Samuel McGee

2.2k total citations
19 papers, 1.5k citations indexed

About

Samuel McGee is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Samuel McGee has authored 19 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Immunology and 5 papers in Surgery. Recurrent topics in Samuel McGee's work include Glycosylation and Glycoproteins Research (6 papers), Helicobacter pylori-related gastroenterology studies (4 papers) and Lymphatic System and Diseases (3 papers). Samuel McGee is often cited by papers focused on Glycosylation and Glycoproteins Research (6 papers), Helicobacter pylori-related gastroenterology studies (4 papers) and Lymphatic System and Diseases (3 papers). Samuel McGee collaborates with scholars based in United States, China and Belgium. Samuel McGee's co-authors include Lijun Xia, J. Michael McDaniel, Jianxin Fu, Xiaowei Liu, Tadayuki Yago, Kirk Bergstrom, Jonathan Braun, Florea Lupu, Robert Silasi‐Mansat and Malin Johansson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Samuel McGee

19 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samuel McGee United States 14 795 524 302 286 206 19 1.5k
Robert Liwski Canada 26 562 0.7× 669 1.3× 278 0.9× 367 1.3× 293 1.4× 89 1.9k
Alberto Cascón Spain 31 918 1.2× 341 0.7× 523 1.7× 915 3.2× 79 0.4× 70 2.7k
Laetitia Furio France 20 549 0.7× 474 0.9× 167 0.6× 205 0.7× 38 0.2× 29 1.6k
Yasunobu Matsuda Japan 29 919 1.2× 434 0.8× 577 1.9× 400 1.4× 69 0.3× 79 2.2k
Anneliese O. Speak United Kingdom 21 611 0.8× 1.4k 2.7× 361 1.2× 126 0.4× 178 0.9× 40 2.2k
Rachel E. Simmonds United Kingdom 24 415 0.5× 393 0.8× 92 0.3× 121 0.4× 633 3.1× 43 1.8k
Harald Thidemann Johansen Norway 22 445 0.6× 247 0.5× 256 0.8× 133 0.5× 218 1.1× 72 1.4k
Tracy L. Burcin United States 10 499 0.6× 1.1k 2.1× 148 0.5× 144 0.5× 91 0.4× 10 1.7k
Malte Bachmann Germany 22 592 0.7× 610 1.2× 474 1.6× 74 0.3× 115 0.6× 40 1.6k

Countries citing papers authored by Samuel McGee

Since Specialization
Citations

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

Fields of papers citing papers by Samuel McGee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuel McGee

