Mitsuko Kosaka

736 total citations
31 papers, 579 citations indexed

About

Mitsuko Kosaka is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Mitsuko Kosaka has authored 31 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Oncology and 5 papers in Genetics. Recurrent topics in Mitsuko Kosaka's work include Retinal Development and Disorders (5 papers), Pluripotent Stem Cells Research (4 papers) and Retinoids in leukemia and cellular processes (4 papers). Mitsuko Kosaka is often cited by papers focused on Retinal Development and Disorders (5 papers), Pluripotent Stem Cells Research (4 papers) and Retinoids in leukemia and cellular processes (4 papers). Mitsuko Kosaka collaborates with scholars based in Japan, United Kingdom and Italy. Mitsuko Kosaka's co-authors include Maki Asami, Guangwei Sun, Masayo Takahashi, Masatoshi Haruta, Goro Eguchi, Hiroshi Ohta, Nobuhiko Mizuno, Yoshitake Nishimune, Yumi Kanegae and Akihiro Nishida and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Neuroscience.

In The Last Decade

Mitsuko Kosaka

31 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitsuko Kosaka Japan 13 468 109 100 97 63 31 579
Brigitte Angénieux Switzerland 4 405 0.9× 141 1.3× 39 0.4× 124 1.3× 87 1.4× 4 556
Sowmya Parameswaran India 14 451 1.0× 112 1.0× 30 0.3× 116 1.2× 86 1.4× 40 637
Petr Baranov United States 15 509 1.1× 144 1.3× 37 0.4× 174 1.8× 21 0.3× 42 678
Xing Zhao United States 16 853 1.8× 305 2.8× 104 1.0× 249 2.6× 207 3.3× 29 1.0k
Sarah Decembrini Switzerland 14 621 1.3× 238 2.2× 50 0.5× 98 1.0× 57 0.9× 18 777
Naoko Yoshimura Japan 12 300 0.6× 64 0.6× 45 0.5× 35 0.4× 27 0.4× 23 510
Stephanie B. Donaldson United Kingdom 8 306 0.7× 62 0.6× 60 0.6× 202 2.1× 14 0.2× 8 653
Karen Kinder United States 6 702 1.5× 120 1.1× 66 0.7× 250 2.6× 24 0.4× 8 855
Daniela Sanges Italy 12 768 1.6× 215 2.0× 148 1.5× 72 0.7× 37 0.6× 12 861
Qihong Xu United States 11 500 1.1× 70 0.6× 101 1.0× 18 0.2× 18 0.3× 15 817

Countries citing papers authored by Mitsuko Kosaka

Since Specialization
Citations

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

Fields of papers citing papers by Mitsuko Kosaka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuko Kosaka

