Shiro Komba

1.0k total citations
61 papers, 836 citations indexed

About

Shiro Komba is a scholar working on Molecular Biology, Organic Chemistry and Biotechnology. According to data from OpenAlex, Shiro Komba has authored 61 papers receiving a total of 836 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 27 papers in Organic Chemistry and 13 papers in Biotechnology. Recurrent topics in Shiro Komba's work include Glycosylation and Glycoproteins Research (27 papers), Carbohydrate Chemistry and Synthesis (24 papers) and Enzyme Production and Characterization (12 papers). Shiro Komba is often cited by papers focused on Glycosylation and Glycoproteins Research (27 papers), Carbohydrate Chemistry and Synthesis (24 papers) and Enzyme Production and Characterization (12 papers). Shiro Komba collaborates with scholars based in Japan, Denmark and Slovakia. Shiro Komba's co-authors include Hideharu Ishida, Makoto Kiso, Ten Feizi, Sachiko Machida, Christine Galustian, Wakako Tsuzuki, Eiichi Kotake‐Nara, Makoto Kiso, Reiji Kannagi and Akira Hasegawa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Shiro Komba

58 papers receiving 813 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shiro Komba Japan 16 582 380 190 104 96 61 836
Hideko Ishihara Japan 10 528 0.9× 227 0.6× 102 0.5× 55 0.5× 96 1.0× 28 713
Hiroyuki Kumagai Japan 15 468 0.8× 118 0.3× 40 0.2× 163 1.6× 33 0.3× 47 792
Douglas M. Sheeley United States 14 568 1.0× 116 0.3× 58 0.3× 98 0.9× 103 1.1× 20 1.3k
Ryoji Hirose Japan 15 481 0.8× 215 0.6× 78 0.4× 217 2.1× 29 0.3× 28 1.1k
Noël R. Peters United States 18 832 1.4× 345 0.9× 226 1.2× 79 0.8× 23 0.2× 21 1.2k
Noeen Malik United States 15 682 1.2× 121 0.3× 48 0.3× 41 0.4× 192 2.0× 34 1.3k
T. Bito Japan 9 310 0.5× 39 0.1× 107 0.6× 156 1.5× 44 0.5× 12 1.1k
Maciej Stawikowski United States 14 446 0.8× 112 0.3× 33 0.2× 23 0.2× 36 0.4× 31 663
Xiaoman Zhou China 14 416 0.7× 54 0.1× 119 0.6× 30 0.3× 26 0.3× 36 613
Stephen W. Carper United States 19 633 1.1× 89 0.2× 48 0.3× 82 0.8× 34 0.4× 37 1.0k

Countries citing papers authored by Shiro Komba

Since Specialization
Citations

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

Fields of papers citing papers by Shiro Komba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shiro Komba

