Naruyoshi Fujiwara

671 total citations
20 papers, 515 citations indexed

About

Naruyoshi Fujiwara is a scholar working on Molecular Biology, Developmental Neuroscience and Ophthalmology. According to data from OpenAlex, Naruyoshi Fujiwara has authored 20 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Developmental Neuroscience and 5 papers in Ophthalmology. Recurrent topics in Naruyoshi Fujiwara's work include Neurogenesis and neuroplasticity mechanisms (6 papers), Pluripotent Stem Cells Research (5 papers) and Ocular Diseases and Behçet’s Syndrome (5 papers). Naruyoshi Fujiwara is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (6 papers), Pluripotent Stem Cells Research (5 papers) and Ocular Diseases and Behçet’s Syndrome (5 papers). Naruyoshi Fujiwara collaborates with scholars based in Japan and United States. Naruyoshi Fujiwara's co-authors include Nagisa Arimitsu, Noboru Suzuki, Jun Shimizu, Tomoko Suzuki, Sueshige Wakisaka, Kenji Takai, Yuji Ueda, Erika Takada, Takao Kubota and Yutaka Ueda and has published in prestigious journals such as PLoS ONE, FEBS Letters and International Journal of Molecular Sciences.

In The Last Decade

Naruyoshi Fujiwara

19 papers receiving 509 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naruyoshi Fujiwara Japan 11 260 158 87 82 73 20 515
Nagisa Arimitsu Japan 16 489 1.9× 165 1.0× 92 1.1× 137 1.7× 103 1.4× 40 874
Erika Takada Japan 10 254 1.0× 110 0.7× 44 0.5× 47 0.6× 54 0.7× 18 467
Ruotong Ren China 12 526 2.0× 55 0.3× 34 0.4× 201 2.5× 104 1.4× 22 822
Xiu Jun Song United States 6 121 0.5× 298 1.9× 31 0.4× 63 0.8× 12 0.2× 6 1.2k
Anna Garefalaki United Kingdom 7 260 1.0× 13 0.1× 53 0.6× 53 0.6× 55 0.8× 7 1.2k
Steven B. Koevary United States 13 104 0.4× 144 0.9× 16 0.2× 25 0.3× 26 0.4× 27 574
M. J. Leboutet France 14 187 0.7× 13 0.1× 30 0.3× 57 0.7× 64 0.9× 35 654
Yangfan Yang China 15 173 0.7× 308 1.9× 15 0.2× 36 0.4× 33 0.5× 45 613
Alexandra Monastirli Greece 13 146 0.6× 49 0.3× 49 0.6× 31 0.4× 113 1.5× 59 493
Nima Milani‐Nejad United States 10 242 0.9× 30 0.2× 33 0.4× 29 0.4× 50 0.7× 33 653

Countries citing papers authored by Naruyoshi Fujiwara

Since Specialization
Citations

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

Fields of papers citing papers by Naruyoshi Fujiwara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naruyoshi Fujiwara

