Teruhisa Miike

2.7k total citations · 1 hit paper
61 papers, 2.0k citations indexed

About

Teruhisa Miike is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Physiology. According to data from OpenAlex, Teruhisa Miike has authored 61 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 13 papers in Cardiology and Cardiovascular Medicine and 12 papers in Physiology. Recurrent topics in Teruhisa Miike's work include Muscle Physiology and Disorders (41 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (10 papers). Teruhisa Miike is often cited by papers focused on Muscle Physiology and Disorders (41 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (10 papers). Teruhisa Miike collaborates with scholars based in Japan, United States and Netherlands. Teruhisa Miike's co-authors include Akemi Tomoda, Kowashi Yoshioka, A. Ishikawa, Reiji Koide, Fusahiro Ikuta, Takafumi Hayashi, Hitoshi Takahashi, Osamu Onodera, Takeshi Ikeuchi and Haruhiko Naito and has published in prestigious journals such as Nature Genetics, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Teruhisa Miike

60 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

1994 904 citations Reiji Koide, Takeshi Ikeuchi et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Teruhisa Miike Japan	21	1.6k	973	365	260	234	61	2.0k
H. F. M. Busch Netherlands	22	964 0.6×	646 0.7×	495 1.4×	242 0.9×	130 0.6×	58	1.8k
Atle Melberg Sweden	25	1.4k 0.9×	432 0.4×	285 0.8×	131 0.5×	239 1.0×	44	2.1k
Sabrina W. Yum United States	25	880 0.6×	543 0.6×	297 0.8×	163 0.6×	138 0.6×	63	1.8k
Grace Yoon Canada	25	1.4k 0.9×	632 0.6×	212 0.6×	136 0.5×	364 1.6×	97	2.1k
Toshiyuki Kumagai Japan	23	852 0.5×	345 0.4×	166 0.5×	152 0.6×	286 1.2×	60	1.5k
N Sunohara Japan	24	1.1k 0.7×	704 0.7×	875 2.4×	460 1.8×	91 0.4×	69	2.2k
Theodoros Kyriakides Cyprus	17	938 0.6×	509 0.5×	221 0.6×	149 0.6×	120 0.5×	47	1.5k
Richard Roxburgh New Zealand	25	1.9k 1.2×	1.3k 1.3×	591 1.6×	234 0.9×	264 1.1×	78	3.0k
Rohit Bhattacharjee New Zealand	5	1.3k 0.8×	519 0.5×	160 0.4×	182 0.7×	127 0.5×	7	1.7k
Victor Ionâşescu United States	35	2.2k 1.4×	1.7k 1.8×	609 1.7×	356 1.4×	392 1.7×	107	3.9k

Countries citing papers authored by Teruhisa Miike

Since Specialization

Citations

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

Fields of papers citing papers by Teruhisa Miike

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teruhisa Miike

This figure shows the co-authorship network connecting the top 25 collaborators of Teruhisa Miike. A scholar is included among the top collaborators of Teruhisa Miike 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 Teruhisa Miike. Teruhisa Miike 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

Ozasa, Shiro, Shigemi Kimura, Kaori Ito, et al.. (2007). Efficient conversion of ES cells into myogenic lineage using the gene-inducible system. Biochemical and Biophysical Research Communications. 357(4). 957–963. 20 indexed citations

Ito, Kaori, Shigemi Kimura, Shiro Ozasa, et al.. (2006). Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice. Human Molecular Genetics. 15(14). 2266–2275. 53 indexed citations

Miike, Teruhisa. (2003). The 19th Annual Conference on Neuromuscular Diseases in Childhood. Brain and Development. 25(5). 376–376. 1 indexed citations

Ikezawa, Makoto, Ichizo Nishino, Yu‐ichi Goto, Teruhisa Miike, & Ikuya Nonaka. (1999). Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Human Mutation. 13(2). 170–170. 22 indexed citations

Ikezawa, Makoto, Narihiro Minami, Miyuki Takahashi, et al.. (1998). Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis. Brain and Development. 20(3). 165–168. 20 indexed citations

Kimura, Shigemi, Shigeto Sugino, Yoshinobu Ohtani, et al.. (1998). Muscle fiber immaturity and inactivity reduce myonecrosis in duchenne muscular dystrophy. Annals of Neurology. 44(6). 967–971. 4 indexed citations

Kimura, Shigemi, Kuniya Abe, Misao Suzuki, et al.. (1997). 2.1 kb 5′-flanking region of the brain type dystrophin gene directs the expression of lacZ in the cerebral cortex, but not in the hippocampus. Journal of the Neurological Sciences. 147(1). 13–20. 9 indexed citations

Koide, Reiji, Takeshi Ikeuchi, Osamu Onodera, et al.. (1994). Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA). Nature Genetics. 6(1). 9–13. 904 indexed citations breakdown →

Uchino, Makoto, et al.. (1994). Dystrophin and dystrophin-related protein in the central nervous system of normal controls and Duchenne muscular dystrophy. Acta Neuropathologica. 87(2). 129–134. 29 indexed citations

10.

Ohtani, Yoshinobu, et al.. (1994). Central nervous system disorders and possible brain type carnitine palmitoyltransferase II deficiency. Brain and Development. 16(2). 139–145. 10 indexed citations

11.

Zhao, Ji-en, et al.. (1991). Dystrophin in control and mdx retina. Brain and Development. 13(2). 135–137. 22 indexed citations

12.

Yoshioka, Kenichi, et al.. (1991). Experimental serotonin myopathy as an animal model of muscle degeneration and regeneration in muscular dystrophy. Acta Neuropathologica. 81(5). 510–516. 9 indexed citations

13.

Sugino, Shigeto, Martin C. Wapenaar, Han‐Xiang Deng, et al.. (1989). Molecular‐genetic study of Duchenne and Becker muscular dystrophies: Deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females. American Journal of Medical Genetics. 34(4). 555–561. 26 indexed citations

14.

Miike, Teruhisa, et al.. (1989). Immunohistochemical dystrophin reaction in synaptic regions. Brain and Development. 11(5). 344–346. 64 indexed citations

15.

Uchino, Miki, S Araki, & Teruhisa Miike. (1988). Correlative study of the incidence of opaque, necrotic and regenerative fibers in Duchenne dystrophy. Acta Neuropathologica. 75(3). 308–312. 4 indexed citations

16.

Miike, Teruhisa, et al.. (1988). Atypical Prader-Willi syndrome with severe developmental delay and emaciation. Brain and Development. 10(3). 186–188. 6 indexed citations

17.

Miike, Teruhisa, et al.. (1987). Vascular endothelial cell injury and platelet embolism in Duchenne muscular dystrophy at the preclinical stage. Journal of the Neurological Sciences. 82(1-3). 67–80. 40 indexed citations

18.

Ohtani, Yoshinobu, et al.. (1986). Carnitine prevents reye-like syndrome in atypical carnitine deficiency. Pediatric Neurology. 2(2). 80–84. 3 indexed citations

19.

Kitano, Akito, Soroku Nishiyama, Teruhisa Miike, et al.. (1986). Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome. Brain and Development. 8(3). 289–295. 15 indexed citations

20.

Miike, Teruhisa. (1983). Maturational defect of regenerating muscle fibers in cases with duchenne and congenital muscular dystrophies. Muscle & Nerve. 6(8). 545–552. 28 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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