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

All Works

19 of 19 papers shown
1.
Shi, Huiping, Jianhua Song, Liang Gao, et al.. (2024). Deletion of Talin1 in Myeloid Cells Facilitates Atherosclerosis in Mice. Arteriosclerosis Thrombosis and Vascular Biology. 44(8). 1799–1812. 2 indexed citations
2.
Shi, Huiping, Liang Gao, Bojing Shao, et al.. (2023). Clearance of VWF by hepatic macrophages is critical for the protective effect of ADAMTS13 in sickle cell anemia mice. Blood. 143(13). 1293–1309. 6 indexed citations
3.
Shao, Bojing, Christopher Hoover, Huiping Shi, et al.. (2022). Deletion of platelet CLEC-2 decreases GPIbα-mediated integrin αIIbβ3 activation and decreases thrombosis in TTP. Blood. 139(16). 2523–2533. 14 indexed citations
4.
Shi, Huiping, Bojing Shao, Liang Gao, et al.. (2022). Endothelial VWF is critical for the pathogenesis of vaso-occlusive episode in a mouse model of sickle cell disease. Proceedings of the National Academy of Sciences. 119(34). e2207592119–e2207592119. 11 indexed citations
5.
Jiang, Yizhi, Yaqiong Tang, Christopher Hoover, et al.. (2021). Kupffer cell receptor CLEC4F is important for the destruction of desialylated platelets in mice. Cell Death and Differentiation. 28(11). 3009–3021. 55 indexed citations
6.
Hoover, Christopher, Yuji Kondo, Bojing Shao, et al.. (2021). Heightened activation of embryonic megakaryocytes causes aneurysms in the developing brain of mice lacking podoplanin. Blood. 137(20). 2756–2769. 15 indexed citations
7.
Liu, Fei, Jianxin Fu, Kirk Bergstrom, et al.. (2019). Core 1–derived mucin-type O-glycosylation protects against spontaneous gastritis and gastric cancer. The Journal of Experimental Medicine. 217(1). 49 indexed citations
8.
Yi, Jun, Kirk Bergstrom, Jianxin Fu, et al.. (2018). Dclk1 in tuft cells promotes inflammation-driven epithelial restitution and mitigates chronic colitis. Cell Death and Differentiation. 26(9). 1656–1669. 73 indexed citations
9.
Song, Kai, Jianxin Fu, Jianhua Song, et al.. (2017). Loss of mucin-type O-glycans impairs the integrity of the glomerular filtration barrier in the mouse kidney. Journal of Biological Chemistry. 292(40). 16491–16497. 22 indexed citations
10.
Li, Yun, Jianxin Fu, Tadayuki Yago, et al.. (2017). Sialylation on O-glycans protects platelets from clearance by liver Kupffer cells. Proceedings of the National Academy of Sciences. 114(31). 8360–8365. 96 indexed citations
11.
Swanson, Kristin R., Nathan Gaw, Andrea Hawkins‐Daarud, et al.. (2017). NIMG-74. RADIOMICS OF TUMOR INVASION 2.0: COMBINING MECHANISTIC TUMOR INVASION MODELS WITH MACHINE LEARNING MODELS TO ACCURATELY PREDICT TUMOR INVASION IN HUMAN GLIOBLASTOMA PATIENTS. Neuro-Oncology. 19(suppl_6). vi159–vi159. 1 indexed citations
12.
Hu, Leland, Hyunsoo Yoon, Jennifer Eschbacher, et al.. (2017). NIMG-68. ACCURATE PATIENT-SPECIFIC MACHINE LEARNING MODELS OF GLIOBLASTOMA INVASION USING TRANSFER LEARNING. Neuro-Oncology. 19(suppl_6). vi157–vi158. 1 indexed citations
13.
Bergstrom, Kirk, Xiaowei Liu, Yiming Zhao, et al.. (2016). Defective Intestinal Mucin-Type O-Glycosylation Causes Spontaneous Colitis-Associated Cancer in Mice. Gastroenterology. 151(1). 152–164.e11. 118 indexed citations
14.
Bergstrom, Kirk, Jianxin Fu, Malin Johansson, et al.. (2016). Core 1– and 3–derived O-glycans collectively maintain the colonic mucus barrier and protect against spontaneous colitis in mice. Mucosal Immunology. 10(1). 91–103. 132 indexed citations
15.
Song, Kai, Brett H. Herzog, Jianxin Fu, et al.. (2015). Loss of Core 1-derived O-Glycans Decreases Breast Cancer Development in Mice. Journal of Biological Chemistry. 290(33). 20159–20166. 26 indexed citations
16.
Herzog, Brett H., Jianxin Fu, Stephen J. Wilson, et al.. (2013). Podoplanin maintains high endothelial venule integrity by interacting with platelet CLEC-2. Nature. 502(7469). 105–109. 250 indexed citations
17.
Fu, Jianxin, Bo Wei, Tao Wen, et al.. (2011). Loss of intestinal core 1–derived O-glycans causes spontaneous colitis in mice. Journal of Clinical Investigation. 121(4). 1657–1666. 274 indexed citations
18.
Fu, Jianxin, Holger Gerhardt, J. Michael McDaniel, et al.. (2008). Endothelial cell O-glycan deficiency causes blood/lymphatic misconnections and consequent fatty liver disease in mice. Journal of Clinical Investigation. 118(11). 3725–3737. 196 indexed citations
19.

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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