This figure shows the co-authorship network connecting the top 25 collaborators of Naruyoshi Fujiwara. A scholar is included among the top collaborators of Naruyoshi Fujiwara 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 Naruyoshi Fujiwara. Naruyoshi Fujiwara 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.
Murayama, Masanori A., Nagisa Arimitsu, Jun Shimizu, et al.. (2021). Dementia model mice exhibited improvements of neuropsychiatric symptoms as well as cognitive dysfunction with neural cell transplantation. EXPERIMENTAL ANIMALS. 70(3). 387–397. 8 indexed citations
2.
Murayama, Masanori A., Nagisa Arimitsu, Jun Shimizu, et al.. (2021). Female dominance of both spatial cognitive dysfunction and neuropsychiatric symptoms in a mouse model of Alzheimer’s disease. EXPERIMENTAL ANIMALS. 70(3). 398–405. 7 indexed citations
3.
5.
Shimizu, Jun, Takao Kubota, Erika Takada, et al.. (2018). Propionate-producing bacteria in the intestine may associate with skewed responses of IL10-producing regulatory T cells in patients with relapsing polychondritis. PLoS ONE. 13(9). e0203657–e0203657. 56 indexed citations
6.
Suzuki, Noboru, Nagisa Arimitsu, Jun Shimizu, et al.. (2017). Neuronal Cell Sheets of Cortical Motor Neuron Phenotype Derived from Human iPSCs. Cell Transplantation. 26(8). 1355–1364. 10 indexed citations
7.
Shimizu, Jun, Takao Kubota, Erika Takada, et al.. (2016). Bifidobacteria Abundance-Featured Gut Microbiota Compositional Change in Patients with Behcet’s Disease. PLoS ONE. 11(4). e0153746–e0153746. 91 indexed citations
9.
Shimizu, Jun, Kenji Takai, Erika Takada, et al.. (2015). Possible association of proinflammatory cytokines including IL1β and TNFα with enhanced Th17 cell differentiation in patients with Behcet’s disease. Clinical Rheumatology. 35(7). 1857–1863. 24 indexed citations
10.
Fujiwara, Naruyoshi, Jun Shimizu, Kenji Takai, et al.. (2015). Cellular and molecular mechanisms of the restoration of human APP transgenic mouse cognitive dysfunction after transplant of human iPS cell-derived neural cells. Experimental Neurology. 271. 423–431. 20 indexed citations
11.
Iinuma, Masahiro, Nagisa Arimitsu, Jun Shimizu, et al.. (2015). Induction of neural cells with spinal motoneuron phenotype from human iPS cells and the transplantation to totally transected spinal cords in mice. Inflammation and Regeneration. 35(3). 154–163. 4 indexed citations
12.
Shimizu, Jun, et al.. (2013). IGFII/Akt Signaling Regulates Myocyte Homeostasis in Human Induced Pluripotent Stem (iPS) Cells. 4(2). 41–48. 1 indexed citations
13.
Shimizu, Jun, Nagisa Arimitsu, Naruyoshi Fujiwara, et al.. (2013). Skewed TGFβ/Smad signalling pathway in T cells in patients with Behçet's disease.. PubMed. 30(3 Suppl 72). S35–9. 15 indexed citations
14.
Fujiwara, Naruyoshi, Jun Shimizu, Kenji Takai, et al.. (2013). Restoration of spatial memory dysfunction of human APP transgenic mice by transplantation of neuronal precursors derived from human iPS cells. Neuroscience Letters. 557. 129–134. 62 indexed citations
15.
Suzuki, Noboru, Jun Shimizu, Kenji Takai, et al.. (2012). Establishment of retinal progenitor cell clones by transfection with Pax6 gene of mouse induced pluripotent stem (iPS) cells. Neuroscience Letters. 509(2). 116–120. 20 indexed citations
16.
Arimitsu, Nagisa, Jun Shimizu, Naruyoshi Fujiwara, et al.. (2012). Role of SDF1/CXCR4 Interaction in Experimental Hemiplegic Models with Neural Cell Transplantation. International Journal of Molecular Sciences. 13(3). 2636–2649. 18 indexed citations
17.
Shimizu, Jun, Naruyoshi Fujiwara, Nagisa Arimitsu, et al.. (2011). Excessive CD4+ T cells co-expressing interleukin-17 and interferon-γ in patients with Behçet's disease. Clinical & Experimental Immunology. 168(1). 68–74. 83 indexed citations
18.
Fujiwara, Naruyoshi, Shinya Hidano, Hiroshi Mamada, et al.. (2006). A novel avian homologue of CD72, chB1r, down modulates BCR-mediated activation signals. International Immunology. 18(5). 775–783. 7 indexed citations
19.
Fujiwara, Naruyoshi, Noemi Fusaki, & Nobumichi Hozumi. (2004). CD72 Stimulation Modulates Anti‐IgM Induced Apoptotic Signaling through the Pathway of NF‐κB, c‐Myc and p27Kip1. Microbiology and Immunology. 48(1). 59–66. 7 indexed citations
20.
Fujii, Yasuyuki, Toru Nakao, Toshifumi Hara, et al.. (2003). Targeting of MIST to Src‐family kinases via SKAP55–SLAP‐130 adaptor complex in mast cells1. FEBS Letters. 540(1-3). 111–116. 20 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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