Kaoru Geddes

2.4k total citations
26 papers, 1.5k citations indexed

About

Kaoru Geddes is a scholar working on Immunology, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Kaoru Geddes has authored 26 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Immunology, 7 papers in Infectious Diseases and 6 papers in Molecular Biology. Recurrent topics in Kaoru Geddes's work include Immune Response and Inflammation (8 papers), Immune Cell Function and Interaction (6 papers) and Salmonella and Campylobacter epidemiology (5 papers). Kaoru Geddes is often cited by papers focused on Immune Response and Inflammation (8 papers), Immune Cell Function and Interaction (6 papers) and Salmonella and Campylobacter epidemiology (5 papers). Kaoru Geddes collaborates with scholars based in Canada, United States and France. Kaoru Geddes's co-authors include Stephen E. Girardin, Dana J. Philpott, João G. Magalhães, Stephen Rubino, Fred Heffron, Micah J. Worley, Joonho Cho, Catherine Streutker, Susan J. Robertson and Lionel Le Bourhis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Gastroenterology.

In The Last Decade

Kaoru Geddes

26 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
Kaoru Geddes Canada 17 724 545 279 277 226 26 1.5k
Matteo Urbano Italy 10 1.2k 1.7× 720 1.3× 307 1.1× 255 0.9× 320 1.4× 10 2.2k
Marinieve Montero Canada 13 450 0.6× 766 1.4× 347 1.2× 222 0.8× 322 1.4× 16 1.6k
Sean Lyons United States 7 981 1.4× 398 0.7× 248 0.9× 298 1.1× 235 1.0× 7 1.6k
Xiubin Gu United States 7 1.0k 1.4× 536 1.0× 161 0.6× 200 0.7× 257 1.1× 13 1.9k
Amit Lahiri India 21 383 0.5× 397 0.7× 204 0.7× 175 0.6× 191 0.8× 32 1.2k
Molly A. Bergman United States 13 639 0.9× 573 1.1× 206 0.7× 319 1.2× 250 1.1× 16 1.7k
Alfredo Menéndez Canada 24 396 0.5× 958 1.8× 236 0.8× 113 0.4× 303 1.3× 48 1.8k
Hugues Lelouard France 22 1.2k 1.6× 723 1.3× 119 0.4× 174 0.6× 142 0.6× 30 2.2k
Jeongmin Song United States 21 300 0.4× 495 0.9× 416 1.5× 471 1.7× 246 1.1× 42 1.6k
Kathrin Endt Switzerland 9 364 0.5× 664 1.2× 331 1.2× 220 0.8× 407 1.8× 13 1.3k

Countries citing papers authored by Kaoru Geddes

Since Specialization
Citations

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

Fields of papers citing papers by Kaoru Geddes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaoru Geddes

