S. Noguchi

21.9k citations

206 papers · 7.0k · h-index 46

Impact in

Cell Biology top 0.5%
Molecular Biology top 1%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Nuclear Structure and Function

Papers in

Molecular Biology 158
- Muscle Physiology and Disorders 95
- RNA Research and Splicing 26
- Nuclear Structure and Function 23
Epidemiology 53
- Inflammatory Myopathies and Dermatomyositis 41

Co-authors: Ichizo Nishino (153 shared papers)Ikuya Nonaka (84 shared papers)Yukiko Hayashi (75 shared papers)Eijiro Ozawa (11 shared papers)Yuji Mizuno (9 shared papers)Mikiharu Yoshida (9 shared papers)May Christine V. Malicdan (29 shared papers)Minoru Nakano (9 shared papers)
Journals: Neuromuscular Disorders (45 papers)Neurology (19 papers)Human Molecular Genetics (9 papers)Muscle & Nerve (7 papers)European Journal of Biochemistry (6 papers)
Partner nations: Japan United States China

In The Last Decade

S. Noguchi

197 papers receiving 6.9k citations

Peers

Countries citing papers authored by S. Noguchi

Since Specialization

Citations

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

Fields of papers citing papers by S. Noguchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside S. Noguchi, 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 S. Noguchi Line = papers co-authored together S. Noguchi 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 206 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy Science ·S. Noguchi, Elizabeth M. McNally, Kamel Ben Othmane, Yasuko Hagiwara, Yuji Mizuno, Mikiharu Yoshida, Hideko Yamamoto, Carsten G. Bönnemann, Emanuela Gussoni, Peter H. Denton, Theodoros Kyriakides, Lefkos Middleton, Fayçal Hentati, Mongi Ben Hamida, Ikuya Nonaka, Jeffery M. Vance, Louis M. Kunkel, Eijiro Ozawa	1995	414
2	β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex Nature Genetics ·Carsten G. Bönnemann, Raju Modi, S. Noguchi, Yuji Mizuno, Mikiharu Yoshida, Emanuela Gussoni, Elizabeth M. McNally, David Duggan, C. Angelini, Eric P. Hoffman, Eijiro Ozawa, Louis M. Kunkel	1995	372
3	Dystrophin-associated proteins in muscular dystrophy Human Molecular Genetics ·E Ozawa, Masaaki Yoshida, Atsushi Suzuki, Yuki Mizuno, Yuriko Hagiwara, S. Noguchi	1995	199
4	From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy Muscle & Nerve ·Eijiro Ozawa, S. Noguchi, Yuji Mizuno, Yasuko Hagiwara, Mikiharu Yoshida	1998	197
5	Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n‐octyl β‐d‐glucoside European Journal of Biochemistry ·Mikiharu Yoshida, Atsushi Suzuki, Hideko Yamamoto, S. Noguchi, Yuji Mizuno, Eijiro Ozawa	1994	187
6	Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy Neurology ·Ichizo Nishino, S. Noguchi, K. Murayama, Adel Driss, Kazuma Sugie, Yasushi Oya, Tetsuya Nagata, Keiji Chida, Tetsuya Takahashi, Yuichi Takusa, Takekazu Ohi, Jin Nishimiya, N Sunohara, Emma Ciafaloni, Mitsuru Kawai, Masashi Aoki, Ikuya Nonaka	2002	175
7	Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy Neurology ·Yukiko Hayashi, Megumu Ogawa, Kazuhiko Tagawa, S. Noguchi, Tadayuki Ishihara, Ikuya Nonaka, Kiichi Arahata	2001	173
8	Autophagic degradation of nuclear components in mammalian cells Autophagy ·Young-Eun Park, Yukiko Hayashi, Gisèle Bonne, Takuro Arimura, S. Noguchi, Ikuya Nonaka, Ichizo Nishino	2009	171
9	Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model Nature Medicine ·May Christine V. Malicdan, S. Noguchi, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino	2009	138
10	Reduction of UDP-N-acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase Activity and Sialylation in Distal Myopathy with Rimmed Vacuoles Journal of Biological Chemistry ·S. Noguchi, Yoko Keira, Kumiko Murayama, Megumu Ogawa, Masako Fujita, Genri Kawahara, Yasushi Oya, Masaoki Imazawa, Yu‐ichi Goto, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino	2004	133
11	Loss of the Sarcoglycan Complex and Sarcospan Leads to Muscular Dystrophy in -Sarcoglycan-Deficient Mice Human Molecular Genetics ·Kenji Araishi, Toshikuni Sasaoka, Michihiro Imamura, S. Noguchi, Hiroko Hama, Eiji Wakabayashi, Masaaki Yoshida, Tsukasa Hori, E Ozawa	1999	133
12	Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca2+ channels Human Molecular Genetics ·Yukari Endo, S. Noguchi, Yuji Hara, Yukiko Hayashi, Kazushi Motomura, Satoko Miyatake, Nobuyuki Murakami, Satsuki Tanaka, Sumimasa Yamashita, Rika Kizu, Masahiro Bamba, Yu‐ichi Goto, Naomichi Matsumoto, Ikuya Nonaka, Ichizo Nishino	2014	126
13	Lysosomal myopathies: An excessive build-up in autophagosomes is too much to handle Neuromuscular Disorders ·May Christine V. Malicdan, S. Noguchi, Ikuya Nonaka, Paul Säftig, Ichizo Nishino	2008	118
14	ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency Neuromuscular Disorders ·Wen‐Chen Liang, Aya Ohkuma, Yukiko Hayashi, Luís C. López, Michio Hirano, Ikuya Nonaka, S. Noguchi, Lianghui Chen, Yuh‐Jyh Jong, Ichizo Nishino	2009	103
15	Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness Annals of Neurology ·Terumi Murakami, Yukiko Hayashi, S. Noguchi, Megumu Ogawa, Ikuya Nonaka, Yuzo Tanabe, Mieko Ogino, Fumio Takada, Makoto Eriguchi, Norihiko Kotooka, Kevin P. Campbell, Makiko Ōsawa, Ichizo Nishino	2006	96
16	TMEM43 mutations in emery‐dreifuss muscular dystrophy‐related myopathy Annals of Neurology ·Wen‐Chen Liang, Hiroaki Mitsuhashi, E. Keduka, Ikuya Nonaka, S. Noguchi, Ichizo Nishino, Yukiko Hayashi	2010	91
17	Structural analysis of the N‐linked carbohydrate chains of the 55‐kDa glycoprotein family (PZP3) from porcine zona pellucida European Journal of Biochemistry ·S. Noguchi, Yumiko Hatanaka, Tohru Tobita, Minoru Nakano	1992	89
18	Malignant Hyperthermia in Japan Anesthesiology ·Carlos A Ibarra, Shiwen Wu, Kumiko Murayama, Narihiro Minami, Yasuko Ichihara, Hirosato Kikuchi, S. Noguchi, Yukiko Hayashi, Ryoichi Ochiai, Ichizo Nishino	2006	89
19	Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy Neurology ·Kohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, Hiroki Masuda, Yukari Sekiguchi, Atsuhiko Sugiyama, Kazumoto Shibuya, Richard J.L.F. Lemmers, Remko Goossens, Megumu Ogawa, Koji Nagao, Chikashi Obuse, S. Noguchi, Yukiko Hayashi, Satoshi Kuwabara, Judit Balog, Ichizo Nishino, Silvère M. van der Maarel	2020	88
20	Emerin-Lacking Mice Show Minimal Motor and Cardiac Dysfunctions with Nuclear-Associated Vacuoles American Journal Of Pathology ·Ritsuko Ozawa, Yukiko Hayashi, Megumu Ogawa, Rumi Kurokawa, Hiroshi Matsumoto, S. Noguchi, Ikuya Nonaka, Ichizo Nishino	2006	84

