David Matallanas

4.0k total citations
67 papers, 2.9k citations indexed

About

David Matallanas is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, David Matallanas has authored 67 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 28 papers in Cell Biology and 9 papers in Oncology. Recurrent topics in David Matallanas's work include Hippo pathway signaling and YAP/TAZ (23 papers), Protein Kinase Regulation and GTPase Signaling (16 papers) and Melanoma and MAPK Pathways (13 papers). David Matallanas is often cited by papers focused on Hippo pathway signaling and YAP/TAZ (23 papers), Protein Kinase Regulation and GTPase Signaling (16 papers) and Melanoma and MAPK Pathways (13 papers). David Matallanas collaborates with scholars based in Ireland, United Kingdom and United States. David Matallanas's co-authors include Walter Kölch, Alex von Kriegsheim, David Romano, Piero Crespo, Eric O’Neill, Jens Rauch, Boris Ν. Kholodenko, Imanol Arozarena, Armin Zebisch and Marc R. Birtwistle and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Nano Letters.

In The Last Decade

David Matallanas

67 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Matallanas Ireland 30 2.1k 1.1k 485 262 169 67 2.9k
Scott T. Eblen United States 24 1.8k 0.8× 552 0.5× 445 0.9× 218 0.8× 138 0.8× 41 2.3k
Jiing‐Dwan Lee United States 21 2.1k 1.0× 450 0.4× 472 1.0× 303 1.2× 157 0.9× 26 2.7k
Karen Lundgren United States 22 2.4k 1.2× 777 0.7× 714 1.5× 196 0.7× 78 0.5× 38 3.1k
Wannian Yang United States 28 1.6k 0.8× 730 0.7× 346 0.7× 236 0.9× 64 0.4× 54 2.1k
Nagi G. Ayad United States 20 1.7k 0.8× 466 0.4× 430 0.9× 321 1.2× 75 0.4× 59 2.2k
Emmanuel Normant United States 22 1.3k 0.6× 417 0.4× 370 0.8× 115 0.4× 122 0.7× 50 2.0k
Caretha L. Creasy United States 27 2.8k 1.3× 716 0.7× 453 0.9× 317 1.2× 87 0.5× 41 3.4k
Jessie M. English United States 19 2.2k 1.1× 348 0.3× 496 1.0× 391 1.5× 185 1.1× 24 2.9k
Gisela Schnapp Germany 19 2.1k 1.0× 928 0.9× 556 1.1× 107 0.4× 139 0.8× 36 3.4k
Fei Gu China 31 1.9k 0.9× 357 0.3× 480 1.0× 707 2.7× 126 0.7× 91 3.0k

Countries citing papers authored by David Matallanas

Since Specialization
Citations

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

Fields of papers citing papers by David Matallanas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Matallanas

