Venus A. Wong

947 total citations
14 papers, 779 citations indexed

About

Venus A. Wong is a scholar working on Immunology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Venus A. Wong has authored 14 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 5 papers in Molecular Biology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Venus A. Wong's work include Immune Response and Inflammation (7 papers), Chemokine receptors and signaling (5 papers) and Immune cells in cancer (4 papers). Venus A. Wong is often cited by papers focused on Immune Response and Inflammation (7 papers), Chemokine receptors and signaling (5 papers) and Immune cells in cancer (4 papers). Venus A. Wong collaborates with scholars based in United States, Taiwan and France. Venus A. Wong's co-authors include Thomas R. Martin, Charles W. Frevert, Richard B. Goodman, Richard H. Goodwin, John Ruzinski, Mark M. Wurfel, Gustavo Matute‐Bello, Joanne Quan, Kenneth P. Steinberg and Janet Lee and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Immunology and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Venus A. Wong

14 papers receiving 768 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Venus A. Wong United States	12	459	203	187	174	159	14	779
Patricia S. Grutkoski United States	17	495 1.1×	83 0.4×	142 0.8×	318 1.8×	197 1.2×	20	851
B. Neumann Germany	9	486 1.1×	80 0.4×	61 0.3×	188 1.1×	180 1.1×	15	800
Rachel L. Robson United Kingdom	12	307 0.7×	139 0.7×	77 0.4×	127 0.7×	81 0.5×	20	716
Tsutomu Shinohara Japan	15	225 0.5×	192 0.9×	219 1.2×	237 1.4×	137 0.9×	109	845
Tolga Barker United States	13	485 1.1×	49 0.2×	81 0.4×	135 0.8×	153 1.0×	16	746
Masakazu Okamoto United States	20	469 1.0×	114 0.6×	208 1.1×	137 0.8×	158 1.0×	35	934
Ludmila N. Drutskaya United States	8	635 1.4×	117 0.6×	38 0.2×	147 0.8×	177 1.1×	9	953
Andreas R. Huber Switzerland	4	383 0.8×	126 0.6×	65 0.3×	164 0.9×	62 0.4×	8	725
Masashi Matsuyama Japan	14	193 0.4×	86 0.4×	201 1.1×	153 0.9×	150 0.9×	42	673
Yngve Raab Sweden	18	300 0.7×	189 0.9×	81 0.4×	84 0.5×	262 1.6×	23	946

Countries citing papers authored by Venus A. Wong

Since Specialization

Citations

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

Fields of papers citing papers by Venus A. Wong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Venus A. Wong. 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 Venus A. Wong. The network helps show where Venus A. Wong may publish in the future.

Co-authorship network of co-authors of Venus A. Wong

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Herrero, Raquel, Mishie Tanino, Lincoln Smith, et al.. (2013). The Fas/FasL pathway impairs the alveolar fluid clearance in mouse lungs. American Journal of Physiology-Lung Cellular and Molecular Physiology. 305(5). L377–L388. 26 indexed citations

Matute‐Bello, Gustavo, et al.. (2011). Death receptors mediate the adverse effects of febrile-range hyperthermia on the outcome of lipopolysaccharide-induced lung injury. American Journal of Physiology-Lung Cellular and Molecular Physiology. 301(1). L60–L70. 9 indexed citations

Matute‐Bello, Gustavo, Raquel Herrero, Kiyoyasu Kurahashi, et al.. (2010). Febrile-Range Hyperthermia Augments Lipopolysaccharide-Induced Lung Injury by a Mechanism of Enhanced Alveolar Epithelial Apoptosis. The Journal of Immunology. 184(7). 3801–3813. 35 indexed citations

Lee, Janet, Charles W. Frevert, Gustavo Matute‐Bello, et al.. (2005). TLR-4 pathway mediates the inflammatory response but not bacterial elimination inE. colipneumonia. American Journal of Physiology-Lung Cellular and Molecular Physiology. 289(5). L731–L738. 51 indexed citations

Lin, Shu‐Min, Charles W. Frevert, Osamu Kajikawa, et al.. (2004). Differential Regulation of Membrane CD14 Expression and Endotoxin-Tolerance in Alveolar Macrophages. American Journal of Respiratory Cell and Molecular Biology. 31(2). 162–170. 40 indexed citations

Lee, Janet, Charles W. Frevert, Mark M. Wurfel, et al.. (2003). Duffy Antigen Facilitates Movement of Chemokine Across the Endothelium In Vitro and Promotes Neutrophil Transmigration In Vitro and In Vivo. The Journal of Immunology. 170(10). 5244–5251. 121 indexed citations

Lee, Janet, Charles W. Frevert, David Thorning, et al.. (2003). Enhanced Expression of Duffy Antigen in the Lungs During Suppurative Pneumonia. Journal of Histochemistry & Cytochemistry. 51(2). 159–166. 30 indexed citations

Frevert, Charles W., et al.. (2002). High and Low Inflammatory Response Phenotypes in 101 Normal Human Subjects. CHEST Journal. 121(3). 87S–88S. 20 indexed citations

Matute‐Bello, Gustavo, Charles W. Frevert, W. Conrad Liles, et al.. (2001). Fas/Fas Ligand System Mediates Epithelial Injury, but Not Pulmonary Host Defenses, in Response to Inhaled Bacteria. Infection and Immunity. 69(9). 5768–5776. 59 indexed citations

10.

Martin, Thomas R., Charles W. Frevert, Joanne Quan, et al.. (1999). Expression and Function of the Chemokine Receptors CXCR1 and CXCR2 in Sepsis. The Journal of Immunology. 162(4). 2341–2346. 179 indexed citations

11.

Frevert, Charles W., Venus A. Wong, Richard B. Goodman, Richard H. Goodwin, & Thomas R. Martin. (1998). Rapid fluorescence-based measurement of neutrophil migration in vitro. Journal of Immunological Methods. 213(1). 41–52. 134 indexed citations

12.

Kajikawa, Osamu, Ellen Caldwell, M. Johnson, et al.. (1997). Pulmonary and Systemic Inflammatory Responses in Rabbits With Gram-Negative Pneumonia. American Journal of Respiratory and Critical Care Medicine. 155(6). 2030–2040. 46 indexed citations

13.

Johnson, Martin, Osamu Kajikawa, Richard B. Goodman, et al.. (1996). Molecular Expression of the α-Chemokine Rabbit GRO in Escherichia coli and Characterization of Its Production by Lung Cells in Vitro and in Vivo. Journal of Biological Chemistry. 271(18). 10853–10858. 21 indexed citations

14.

Johnson, Martin, Richard B. Goodman, Osamu Kajikawa, et al.. (1994). Cloning of two rabbit GRO homologues and their expression in alveolar macrophages. Gene. 151(1-2). 337–338. 8 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.

Explore authors with similar magnitude of impact