Chie Matsuda

2.4k total citations
31 papers, 1.9k citations indexed

About

Chie Matsuda is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Chie Matsuda has authored 31 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Cell Biology and 6 papers in Physiology. Recurrent topics in Chie Matsuda's work include Muscle Physiology and Disorders (15 papers), Nuclear Structure and Function (6 papers) and RNA Research and Splicing (5 papers). Chie Matsuda is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Nuclear Structure and Function (6 papers) and RNA Research and Splicing (5 papers). Chie Matsuda collaborates with scholars based in Japan, United States and Spain. Chie Matsuda's co-authors include Yukiko Hayashi, Kiichi Arahata, Megumu Ogawa, Ichizo Nishino, Ikuya Nonaka, Robert H. Brown, Kanako Goto, Hiromichi Kumagai, Eriko Fujita and Yoriko Kouroku and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Chie Matsuda

31 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chie Matsuda Japan 18 1.5k 610 328 322 228 31 1.9k
Christoph S. Clemen Germany 29 1.4k 0.9× 856 1.4× 198 0.6× 355 1.1× 254 1.1× 89 2.1k
Dimple Bansal United States 11 1.6k 1.0× 395 0.6× 354 1.1× 409 1.3× 206 0.9× 15 1.8k
Vishram Kedar United States 12 1.1k 0.8× 255 0.4× 128 0.4× 313 1.0× 204 0.9× 16 1.4k
Yanmin Yang United States 20 1.2k 0.8× 1.0k 1.7× 96 0.3× 125 0.4× 478 2.1× 31 2.1k
Stéphane Bodin France 21 845 0.6× 562 0.9× 178 0.5× 140 0.4× 132 0.6× 33 1.5k
Bernd Kinzel Switzerland 23 1.4k 0.9× 295 0.5× 207 0.6× 123 0.4× 98 0.4× 30 2.1k
Steve J. Winder United Kingdom 23 1.2k 0.8× 406 0.7× 247 0.8× 119 0.4× 157 0.7× 51 1.5k
Derek Warren United Kingdom 21 1.6k 1.1× 605 1.0× 172 0.5× 177 0.5× 61 0.3× 38 2.0k
Satomi Mitsuhashi Japan 28 1.8k 1.2× 299 0.5× 249 0.8× 333 1.0× 375 1.6× 99 2.4k
Thomas Weide Germany 25 1.1k 0.8× 1.0k 1.7× 186 0.6× 69 0.2× 136 0.6× 56 2.1k

Countries citing papers authored by Chie Matsuda

Since Specialization
Citations

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

Fields of papers citing papers by Chie Matsuda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chie Matsuda

This figure shows the co-authorship network connecting the top 25 collaborators of Chie Matsuda. A scholar is included among the top collaborators of Chie Matsuda 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 Chie Matsuda. Chie Matsuda 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.
Kinose, Yasuto, et al.. (2022). Obstetrical outcomes of labor with and without analgesia in Robson classification groups 1 and 2a: a single-center retrospective study. Journal of Anesthesia. 37(1). 39–48. 4 indexed citations
2.
Ohira, Takashi, Yoko Ino, Yayoi Kimura, et al.. (2021). Effects of microgravity exposure and fructo-oligosaccharide ingestion on the proteome of soleus and extensor digitorum longus muscles in developing mice. npj Microgravity. 7(1). 34–34. 9 indexed citations
3.
Matsuda, Chie, Tamotsu Kato, Jun Kikuchi, et al.. (2019). Dietary intervention of mice using an improved Multiple Artificial-gravity Research System (MARS) under artificial 1 g. npj Microgravity. 5(1). 16–16. 14 indexed citations
4.
Mio, M., Toshihiko Sugiki, Chie Matsuda, et al.. (2019). Structural instability of lamin A tail domain modulates its assembly and higher order function in Emery–Dreifuss muscular dystrophy. Biochemical and Biophysical Research Communications. 512(1). 22–28. 3 indexed citations
5.
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7.
Okada, Tomoko, Kazuhiro Murata, Chie Matsuda, et al.. (2013). Upregulated expression of FGF13/FHF2 mediates resistance to platinum drugs in cervical cancer cells. Scientific Reports. 3(1). 2899–2899. 41 indexed citations
8.
Furihata, Mutsuo, Chie Matsuda, Munehisa Takahashi, et al.. (2012). Augmented autocrine bone morphogenic protein (BMP) 7 signaling increases the metastatic potential of mouse breast cancer cells. Clinical & Experimental Metastasis. 29(4). 327–338. 35 indexed citations
9.
Shalaby, S. W., Hiroaki Mitsuhashi, Chie Matsuda, et al.. (2009). Defective Myotilin Homodimerization Caused by a Novel Mutation in MYOT Exon 9 in the First Japanese Limb Girdle Muscular Dystrophy 1A Patient. Journal of Neuropathology & Experimental Neurology. 68(6). 701–707. 16 indexed citations
10.
Hayashi, Yukiko, Chie Matsuda, Megumu Ogawa, et al.. (2009). Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy. Journal of Clinical Investigation. 119(9). 2623–2633. 296 indexed citations
11.
Hayward, Lawrence J., Ming-Yang Lee, Hongru Zhou, et al.. (2008). Targeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness. Journal of Clinical Investigation. 118(4). 1437–49. 45 indexed citations
12.
Matsuda, Chie, Kimihiko Kameyama, Atsushi Suzuki, et al.. (2008). Affixin activates Rac1 via βPIX in C2C12 myoblast. FEBS Letters. 582(8). 1189–1196. 20 indexed citations
13.
Fujita, Eriko, Yoriko Kouroku, Atsushi Isoai, et al.. (2007). Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II). Human Molecular Genetics. 16(6). 618–629. 265 indexed citations
14.
Yoshimi, Ryusuke, Satoshi Yamaji, Atsushi Suzuki, et al.. (2006). The γ-Parvin-Integrin-Linked Kinase Complex Is Critically Involved in Leukocyte-Substrate Interaction. The Journal of Immunology. 176(6). 3611–3624. 30 indexed citations
15.
Matsuda, Chie, Kimihiko Kameyama, Kazuhiko Tagawa, et al.. (2005). Dysferlin Interacts with Affixin (β-Parvin) at the Sarcolemma. Journal of Neuropathology & Experimental Neurology. 64(4). 334–340. 59 indexed citations
16.
Illa, Isabel, Carmen Serrano, Eduard Gallardo, et al.. (2001). Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype. Annals of Neurology. 49(1). 130–134. 11 indexed citations
17.
Hayashi, Yukiko, Eva Engvall, Megumu Ogawa, et al.. (1998). Mutations in the integrin α7 gene cause congenital myopathy. Nature Genetics. 19(1). 94–97. 281 indexed citations
18.
Ichida, Masaru, Hitoshi Endo, Uichi Ikeda, et al.. (1998). MyoD Is Indispensable for Muscle-specific Alternative Splicing in Mouse Mitochondrial ATP Synthase γ-Subunit Pre-mRNA. Journal of Biological Chemistry. 273(14). 8492–8501. 15 indexed citations
19.
Lee, Je Hyeon, Kanako Goto, Ko Sahashi, et al.. (1995). Cloning and mapping of a very short (10-kb)EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD). Muscle & Nerve. 18(S13). S27–S31. 11 indexed citations
20.
Matsuda, Chie, et al.. (1993). Tissue‐specific isoforms of the bovine mitochondrial ATP synthase γ‐subunit. FEBS Letters. 325(3). 281–284. 17 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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