About S. Noguchi

S. Noguchi is a scholar working on Molecular Biology, Epidemiology, Cell Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience, having authored 206 papers that have together received 7.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (95 papers), Inflammatory Myopathies and Dermatomyositis (41 papers), Cardiomyopathy and Myosin Studies (34 papers), Genetic Neurodegenerative Diseases (32 papers), RNA Research and Splicing (26 papers), Nuclear Structure and Function (23 papers), Cellular transport and secretion (20 papers) and Neurogenetic and Muscular Disorders Research (14 papers). The work is most often cited by research in Cell Biology (1.3k citations), Molecular Biology (5.4k citations), Cellular and Molecular Neuroscience (1.3k citations), Genetics (777 citations) and Cardiology and Cardiovascular Medicine (1.5k citations). S. Noguchi has collaborated with scholars based in Japan, United States and China. Frequent co-authors include Ichizo Nishino, Ikuya Nonaka, Yukiko Hayashi, Eijiro Ozawa, Yuji Mizuno, Mikiharu Yoshida, May Christine V. Malicdan, Minoru Nakano, Megumu Ogawa and Atsushi Suzuki. Their work appears in journals such as Neuromuscular Disorders, Neurology, Human Molecular Genetics, Muscle & Nerve and European Journal of Biochemistry.

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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S. Noguchi

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