En Kimura

3.4k citations

88 papers · 1.8k · h-index 24

Impact in

Genetics top 5%
- Virus-based gene therapy research
- Neurogenetic and Muscular Disorders Research
Neurology top 5%

Papers in

Molecular Biology 51
- Muscle Physiology and Disorders 40
Cellular and Molecular Neuroscience 18
- Genetic Neurodegenerative Diseases 13
- Hereditary Neurological Disorders 4

Co-authors: Satoshi Yamashita (35 shared papers)Makoto Uchino (28 shared papers)Yasushi Maeda (26 shared papers)Jeffrey S. Chamberlain (8 shared papers)B. Fall (5 shared papers)Teruyuki Hirano (22 shared papers)Masatoshi Ishizaki (11 shared papers)Madoka Mori‐Yoshimura (11 shared papers)
Journals: Neuromuscular Disorders (9 papers)Muscle & Nerve (7 papers)Journal of the Neurological Sciences (6 papers)Orphanet Journal of Rare Diseases (5 papers)PLoS ONE (4 papers)
Partner nations: Japan United States United Kingdom

In The Last Decade

En Kimura

82 papers receiving 1.7k citations

Peers

Countries citing papers authored by En Kimura

Since Specialization

Citations

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

Fields of papers citing papers by En Kimura

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside En Kimura, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with En Kimura Line = papers co-authored together En Kimura links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 88 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Efficient and Reproducible Myogenic Differentiation from Human iPS Cells: Prospects for Modeling Miyoshi Myopathy In Vitro PLoS ONE ·Akihito Tanaka, Knut Woltjen, Katsuya Miyake, Akitsu Hotta, Makoto Ikeya, Takuya Yamamoto, Tokiko Nishino, Emi Shoji, Atsuko Sehara‐Fujisawa, Yasuko Manabe, Nobuharu Fujii, Kazunori Hanaoka, Takumi Era, Satoshi Yamashita, Ken‐ichi Isobe, En Kimura, Hidetoshi Sakurai	2013	196
2	Comparison of the Added Value of Contrast-Enhanced 3D Fluid-Attenuated Inversion Recovery and Magnetization-Prepared Rapid Acquisition of Gradient Echo Sequences in Relation to Conventional Postcontrast T1-Weighted Images for the Evaluation of Leptomeningeal Diseases at 3T American Journal of Neuroradiology ·Hirofumi Fukuoka, Toshinori Hirai, Tomoko Okuda, Yosuke Shigematsu, Akira Sasao, En Kimura, Teruyuki Hirano, S. Yano, Ryuji Murakami, Yasuyuki Yamashita	2009	116
3	Female dystrophinopathy: Review of current literature Neuromuscular Disorders ·Masatoshi Ishizaki, Michio Kobayashi, Katsuhito Adachi, Tsuyoshi Matsumura, En Kimura	2018	79
4	Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin Gene Therapy ·Shuowei Li, En Kimura, B. Fall, Morayma Reyes, John C. Angello, Robert E. Welikson, Stephen D. Hauschka, Jeffrey S. Chamberlain	2005	77
5	Mdx respiratory impairment following fibrosis of the diaphragm Neuromuscular Disorders ·Masatoshi Ishizaki, Tomohiro Suga, En Kimura, Tetsuya Shiota, Ryoko Kawano, Y. Uchida, Katsuhisa Uchino, Satoshi Yamashita, Yasushi Maeda, Makoto Uchino	2008	66
6	Dystrophin Delivery to Muscles of mdx Mice Using Lentiviral Vectors Leads to Myogenic Progenitor Targeting and Stable Gene Expression Molecular Therapy ·En Kimura, Sheng Li, Paul Gregorevic, B. Fall, Jeffrey S. Chamberlain	2009	58
7	Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy Human Molecular Genetics ·En Kimura, Jiajia Han, Sheng Li, B. Fall, Joyce Ra, Miki Haraguchi, Stephen J. Tapscott, Jeffrey S. Chamberlain	2008	57
8	Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy) Orphanet Journal of Rare Diseases ·Harumasa Nakamura, En Kimura, Madoka Mori‐Yoshimura, Hirofumi Komaki, Yu Matsuda, Kanako Goto, Yukiko Hayashi, Ichizo Nishino, Shin’ichi Takeda, Mitsuru Kawai	2013	56
9	Correction: Efficient and Reproducible Myogenic Differentiation from Human iPS Cells: Prospects for Modeling Miyoshi Myopathy In Vitro PLoS ONE ·Akihito Tanaka, Knut Woltjen, Katsuya Miyake, Akitsu Hotta, Makoto Ikeya, Takuya Yamamoto, Tokiko Nishino, Emi Shoji, Atsuko Sehara‐Fujisawa, Yasuko Manabe, Nobuharu Fujii, Kazunori Hanaoka, Takumi Era, Satoshi Yamashita, Ken‐ichi Isobe, En Kimura, Hidetoshi Sakurai	2013	49