This figure shows the co-authorship network connecting the top 25 collaborators of Shiro Komba. A scholar is included among the top collaborators of Shiro Komba 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 Shiro Komba. Shiro Komba 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.
Kikkawa, Yoshihiro, et al.. (2023). Two-dimensional assemblies of saccharide-derived molecules on highly oriented pyrolytic graphite revealed by scanning tunneling microscopy. Colloids and Surfaces A Physicochemical and Engineering Aspects. 674. 131900–131900. 2 indexed citations
2.
Saburi, Wataru, et al.. (2023). Chemical synthesis of oligosaccharide derivatives with partial structure of β1-3/1-6 glucan, using monomeric units for the formation of β1-3 and β1-6 glucosidic linkages. Bioscience Biotechnology and Biochemistry. 87(10). 1111–1121. 1 indexed citations
3.
Saburi, Wataru, Takayoshi Tagami, Jian Yu, et al.. (2023). Molecular mechanism for endo-type action of glycoside hydrolase family 55 endo-β-1,3-glucanase on β1-3/1-6-glucan. Journal of Biological Chemistry. 299(11). 105294–105294. 3 indexed citations
5.
Tsuzuki, Wakako, Shiro Komba, & Eiichi Kotake‐Nara. (2019). Diversity in γ-oryzanol profiles of Japanese black-purple rice varieties. Journal of Food Science and Technology. 56(5). 2778–2786. 13 indexed citations
6.
Tanaka, Nobukiyo, Masahiro Nakajima, Shinji Kamisuki, et al.. (2019). Identification, characterization, and structural analyses of a fungal endo-β-1,2-glucanase reveal a new glycoside hydrolase family. Journal of Biological Chemistry. 294(19). 7942–7965. 15 indexed citations
7.
Tanaka, Nobukiyo, Masahiro Nakajima, Hiroyuki Nakai, et al.. (2018). Synthesis of three deoxy-sophorose derivatives for evaluating the requirement of hydroxy groups at position 3 and/or 3’ of sophorose by 1,2-β-oligoglucan phosphorylases. Carbohydrate Research. 468. 13–22. 3 indexed citations
8.
Tsuzuki, Wakako, et al.. (2018). The unique compositions of steryl ferulates in foxtail millet, barnyard millet and naked barley. Journal of Cereal Science. 81. 153–160. 11 indexed citations
9.
Fujimura, Takashi, et al.. (2016). Screening, expression, and characterization of an anti-human oxidized low-density lipoprotein single-chain variable fragment. Journal of Bioscience and Bioengineering. 122(3). 287–293. 5 indexed citations
10.
Xie, Qiuhong, et al.. (2013). Lectin-like oxidized LDL receptor-1 is palmitoylated and internalizes ligands via caveolae/raft-dependent endocytosis. Biochemical and Biophysical Research Communications. 434(3). 594–599. 18 indexed citations
11.
Ohnishi‐Kameyama, Mayumi, et al.. (2009). Minimum stable structure of the receptor for advanced glycation end product possesses multi ligand binding ability. Biochemical and Biophysical Research Communications. 386(1). 130–134. 13 indexed citations
12.
Matsunaga, Shigeru, Qiuhong Xie, Miyuki Kumano, et al.. (2007). Lectin-like oxidized low-density lipoprotein receptor (LOX-1) functions as an oligomer and oligomerization is dependent on receptor density. Experimental Cell Research. 313(6). 1203–1214. 29 indexed citations
13.
Campanero‐Rhodes, María Asunción, Robert A. Childs, M. KISO, et al.. (2006). Carbohydrate microarrays reveal sulphation as a modulator of siglec binding. Biochemical and Biophysical Research Communications. 344(4). 1141–1146. 84 indexed citations
14.
15.
Komba, Shiro, Masanori Yamaguchi, Hideharu Ishida, & Makoto Kiso. (2001). 6-O-Sulfo De-N-Acetylsialyl Lewis X as a Novel High-Affinity Ligand for Human L-Selectin: Total Synthesis and Structural Characterization. Biological Chemistry. 382(2). 233–40. 17 indexed citations
16.
Komba, Shiro, Ole Werdelin, Teis Jensen, & Morten Meldal. (2000). Synthesis of tumor associated sialyl-T-glycopeptides and their immunogenicity. Journal of Peptide Science. 6(12). 585–593. 13 indexed citations
17.
Komba, Shiro, Christine Galustian, H. Ishida, et al.. (1999). The First Total Synthesis of 6-Sulfo-de-N-acetylsialyl Lewisx Ganglioside: A Superior Ligand for Human L-Selectin. Angewandte Chemie International Edition. 38(8). 1131–1133. 62 indexed citations
18.
Tokuda, Akira, Toshio Ariga, Yukihiro Isogai, et al.. (1998). On the Specificity of Anti-Sulfoglucuronosyl Glycolipid Antibodies. Journal of Carbohydrate Chemistry. 17(4-5). 535–546. 19 indexed citations
19.
Galustian, Christine, Alexander Lawson, Shiro Komba, et al.. (1997). Sialyl-LewisxSequence 6-O-Sulfated atN-Acetylglucosamine Rather Than at Galactose Is the Preferred Ligand forl-Selectin and De-N-acetylation of the Sialic Acid Enhances the Binding Strength. Biochemical and Biophysical Research Communications. 240(3). 748–751. 73 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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