Daigo Inoue

3.8k total citations
17 papers, 704 citations indexed

About

Daigo Inoue is a scholar working on Cell Biology, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Daigo Inoue has authored 17 papers receiving a total of 704 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cell Biology, 10 papers in Molecular Biology and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Daigo Inoue's work include Microtubule and mitosis dynamics (9 papers), Reproductive Biology and Fertility (5 papers) and Epigenetics and DNA Methylation (4 papers). Daigo Inoue is often cited by papers focused on Microtubule and mitosis dynamics (9 papers), Reproductive Biology and Fertility (5 papers) and Epigenetics and DNA Methylation (4 papers). Daigo Inoue collaborates with scholars based in Germany, Japan and United States. Daigo Inoue's co-authors include Noriyuki Sagata, Joachim Wittbrodt, Yoshinori Kanemori, Nobushige Nakajo, Katsuhiro Uto, Oliver J. Gruß, Satchidananda Panda, Juan Ramón Martínez‐Morales, Lázaro Centanin and Stephan Kirchmaier and has published in prestigious journals such as Nature, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Daigo Inoue

17 papers receiving 704 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daigo Inoue Germany	12	513	330	115	87	65	17	704
Marco C. Betist Netherlands	16	892 1.7×	439 1.3×	83 0.7×	30 0.3×	113 1.7×	22	1.2k
Ahna R. Skop United States	16	1.0k 2.0×	966 2.9×	81 0.7×	46 0.5×	70 1.1×	27	1.5k
Manuela Melchionda United Kingdom	8	465 0.9×	195 0.6×	45 0.4×	29 0.3×	109 1.7×	8	743
Karsten H. Siller United States	12	775 1.5×	667 2.0×	35 0.3×	56 0.6×	167 2.6×	24	1.1k
Christian E. Rocheleau Canada	14	1.1k 2.1×	288 0.9×	288 2.5×	38 0.4×	64 1.0×	22	1.4k
Haigen Huang United States	15	561 1.1×	218 0.7×	60 0.5×	33 0.4×	33 0.5×	23	825
Iva Greenwald United States	9	684 1.3×	209 0.6×	75 0.7×	38 0.4×	158 2.4×	9	1.1k
Raghavendra Nagaraj United States	12	958 1.9×	225 0.7×	92 0.8×	41 0.5×	221 3.4×	16	1.1k
Diane G. Morton United States	15	1.4k 2.8×	469 1.4×	166 1.4×	101 1.2×	89 1.4×	17	1.9k
Gordon Polevoy Canada	10	923 1.8×	445 1.3×	45 0.4×	42 0.5×	112 1.7×	13	1.2k

Countries citing papers authored by Daigo Inoue

Since Specialization

Citations

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

Fields of papers citing papers by Daigo Inoue

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daigo Inoue

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

All Works

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17 of 17 papers shown

1.

Aghaallaei, Narges, Erika Tsingos, Daigo Inoue, et al.. (2021). αβ/γδ T cell lineage outcome is regulated by intrathymic cell localization and environmental signals. Science Advances. 7(29). 9 indexed citations

2.

Aghaallaei, Narges, et al.. (2021). Notch1 deficiency alters the migratory behavior of developing T cells and calcium signaling in the thymus of medaka. European Journal of Immunology. 52(2). 261–269. 1 indexed citations

3.

Takahashi, Eiichi, et al.. (2019). Dracena: A Real-Time IoT Service Platform Based on Flexible Composition of Data Streams. 596–601. 13 indexed citations

4.

Inoue, Daigo, Joachim Wittbrodt, & Oliver J. Gruß. (2018). Loss and Rebirth of the Animal Microtubule Organizing Center: How Maternal Expression of Centrosomal Proteins Cooperates with the Sperm Centriole in Zygotic Centrosome Reformation. BioEssays. 40(4). e1700135–e1700135. 8 indexed citations

5.

Inoue, Daigo, Manuel Stemmer, Thomas Thumberger, et al.. (2017). Expression of the novel maternal centrosome assembly factor Wdr8 is required for vertebrate embryonic mitoses. Nature Communications. 8(1). 14090–14090. 9 indexed citations

6.

Reinhardt, Robert, Lázaro Centanin, Daigo Inoue, et al.. (2015). Sox2, Tlx, Gli3, and Her9 converge on Rx2 to define retinal stem cells in vivo. The EMBO Journal. 34(11). 1572–1588. 50 indexed citations

7.

Bajoghli, Baubak, Paola Kuri, Daigo Inoue, et al.. (2015). Noninvasive In Toto Imaging of the Thymus Reveals Heterogeneous Migratory Behavior of Developing T Cells. The Journal of Immunology. 195(5). 2177–2186. 21 indexed citations

8.

Fischer, Ruth M., Bruno M. Fontinha, Stephan Kirchmaier, et al.. (2013). Co-Expression of VAL- and TMT-Opsins Uncovers Ancient Photosensory Interneurons and Motorneurons in the Vertebrate Brain. PLoS Biology. 11(6). e1001585–e1001585. 58 indexed citations

9.

Bärenz, Felix, Daigo Inoue, Hideki Yokoyama, et al.. (2013). The centriolar satellite protein SSX2IP promotes centrosome maturation. The Journal of Cell Biology. 202(1). 81–95. 52 indexed citations

10.

Isoda, Michitaka, Kazuhiro Suzuki, Kazuaki Nishino, et al.. (2011). Dynamic Regulation of Emi2 by Emi2-Bound Cdk1/Plk1/CK1 and PP2A-B56 in Meiotic Arrest of Xenopus Eggs. Developmental Cell. 21(3). 597–598. 1 indexed citations

11.

Inoue, Daigo & Joachim Wittbrodt. (2011). One for All—A Highly Efficient and Versatile Method for Fluorescent Immunostaining in Fish Embryos. PLoS ONE. 6(5). e19713–e19713. 118 indexed citations

12.

Isoda, Michitaka, Kazuhiro Suzuki, Kazuaki Nishino, et al.. (2011). Dynamic Regulation of Emi2 by Emi2-Bound Cdk1/Plk1/CK1 and PP2A-B56 in Meiotic Arrest of Xenopus Eggs. Developmental Cell. 21(3). 506–519. 34 indexed citations

13.

Ueno, Hiroyuki, Daigo Inoue, Yoshinori Kanemori, et al.. (2010). Emi2 Inhibition of the Anaphase-promoting Complex/Cyclosome Absolutely Requires Emi2 Binding via the C-Terminal RL Tail. Molecular Biology of the Cell. 21(6). 905–913. 25 indexed citations

14.

Inoue, Daigo, et al.. (2007). A direct link of the Mos–MAPK pathway to Erp1/Emi2 in meiotic arrest of Xenopus laevis eggs. Nature. 446(7139). 1100–1104. 104 indexed citations

15.

Inoue, Daigo, et al.. (2006). Erp1/Emi2 is essential for the meiosis I to meiosis II transition in Xenopus oocytes. Developmental Biology. 303(1). 157–164. 42 indexed citations

16.

Inoue, Daigo & Noriyuki Sagata. (2005). The Polo‐like kinase Plx1 interacts with and inhibits Myt1 after fertilization of Xenopus eggs. The EMBO Journal. 24(5). 1057–1067. 65 indexed citations

17.

Uto, Katsuhiro, et al.. (2004). Chk1, but not Chk2, inhibits Cdc25 phosphatases by a novel common mechanism. The EMBO Journal. 23(16). 3386–3396. 94 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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