Jun Shinga
About
Jun Shinga is a scholar working on Molecular Biology, Immunology and Oncology.
According to data from OpenAlex, Jun Shinga has authored 28 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Immunology and 6 papers in Oncology. Recurrent topics in Jun Shinga's work include Epigenetics and DNA Methylation (10 papers), Immune Cell Function and Interaction (9 papers) and Immunotherapy and Immune Responses (6 papers). Jun Shinga is often cited by papers focused on Epigenetics and DNA Methylation (10 papers), Immune Cell Function and Interaction (9 papers) and Immunotherapy and Immune Responses (6 papers). Jun Shinga collaborates with scholars based in Japan, United States and United Kingdom. Jun Shinga's co-authors include Haruhiko Koseki, Takaho A. Endo, Tetsuro Toyoda, Yoko Mizutani-Koseki, Jafar Sharif, Akihiro Iwamatsu, Shoji Tajima, Masaki Okano, Masahiro Muto and Shin‐ichiro Takebayashi and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.
In The Last Decade
Jun Shinga
28 papers receiving 2.4k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Jun Shinga Japan | 19 | 2.0k | 549 | 304 | 216 | 170 | 28 | 2.4k | ||
| David J. Picketts Canada | 28 | 2.2k 1.1× | 934 1.7× | 241 0.8× | 147 0.7× | 213 1.3× | 64 | 2.7k | ||
| Andrei Kuzmichev United States | 9 | 2.6k 1.3× | 373 0.7× | 120 0.4× | 209 1.0× | 264 1.6× | 9 | 2.9k | ||
| Véronique Azuara United Kingdom | 21 | 2.5k 1.2× | 398 0.7× | 574 1.9× | 167 0.8× | 164 1.0× | 30 | 3.1k | ||
| Dimitrina D. Pravtcheva United States | 24 | 1.2k 0.6× | 563 1.0× | 380 1.3× | 280 1.3× | 116 0.7× | 54 | 1.8k | ||
| Mark Wijgerde Netherlands | 17 | 1.9k 0.9× | 514 0.9× | 111 0.4× | 108 0.5× | 97 0.6× | 21 | 2.1k | ||
| Sumiyo Morita Japan | 25 | 1.7k 0.9× | 501 0.9× | 365 1.2× | 384 1.8× | 383 2.3× | 48 | 2.2k | ||
| Suzana Hadjur United Kingdom | 15 | 2.5k 1.3× | 389 0.7× | 282 0.9× | 107 0.5× | 203 1.2× | 22 | 2.8k | ||
| Dana J. Huebert United States | 8 | 5.0k 2.5× | 833 1.5× | 313 1.0× | 221 1.0× | 459 2.7× | 8 | 5.5k | ||
| Jafar Sharif Japan | 26 | 3.1k 1.5× | 706 1.3× | 179 0.6× | 124 0.6× | 382 2.2× | 44 | 3.4k | ||
| Stéphan Gasca France | 13 | 1.5k 0.8× | 480 0.9× | 259 0.9× | 172 0.8× | 124 0.7× | 18 | 1.8k |
Countries citing papers authored by Jun Shinga
Since
Specialization
Citations
This map shows the geographic impact of Jun Shinga'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 Jun Shinga with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jun Shinga more than expected).
Fields of papers citing papers by Jun Shinga
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Jun Shinga. 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 Jun Shinga. The network helps show where Jun Shinga may publish in the future.
Co-authorship network of co-authors of Jun Shinga
This figure shows the co-authorship network connecting the top 25 collaborators of Jun Shinga. A scholar is included among the top collaborators of Jun Shinga 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 Jun Shinga. Jun Shinga is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Kumagai, Jin, Masahiro Kiuchi, Kota Kokubo, et al.. (2023). The USP7-STAT3-granzyme-Par-1 axis regulates allergic inflammation by promoting differentiation of IL-5-producing Th2 cells. Proceedings of the National Academy of Sciences. 120(49). e2302903120–e2302903120.
2.
Iyoda, Tomonori, Kanako Shimizu, Masami Kawamura, et al.. (2023). Augmenting Granzyme B–Expressing NK Cells by Invariant NKT Ligand–Loaded APCs in Patients with Postoperative Early Stage Non–Small Cell Lung Cancer: Results of a Randomized Phase II Study. ImmunoHorizons. 7(1). 1–16.
3.
Fujii, Shin‐ichiro, Toyotaka Kawamata, Kanako Shimizu, et al.. (2022). Reinvigoration of innate and adaptive immunity via therapeutic cellular vaccine for patients with AML. Molecular Therapy — Oncolytics. 27. 315–332.
4.
