Murat Tekgüç

737 total citations · 1 hit paper
7 papers, 480 citations indexed

About

Murat Tekgüç is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Murat Tekgüç has authored 7 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Immunology and 2 papers in Surgery. Recurrent topics in Murat Tekgüç's work include Immune Cell Function and Interaction (3 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Immunotherapy and Immune Responses (2 papers). Murat Tekgüç is often cited by papers focused on Immune Cell Function and Interaction (3 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Immunotherapy and Immune Responses (2 papers). Murat Tekgüç collaborates with scholars based in Japan and United States. Murat Tekgüç's co-authors include Shimon Sakaguchi, James B. Wing, Motonao Osaki, Navin Gupta, Sebastien G. M. Uzel, Mehmet E. Yalvaç, И. И. Салафутдинов, A. P. Kiyasov, András Palotás and Ryuji Morizane and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Frontiers in Immunology and Cancer Letters.

In The Last Decade

Murat Tekgüç

7 papers receiving 478 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Treg-expressed CTLA-4 depletes CD80/CD86 by trogocytosis, releasing free PD-L1 on antigen-presenting cells

2021 286 citations Murat Tekgüç, James B. Wing et al. Proceedings of the National Academy of Sciences profile →

Peers

Murat Tekgüç

IMMUN

ONCOL

MB

PRM

GENET

Zhilei Bian China

Brile Chung United States

Rongqun Guo China

Petra Aigner Austria

Ana Carolina Leal Brazil

Andrea Acebes‐Huerta Spain

Giulia Fregni France

Jianqiu Wu China

Shriram K. Sundararaman United States

Mike Keeney Canada

Zhilei Bian China

Murat Tekgüç

327 ×1.1

IMMUN

198 ×1.3

ONCOL

174 ×1.4

MB

34 ×0.7

PRM

29 ×0.6

GENET

Citations per year, relative to Murat Tekgüç Murat Tekgüç (= 1×) peers Zhilei Bian

Countries citing papers authored by Murat Tekgüç

Since Specialization

Citations

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

Fields of papers citing papers by Murat Tekgüç

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Murat Tekgüç

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

All Works

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7 of 7 papers shown

1.

Borges, Thiago J., Sebastien G. M. Uzel, Ivy A. Rosales, et al.. (2024). Exploring immune response toward transplanted human kidney tissues assembled from organoid building blocks. iScience. 27(10). 110957–110957. 4 indexed citations

2.

Tekgüç, Murat, Sebastien G. M. Uzel, Navin Gupta, et al.. (2022). Kidney organoids: a pioneering model for kidney diseases. Translational research. 250. 1–17. 29 indexed citations

3.

Tekgüç, Murat, James B. Wing, Ari Hashimoto, et al.. (2021). Arid5a Promotes Immune Evasion by Augmenting Tryptophan Metabolism and Chemokine Expression. Cancer Immunology Research. 9(8). 862–876. 21 indexed citations

4.

Nyati, Kishan Kumar, Shigeru Hashimoto, Shailendra Kumar Singh, et al.. (2021). The novel long noncoding RNA AU021063, induced by IL-6/Arid5a signaling, exacerbates breast cancer invasion and metastasis by stabilizing Trib3 and activating the Mek/Erk pathway. Cancer Letters. 520. 295–306. 23 indexed citations

5.

Tekgüç, Murat, et al.. (2021). Treg-expressed CTLA-4 depletes CD80/CD86 by trogocytosis, releasing free PD-L1 on antigen-presenting cells. Proceedings of the National Academy of Sciences. 118(30). 286 indexed citations breakdown →

6.

Wing, James B., Murat Tekgüç, & Shimon Sakaguchi. (2018). Control of Germinal Center Responses by T-Follicular Regulatory Cells. Frontiers in Immunology. 9. 1910–1910. 74 indexed citations

7.

Yalvaç, Mehmet E., Murat Tekgüç, Ömer Faruk Bayrak, et al.. (2010). Human Tooth Germ Stem Cells Preserve Neuro-Protective Effects after Long-Term Cryo-Preservation. Current Neurovascular Research. 7(1). 49–58. 43 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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