Manuela Carvalho‐Gaspar

942 total citations
14 papers, 619 citations indexed

About

Manuela Carvalho‐Gaspar is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Manuela Carvalho‐Gaspar has authored 14 papers receiving a total of 619 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Immunology, 4 papers in Oncology and 2 papers in Molecular Biology. Recurrent topics in Manuela Carvalho‐Gaspar's work include Immune Cell Function and Interaction (8 papers), Immunotherapy and Immune Responses (7 papers) and T-cell and B-cell Immunology (7 papers). Manuela Carvalho‐Gaspar is often cited by papers focused on Immune Cell Function and Interaction (8 papers), Immunotherapy and Immune Responses (7 papers) and T-cell and B-cell Immunology (7 papers). Manuela Carvalho‐Gaspar collaborates with scholars based in United Kingdom, United States and Germany. Manuela Carvalho‐Gaspar's co-authors include Kathryn J. Wood, Nick D. Jones, Matthew O. Brook, Mohamed H. Sayegh, Jaeseok Yang, Jidong Zhang, Laurence A. Turka, Hilda E. Ramón, Shiqiao Luo and Laurent Martin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and Journal of Clinical Oncology.

In The Last Decade

Manuela Carvalho‐Gaspar

13 papers receiving 616 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Carvalho‐Gaspar United Kingdom 11 463 139 105 76 71 14 619
Oliver Kim United States 11 519 1.1× 69 0.5× 66 0.6× 81 1.1× 35 0.5× 11 647
Trishan Vaikunthanathan United Kingdom 8 268 0.6× 95 0.7× 86 0.8× 79 1.0× 39 0.5× 13 403
Masaaki Zaitsu Japan 10 267 0.6× 92 0.7× 160 1.5× 180 2.4× 60 0.8× 21 502
E. Dijke Netherlands 13 350 0.8× 65 0.5× 199 1.9× 140 1.8× 74 1.0× 35 547
Jennifer Woodward United States 13 327 0.7× 54 0.4× 115 1.1× 174 2.3× 39 0.5× 24 571
Hilda E. Ramón United States 8 538 1.2× 103 0.7× 46 0.4× 36 0.5× 53 0.7× 9 651
NICHOLAS W. PEARCE Australia 8 489 1.1× 51 0.4× 129 1.2× 108 1.4× 37 0.5× 13 594
Tara M. Engeman United States 9 399 0.9× 184 1.3× 57 0.5× 107 1.4× 28 0.4× 9 580
Hector A. DePaz United States 10 237 0.5× 58 0.4× 37 0.4× 101 1.3× 27 0.4× 36 397
Sarah C. Spencer United Kingdom 12 392 0.8× 34 0.2× 85 0.8× 124 1.6× 30 0.4× 18 539

Countries citing papers authored by Manuela Carvalho‐Gaspar

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Carvalho‐Gaspar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manuela Carvalho‐Gaspar. 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 Manuela Carvalho‐Gaspar. The network helps show where Manuela Carvalho‐Gaspar may publish in the future.

Co-authorship network of co-authors of Manuela Carvalho‐Gaspar

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

All Works

14 of 14 papers shown
1.
James, Kieran D., Emilie J. Cosway, Beth Lucas, et al.. (2018). Endothelial cells act as gatekeepers for LTβR-dependent thymocyte emigration. The Journal of Experimental Medicine. 215(12). 2984–2993. 22 indexed citations
2.
Cosway, Emilie J., Beth Lucas, Kieran D. James, et al.. (2017). Redefining thymus medulla specialization for central tolerance. The Journal of Experimental Medicine. 214(11). 3183–3195. 61 indexed citations
3.
Brunner, Thomas, Serena Lunardi, Nigel B. Jamieson, et al.. (2015). Influence of IP-10/CXCL10 induction in human pancreatic cancer stroma on lymphocytes recruitment and correlation with survival.. Journal of Clinical Oncology. 33(3_suppl). 290–290. 1 indexed citations
4.
Lunardi, Serena, Nigel B. Jamieson, Su Yin Lim, et al.. (2014). IP-10/CXCL10 induction in human pancreatic cancer stroma influences lymphocytes recruitment and correlates with poor survival. Oncotarget. 5(22). 11064–11080. 103 indexed citations
5.
Taylor, Stephen L., James A. Guggenheim, Iain B. Styles, et al.. (2014). Importance of Free Space Modelling on Quantitative Non-Contact Imaging. University of Birmingham Research Portal (University of Birmingham). BM3A.46–BM3A.46.
6.
Ross, Ewan A., Adriana Flores‐Langarica, Saeeda Bobat, et al.. (2014). Resolving Salmonella infection reveals dynamic and persisting changes in murine bone marrow progenitor cell phenotype and function. European Journal of Immunology. 44(8). 2318–2330. 9 indexed citations
7.
Texier, Laëtitia Le, Paméla Thébault, Manuela Carvalho‐Gaspar, et al.. (2012). Immunoregulatory Function of IL-27 and TGF-β1 in Cardiac Allograft Transplantation. Transplantation. 94(3). 226–233. 16 indexed citations
8.
Hester, Joanna, Natalie Mills, Sushma Shankar, et al.. (2011). Th17 Cells in Alemtuzumab-Treated Patients: The Effect of Long-Term Maintenance Immunosuppressive Therapy. Transplantation. 91(7). 744–750. 28 indexed citations
9.
Trzonkowski, Piotr, Alicja Dębska‐Ślizień, Magdalena Jankowska, et al.. (2010). Immunosenescence increases the rate of acceptance of kidney allotransplants in elderly recipients through exhaustion of CD4+ T-cells. Mechanisms of Ageing and Development. 131(2). 96–104. 56 indexed citations
10.
Jones, Nick D., et al.. (2010). Regulatory T cells can prevent memory CD8+ T‐cell‐mediated rejection following polymorphonuclear cell depletion. European Journal of Immunology. 40(11). 3107–3116. 28 indexed citations
11.
Carvalho‐Gaspar, Manuela, Nick D. Jones, Shiqiao Luo, et al.. (2008). Location and Time-Dependent Control of Rejection by Regulatory T Cells Culminates in a Failure to Generate Memory T Cells. The Journal of Immunology. 180(10). 6640–6648. 49 indexed citations
12.
Yang, Jaeseok, Matthew O. Brook, Manuela Carvalho‐Gaspar, et al.. (2007). Allograft rejection mediated by memory T cells is resistant to regulation. Proceedings of the National Academy of Sciences. 104(50). 19954–19959. 171 indexed citations
13.
Jones, Nick D., Manuela Carvalho‐Gaspar, Shiqiao Luo, et al.. (2006). Effector and Memory CD8+ T Cells Can Be Generated in Response to Alloantigen Independently of CD4+ T Cell Help. The Journal of Immunology. 176(4). 2316–2323. 39 indexed citations
14.
Carvalho‐Gaspar, Manuela, et al.. (2005). Chemokine gene expression during allograft rejection: Comparison of two quantitative PCR techniques. Journal of Immunological Methods. 301(1-2). 41–52. 36 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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