This figure shows the co-authorship network connecting the top 25 collaborators of Mitsuko Kosaka. A scholar is included among the top collaborators of Mitsuko Kosaka 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 Mitsuko Kosaka. Mitsuko Kosaka 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.
Kosaka, Mitsuko, Nobuhiko Mizuno, Hiromasa Yamamoto, et al.. (2020). Prognostic value of OCT4A and SPP1C transcript variant co-expression in early-stage lung adenocarcinoma. BMC Cancer. 20(1). 521–521. 3 indexed citations
2.
Kagiwada, Satoshi, et al.. (2014). Immediate differentiation of neuronal cells from stem/progenitor-like cells in the avian iris tissues. Experimental Eye Research. 123. 16–26. 9 indexed citations
3.
Shinaoka, Akira, Ryusuke Momota, Mitsuko Kosaka, et al.. (2013). Architecture of the Subendothelial Elastic Fibers of Small Blood Vessels and Variations in Vascular Type and Size. Microscopy and Microanalysis. 19(2). 406–414. 10 indexed citations
4.
Mizuno, Nobuhiko & Mitsuko Kosaka. (2008). Novel Variants of Oct-3/4 Gene Expressed in Mouse Somatic Cells. Journal of Biological Chemistry. 283(45). 30997–31004. 26 indexed citations
5.
Ohta, Kunimasa, Ayako Ito, Sei Kuriyama, et al.. (2007). Tsukushi inhibits the proliferation of retinal stem/progenitor cells. Developmental Biology. 306(1). 391–391. 1 indexed citations
6.
Asami, Maki, Guangwei Sun, Masahiro Yamaguchi, & Mitsuko Kosaka. (2006). Multipotent cells from mammalian iris pigment epithelium. Developmental Biology. 304(1). 433–446. 45 indexed citations
7.
Sun, Guangwei, Maki Asami, Hiroshi Ohta, Jun Kosaka, & Mitsuko Kosaka. (2005). Retinal stem/progenitor properties of iris pigment epithelial cells. Developmental Biology. 289(1). 243–252. 59 indexed citations
8.
Haruta, Masatoshi, Mitsuko Kosaka, Yumi Kanegae, et al.. (2001). Induction of photoreceptor-specific phenotypes in adult mammalian iris tissue. Nature Neuroscience. 4(12). 1163–1164. 114 indexed citations
9.
Kosaka, Mitsuko, et al.. (1999). Localization of FGFR-1 in axotomized and peripheral nerve transplanted ferret retina. Neuroreport. 10(18). 3903–3907. 6 indexed citations
10.
Kosaka, Mitsuko, Ryuji Kodama, & Goro Eguchi. (1998). In VitroCulture System for Iris-Pigmented Epithelial Cells for Molecular Analysis of Transdifferentiation. Experimental Cell Research. 245(2). 245–251. 28 indexed citations
11.
Kosaka, Mitsuko, et al.. (1995). Induction of teratocarcinoma F9 cell differentiation with cis-diammine dichloroplatinum(II) (CDDP). Cancer Letters. 88(1). 81–86. 5 indexed citations
12.
Kosaka, Mitsuko, Masashi Takeda, Keishi Matsumoto, & Yoshitake Nishimune. (1994). F9 Cells Can be Differentiated toward Two Distinct, Mutually Exclusive Pathways by Retinoic Acid and Sodium Butyrate. Development Growth & Differentiation. 36(2). 223–230. 2 indexed citations
13.
14.
Kosaka, Mitsuko, et al.. (1993). The Induction of jun Genes during the Reversible Changes Induced with Sodium Butyrate on the Differentiation of F9 Cells. Experimental Cell Research. 208(2). 492–497. 14 indexed citations
15.
Kosaka, Mitsuko, et al.. (1993). Changes in Hox1.6, c-jun, and Oct-3 Gene Expressions Are Associated with Teratocarcinoma F9 Cell Differentiation in Three Different Ways of Induction. Experimental Cell Research. 205(1). 39–43. 12 indexed citations
16.
Nishina, Yukio, et al.. (1992). Expression of c-kit protooncogene is stimulated by cAMP in differentiated F9 mouse teratocarcinoma cells. Experimental Cell Research. 198(2). 352–356. 7 indexed citations
17.
Kosaka, Mitsuko, et al.. (1991). Reversible effects of sodium butyrate on the differentiation of F9 embryonal carcinoma cells. Experimental Cell Research. 192(1). 46–51. 23 indexed citations
18.
Nakao, Kazuhiko, Mitsuko Kosaka, & Shinichi Saito. (1991). Effects of erythroid differentiation factor (EDF) on proliferation and differentiation of human hematopoietic progenitors.. PubMed. 19(11). 1090–5. 21 indexed citations
19.
Nishimune, Yoshitake, Yukio Nishina, Mitsuko Kosaka, et al.. (1989). Isolation of mutants showing temperature-sensitive cell growth from embryonal carcinoma cells: Control of stem cell differentiation by incubation temperatures. Biochemical and Biophysical Research Communications. 165(1). 65–72. 3 indexed citations
20.
Watanabe, Tomoko, et al.. (1953). STUDIES ON THE REPRODUCTION OF THE SAURY, COLOLABIS SAIRA (BREVOORT), OF THE PACIFIC COAST OF JAPAN. Tohoku Journal of Agricultural Research. 3(2). 293–302. 3 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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