Shimizu, Kanako, Satoru Yamasaki, Jun Shinga, et al.. (2016). Systemic DC Activation Modulates the Tumor Microenvironment and Shapes the Long-Lived Tumor-Specific Memory Mediated by CD8+ T Cells. Cancer Research. 76(13). 3756–3766.
5.
Shimizu, Kanako, Jun Shinga, Satoru Yamasaki, et al.. (2015). Transfer of mRNA Encoding Invariant NKT Cell Receptors Imparts Glycolipid Specific Responses to T Cells and γδT Cells. PLoS ONE. 10(6). e0131477–e0131477.
6.
Sato, Yusuke, Kanako Shimizu, Jun Shinga, et al.. (2015). Characterization of the myeloid-derived suppressor cell subset regulated by NK cells in malignant lymphoma. OncoImmunology. 4(3). e995541–e995541.
7.
Hirabayashi, Yusuke, Kelsey M. Tyssowski, Jun Shinga, et al.. (2014). The polycomb component Ring1B regulates the timed termination of subcerebral projection neuron production during mouse neocortical development. Development. 141(22). 4343–4353.
8.
Shimizu, Kanako, Takuya Mizuno, Jun Shinga, et al.. (2012). Vaccination with Antigen-Transfected, NKT Cell Ligand–Loaded, Human Cells Elicits Robust In Situ Immune Responses by Dendritic Cells. Cancer Research. 73(1). 62–73.
9.
Mochizuki‐Kashio, Makiko, Yuta Mishima, Satoru Miyagi, et al.. (2011). Dependency on the polycomb gene Ezh2 distinguishes fetal from adult hematopoietic stem cells. Blood. 118(25). 6553–6561.
10.
Li, Xiangzhi, Kyoichi Isono, Daisuke Yamada, et al.. (2010). Mammalian Polycomb-Like Pcl2/Mtf2 Is a Novel Regulatory Component of PRC2 That Can Differentially Modulate Polycomb Activity both at the Hox Gene Cluster and at Cdkn2a Genes. Molecular and Cellular Biology. 31(2). 351–364.
11.
Hirabayashi, Yusuke, Masafumi Tsuboi, Takaho A. Endo, et al.. (2009). Polycomb Limits the Neurogenic Competence of Neural Precursor Cells to Promote Astrogenic Fate Transition. Neuron. 63(5). 600–613.
12.
Takahashi, Noriyuki, Shin’ya Ohmori, Hiroshi Mamada, et al.. (2005). Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development. The International Journal of Developmental Biology. 49(8). 939–951.
13.
Shinga, Jun, et al.. (2001). Early patterning of the prospective midbrain–hindbrain boundary by the HES-related gene XHR1 in Xenopus embryos. Mechanisms of Development. 109(2). 225–239.
14.
Shibata, Mikihito, Mari Itoh, Shin’ya Ohmori, Jun Shinga, & Masanori Taira. (2001). Systematic Screening and Expression Analysis of the Head Organizer Genes in Xenopus Embryos. Developmental Biology. 239(2). 241–256.
15.
Shibata, Mikihito, Hirofumi Ono, Hiroki Hikasa, Jun Shinga, & Masanori Taira. (2000). Xenopus crescent encoding a Frizzled-like domain is expressed in the Spemann organizer and pronephros. Mechanisms of Development. 96(2). 243–246.
16.
Kai, Masatake, Takayasu Higo, Chikara Kaito, et al.. (2000). Maternal program of apoptosis activated shortly after midblastula transition by overexpression of S-adenosylmethionine decarboxylase in Xenopus early embryos. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 126(2). 149–155.
17.
Shibata, Maho, Jun Shinga, Yukuto Yasuhiko, et al.. (1998). Overexpression of S-adenosylmethionine decarboxylase (SAMDC) in early Xenopus embryos induces cell dissociation and inhibits transition from the blastula to gastrula stage. The International Journal of Developmental Biology. 42(5). 675–686.
18.
Shinga, Jun, et al.. (1996). Maternal and zygotic expression of mRNA for S-adenosylmethionine decarboxylase and its relevance to the unique polyamine composition in Xenopus oocytes and embryos. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1308(1). 31–40.
19.
Shinga, Jun, et al.. (1996). Cloning ofXenopusTFIIS and Its Expression in Oocytes and Early Embryos. Biochemical and Biophysical Research Communications. 222(2). 541–546.
20.
Shiokawa, K., Rick Kurashima, & Jun Shinga. (1994). Temporal control of gene expression from endogenous and exogenously-introduced DNAs in early embryogenesis of Xenopus laevis. The International Journal of Developmental Biology. 38(2). 249–255.
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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