This figure shows the co-authorship network connecting the top 25 collaborators of Kaoru Geddes. A scholar is included among the top collaborators of Kaoru Geddes 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 Kaoru Geddes. Kaoru Geddes 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.
Maisonneuve, Charles, Elisabeth G. Foerster, Tapas Mukherjee, et al.. (2021). Nod1 promotes colorectal carcinogenesis by regulating the immunosuppressive functions of tumor-infiltrating myeloid cells. Cell Reports. 34(4). 108677–108677. 63 indexed citations
2.
Maisonneuve, Charles, Derek S. Tsang, Elisabeth G. Foerster, et al.. (2020). Nod1 Promotes Colorectal Carcinogenesis by Regulating the Immunosuppressive Functions of Tumor-Infiltrating Myeloid Cells. SSRN Electronic Journal. 4 indexed citations
3.
Robertson, Susan J., Kaoru Geddes, Charles Maisonneuve, Catherine Streutker, & Dana J. Philpott. (2016). Resilience of the intestinal microbiota following pathogenic bacterial infection is independent of innate immunity mediated by NOD1 or NOD2. Microbes and Infection. 18(7-8). 460–471. 15 indexed citations
4.
Wang, Chao, et al.. (2016). Irreversible splenic atrophy following chronic LCMV infection is associated with compromised immunity in mice. European Journal of Immunology. 47(1). 94–106. 11 indexed citations
5.
Steck, Natalie, Ulrich Zähringer, Simone Lipinski, et al.. (2014). Salmonella enterica serovar Typhimurium ΔmsbB Triggers Exacerbated Inflammation in Nod2 Deficient Mice. PLoS ONE. 9(11). e113645–e113645. 15 indexed citations
6.
Zanello, Galliano, Ashleigh Goethel, Katharina Förster, et al.. (2013). Nod2 Activates NF-kB in CD4+ T Cells but Its Expression Is Dispensable for T Cell-Induced Colitis. PLoS ONE. 8(12). e82623–e82623. 29 indexed citations
7.
Robertson, Susan J., Jun Zhou, Kaoru Geddes, et al.. (2013). Nod1 and Nod2 signaling does not alter the composition of intestinal bacterial communities at homeostasis. Gut Microbes. 4(3). 222–231. 111 indexed citations
8.
Chege, Duncan, Sarah J. Higgins, Chloë R. McDonald, et al.. (2013). Murine Plasmodium chabaudi Malaria Increases Mucosal Immune Activation and the Expression of Putative HIV Susceptibility Markers in the Gut and Genital Mucosae. JAIDS Journal of Acquired Immune Deficiency Syndromes. 65(5). 517–525. 7 indexed citations
9.
Robertson, Susan J., Stephen Rubino, Kaoru Geddes, & Dana J. Philpott. (2012). Examining host–microbial interactions through the lens of NOD: From plants to mammals. Seminars in Immunology. 24(1). 9–16. 21 indexed citations
10.
Rubino, Stephen, Kaoru Geddes, & Stephen E. Girardin. (2012). Innate IL-17 and IL-22 responses to enteric bacterial pathogens. Trends in Immunology. 33(3). 112–118. 78 indexed citations
11.
Lee, Jooeun, Kaoru Geddes, Catherine Streutker, Dana J. Philpott, & Stephen E. Girardin. (2012). Role of Mouse Peptidoglycan Recognition Protein PGLYRP2 in the Innate Immune Response to Salmonella enterica Serovar Typhimurium Infection In Vivo. Infection and Immunity. 80(8). 2645–2654. 23 indexed citations
12.
Magalhães, João G., Stephen Rubino, Leonardo H. Travassos, et al.. (2011). Nucleotide oligomerization domain-containing proteins instruct T cell helper type 2 immunity through stromal activation. Proceedings of the National Academy of Sciences. 108(36). 14896–14901. 64 indexed citations
13.
Geddes, Kaoru, Stephen Rubino, João G. Magalhães, et al.. (2011). Identification of an innate T helper type 17 response to intestinal bacterial pathogens. Nature Medicine. 17(7). 837–844. 192 indexed citations
14.
Geddes, Kaoru, Stephen Rubino, João G. Magalhães, et al.. (2011). Geddes K, Rubino SJ, Magalhaes JG, et al.. Identification of an innate T helper type 17 response to intestinal bacterial pathogens. 1 indexed citations
15.
Magalhães, João G., Stephen Rubino, Leonardo H. Travassos, et al.. (2011). Magalhaes JG, Rubino SJ, Travassos LH et al.Nucleotide oligomerization domain-containing proteins instruct T cell helper type 2 immunity through stromal activation. Proc Natl Acad Sci USA 108:14896-14901. 2 indexed citations
16.
Magalhães, João G., Jooeun Lee, Kaoru Geddes, et al.. (2011). Essential role of RIP2 in the modulation of innate and adaptive immunity triggered by NOD2 and NOD2 ligands. 1 indexed citations
17.
Magalhães, João G., Jooeun Lee, Kaoru Geddes, et al.. (2011). Essential role of Rip2 in the modulation of innate and adaptive immunity triggered by Nod1 and Nod2 ligands. European Journal of Immunology. 41(5). 1445–1455. 90 indexed citations
18.
Geddes, Kaoru, João G. Magalhães, & Stephen E. Girardin. (2009). Unleashing the therapeutic potential of NOD-like receptors. Nature Reviews Drug Discovery. 8(6). 465–479. 183 indexed citations
19.
Geddes, Kaoru, et al.. (2007). Analysis of Cells Targeted by Salmonella Type III Secretion In Vivo. PLoS Pathogens. 3(12). e196–e196. 115 indexed citations
20.
Worley, Micah J., et al.. (2006). Salmonella typhimurium disseminates within its host by manipulating the motility of infected cells. Proceedings of the National Academy of Sciences. 103(47). 17915–17920. 107 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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