Mamiko Yajima

1.7k total citations
45 papers, 1.2k citations indexed

About

Mamiko Yajima is a scholar working on Molecular Biology, Aquatic Science and Ocean Engineering. According to data from OpenAlex, Mamiko Yajima has authored 45 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 11 papers in Aquatic Science and 11 papers in Ocean Engineering. Recurrent topics in Mamiko Yajima's work include Developmental Biology and Gene Regulation (14 papers), Marine Ecology and Invasive Species (11 papers) and Echinoderm biology and ecology (11 papers). Mamiko Yajima is often cited by papers focused on Developmental Biology and Gene Regulation (14 papers), Marine Ecology and Invasive Species (11 papers) and Echinoderm biology and ecology (11 papers). Mamiko Yajima collaborates with scholars based in United States, Japan and Italy. Mamiko Yajima's co-authors include Gary M. Wessel, Celina E. Juliano, Masato Kiyomoto, Eric A. Gustafson, David A. Barbie, Shunsuke Kitajima, Tran C. Thai, Sujuan Guo, Yoichiro Mitsuishi and Brandon Piel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Development.

In The Last Decade

Mamiko Yajima

42 papers receiving 1.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Mamiko Yajima 651 259 253 195 191 45 1.2k
Jia L. Song 1.2k 1.8× 138 0.5× 165 0.7× 73 0.4× 64 0.3× 48 1.8k
Mariano Loza‐Coll 565 0.9× 209 0.8× 775 3.1× 52 0.3× 104 0.5× 17 1.4k
Carol L. Reinisch 409 0.6× 43 0.2× 502 2.0× 131 0.7× 244 1.3× 67 1.6k
Ian Robbins 444 0.7× 55 0.2× 92 0.4× 91 0.5× 100 0.5× 34 998
Lydia Besnardeau 1.2k 1.8× 378 1.5× 99 0.4× 281 1.4× 43 0.2× 33 1.9k
Kouichi Kawamura 411 0.6× 164 0.6× 122 0.5× 28 0.1× 29 0.2× 62 1.3k
Alessandro Coppe 604 0.9× 100 0.4× 191 0.8× 25 0.1× 39 0.2× 29 1.1k
Fabio Iannelli 1.3k 1.9× 27 0.1× 95 0.4× 46 0.2× 194 1.0× 35 1.8k
Kohji Nomura 329 0.5× 125 0.5× 120 0.5× 58 0.3× 86 0.5× 34 729
Giovanni Spinelli 775 1.2× 138 0.5× 36 0.1× 97 0.5× 32 0.2× 58 1.0k

Countries citing papers authored by Mamiko Yajima

Since Specialization
Citations

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

Fields of papers citing papers by Mamiko Yajima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mamiko Yajima

This figure shows the co-authorship network connecting the top 25 collaborators of Mamiko Yajima. A scholar is included among the top collaborators of Mamiko Yajima 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 Mamiko Yajima. Mamiko Yajima 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.
Yajima, Mamiko, et al.. (2024). Visualizing metabolic regulation using metabolic biosensors during sea urchin embryogenesis. Developmental Biology. 516. 122–129.
3.
Yajima, Mamiko, et al.. (2023). Characterization of p53/p63/p73 and Myc expressions during embryogenesis of the sea urchin. Developmental Dynamics. 253(3). 333–350. 3 indexed citations
4.
Kitajima, Shunsuke, Fengkai Li, Nagib Ahsan, et al.. (2023). The germline factor DDX4 contributes to the chemoresistance of small cell lung cancer cells. Communications Biology. 6(1). 65–65. 7 indexed citations
5.
Yajima, Mamiko, et al.. (2023). Vasa, a regulator of localized mRNA translation on the spindle. BioEssays. 45(4). e2300004–e2300004. 3 indexed citations
6.
Sakuma, Tetsushi, Naoaki Sakamoto, Takashi Yamamoto, et al.. (2021). CRISPR-Cas9 editing of non-coding genomic loci as a means of controlling gene expression in the sea urchin. Developmental Biology. 472. 85–97. 12 indexed citations
7.
Wessel, Gary M., et al.. (2021). Light-induced, spatiotemporal control of protein in the developing embryo of the sea urchin. Developmental Biology. 478. 13–24. 3 indexed citations
8.
Yajima, Mamiko, et al.. (2020). Localized translation on the mitotic apparatus: A history and perspective. Developmental Biology. 468(1-2). 55–58. 10 indexed citations
9.
Yajima, Mamiko, et al.. (2020). Diversity of activator of G-protein signaling (AGS)-family proteins and their impact on asymmetric cell division across taxa. Developmental Biology. 465(2). 89–99. 6 indexed citations
10.
Wessel, Gary M., Masato Kiyomoto, Tun‐Li Shen, & Mamiko Yajima. (2020). Genetic manipulation of the pigment pathway in a sea urchin reveals distinct lineage commitment prior to metamorphosis in the bilateral to radial body plan transition. Scientific Reports. 10(1). 1973–1973. 25 indexed citations
11.
Wessel, Gary M., et al.. (2019). Evolutionary modification of AGS protein contributes to formation of micromeres in sea urchins. Nature Communications. 10(1). 3779–3779. 19 indexed citations
12.
Kitajima, Shunsuke, Elena V. Ivanova, Sujuan Guo, et al.. (2018). Suppression of STING Associated with LKB1 Loss in KRAS-Driven Lung Cancer. Cancer Discovery. 9(1). 34–45. 348 indexed citations
13.
Yajima, Mamiko, et al.. (2018). An optogenetic approach to control protein localization during embryogenesis of the sea urchin. Developmental Biology. 441(1). 19–30. 8 indexed citations
14.
Oulhen, Nathalie, T. Yoshida, Mamiko Yajima, et al.. (2013). The 3′UTR of nanos2 directs enrichment in the germ cell lineage of the sea urchin. Developmental Biology. 377(1). 275–283. 23 indexed citations
15.
Gustafson, Eric A., Mamiko Yajima, Celina E. Juliano, & Gary M. Wessel. (2010). Post-translational regulation by gustavus contributes to selective Vasa protein accumulation in multipotent cells during embryogenesis. Developmental Biology. 349(2). 440–450. 51 indexed citations
16.
Yajima, Mamiko, et al.. (2010). Implication ofHpEtsin Gene Regulatory Networks Responsible for Specification of Sea Urchin Skeletogenic Primary Mesenchyme Cells. ZOOLOGICAL SCIENCE. 27(8). 638–646. 13 indexed citations
17.
Sasakura, Yasunori, Junko Yaguchi, Shunsuke Yaguchi, & Mamiko Yajima. (2010). Excision and Transposition Activity of Tc1/marinerSuperfamily Transposons in Sea Urchin Embryos. ZOOLOGICAL SCIENCE. 27(3). 256–262. 4 indexed citations
18.
Juliano, Celina E., Mamiko Yajima, & Gary M. Wessel. (2009). Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo. Developmental Biology. 337(2). 220–232. 62 indexed citations
19.
Yajima, Mamiko. (2007). A switch in the cellular basis of skeletogenesis in late-stage sea urchin larvae. Developmental Biology. 307(2). 272–281. 31 indexed citations
20.
Yajima, Mamiko, Masato Kiyomoto, & Koji Akasaka. (2007). Ars insulator protects transgenes from long-term silencing in sea urchin larva. Development Genes and Evolution. 217(4). 331–336. 14 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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