Anna Valujskikh

4.1k total citations
89 papers, 3.2k citations indexed

About

Anna Valujskikh is a scholar working on Immunology, Transplantation and Surgery. According to data from OpenAlex, Anna Valujskikh has authored 89 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Immunology, 33 papers in Transplantation and 20 papers in Surgery. Recurrent topics in Anna Valujskikh's work include T-cell and B-cell Immunology (56 papers), Immune Cell Function and Interaction (51 papers) and Renal Transplantation Outcomes and Treatments (33 papers). Anna Valujskikh is often cited by papers focused on T-cell and B-cell Immunology (56 papers), Immune Cell Function and Interaction (51 papers) and Renal Transplantation Outcomes and Treatments (33 papers). Anna Valujskikh collaborates with scholars based in United States, Japan and France. Anna Valujskikh's co-authors include Peter S. Heeger, Robert L. Fairchild, Gilles Bénichou, Birte Pantenburg, William M. Baldwin, Ran Fan, Li X, Victoria Gorbacheva, Yifa Chen and Qiwei Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Experimental Medicine.

In The Last Decade

Anna Valujskikh

84 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Valujskikh United States 32 2.3k 1.0k 695 405 375 89 3.2k
Nicolas Degauque France 31 2.1k 0.9× 969 0.9× 645 0.9× 369 0.9× 425 1.1× 87 3.3k
Sebastiaan Heidt Netherlands 30 1.1k 0.5× 1.2k 1.1× 802 1.2× 325 0.8× 386 1.0× 130 2.5k
Ewa Jankowska−Gan United States 25 1.3k 0.6× 548 0.5× 577 0.8× 268 0.7× 351 0.9× 61 2.4k
Marc Martínez‐Llordella United Kingdom 25 2.6k 1.1× 815 0.8× 884 1.3× 585 1.4× 483 1.3× 42 4.2k
Eric T. Elwood United States 16 1.8k 0.8× 591 0.6× 1.1k 1.6× 320 0.8× 211 0.6× 37 3.1k
George Vlad United States 27 1.6k 0.7× 445 0.4× 404 0.6× 194 0.5× 126 0.3× 60 2.3k
Catharine M. Chase United States 22 1.1k 0.5× 726 0.7× 860 1.2× 241 0.6× 158 0.4× 39 2.0k
Sylvie Ferrari‐Lacraz Switzerland 20 1.0k 0.4× 320 0.3× 338 0.5× 352 0.9× 310 0.8× 60 1.9k
T. Mohanakumar United States 31 815 0.4× 716 0.7× 1.5k 2.2× 435 1.1× 261 0.7× 106 2.7k
Andrés Jaramillo United States 28 1.3k 0.6× 522 0.5× 1.2k 1.7× 325 0.8× 411 1.1× 96 2.9k

Countries citing papers authored by Anna Valujskikh

Since Specialization
Citations

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

Fields of papers citing papers by Anna Valujskikh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Valujskikh

