David R. Gibb

1.5k total citations
41 papers, 1.1k citations indexed

About

David R. Gibb is a scholar working on Physiology, Hematology and Immunology. According to data from OpenAlex, David R. Gibb has authored 41 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Physiology, 19 papers in Hematology and 14 papers in Immunology. Recurrent topics in David R. Gibb's work include Blood groups and transfusion (18 papers), Erythrocyte Function and Pathophysiology (17 papers) and Diabetes and associated disorders (6 papers). David R. Gibb is often cited by papers focused on Blood groups and transfusion (18 papers), Erythrocyte Function and Pathophysiology (17 papers) and Diabetes and associated disorders (6 papers). David R. Gibb collaborates with scholars based in United States, France and Japan. David R. Gibb's co-authors include Daniel H. Conrad, Jamie Sturgill, Jeanne E. Hendrickson, Sheinei Saleem, Paul Säftig, Jill Ford, Daniel Lundell, Keisuke Horiuchi, Karina Reiß and Carl Blobel and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

David R. Gibb

40 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David R. Gibb United States 17 405 336 320 281 203 41 1.1k
Frank C. Stomski Australia 23 800 2.0× 130 0.4× 727 2.3× 254 0.9× 192 0.9× 35 1.8k
Hendra Setiadi United States 17 383 0.9× 103 0.3× 374 1.2× 217 0.8× 518 2.6× 31 1.1k
Jennifer Cairns United Kingdom 17 1.1k 2.7× 365 1.1× 336 1.1× 206 0.7× 369 1.8× 29 1.7k
Palaniswami Rathanaswami Canada 16 420 1.0× 93 0.3× 358 1.1× 99 0.4× 101 0.5× 21 1.2k
Amanda J. Stranks United Kingdom 12 579 1.4× 232 0.7× 623 1.9× 219 0.8× 175 0.9× 14 1.6k
Julio Gómez‐Rodríguez United States 19 1.3k 3.2× 156 0.5× 300 0.9× 168 0.6× 116 0.6× 29 1.8k
Tim Vanden Bos Canada 12 1.2k 2.9× 184 0.5× 630 2.0× 294 1.0× 144 0.7× 13 2.0k
Tomáš Cinek United States 12 483 1.2× 151 0.4× 522 1.6× 77 0.3× 204 1.0× 14 1.1k
Majed M. Hamawy United States 24 925 2.3× 127 0.4× 405 1.3× 118 0.4× 405 2.0× 56 1.8k
Daocheng Zhu United States 16 622 1.5× 291 0.9× 270 0.8× 54 0.2× 422 2.1× 37 1.1k

Countries citing papers authored by David R. Gibb

Since Specialization
Citations

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

Fields of papers citing papers by David R. Gibb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David R. Gibb. 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 David R. Gibb. The network helps show where David R. Gibb may publish in the future.

