuki, Yasuyuki, Mizue Iai, Atsushi Kamei, et al.. (2002). Peroxisomal acyl CoA oxidase deficiency. The Journal of Pediatrics. 140(1). 128–130. 33 indexed citations
9.
Inoue, Ken, Makoto Kanai, Yuzo Tanabe, et al.. (2001). Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus–Merzbacher disease. Prenatal Diagnosis. 21(13). 1133–1136. 21 indexed citations
10.
Kubota, Hiroaki, et al.. (2001). Q FEVER ENCEPHALITIS WITH CYTOKINE PROFILES IN SERUM AND CEREBROSPINAL FLUID. The Pediatric Infectious Disease Journal. 20(3). 318–319. 8 indexed citations
11.
Iwamaru, Yoshifumi, Masami Miyake, Junko Arii, Yuzo Tanabe, & Masatoshi Noda. (2001). An inhibitory factor for cell-free protein synthesis from Salmonella enteritidis exhibits cytopathic activity against Chinese hamster ovary cells. Microbial Pathogenesis. 31(6). 283–293. 4 indexed citations
12.
Inoue, Ken, Yuzo Tanabe, & James R. Lupski. (1999). Myelin deficiencies in both the central and the peripheral nervous systems associated with aSOX10 mutation. Annals of Neurology. 46(3). 313–318. 144 indexed citations
13.
Takanashi, Jun‐ichi, Katsuo Sugita, Yuzo Tanabe, & Hiroo Niimi. (1998). Adolescent case of Alexander disease: MR imaging and MR spectroscopy. Pediatric Neurology. 18(1). 67–70. 20 indexed citations
14.
Takanashi, Jun‐ichi, et al.. (1997). Dichloroacetate treatment in Leigh syndrome caused by mitochondrial DNA mutation. Journal of the Neurological Sciences. 145(1). 83–86. 18 indexed citations
15.
Kobayashi, Osamu, et al.. (1996). Basement membrane abnormality in merosin-negative congenital muscular dystrophy. Acta Neuropathologica. 91(4). 332–336. 27 indexed citations
16.
Kadowaki, Takashi, Hiroko Kadowaki, Yasumichi Mori, et al.. (1994). A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNA. New England Journal of Medicine. 330(14). 962–968. 402 indexed citations
17.
Ishikiriyama, Satoshi, Mizue Iai, & Yuzo Tanabe. (1993). Lack of X inactivation: Loss of one X inactivation center in a case with mos45,X, –21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2). American Journal of Medical Genetics. 47(1). 41–44. 6 indexed citations
18.
Sugita, Katsuo, Akio Takeuchi, Mizue Iai, & Yuzo Tanabe. (1989). Neurologic sequelae and MRI in low-birth weight patients. Pediatric Neurology. 5(6). 365–369. 17 indexed citations
19.
Tanabe, Yuzo, Shigeki Miyamoto, Kazutaka Yamada, et al.. (1988). Diabetes mellitus in Kearns-Sayre Syndrome. European Neurology. 28(1). 34–38. 23 indexed citations
20.
Woo, Man, et al.. (1987). Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx mice. Journal of the Neurological Sciences. 82(1-3). 111–122. 25 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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