Taichi Noda

3.5k total citations
56 papers, 1.2k citations indexed

About

Taichi Noda is a scholar working on Reproductive Medicine, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Taichi Noda has authored 56 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Reproductive Medicine, 26 papers in Public Health, Environmental and Occupational Health and 23 papers in Molecular Biology. Recurrent topics in Taichi Noda's work include Sperm and Testicular Function (30 papers), Reproductive Biology and Fertility (25 papers) and CRISPR and Genetic Engineering (10 papers). Taichi Noda is often cited by papers focused on Sperm and Testicular Function (30 papers), Reproductive Biology and Fertility (25 papers) and CRISPR and Genetic Engineering (10 papers). Taichi Noda collaborates with scholars based in Japan, United States and Sweden. Taichi Noda's co-authors include Masahito Ikawa, Yoshitaka Fujihara, Martin M. Matzuk, Seiya Oura, Hiroshi Harayama, Yonggang Lu, Takafumi Matsumura, Sumire Kobayashi, Asami Oji and Kaori Nozawa and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Taichi Noda

54 papers receiving 1.2k citations

Peers

Taichi Noda

PHEOH

GENET

David L’Hôte France

Chizuru Ito Japan

Venkataraman Sriraman United States

Yang Zeng United States

Paula R. Brown United States

Giovanna Berruti Italy

Stephen Palmer United States

Adrien Georges France

Misung Jo United States

Geert Hamer Netherlands

David L’Hôte France

Taichi Noda

504 ×0.8

354 ×0.6

325 ×0.7

PHEOH

412 ×1.2

GENET

121 ×1.4

Citations per year, relative to Taichi Noda Taichi Noda (= 1×) peers David L’Hôte

Countries citing papers authored by Taichi Noda

Since Specialization

Citations

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

Fields of papers citing papers by Taichi Noda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taichi Noda

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Noda, Taichi, Daisuke Mashiko, Yongcun Qu, et al.. (2025). GALNTL5 binds GalNAc and is required for migration through the uterotubal junction and sperm-zona pellucida binding. Nature Communications. 16(1). 8264–8264.

Hirashima, Tsuyoshi, et al.. (2024). Collective sperm movement in mammalian reproductive tracts. Seminars in Cell and Developmental Biology. 166. 13–21.

Kobayashi, Hiroko, Keisuke Shimada, Seiya Oura, et al.. (2024). MYCBPAP is a central apparatus protein required for centrosome–nuclear envelope docking and sperm tail biogenesis in mice. Journal of Cell Science. 137(16). 4 indexed citations

Kim, Jae‐Beom, Young Suk Yu, Taichi Noda, et al.. (2024). USF2 and TFEB compete in regulating lysosomal and autophagy genes. Nature Communications. 15(1). 8334–8334. 12 indexed citations

Noda, Taichi, et al.. (2024). Multiple genes in the Pate5–13 genomic region contribute to ADAM3 processing. Biology of Reproduction. 110(4). 750–760. 2 indexed citations

Noda, Taichi, et al.. (2023). The testis-, epididymis-, or seminal vesicle-enriched genes Aldoart2, Serpina16, Aoc1l3, and Pate14 are not essential for male fertility in mice. EXPERIMENTAL ANIMALS. 72(3). 314–323. 4 indexed citations

Lu, Yonggang, Kentaro Shimada, Shaogeng Tang, et al.. (2023). 1700029I15Rik orchestrates the biosynthesis of acrosomal membrane proteins required for sperm–egg interaction. Proceedings of the National Academy of Sciences. 120(8). e2207263120–e2207263120. 10 indexed citations

Kiyozumi, Daiji, Kentaro Shimada, Chihiro Emori, et al.. (2023). A small secreted protein NICOL regulates lumicrine-mediated sperm maturation and male fertility. Nature Communications. 14(1). 2354–2354. 18 indexed citations

Noda, Taichi, Andreas Blaha, Yoshitaka Fujihara, et al.. (2022). Sperm membrane proteins DCST1 and DCST2 are required for sperm-egg interaction in mice and fish. Communications Biology. 5(1). 332–332. 26 indexed citations

10.

Lu, Yonggang, Jintao Zhang, Keisuke Shimada, et al.. (2021). LRRC23 is a conserved component of the radial spoke that is necessary for sperm motility and male fertility in mice. Journal of Cell Science. 134(20). 21 indexed citations

11.

Morohoshi, Akane, et al.. (2021). FAM71F1 binds to RAB2A and RAB2B and is essential for acrosome formation and male fertility in mice. Development. 148(21). 23 indexed citations

12.

Oura, Seiya, Taichi Noda, Naoko Morimura, et al.. (2021). Precise CAG repeat contraction in a Huntington’s Disease mouse model is enabled by gene editing with SpCas9-NG. Communications Biology. 4(1). 771–771. 23 indexed citations

13.

Kim, Chang Rok, Taichi Noda, Yuki Okada, Masahito Ikawa, & Sung Hee Baek. (2021). Protocol for isolation of spermatids from mouse testes. STAR Protocols. 2(1). 100254–100254. 4 indexed citations

14.

Kim, Chang Rok, Taichi Noda, Hyun-Kyung Kim, et al.. (2020). PHF7 Modulates BRDT Stability and Histone-to-Protamine Exchange during Spermiogenesis. Cell Reports. 32(4). 107950–107950. 30 indexed citations

15.

Kiyozumi, Daiji, Taichi Noda, Ryo Yamaguchi, et al.. (2020). NELL2-mediated lumicrine signaling through OVCH2 is required for male fertility. Science. 368(6495). 1132–1135. 77 indexed citations

16.

Noda, Taichi, Yonggang Lu, Yoshitaka Fujihara, et al.. (2020). Sperm proteins SOF1, TMEM95, and SPACA6 are required for sperm−oocyte fusion in mice. Proceedings of the National Academy of Sciences. 117(21). 11493–11502. 103 indexed citations

17.

Akıncılar, Semih Can, Lele Wu, Bilal Unal, et al.. (2020). NAIL: an evolutionarily conserved lncRNA essential for licensing coordinated activation of p38 and NFκB in colitis. Gut. 70(10). 1857–1871. 48 indexed citations

18.

Noda, Taichi, Yoshitaka Fujihara, Takafumi Matsumura, et al.. (2018). Seminal vesicle secretory protein 7, PATE4, is not required for sperm function but for copulatory plug formation to ensure fecundity†. Biology of Reproduction. 100(4). 1035–1045. 21 indexed citations

19.

Kondo, Natsuko, Akihisa Takahashi, Eiichiro Mori, et al.. (2011). FANCD1/BRCA2 Plays Predominant Role in the Repair of DNA Damage Induced by ACNU or TMZ. PLoS ONE. 6(5). e19659–e19659. 35 indexed citations

20.

Kondo, Natsuko, Akihisa Takahashi, Eiichiro Mori, et al.. (2010). DNA ligase IV is a potential molecular target in ACNU sensitivity. Cancer Science. 101(8). 1881–1885. 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.

Explore authors with similar magnitude of impact