10	A highly functional mini-dystrophin / GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy Human Molecular Genetics ·Sheng Li, En Kimura, Rainer Ng, B. Fall, Leonard Meuse, Morayma Reyes, John A. Faulkner, Jeffrey S. Chamberlain	2006	45
11	Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in Japan Neuromuscular Disorders ·Toshio Saito, Mitsuru Kawai, En Kimura, Katsuhisa Ogata, Toshiaki Takahashi, Michio Kobayashi, Hiroto Takada, Satoshi Kuru, Takashi Mikata, Tsuyoshi Matsumura, Naohiro Yonemoto, Harutoshi Fujimura, Saburo Sakoda	2016	45
12	Nationwide patient registry for GNE myopathy in Japan Orphanet Journal of Rare Diseases ·Madoka Mori‐Yoshimura, Yukiko Hayashi, Naohiro Yonemoto, Harumasa Nakamura, Miho Murata, Shin’ichi Takeda, Ichizo Nishino, En Kimura	2014	42
13	Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan Orphanet Journal of Rare Diseases ·Mariko Okubo, Kanako Goto, Hirofumi Komaki, Harumasa Nakamura, Madoka Mori‐Yoshimura, Yukiko Hayashi, Satomi Mitsuhashi, S. Noguchi, En Kimura, Ichizo Nishino	2017	38
14	DJ‐1 forms complexes with mutant SOD1 and ameliorates its toxicity Journal of Neurochemistry ·Satoshi Yamashita, Akira Mori, En Kimura, Shuji Mita, Yasushi Maeda, Teruyuki Hirano, Makoto Uchino	2010	35
15	Cerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature Journal of Neuroinflammation ·Hideya Sakaguchi, Akihiko Ueda, Takayuki Kosaka, Satoshi Yamashita, En Kimura, Taro Yamashita, Yasushi Maeda, Teruyuki Hirano, Makoto Uchino	2011	34
16	Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation Neurochemistry International ·Akira Mori, Satoshi Yamashita, Katsuhisa Uchino, Tomohiro Suga, Tokunori Ikeda, Koutaro Takamatsu, Masatoshi Ishizaki, Tatsuya Koide, En Kimura, Shuji Mita, Yasushi Maeda, Teruyuki Hirano, Makoto Uchino	2010	33
17	Exon skipping for Duchenne muscular dystrophy: a systematic review and meta-analysis Orphanet Journal of Rare Diseases ·Yuko Shimizu‐Motohashi, Terumi Murakami, En Kimura, Hirofumi Komaki, Norio Watanabe	2018	32
18	Multicenter questionnaire survey for sporadic inclusion body myositis in Japan Orphanet Journal of Rare Diseases ·Naoki Suzuki, Madoka Mori‐Yoshimura, Satoshi Yamashita, Satoshi Nakano, Ken-ya Murata, Yukie Inamori, Naoko Matsui, En Kimura, Hirofumi Kusaka, Tomoyoshi Kondo, Itsuro Higuchi, Ryuji Kaji, M. Tateyama, Rumiko Izumi, Hiroya Ono, Masaaki Kato, Hitoshi Warita, Toshiaki Takahashi, Ichizo Nishino, Masashi Aoki	2016	31
19	Transduction of Full-length Dystrophin to Multiple Skeletal Muscles Improves Motor Performance and Life Span in Utrophin/Dystrophin Double Knockout Mice Molecular Therapy ·Ryoko Kawano, Masatoshi Ishizaki, Yasushi Maeda, Y. Uchida, En Kimura, Makoto Uchino	2008	30
20	Full‐length dystrophin cDNA transfer into skeletal muscle of adult mdx mice by electroporation Muscle & Nerve ·T. Murakami, Toru Nishi, En Kimura, Tomoaki Goto, Yasushi Maeda, Yukitaka Ushio, Makoto Uchino, Yoshihide Sunada	2002	29

About En Kimura

En Kimura is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Genetics, having authored 88 papers that have together received 1.8k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (40 papers), Genetic Neurodegenerative Diseases (13 papers), Virus-based gene therapy research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers), Amyotrophic Lateral Sclerosis Research (6 papers), Inflammatory Myopathies and Dermatomyositis (6 papers), Exercise and Physiological Responses (4 papers) and Hereditary Neurological Disorders (4 papers). The work is most often cited by research in Genetics (230 citations), Neurology (233 citations), Molecular Biology (1.1k citations), Aging (23 citations) and Rehabilitation (69 citations). En Kimura has collaborated with scholars based in Japan, United States and United Kingdom. Frequent co-authors include Satoshi Yamashita, Makoto Uchino, Yasushi Maeda, Jeffrey S. Chamberlain, B. Fall, Teruyuki Hirano, Masatoshi Ishizaki, Madoka Mori‐Yoshimura, Ichizo Nishino and Harumasa Nakamura. Their work appears in journals such as Neuromuscular Disorders, Muscle & Nerve, Journal of the Neurological Sciences, Orphanet Journal of Rare Diseases and PLoS ONE.

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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