Narihiro Minami

2.2k citations

58 papers · 1.3k indexed · h-index 21

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 23
Cell Biology top 5%
- Calpain Protease Function and Regulation 6
Aging top 10%
Cardiology and Cardiovascular Medicine top 10%
- Cardiomyopathy and Myosin Studies 9
Molecular Biology top 10%
- Muscle Physiology and Disorders 37
- RNA regulation and disease 6
- RNA modifications and cancer 5
- Mitochondrial Function and Pathology 4
Genetics
- Neurogenetic and Muscular Disorders Research 6

Co-authors: Ichizo Nishino Ikuya Nonaka Hiroshi Abe Takashi Obinata Yu‐ichi Goto S. Noguchi Shoichiro Ono Yukiko Hayashi
Cited by: Cellular and Molecular Neuroscience Cell Biology Aging
Journals: Journal of Biological Chemistry (1 paper)The Journal of Immunology (1 paper)PLoS ONE (1 paper)
Partner nations: Japan United States Taiwan

In The Last Decade

Narihiro Minami

57 papers receiving 1.2k citations

Peers

Countries citing papers authored by Narihiro Minami

Since Specialization

Citations

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

Fields of papers citing papers by Narihiro Minami

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Narihiro Minami, 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 Narihiro Minami Line = papers co-authored together Narihiro Minami links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A Case of Oculopharyngeal Muscular Dystrophy Caused by a Novel PABPN1 c.34G > T (p.Gly12Trp) Point Mutation without Polyalanine Expansion Journal of Neuromuscular Diseases ·Yoshiaki Takahashi,Nobutoshi Morimoto,Tomoaki Nada,Mizuki Morimoto,Nobuyuki Eura,Narihiro Minami,Ichizo Nishino	2023	2
2	Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy Acta Neuropathologica Communications ·Masashi Ogasawara,Nobuyuki Eura,Aritoshi Iida,Theerawat Kumutpongpanich,Narihiro Minami,Ikuya Nonaka,Shinichiro Hayashi,S. Noguchi,Ichizo Nishino	2022	6
3	Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathy Neuropathology and Applied Neurobiology ·Masashi Ogasawara,Nobuyuki Eura,Utako Nagaoka,Tatsuro Sato,Hajime Arahata,Tomohiro Hayashi,Tomoko Okamoto,Yuji Takahashi,Madoka Mori‐Yoshimura,Yasushi Oya,Akinori Nakamura,Rui Shimazaki,Terunori Sano,Theerawat Kumutpongpanich,Narihiro Minami,Shinichiro Hayashi,S. Noguchi,Aritoshi Iida,Masaki Takao,Ichizo Nishino	2021	14
4	Severe cardiac involvement with preserved truncated dystrophin expression in Becker muscular dystrophy by +1G>A DMD splice-site mutation: a case report Journal of Human Genetics ·Ryouhei Komaki,Yasumasa Hashimoto,Madoka Mori‐Yoshimura,Yasushi Oya,Hotake Takizawa,Narihiro Minami,Ichizo Nishino,Yoshitsugu Aoki,Yuji Takahashi	2020	4
5	Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy Orphanet Journal of Rare Diseases ·Wen‐Chen Liang,Yuh‐Jyh Jong,Chien-Hua Wang,Chen‐Hua Wang,Tian Xia,Wan-Zi Chen,Tzu-Min Kan,Narihiro Minami,Ichizo Nishino,Lee‐Jun C. Wong	2020	14
6	Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy Neuromuscular Disorders ·Madoka Mori‐Yoshimura,Y Mizuno,Sumiko Yoshida,Naoko Ishihara,Narihiro Minami,Emiko Morimoto,Kazushi Maruo,Ikuya Nonaka,Hirofumi Komaki,Ichizo Nishino,Masayuki Sekiguchi,Noriko Sato,Shin’ichi Takeda,Yuji Takahashi	2019	28
7	Induction of Pluripotent Stem Cells from a Manifesting Carrier of Duchenne Muscular Dystrophy and Characterization of Their X-Inactivation Status Stem Cells International ·Yuko Miyagoe‐Suzuki,Takashi Nishiyama,Miho Nakamura,Asako Narita,Fusako Sakai‐Takemura,S. Masuda,Narihiro Minami,Kumiko Murayama,Hirofumi Komaki,Yu‐ichi Goto,Shin’ichi Takeda	2017	6
8	Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions Neuromuscular Disorders ·Eri Takeshita,Narihiro Minami,Kumiko Minami,Mikiya Suzuki,Takeya Awashima,Akihiko Ishiyama,Hirofumi Komaki,Ichizo Nishino,Masayuki Sasaki	2017	9
9	Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations Journal of Human Genetics ·Mariko Okubo,Narihiro Minami,Kanako Goto,Yu‐ichi Goto,S. Noguchi,Satomi Mitsuhashi,Ichizo Nishino	2016	76
