Aihao Ding

17.1k total citations · 6 hit papers
66 papers, 13.2k citations indexed

About

Aihao Ding is a scholar working on Immunology, Molecular Biology and Cancer Research. According to data from OpenAlex, Aihao Ding has authored 66 papers receiving a total of 13.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Immunology, 23 papers in Molecular Biology and 14 papers in Cancer Research. Recurrent topics in Aihao Ding's work include Immune Response and Inflammation (24 papers), Immune cells in cancer (12 papers) and Neuroinflammation and Neurodegeneration Mechanisms (7 papers). Aihao Ding is often cited by papers focused on Immune Response and Inflammation (24 papers), Immune cells in cancer (12 papers) and Neuroinflammation and Neurodegeneration Mechanisms (7 papers). Aihao Ding collaborates with scholars based in United States, Canada and China. Aihao Ding's co-authors include Carl Nathan, Dennis J. Stuehr, Q W Xie, Michael B. Sporn, Shohko Tsunawaki, Hearn Jay Cho, Jimmy Calaycay, Terry D. Lee, Richard A. Mumford and Kristine M. Swiderek and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Aihao Ding

65 papers receiving 12.9k citations

Hit Papers

Release of reactive nitrogen intermediates and reactive o... 1988 2026 2000 2013 1988 2010 1992 1988 2006 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aihao Ding United States 43 5.0k 3.8k 3.0k 1.5k 1.3k 66 13.2k
Walter Malorni Italy 66 3.4k 0.7× 6.4k 1.7× 1.8k 0.6× 2.2k 1.5× 1.6k 1.3× 370 14.9k
Søren K. Moestrup Denmark 85 3.9k 0.8× 7.7k 2.0× 3.1k 1.0× 2.2k 1.5× 1.8k 1.4× 246 20.0k
Babette B. Weksler United States 72 1.9k 0.4× 4.4k 1.2× 2.0k 0.7× 1.4k 0.9× 1.8k 1.4× 214 15.5k
Horst Bluethmann Switzerland 64 8.1k 1.6× 6.4k 1.7× 2.5k 0.8× 2.0k 1.4× 2.0k 1.6× 132 19.6k
Yoshiki Miyachi Japan 65 4.6k 0.9× 3.8k 1.0× 1.7k 0.6× 1.3k 0.9× 1.3k 1.1× 506 15.9k
Davide Ferrari Italy 67 4.5k 0.9× 6.0k 1.6× 2.1k 0.7× 1.5k 1.0× 1.0k 0.8× 148 17.2k
Michael J. Holtzman United States 72 5.0k 1.0× 3.2k 0.8× 4.4k 1.5× 2.4k 1.6× 1.2k 0.9× 226 15.1k
C A Dinarello United States 65 7.1k 1.4× 3.8k 1.0× 1.9k 0.6× 2.7k 1.8× 1.5k 1.2× 138 16.3k
Morley D. Hollenberg Canada 78 3.3k 0.7× 6.9k 1.8× 2.8k 0.9× 804 0.5× 1.7k 1.4× 425 20.8k
John Savill United Kingdom 60 11.2k 2.3× 6.0k 1.6× 2.5k 0.8× 1.4k 0.9× 1.1k 0.9× 110 18.0k