Co-authorship network of co-authors of David R. Gibb

This figure shows the co-authorship network connecting the top 25 collaborators of David R. Gibb. A scholar is included among the top collaborators of David R. Gibb 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 David R. Gibb. David R. Gibb 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.
Tumurkhuu, Gantsetseg, Richard E. Moore, Lihong Huo, et al.. (2025). Loss of Tripartite Motif–Containing Protein 21 and UVB ‐Induced Systemic Inflammation by Regulating DNA ‐Sensing Pathways. Arthritis & Rheumatology. 78(1). 172–183. 2 indexed citations
2.
Lee, Juneyoung, Che‐Yu Chang, Tomohiro Shibata, et al.. (2024). Distinct RBC alloantibody responses in type 1 interferon-dependent and -independent lupus mouse models. Frontiers in Immunology. 14. 1304086–1304086. 5 indexed citations
3.
Gragert, Loren, Denise Biagini, J. Patel, et al.. (2023). IgM marks persistent IgG anti-human leukocyte antigen antibodies in highly sensitized heart transplant patients. The Journal of Heart and Lung Transplantation. 43(2). 314–323. 2 indexed citations
4.
Maier, Cheryl L., Ryan Philip Jajosky, Seema R. Patel, et al.. (2023). Storage differentially impacts alloimmunization to distinct red cell antigens following transfusion in mice. Transfusion. 63(3). 457–462. 11 indexed citations
5.
Veiras, Luciana C., Ellen A. Bernstein, Duo‐Yao Cao, et al.. (2022). Tubular IL-1β Induces Salt Sensitivity in Diabetes by Activating Renal Macrophages. Circulation Research. 131(1). 59–73. 34 indexed citations
6.
Veiras, Luciana C., Ellen A. Bernstein, Giovanna C. Regis, et al.. (2021). Renal Inflammation Induces Salt Sensitivity in Male db/db Mice through Dysregulation of ENaC. Journal of the American Society of Nephrology. 32(5). 1131–1149. 26 indexed citations
7.
Okwan‐Duodu, Derick, et al.. (2021). Potential Implications of a Type 1 Interferon Gene Signature on COVID-19 Severity and Chronic Inflammation in Sickle Cell Disease. Frontiers in Medicine. 8. 679030–679030. 3 indexed citations
8.
Liu, Jingchun, David R. Gibb, Manjula Santhanakrishnan, et al.. (2020). Poly(I:C) causes failure of immunoprophylaxis to red blood cells expressing the KEL glycoprotein in mice. Blood. 135(22). 1983–1993. 5 indexed citations
9.
Patel, Seema R., David R. Gibb, Kathryn R. Girard‐Pierce, et al.. (2018). Marginal Zone B Cells Induce Alloantibody Formation Following RBC Transfusion. Frontiers in Immunology. 9. 2516–2516. 34 indexed citations
10.
Gibb, David R., Jingchun Liu, P Natarajan, et al.. (2017). Type I IFN Is Necessary and Sufficient for Inflammation-Induced Red Blood Cell Alloimmunization in Mice. The Journal of Immunology. 199(3). 1041–1050. 44 indexed citations
11.
Natarajan, P, Dong Liu, Seema R. Patel, et al.. (2017). CD4 Depletion or CD40L Blockade Results in Antigen-Specific Tolerance in a Red Blood Cell Alloimmunization Model. Frontiers in Immunology. 8. 907–907. 14 indexed citations
12.
Natarajan, P, Jingchun Liu, Manjula Santhanakrishnan, et al.. (2016). Bortezomib decreases the magnitude of a primary humoral immune response to transfused red blood cells in a murine model. Transfusion. 57(1). 82–92. 6 indexed citations
13.
Gibb, David R., Samuele Calabrό, Christopher A. Tormey, et al.. (2016). The Nlrp3 Inflammasome Does Not Regulate Alloimmunization to Transfused Red Blood Cells in Mice. EBioMedicine. 9. 77–86. 16 indexed citations
14.
Saleem, Sheinei, Rebecca Martin, Johanna K. Morales, et al.. (2012). Cutting Edge: Mast Cells Critically Augment Myeloid-Derived Suppressor Cell Activity. The Journal of Immunology. 189(2). 511–515. 72 indexed citations
15.
Loria, Roger M., et al.. (2011). Beta Androstenediol Mitigates the Damage of 1 GeV/n Fe Ion Particle Radiation to the Hematopoietic System. Cancer Biotherapy and Radiopharmaceuticals. 26(4). 453–459. 3 indexed citations
16.
Gibb, David R., et al.. (2011). ADAM10 Overexpression Shifts Lympho- and Myelopoiesis by Dysregulating Site 2/Site 3 Cleavage Products of Notch. The Journal of Immunology. 186(7). 4244–4252. 47 indexed citations
17.
Mathews, Joel, Jill Ford, Sarah K. Norton, et al.. (2011). A potential new target for asthma therapy: A Disintegrin and Metalloprotease 10 (ADAM10) involvement in murine experimental asthma. Allergy. 66(9). 1193–1200. 40 indexed citations
18.
Gibb, David R., Mohey Eldin El Shikh, Rania Sayed, et al.. (2010). ADAM10 is essential for Notch2-dependent marginal zone B cell development and CD23 cleavage in vivo. The Journal of Experimental Medicine. 207(3). 623–635. 127 indexed citations
19.
Gall, Sylvain M. Le, Pierre Bobé, Karina Reiß, et al.. (2009). ADAMs 10 and 17 Represent Differentially Regulated Components of a General Shedding Machinery for Membrane Proteins Such as Transforming Growth Factor α, L-Selectin, and Tumor Necrosis Factor α. Molecular Biology of the Cell. 20(6). 1785–1794. 214 indexed citations
20.
Morris, Margaret, David R. Gibb, Franck Picard, et al.. (2005). Transient T cell accumulation in lymph nodes and sustained lymphopenia in mice treated with FTY720. European Journal of Immunology. 35(12). 3570–3580. 69 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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