Shoko Ishibashi

1.1k total citations
19 papers, 834 citations indexed

About

Shoko Ishibashi is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Shoko Ishibashi has authored 19 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Shoko Ishibashi's work include CRISPR and Genetic Engineering (8 papers), Animal Genetics and Reproduction (7 papers) and Developmental Biology and Gene Regulation (4 papers). Shoko Ishibashi is often cited by papers focused on CRISPR and Genetic Engineering (8 papers), Animal Genetics and Reproduction (7 papers) and Developmental Biology and Gene Regulation (4 papers). Shoko Ishibashi collaborates with scholars based in United Kingdom, United States and Spain. Shoko Ishibashi's co-authors include Enrique Amaya, Nick R. Love, Yaoyao Chen, Karel Dorey, Jennifer L. Gallop, Paraskevi Kritsiligkou, Robert Lea, Yvette W. H. Koh, Kristen L. Kroll and Javier Iglesias‐González and has published in prestigious journals such as Nature Cell Biology, Molecular and Cellular Biology and Development.

In The Last Decade

Shoko Ishibashi

19 papers receiving 831 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shoko Ishibashi United Kingdom 12 598 129 111 105 99 19 834
Nick R. Love United Kingdom 10 506 0.8× 110 0.9× 49 0.4× 78 0.7× 90 0.9× 11 732
Ziad Al Tanoury France 14 752 1.3× 88 0.7× 103 0.9× 94 0.9× 61 0.6× 16 946
José M. Brito Brazil 16 479 0.8× 61 0.5× 155 1.4× 191 1.8× 139 1.4× 28 1.1k
Ashim Mukherjee India 15 755 1.3× 152 1.2× 118 1.1× 182 1.7× 118 1.2× 50 970
Tsutomu Kinoshita Japan 16 414 0.7× 125 1.0× 121 1.1× 76 0.7× 61 0.6× 61 700
Barbara H. Jennings United Kingdom 13 756 1.3× 88 0.7× 137 1.2× 200 1.9× 76 0.8× 18 1.1k
Yasuko Onuma Japan 20 1.2k 2.0× 106 0.8× 185 1.7× 94 0.9× 127 1.3× 44 1.5k
Tatsuo S. Hamazaki Japan 24 581 1.0× 188 1.5× 295 2.7× 78 0.7× 73 0.7× 36 1.5k
Raghavendra Nagaraj United States 12 958 1.6× 225 1.7× 112 1.0× 221 2.1× 100 1.0× 16 1.1k
Gabriela Nica Germany 9 815 1.4× 144 1.1× 298 2.7× 80 0.8× 126 1.3× 9 1.1k

Countries citing papers authored by Shoko Ishibashi

Since Specialization
Citations

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

Fields of papers citing papers by Shoko Ishibashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shoko Ishibashi

This figure shows the co-authorship network connecting the top 25 collaborators of Shoko Ishibashi. A scholar is included among the top collaborators of Shoko Ishibashi 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 Shoko Ishibashi. Shoko Ishibashi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Ishibashi, Shoko, et al.. (2023). Duox is the primary NADPH oxidase responsible for ROS production during adult caudal fin regeneration in zebrafish. iScience. 26(3). 106147–106147. 8 indexed citations
2.
Ishibashi, Shoko & Enrique Amaya. (2020). How to Grow Xenopus laevis Tadpole Stages to Adult. Cold Spring Harbor Protocols. 2021(3). pdb.prot106245–pdb.prot106245. 5 indexed citations
3.
Ishibashi, Shoko, et al.. (2019). Zebrafish duox mutations provide a model for human congenital hypothyroidism. Biology Open. 8(2). 18 indexed citations
4.
Han, Yue, Shoko Ishibashi, Javier Iglesias‐González, et al.. (2018). Ca2+-Induced Mitochondrial ROS Regulate the Early Embryonic Cell Cycle. Cell Reports. 22(1). 218–231. 78 indexed citations
5.
Paredes, Roberto, et al.. (2015). Xenopus: An in vivo model for imaging the inflammatory response following injury and bacterial infection. Developmental Biology. 408(2). 213–228. 31 indexed citations
6.
Love, Nick R., Yaoyao Chen, Shoko Ishibashi, et al.. (2013). Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration. Nature Cell Biology. 15(2). 222–228. 378 indexed citations
7.
Zhao, Yanan, Shoko Ishibashi, & Enrique Amaya. (2012). Reverse Genetic Studies Using Antisense Morpholino Oligonucleotides. Methods in molecular biology. 917. 143–154. 10 indexed citations
8.
Ishibashi, Shoko, Kristen L. Kroll, & Enrique Amaya. (2012). Generating Transgenic Frog Embryos by Restriction Enzyme Mediated Integration (REMI). Methods in molecular biology. 917. 185–203. 12 indexed citations
9.
Ishibashi, Shoko, Nick R. Love, & Enrique Amaya. (2012). A Simple Method of Transgenesis Using I-Sce I Meganuclease in Xenopus. Methods in molecular biology. 917. 205–218. 14 indexed citations
10.
Ishibashi, Shoko, et al.. (2012). Highly efficient bi-allelic mutation rates using TALENs in Xenopus tropicalis. Biology Open. 1(12). 1273–1276. 63 indexed citations
11.
Love, Nick R., Raphaël Thuret, Yaoyao Chen, et al.. (2011). pTransgenesis: a cross-species, modular transgenesis resource. Development. 138(24). 5451–5458. 46 indexed citations
12.
Göttgens, Berthold, Rita Ferreira, María J. Sánchez, et al.. (2010). cis-Regulatory Remodeling of the SCL Locus during Vertebrate Evolution. Molecular and Cellular Biology. 30(24). 5741–5751. 14 indexed citations
13.
Ishibashi, Shoko, Kristen L. Kroll, & Enrique Amaya. (2008). A Method for Generating Transgenic Frog Embryos. Methods in molecular biology. 461. 447–466. 62 indexed citations
14.
Ishibashi, Shoko, et al.. (2007). Generation of Transgenic Xenopus laevis: I. High-Speed Preparation of Egg Extracts. Cold Spring Harbor Protocols. 2007(9). pdb.prot4838–pdb.prot4838. 3 indexed citations
15.
Huang, Jeffrey K., Karel Dorey, Shoko Ishibashi, & Enrique Amaya. (2007). BDNF promotes target innervation of Xenopus mandibular trigeminal axons in vivo. BMC Developmental Biology. 7(1). 59–59. 23 indexed citations
16.
Ishibashi, Shoko, et al.. (2007). Generation of Transgenic Xenopus laevis: II. Sperm Nuclei Preparation. Cold Spring Harbor Protocols. 2007(9). pdb.prot4839–pdb.prot4839. 3 indexed citations
17.
Ishibashi, Shoko, et al.. (2007). Generation of Transgenic Xenopus laevis: III. Sperm Nuclear Transplantation. Cold Spring Harbor Protocols. 2007(9). pdb.prot4840–pdb.prot4840. 4 indexed citations
18.
Ishii, Yasuyuki, Shuichi Asakawa, Yusuke Taguchi, et al.. (2004). Construction of BAC library for the amphibian Xenopus tropicalis. Genes & Genetic Systems. 79(1). 49–51. 6 indexed citations
19.
Ishibashi, Shoko, et al.. (2001). Distinct roles of maf genes during Xenopus lens development. Mechanisms of Development. 101(1-2). 155–166. 56 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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