10	Nuclear inclusions mimicking poly(A)-binding protein nuclear 1 inclusions in a case of inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia with a novel mutation in the valosin-containing protein gene Neuromuscular Disorders ·Shiro Matsubara,Toshio Shimizu,Takashi Komori,Madoka Mori‐Yoshimura,Narihiro Minami,Yukiko Hayashi	2016	11
11	Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines The American Journal of Human Genetics ·Jun Mitsui,Yuji Takahashi,Jun Goto,Hiroyuki Tomiyama,Shunpei Ishikawa,Hiroyo Yoshino,Narihiro Minami,Jeremy C. Smith,Suzanne Lesage,Hiroyuki Aburatani,Ichizo Nishino,Alexis Brice,Nobutaka Hattori,Shoji Tsuji	2010	73
12	Homozygous female Becker muscular dystrophy American Journal of Medical Genetics Part A ·Katsunori Fujii,Narihiro Minami,Yukiko Hayashi,Ichizo Nishino,Ikuya Nonaka,Yuzo Tanabe,Jun‐ichi Takanashi,Yoichi Kohno	2009	26
13	Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling Neuroscience Research ·Yoko Keira,S. Noguchi,Rumi Kurokawa,Masako Fujita,Narihiro Minami,Yukiko Hayashi,Takashi Kato,Ichizo Nishino	2007	21
14	A unique case of limb‐girdle muscular dystrophy type 2A carrying novel compound heterozygous mutations in the human CAPN3 gene European Journal of Neurology ·E. Matsubara,Akiko Tsuchiya,Narihiro Minami,Ichizo Nishino,Miguel A. Pappolla,Mikio Shoji,Kōji Abe	2007	3
15	Dysferlinopathy associated with rigid spine syndrome Neuropathology ·Toshiko Nagashima,Takayo Chuma,Yukio Mano,Yu‐ichi Goto,Yukiko Hayashi,Narihiro Minami,Ichizo Nishino,Ikuya Nonaka,Toshiaki Takahashi,Hirofumi Sawa,Masashi Aoki,Kazuo Nagashima	2004	23
16	Six Novel Nonsynonymous CYP1A2 Gene Polymorphisms: Catalytic Activities of the Naturally Occurring Variant Enzymes Journal of Pharmacology and Experimental Therapeutics ·Norie Murayama,Akiko Soyama,Yoshiro Saito,Yukiko Nakajima,Kazuo Komamura,Kazuyuki Ueno,Shiro Kamakura,Masafumi Kitakaze,Hideo Kimura,Yu‐ichi Goto,Osamu Saitoh,Masaaki Katoh,Teiichi Ohnuma,Mitsuru Kawai,Kenji Sugai,Taisuke Ohtsuki,Chieko Suzuki,Narihiro Minami,Shogo Ozawa,Jun‐ichi Sawada	2004	71
17	Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy Neuromuscular Disorders ·Narihiro Minami,Koji Ikezoe,Hirotaka Kuroda,Haruo Nakabayashi,E Satoyoshi,Ikuya Nonaka	2001	31
18	Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)11 in PABP2 gene Neuromuscular Disorders ·Toshiko Nagashima,Hideo Kato,Manabu Kase,Shiroh Maguchi,Yasuyuki Mizutani,Katsuhiro Matsuda,Takayo Chuma,Yukio Mano,Yu‐ichi Goto,Narihiro Minami,Ikuya Nonaka,Kazuo Nagashima	2000	26
19	Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan Journal of the Neurological Sciences ·Narihiro Minami,Ichizo Nishino,Osamu Kobayashi,Koji Ikezoe,Yu‐ichi Goto,Ikuya Nonaka	1999	29
20	Quantitative analysis of low molecular weight G-actin-binding proteins, cofilin, ADF and profilin, expressed in developing and degenerating chicken skeletal muscles Journal of Muscle Research and Cell Motility ·R. Nagaoka,Narihiro Minami,Kimihide Hayakawa,Hiroshi Abe,Takashi Obinata	1996	30

About Narihiro Minami

Narihiro Minami is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology, having authored 58 papers that have together received 1.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (37 papers), Genetic Neurodegenerative Diseases (23 papers), Cardiomyopathy and Myosin Studies (9 papers), Calpain Protease Function and Regulation (6 papers), RNA regulation and disease (6 papers), Neurogenetic and Muscular Disorders Research (6 papers), RNA modifications and cancer (5 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (329 citations), Cell Biology (294 citations) and Aging (25 citations). Narihiro Minami has collaborated with scholars based in Japan, United States and Taiwan. Frequent co-authors include Ichizo Nishino, Ikuya Nonaka, Hiroshi Abe, Takashi Obinata, Yu‐ichi Goto, S. Noguchi, Shoichiro Ono, Yukiko Hayashi, Kumiko Murayama and Kanako Goto. Their work appears in journals such as Journal of Biological Chemistry, The Journal of Immunology and PLoS ONE.

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