Toshiaki Noce

5.9k total citations · 2 hit papers
60 papers, 4.9k citations indexed

About

Toshiaki Noce is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Toshiaki Noce has authored 60 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 22 papers in Genetics and 12 papers in Reproductive Medicine. Recurrent topics in Toshiaki Noce's work include Pluripotent Stem Cells Research (16 papers), Animal Genetics and Reproduction (16 papers) and CRISPR and Genetic Engineering (14 papers). Toshiaki Noce is often cited by papers focused on Pluripotent Stem Cells Research (16 papers), Animal Genetics and Reproduction (16 papers) and CRISPR and Genetic Engineering (14 papers). Toshiaki Noce collaborates with scholars based in Japan, United States and Netherlands. Toshiaki Noce's co-authors include Naoki Tsunekawa, Yayoi Toyooka, Yasuhisa Matsui, Norio Nakatsuji, Shinichiro Chuma, Yoshihiko Takahashi, Yûkô Fukui, Hirokazu Fujimoto, Yuko Fujiwara and Yasuhiro Sakai and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Toshiaki Noce

60 papers receiving 4.8k citations

Hit Papers

The mouse homolog of Drosophila Vasa is required for the ... 2000 2026 2008 2017 2000 2003 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toshiaki Noce Japan 29 3.7k 2.0k 985 903 783 60 4.9k
Shogo Matoba Japan 32 5.5k 1.5× 2.0k 1.0× 1.4k 1.4× 710 0.8× 394 0.5× 76 6.4k
Shinichiro Chuma Japan 37 3.7k 1.0× 1.3k 0.7× 779 0.8× 840 0.9× 1.8k 2.4× 54 4.7k
Willy M. Baarends Netherlands 33 3.1k 0.9× 1.6k 0.8× 1.2k 1.2× 1.3k 1.5× 605 0.8× 75 4.5k
Vivian J. Bardwell United States 42 4.6k 1.3× 3.3k 1.7× 593 0.6× 1.2k 1.4× 403 0.5× 64 7.0k
Satoru Kobayashi Japan 40 4.4k 1.2× 1.7k 0.9× 483 0.5× 352 0.4× 583 0.7× 142 6.1k
E. M. Eddy United States 32 2.2k 0.6× 1.2k 0.6× 917 0.9× 1.3k 1.4× 299 0.4× 53 4.1k
Reiner A. Veitia France 54 5.6k 1.5× 3.8k 1.9× 1.5k 1.6× 1.3k 1.4× 2.1k 2.7× 187 8.7k
Silvia Garagna Italy 36 2.1k 0.6× 1.1k 0.6× 1.4k 1.4× 687 0.8× 1.0k 1.3× 161 3.8k
Ryohei Sekido United Kingdom 25 3.0k 0.8× 2.9k 1.5× 486 0.5× 1.1k 1.2× 170 0.2× 30 4.2k
Laura L. Tres United States 36 2.0k 0.5× 1.5k 0.7× 1.5k 1.6× 2.2k 2.4× 370 0.5× 91 4.1k

Countries citing papers authored by Toshiaki Noce

Since Specialization
Citations

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

Fields of papers citing papers by Toshiaki Noce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshiaki Noce