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Valujskikh. A scholar is included among the top collaborators of Anna Valujskikh 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 Anna Valujskikh. Anna Valujskikh 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.
Fan, Ran, Juyeun Lee, Victoria Gorbacheva, et al.. (2025). LAG3 regulates antibody responses in a murine model of kidney transplantation. Journal of Clinical Investigation. 135(13).
2.
Gorbacheva, Victoria, et al.. (2023). Autoantibodies against DNA topoisomerase I promote renal allograft rejection by increasing alloreactive T cell responses. American Journal of Transplantation. 23(9). 1307–1318. 1 indexed citations
3.
Lee, Juyeun, Danielle D. Kish, George W. Farr, et al.. (2023). Water channel aquaporin 4 is required for T cell receptor mediated lymphocyte activation. Journal of Leukocyte Biology. 113(6). 544–554. 2 indexed citations
4.
Fan, Ran, et al.. (2020). B cell–derived IL-1β and IL-6 drive T cell reconstitution following lymphoablation. American Journal of Transplantation. 20(10). 2740–2754. 14 indexed citations
5.
Gorbacheva, Victoria, et al.. (2019). Anti-donor MHC Class II Alloantibody Induces Glomerular Injury in Mouse Renal Allografts Subjected to Prolonged Cold Ischemia. Journal of the American Society of Nephrology. 30(12). 2413–2425. 11 indexed citations
6.
Ayasoufi, Katayoun, Naoki Kohei, Ran Fan, et al.. (2017). Aquaporin 4 blockade improves survival of murine heart allografts subjected to prolonged cold ischemia. American Journal of Transplantation. 18(5). 1238–1246. 19 indexed citations
7.
Kohei, Naoki, Toshiaki Tanaka, Kazunari Tanabe, et al.. (2016). Natural killer cells play a critical role in mediating inflammation and graft failure during antibody-mediated rejection of kidney allografts. Kidney International. 89(6). 1293–1306. 54 indexed citations
8.
Kaul, Artur, Sravan K. Goparaju, Nina Dvorina, et al.. (2015). Acute and Chronic Rejection: Compartmentalization and Kinetics of Counterbalancing Signals in Cardiac Transplants. American Journal of Transplantation. 15(2). 333–345. 28 indexed citations
9.
Abe, Toyofumi, Daisuke Ishii, Victoria Gorbacheva, et al.. (2015). Anti-huCD20 Antibody Therapy for Antibody-Mediated Rejection of Renal Allografts in a Mouse Model. American Journal of Transplantation. 15(5). 1192–1204. 28 indexed citations
10.
Zhang, Qiwei, Yi-fa Chen, Robert L. Fairchild, Peter S. Heeger, & Anna Valujskikh. (2006). Lymphoid Sequestration of Alloreactive Memory CD4 T Cells Promotes Cardiac Allograft Survival. The Journal of Immunology. 176(2). 770–777. 91 indexed citations
11.
Valujskikh, Anna, Qiwei Zhang, & Peter S. Heeger. (2006). CD8 T Cells Specific for a Donor-Derived, Self-Restricted Transplant Antigen Are Nonpathogenic Bystanders after Vascularized Heart Transplantation in Mice. The Journal of Immunology. 176(4). 2190–2196. 19 indexed citations
12.
Valujskikh, Anna, David H. Canaday, Erin Bailey, et al.. (2005). Mouse Endothelial Cells Cross-Present Lymphocyte-Derived Antigen on Class I MHC via a TAP1- and Proteasome-Dependent Pathway. The Journal of Immunology. 174(12). 7711–7715. 46 indexed citations
13.
Heeger, Peter S., Peter N. Lalli, Feng Lin, et al.. (2005). Decay-accelerating factor modulates induction of T cell immunity. The Journal of Experimental Medicine. 201(10). 1523–1530. 242 indexed citations
14.
Schenk, Sören, Qiwei Zhang, Anna Valujskikh, et al.. (2004). Effects of T Cell Frequency and Graft Size on Transplant Outcome in Mice. The Journal of Immunology. 172(1). 240–247. 59 indexed citations
15.
Chen, Yi-fa, et al.. (2003). The Male Minor Transplantation Antigen Preferentially Activates Recipient CD4+ T Cells through the Indirect Presentation Pathway In Vivo. The Journal of Immunology. 171(12). 6510–6518. 44 indexed citations
16.
Valujskikh, Anna & Peter S. Heeger. (2003). Emerging roles of endothelial cells in transplant rejection. Current Opinion in Immunology. 15(5). 493–498. 46 indexed citations
17.
Pantenburg, Birte, et al.. (2002). T Cells Primed by Leishmania major Infection Cross-React with Alloantigens and Alter the Course of Allograft Rejection. The Journal of Immunology. 169(7). 3686–3693. 138 indexed citations
18.
Illigens, Ben, Akira Yamada, Eugenia V. Fedoseyeva, et al.. (2002). The relative contribution of direct and indirect antigen recognition pathways to the alloresponse and graft rejection depends upon the nature of the transplant. Human Immunology. 63(10). 912–925. 42 indexed citations
19.
Valujskikh, Anna, et al.. (2001). INDIRECTLY PRIMED CD8+ T CELLS ARE A PROMINENT COMPONENT OF THE ALLOGENEIC T-CELL REPERTOIRE AFTER SKIN GRAFT REJECTION IN MICE1. Transplantation. 71(3). 418–421. 18 indexed citations
20.
Heeger, Peter S., Anna Valujskikh, & Paul Lehmann. (2000). Comprehensive Assessment of Determinant Specificity, Frequency, and Cytokine Signature of the Primed CD8 Cell Repertoire Induced by a Minor Transplantation Antigen. The Journal of Immunology. 165(3). 1278–1284. 21 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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