Countries citing papers authored by Aihao Ding

Since Specialization
Citations

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

Fields of papers citing papers by Aihao Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aihao Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Aihao Ding. A scholar is included among the top collaborators of Aihao Ding 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 Aihao Ding. Aihao Ding 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.
Chou, Szu‐Yi, Kuo‐Shun Hsu, Wataru Otsu, et al.. (2016). CLIC4 regulates apical exocytosis and renal tube luminogenesis through retromer- and actin-mediated endocytic trafficking. Nature Communications. 7(1). 10412–10412. 41 indexed citations
2.
He, Guoan, et al.. (2012). The Protein Zfand5 Binds and Stabilizes mRNAs with AU-rich Elements in Their 3′-Untranslated Regions. Journal of Biological Chemistry. 287(30). 24967–24977. 15 indexed citations
3.
He, Guoan, Yao Ma, Szu‐Yi Chou, et al.. (2011). Role of CLIC4 in the host innate responses to bacterial lipopolysaccharide. European Journal of Immunology. 41(5). 1221–1230. 45 indexed citations
4.
Marino, Rafael, Thusanth Thuraisingam, Pierre Camateros, et al.. (2011). Secretory Leukocyte Protease Inhibitor Plays an Important Role in the Regulation of Allergic Asthma in Mice. The Journal of Immunology. 186(7). 4433–4442. 33 indexed citations
5.
Nathan, Carl & Aihao Ding. (2010). Nonresolving Inflammation. Cell. 140(6). 871–882. 1637 indexed citations breakdown →
6.
Xu, Weifeng, Bing He, April Chiu, et al.. (2007). Epithelial cells trigger frontline immunoglobulin class switching through an SLPI-regulated pathway (41.7). The Journal of Immunology. 178(1_Supplement). S31–S31. 1 indexed citations
8.
Thuraisingam, Thusanth, et al.. (2006). Delayed Cutaneous Wound Healing in Mice Lacking Solute Carrier 11a1 (Formerly Nramp1): Correlation with Decreased Expression of Secretory Leukocyte Protease Inhibitor. Journal of Investigative Dermatology. 126(4). 890–901. 21 indexed citations
9.
Sun, Dongxu & Aihao Ding. (2006). MyD88-mediated stabilization of interferon-γ-induced cytokine and chemokine mRNA. Nature Immunology. 7(4). 375–381. 181 indexed citations
10.
Shi, Shuangping, Carl Nathan, Dirk Schnappinger, et al.. (2003). MyD88 Primes Macrophages for Full-Scale Activation by Interferon-γ yet Mediates Few Responses to Mycobacterium tuberculosis. The Journal of Experimental Medicine. 198(7). 987–997. 123 indexed citations
11.
Odaka, Chikako, Toshiaki Mizuochi, Jingxuan Yang, & Aihao Ding. (2003). Murine Macrophages Produce Secretory Leukocyte Protease Inhibitor During Clearance of Apoptotic Cells: Implications for Resolution of the Inflammatory Response. The Journal of Immunology. 171(3). 1507–1514. 89 indexed citations
12.
Mukherjee, Shankar, Thomas J. Belbin, David C. Spray, et al.. (2003). Microarray analysis of changes in gene expression in a murine model of chronic chagasic cardiomyopathy. Parasitology Research. 91(3). 187–196. 65 indexed citations
13.
Nathan, Carl & Aihao Ding. (2001). TREM-1: A new regulator of innate immunity in sepsis syndrome. Nature Medicine. 7(5). 530–532. 89 indexed citations
14.
Nathan, Carl, et al.. (1999). Paradoxical Preservation of a Lipopolysaccharide Response in C3H/HeJ Macrophages: Induction of Matrix Metalloproteinase-9. The Journal of Immunology. 162(6). 3596–3600. 20 indexed citations
15.
16.
Ding, Aihao, Shen-An Hwang, & R. Schwab. (1994). Effect of aging on murine macrophages. Diminished response to IFN-gamma for enhanced oxidative metabolism.. The Journal of Immunology. 153(5). 2146–2152. 83 indexed citations
17.
Ding, Aihao & Françoise Porteu. (1992). Regulation of Tumor Necrosis Factor Receptors on Phagocytes. Experimental Biology and Medicine. 200(4). 458–465. 17 indexed citations
18.
Ding, Aihao & Carl Nathan. (1988). Analysis of the nonfunctional respiratory burst in murine Kupffer cells.. The Journal of Experimental Medicine. 167(3). 1154–1170. 33 indexed citations
19.
Tsunawaki, Shohko, Michael B. Sporn, Aihao Ding, & Carl Nathan. (1988). Deactivation of macrophages by transforming growth factor-β. Nature. 334(6179). 260–262. 744 indexed citations breakdown →
20.
Ding, Aihao & Carl Nathan. (1988). The measurement of cytochrome b559 in polymorphonuclear leukocytes and macrophages in the presence of hemoglobin or mitochondrial cytochromes. Analytical Biochemistry. 175(1). 22–29. 12 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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