This figure shows the co-authorship network connecting the top 25 collaborators of Toshiaki Noce. A scholar is included among the top collaborators of Toshiaki Noce 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 Toshiaki Noce. Toshiaki Noce 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.
Yamazaki, Atsushi, Kazuya EDAMURA, Hisashi Shibuya, et al.. (2022). Step‐by‐step protocols for non‐viral derivation of transgene‐free induced pluripotent stem cells from somatic fibroblasts of multiple mammalian species. Development Growth & Differentiation. 64(6). 325–341. 2 indexed citations
2.
Yamamoto, Masafumi, et al.. (2021). Generation of a common marmoset embryonic stem cell line CMES40-OC harboring a POU5F1 (OCT4)-2A-mCerulean3 knock-in reporter allele. Stem Cell Research. 53. 102308–102308. 5 indexed citations
3.
Okano, Hideyuki, et al.. (2016). JMJD1C Exhibits Multiple Functions in Epigenetic Regulation during Spermatogenesis. PLoS ONE. 11(9). e0163466–e0163466. 15 indexed citations
4.
Hayashi, Yohei, et al.. (2016). Selective de-repression of germ cell-specific genes in mouse embryonic fibroblasts in a permissive epigenetic environment. Scientific Reports. 6(1). 32932–32932. 4 indexed citations
5.
Okamura, Daiji, Makiko Ikeda, Keiko Ozato, et al.. (2012). Cell cycle gene-specific control of transcription has a critical role in proliferation of primordial germ cells. Genes & Development. 26(22). 2477–2482. 27 indexed citations
6.
Shoji, Masanobu, Takashi Tanaka, Mihoko Hosokawa, et al.. (2009). The TDRD9-MIWI2 Complex Is Essential for piRNA-Mediated Retrotransposon Silencing in the Mouse Male Germline. Developmental Cell. 17(6). 775–787. 273 indexed citations
7.
Mizukami, Takuo, Madoka Kuramitsu, Kazuya Takizawa, et al.. (2008). Identification of Transcripts Commonly Expressed in Both Hematopoietic and Germ-Line Stem Cells. Stem Cells and Development. 17(1). 67–80. 13 indexed citations
8.
Mise, Nathan, Michihiko Sugimoto, Takehiko Ogawa, et al.. (2008). Differences and similarities in the developmental status of embryo‐derived stem cells and primordial germ cells revealed by global expression profiling. Genes to Cells. 13(8). 863–877. 45 indexed citations
9.
Hosokawa, Mihoko, Masanobu Shoji, K Kitamura, et al.. (2006). Tudor-related proteins TDRD1/MTR-1, TDRD6 and TDRD7/TRAP: Domain composition, intracellular localization, and function in male germ cells in mice. Developmental Biology. 301(1). 38–52. 131 indexed citations
10.
Yoshioka, Hidefumi, Yoshiyasu Ishimaru, Noriyuki Sugiyama, et al.. (2005). Mesonephric FGF signaling is associated with the development of sexually indifferent gonadal primordium in chick embryos. Developmental Biology. 280(1). 150–161. 25 indexed citations
11.
Nakamura, Takahisa, Ryoji Yao, Takehiko Ogawa, et al.. (2004). Oligo-astheno-teratozoospermia in mice lacking Cnot7, a regulator of retinoid X receptor beta. Nature Genetics. 36(5). 528–533. 113 indexed citations
12.
Toyooka, Yayoi, et al.. (2003). Embryonic stem cells can form germ cells in vitro. Proceedings of the National Academy of Sciences. 100(20). 11457–11462. 534 indexed citations breakdown →
13.
Toyooka, Yayoi, et al.. (2000). Expression and intracellular localization of mouse Vasa-homologue protein during germ cell development. Mechanisms of Development. 93(1-2). 139–149. 467 indexed citations
14.
Yamazaki, Yukiko, Hirokazu Fujimoto, Hironori Ando, et al.. (1998). In Vivo Gene Transfer to Mouse Spermatogenic Cells by Deoxyribonucleic Acid Injection into Seminiferous Tubules and Subsequent Electroporation1. Biology of Reproduction. 59(6). 1439–1444. 80 indexed citations
15.
Abe, Kuniya & Toshiaki Noce. (1997). A DEAD-family protein gene, Ddx4, encoding a murine homolog of Drosophila vasa maps to the distal end of mouse Chromosome 13. Mammalian Genome. 8(8). 622–623. 9 indexed citations
16.
Noce, Toshiaki, Yuko Fujiwara, Michihiko Ito, et al.. (1993). A Novel Murine Zinc Finger Gene Mapped within the tw18 Deletion Region Expresses in Germ Cells and Embryonic Nervous System. Developmental Biology. 155(2). 409–422. 30 indexed citations
17.
Fukui, Yûkô, Toshiaki Noce, Tetsuya Ueda, et al.. (1992). Isolation and characterization of cDNA encoding a spicule matrix protein in Hemicentrotus pulcherrimus micromeres. The International Journal of Developmental Biology. 36(3). 353–361. 18 indexed citations
18.
Tsang, Adrian, Caroline E. Grant, Gerard Bain, et al.. (1988). Characterization of an unusual cAMP receptor and its related polypeptides in Dictyostelium discoideum. Developmental Genetics. 9(4-5). 237–245. 7 indexed citations
19.
Noce, Toshiaki & Ikuo Takeuchi. (1985). Prestalk/prespore differentiation tendency of Dictyostelium discoideum cells as detected by a stalk-specific monoclonal antibody. Developmental Biology. 109(1). 157–164. 19 indexed citations
20.
Nakahara, Yasuo, Toshiaki Noce, & Ikuo Takeuchi. (1985). Prestalk/prespore Differentiation of Dictyostelium Cells under the Conditions Favoring Stalk or Spore Cell Formation*. Development Growth & Differentiation. 27(5). 591–597. 1 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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