This figure shows the co-authorship network connecting the top 25 collaborators of David Matallanas. A scholar is included among the top collaborators of David Matallanas 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 David Matallanas. David Matallanas 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.
Cassidy, Hilary, et al.. (2025). Single- vs. Multi-Walled Carbon Nanotubes: Differential Cellular Stress and Lipid Metabolism Effects in Macrophage Models. Nanomaterials. 15(18). 1401–1401. 1 indexed citations
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Romano, David, Lucia García-Gutiérrez, David J. Duffy, et al.. (2022). Proteasomal down-regulation of the proapoptotic MST2 pathway contributes to BRAF inhibitor resistance in melanoma. Life Science Alliance. 5(10). e202201445–e202201445. 5 indexed citations
5.
García-Gutiérrez, Lucia, et al.. (2022). Interaction of LATS1 with SMAC links the MST2/Hippo pathway with apoptosis in an IAP-dependent manner. Cell Death and Disease. 13(8). 692–692. 7 indexed citations
6.
García-Gutiérrez, Lucia, et al.. (2021). BAX and SMAC regulate bistable properties of the apoptotic caspase system. Scientific Reports. 11(1). 20 indexed citations
7.
Kölch, Walter, et al.. (2021). Hidden Targets in RAF Signalling Pathways to Block Oncogenic RAS Signalling. Genes. 12(4). 553–553. 18 indexed citations
8.
Marcone, Simone, Amy Buckley, Colm J. Ryan, et al.. (2021). Proteomic signatures of radioresistance: Alteration of inflammation, angiogenesis and metabolism-related factors in radioresistant oesophageal adenocarcinoma. Cancer Treatment and Research Communications. 27. 100376–100376. 7 indexed citations
9.
Nováček, Vít, David Matallanas, Alfonso Blanco, et al.. (2020). Accurate prediction of kinase-substrate networks using knowledge graphs. PLoS Computational Biology. 16(12). e1007578–e1007578. 17 indexed citations
10.
Leroux, M., Hilary Cassidy, David Matallanas, et al.. (2019). Protein and lipid homeostasis altered in rat macrophages after exposure to metallic oxide nanoparticles. Cell Biology and Toxicology. 36(1). 65–82. 23 indexed citations
11.
Urbančič, Iztok, Maja Garvas, Polona Umek, et al.. (2018). Nanoparticles Can Wrap Epithelial Cell Membranes and Relocate Them Across the Epithelial Cell Layer. Nano Letters. 18(8). 5294–5305. 29 indexed citations
12.
Schaible, Bettina, Scott V. Nguyen, Daniel Hurley, et al.. (2018). Increased Virulence of Bloodstream Over Peripheral Isolates of P. aeruginosa Identified Through Post-transcriptional Regulation of Virulence Factors. Frontiers in Cellular and Infection Microbiology. 8. 357–357. 16 indexed citations
13.
Ryan, Colm J., Susan Kennedy, Ilirjana Bajrami, David Matallanas, & Christopher J. Lord. (2017). A Compendium of Co-regulated Protein Complexes in Breast Cancer Reveals Collateral Loss Events. Cell Systems. 5(4). 399–409.e5. 28 indexed citations
14.
Matallanas, David, Marc R. Birtwistle, Diego Romano, et al.. (2011). Raf Family Kinases: Old Dogs Have Learned New Tricks. Genes & Cancer. 2(3). 232–260. 288 indexed citations
15.
Romano, David, David Matallanas, Gregory Weitsman, et al.. (2010). Proapoptotic Kinase MST2 Coordinates Signaling Crosstalk between RASSF1A, Raf-1, and Akt. Cancer Research. 70(3). 1195–1203. 81 indexed citations
16.
Lock, Frances E., Thomas L. Dunwell, David Matallanas, et al.. (2010). The RASSF8 candidate tumor suppressor inhibits cell growth and regulates the Wnt and NF-κB signaling pathways. Oncogene. 29(30). 4307–4316. 68 indexed citations
17.
Preisinger, Christian, Alex von Kriegsheim, David Matallanas, & Walter Kölch. (2008). Proteomics and phosphoproteomics for the mapping of cellular signalling networks. PROTEOMICS. 8(21). 4402–4415. 30 indexed citations
18.
Matallanas, David, Victoria Sanz‐Moreno, Imanol Arozarena, et al.. (2005). Distinct Utilization of Effectors and Biological Outcomes Resulting from Site-Specific Ras Activation: Ras Functions in Lipid Rafts and Golgi Complex Are Dispensable for Proliferation and Transformation. Molecular and Cellular Biology. 26(1). 100–116. 107 indexed citations
19.
Arozarena, Imanol, David Matallanas, Marı́a T. Berciano, et al.. (2004). Activation of H-Ras in the Endoplasmic Reticulum by the RasGRF Family Guanine Nucleotide Exchange Factors. Molecular and Cellular Biology. 24(4). 1516–1530. 83 indexed citations
20.
Matallanas, David, Imanol Arozarena, Marı́a T. Berciano, et al.. (2003). Differences on the Inhibitory Specificities of H-Ras, K-Ras, and N-Ras (N17) Dominant Negative Mutants Are Related to Their Membrane Microlocalization. Journal of Biological Chemistry. 278(7). 4572–4581. 100 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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