Manuel O. Landázuri

8.3k total citations
109 papers, 6.9k citations indexed

About

Manuel O. Landázuri is a scholar working on Immunology, Molecular Biology and Cancer Research. According to data from OpenAlex, Manuel O. Landázuri has authored 109 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Immunology, 40 papers in Molecular Biology and 37 papers in Cancer Research. Recurrent topics in Manuel O. Landázuri's work include Cancer, Hypoxia, and Metabolism (31 papers), Immune Cell Function and Interaction (28 papers) and T-cell and B-cell Immunology (26 papers). Manuel O. Landázuri is often cited by papers focused on Cancer, Hypoxia, and Metabolism (31 papers), Immune Cell Function and Interaction (28 papers) and T-cell and B-cell Immunology (26 papers). Manuel O. Landázuri collaborates with scholars based in Spain, United States and United Kingdom. Manuel O. Landázuri's co-authors include Francisco Sánchez‐Madrid, Miguel López‐Botet, Julián Aragonés, Luis del Peso, Marta Cebrián, Ana C. Carrera, Antonio Postigo, Arántzazu Alfranca, Ronald B. Herberman and Mercedes Rincón and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The Journal of Experimental Medicine.

In The Last Decade

Manuel O. Landázuri

109 papers receiving 6.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuel O. Landázuri Spain 47 2.8k 2.7k 1.8k 1.2k 900 109 6.9k
Catherine Hession United States 33 3.3k 1.2× 4.0k 1.5× 1.3k 0.7× 1.7k 1.4× 880 1.0× 49 9.6k
Carl J. Kozlosky United States 18 2.1k 0.8× 3.1k 1.1× 1.2k 0.7× 1.4k 1.1× 2.0k 2.2× 20 6.8k
Gray D. Shaw United States 29 2.2k 0.8× 4.1k 1.5× 744 0.4× 1.5k 1.2× 960 1.1× 52 8.0k
Beverly J. Castner United States 13 1.3k 0.5× 2.5k 0.9× 1.2k 0.7× 1.4k 1.1× 1.8k 2.0× 18 5.8k
Jeffrey N. Fitzner United States 13 1.3k 0.5× 2.1k 0.8× 1.1k 0.6× 1.2k 1.0× 1.6k 1.7× 14 5.1k
Martin F. Wolfson United States 13 1.7k 0.6× 2.0k 0.7× 1.0k 0.6× 1.1k 0.9× 1.6k 1.7× 19 5.1k
Amnon Altman United States 62 6.2k 2.2× 5.1k 1.9× 1.1k 0.6× 828 0.7× 2.1k 2.3× 171 11.0k
Bernard Sordat Switzerland 37 1.6k 0.6× 2.3k 0.8× 1.0k 0.6× 442 0.4× 1.7k 1.9× 111 5.7k
G H Wong United States 26 3.8k 1.3× 3.3k 1.2× 1.1k 0.6× 347 0.3× 917 1.0× 54 7.7k
Mary Gerhart United States 14 1.4k 0.5× 1.7k 0.6× 902 0.5× 808 0.7× 1.2k 1.4× 22 4.2k

Countries citing papers authored by Manuel O. Landázuri

Since Specialization
Citations

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

Fields of papers citing papers by Manuel O. Landázuri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Manuel O. Landázuri. 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 Manuel O. Landázuri. The network helps show where Manuel O. Landázuri may publish in the future.

