Tohru Ibi

1.3k total citations
33 papers, 554 citations indexed

About

Tohru Ibi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Tohru Ibi has authored 33 papers receiving a total of 554 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Tohru Ibi's work include Muscle Physiology and Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Tohru Ibi is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Tohru Ibi collaborates with scholars based in Japan, United States and France. Tohru Ibi's co-authors include Ko Sahashi, Kinji Ohno, Akira Takahashi, Mikako Ito, Naoki Nakao, Masafumi Ito, S. Igarashi, Kimiyasu Sato, Yoshinori Tanno and Takahisa Miyatake and has published in prestigious journals such as Neurology, Annals of Neurology and Acta Neuropathologica.

In The Last Decade

Tohru Ibi

33 papers receiving 542 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tohru Ibi Japan 12 363 215 104 84 80 33 554
Ko Sahashi Japan 16 535 1.5× 247 1.1× 289 2.8× 119 1.4× 88 1.1× 42 857
Karlla W. Brigatti United States 13 364 1.0× 180 0.8× 86 0.8× 45 0.5× 60 0.8× 19 511
J. Bautista Spain 14 264 0.7× 99 0.5× 44 0.4× 57 0.7× 22 0.3× 29 456
Robyn Labrum United Kingdom 14 488 1.3× 400 1.9× 175 1.7× 54 0.6× 28 0.3× 21 772
Linton C. Hopkins United States 14 729 2.0× 168 0.8× 221 2.1× 337 4.0× 64 0.8× 15 1.1k
J. Colomer Spain 17 479 1.3× 214 1.0× 213 2.0× 50 0.6× 137 1.7× 42 934
Eduardo Gutiérrez‐Rivas Spain 14 233 0.6× 148 0.7× 142 1.4× 51 0.6× 25 0.3× 25 620
B. Lemieux Canada 12 339 0.9× 347 1.6× 126 1.2× 120 1.4× 18 0.2× 29 532
Luca Chiveri Italy 9 291 0.8× 61 0.3× 199 1.9× 35 0.4× 28 0.3× 13 540
Alexander Shtilbans United States 12 358 1.0× 83 0.4× 125 1.2× 189 2.3× 24 0.3× 16 566

Countries citing papers authored by Tohru Ibi

Since Specialization
Citations

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

Fields of papers citing papers by Tohru Ibi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tohru Ibi

This figure shows the co-authorship network connecting the top 25 collaborators of Tohru Ibi. A scholar is included among the top collaborators of Tohru Ibi 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 Tohru Ibi. Tohru Ibi 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.
Niwa, Jun‐ichi, et al.. (2015). Dyskinesia-hyperpyrexia syndrome in a patient with Parkinson’s disease: a case report. Rinsho Shinkeigaku. 55(3). 182–184. 11 indexed citations
2.
Yamashita, Yoshihiro, Tohru Matsuura, Tatsuaki Kurosaki, et al.. (2014). LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinity. Neurobiology of Disease. 69. 200–205. 26 indexed citations
3.
Yamashita, Yoshihiro, Tohru Matsuura, Akio Masuda, et al.. (2012). Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy. Journal of Human Genetics. 57(6). 368–374. 14 indexed citations
4.
Kokunai, Yosuke, Keigo Goto, Tomoya Kubota, et al.. (2012). A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis. Neuroscience Letters. 519(1). 67–72. 9 indexed citations
5.
6.
Nishigaki, Yutaka, Hitomi Ueno, Jorida Çoku, et al.. (2010). Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion. 10(3). 300–308. 24 indexed citations
7.
Hoshino, Akira, Yasushi Iwasaki, Shinya Kimura, et al.. (2008). MM1‐type sporadic Creutzfeldt‐Jakob disease with unusually prolonged disease duration presenting with panencephalopathic‐type pathology. Neuropathology. 28(3). 326–332. 5 indexed citations
8.
Sahashi, Ko, Tohru Ibi, Kinji Ohno, Naoki Nakao, & Hirohito M. Kondo. (2004). Progressive myopathy with circulating autoantibody against giantin in the Golgi apparatus. Neurology. 62(10). 1891–1893. 4 indexed citations
9.
Nishida, Hiroshi, Hirotaka Shimizu, Yuji Tanaka, Tohru Ibi, & Ko Sahashi. (2001). A case with deep cerebral venous thrombosis showing chronic neurological deficits of the frontal lobe.. Nosotchu. 23(2). 204–207. 1 indexed citations
10.
Ibi, Tohru, et al.. (2001). [Myasthenia gravis, giant cell polymyositis and cardiomyositis associated with thymoma].. PubMed. 344–6. 3 indexed citations
11.
Ibi, Tohru, Jing Ling, Naoki Nakao, Narihiro Minami, & Ko Sahashi. (2000). [A case of LGMD2A identified with both western blot analysis and immunostaining of calpain 3 in biopsied muscle].. PubMed. 40(10). 1023–7. 2 indexed citations
12.
Naoi, Makoto, Wakako Maruyama, Naoki Nakao, et al.. (1998). (R) salsolinol N‐methyltransferase activity increases in parkinsonian lymphocytes. Annals of Neurology. 43(2). 212–216. 49 indexed citations
13.
Nakao, Naoki, Ko Sahashi, Masahiko Takahashi, Tohru Ibi, & Yoshio Hashizume. (1995). Clinical and neuropathological features of a neurodegenerative disorder in the central nervous system with progressive head drooping (Kubisagari). Acta Neuropathologica. 90(2). 208–212. 2 indexed citations
14.
Ibi, Tohru, et al.. (1995). [Expression of the heat shock protein 70 in inflammatory myopathies].. PubMed. 35(10). 1163–6. 4 indexed citations
15.
Hori, Shinichiro, et al.. (1994). Multiplicity of abnormal dystrophin in Becker muscular dystrophy. Journal of the Neurological Sciences. 121(2). 183–189. 2 indexed citations
16.
Igarashi, S., Yoshinori Tanno, Osamu Onodera, et al.. (1992). Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. Neurology. 42(12). 2300–2300. 148 indexed citations
17.
Sahashi, Ko, et al.. (1992). Increased Mitochondrial DNA Deletions in the Skeletal Muscle of Myotonic Dystrophy. Gerontology. 38(1-2). 18–29. 20 indexed citations
18.
Ohno, Kinji, Masashi Tanaka, Ko Sahashi, et al.. (1991). Mitochondrial DNA deletions in inherited recurrent myoglobinuria. Annals of Neurology. 29(4). 364–369. 64 indexed citations
19.
Ohno, Kinji, Masashi Tanaka, Hidekazu Ino, et al.. (1991). Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1090(1). 9–16. 6 indexed citations
20.
Sahashi, Ko, Kinji Ohno, Masashi Tanaka, et al.. (1990). Cytoplasmic body and mitochondrial DNA deletion. Journal of the Neurological Sciences. 99(2-3). 291–300. 4 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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