Co-authorship network of co-authors of Manuel O. Landázuri

This figure shows the co-authorship network connecting the top 25 collaborators of Manuel O. Landázuri. A scholar is included among the top collaborators of Manuel O. Landázuri 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 Manuel O. Landázuri. Manuel O. Landázuri 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.
Elorza, Ainara, Inés Soro-Arnáiz, Florinda Meléndez‐Rodríguez, et al.. (2012). HIF2α Acts as an mTORC1 Activator through the Amino Acid Carrier SLC7A5. Molecular Cell. 48(5). 681–691. 161 indexed citations
2.
Acosta‐Iborra, Bárbara, Ainara Elorza, Isabel M. Olazabal, et al.. (2009). Macrophage Oxygen Sensing Modulates Antigen Presentation and Phagocytic Functions Involving IFN-γ Production through the HIF-1α Transcription Factor. The Journal of Immunology. 182(5). 3155–3164. 83 indexed citations
3.
Calzada, Marı́a J., Miguel A. Esteban, María C. Castellanos, et al.. (2006). von Hippel-Lindau Tumor Suppressor Protein Regulates the Assembly of Intercellular Junctions in Renal Cancer Cells through Hypoxia-Inducible Factor–Independent Mechanisms. Cancer Research. 66(3). 1553–1560. 60 indexed citations
4.
Landázuri, Manuel O., et al.. (2006). Analysis of HIF-prolyl hydroxylases binding to substrates. Biochemical and Biophysical Research Communications. 351(2). 313–320. 31 indexed citations
5.
Pescador, Nuria, et al.. (2005). Identification of a functional hypoxia-responsive element that regulates the expression of the egl nine homologue 3 (egln3/phd3) gene. Biochemical Journal. 390(1). 189–197. 181 indexed citations
6.
Martı́n-Puig, Silvia, Julián Aragonés, David Jones, et al.. (2004). Role of diacylglycerol induced by hypoxia in the regulation of HIF-1α activity. Biochemical and Biophysical Research Communications. 315(1). 44–50. 31 indexed citations
7.
Naranjo‐Suarez, Salvador, et al.. (2003). Down-regulation of Hypoxia-inducible Factor-2 in PC12 Cells by Nerve Growth Factor Stimulation. Journal of Biological Chemistry. 278(34). 31895–31901. 30 indexed citations
8.
Pinto-Vidal, Felipe Augusto, Julián Aragonés, Arántzazu Alfranca, & Manuel O. Landázuri. (2000). Up-regulation of vascular endothelial growth factor receptor Flt-1 after endothelial denudation: role of transcription factor Egr-1. Blood. 95(11). 3387–3395. 46 indexed citations
9.
Yáñez-Mó, Marı́a, Arántzazu Alfranca, Carlos Cabañas, et al.. (1998). Regulation of Endothelial Cell Motility by Complexes of Tetraspan Molecules CD81/TAPA-1 and CD151/PETA-3 with α3β1 Integrin Localized at Endothelial Lateral Junctions. The Journal of Cell Biology. 141(3). 791–804. 240 indexed citations
10.
Montoya, Marı́a C., Francis W. Luscinskas, Miguel Á. del Pozo, Julián Aragonés, & Manuel O. Landázuri. (1997). Reduced intracellular oxidative metabolism promotes firm adhesion of human polymorphonuclear leukocytes to vascular endothelium under flow conditions. European Journal of Immunology. 27(8). 1942–1951. 18 indexed citations
11.
Postigo, Antonio, Paloma Sánchez‐Mateos, A I Lazarovits, Francisco Sánchez‐Madrid, & Manuel O. Landázuri. (1993). Alpha 4 beta 7 integrin mediates B cell binding to fibronectin and vascular cell adhesion molecule-1. Expression and function of alpha 4 integrins on human B lymphocytes.. The Journal of Immunology. 151(5). 2471–2483. 118 indexed citations
12.
Postigo, Antonio, Rosario García‐Vicuña, Federico Díaz‐González, et al.. (1992). Increased binding of synovial T lymphocytes from rheumatoid arthritis to endothelial-leukocyte adhesion molecule-1 (ELAM-1) and vascular cell adhesion molecule-1 (VCAM-1).. Journal of Clinical Investigation. 89(5). 1445–1452. 75 indexed citations
13.
Campanero, Miguel R., Alicia G. Arroyo, Rafael Pulido, et al.. (1992). Functional role of α2/β1 and α4/β1 integrins in leukocyte intercellular adhesion induced through the common β1 subunit. European Journal of Immunology. 22(12). 3111–3119. 61 indexed citations
14.
Aramburu, J., Marı́a A. Balboa, Agustín Acevedo, et al.. (1990). A novel functional cell surface dimer (Kp43) expressed by natural killer cells and T cell receptor-gamma/delta+ T lymphocytes. I. Inhibition of the IL-2-dependent proliferation by anti-Kp43 monoclonal antibody.. The Journal of Immunology. 144(8). 3238–3247. 115 indexed citations
15.
Sánchez‐Mateos, Paloma, et al.. (1989). Expression of a gp33/27,000 MW activation inducer molecule (AIM) on human lymphoid tissues. Induction of cell proliferation on thymocytes and B lymphocytes by anti-AIM antibodies.. PubMed. 68(1). 72–9. 42 indexed citations
16.
Carrera, Ana C., Mercedes Rincón, Francisco Sánchez‐Madrid, Miguel López‐Botet, & Manuel O. Landázuri. (1988). Triggering of co-mitogenic signals in T cell proliferation by anti-LFA-1 (CD18, CD11a), LFA-3, and CD7 monoclonal antibodies.. The Journal of Immunology. 141(6). 1919–1924. 107 indexed citations
17.
Pulido, Rafael, et al.. (1988). Comparative biochemical and tissue distribution study of four distinct CD45 antigen specificities.. The Journal of Immunology. 140(11). 3851–3857. 90 indexed citations
18.
Cebrián, Marta, et al.. (1988). Triggering of T cell proliferation through AIM, an activation inducer molecule expressed on activated human lymphocytes.. The Journal of Experimental Medicine. 168(5). 1621–1637. 256 indexed citations
19.
Bernabéu, Carmelo, Ana C. Carrera, Manuel O. Landázuri, & Francisco Sánchez‐Madrid. (1987). Interaction between the CD45 antigen and phytohemagglutinin. Inhibitory effect on the lectininduced T cell proliferation by anti‐CD45 monoclonal antibody. European Journal of Immunology. 17(10). 1461–1466. 56 indexed citations
20.
Sánchez‐Madrid, Francisco, et al.. (1986). VLA‐3: A novel polypeptide association within the VLA molecular complex: cell distribution and biochemical characterization. European Journal of Immunology. 16(11). 1343–1349. 200 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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