Jesús Pérez‐Losada

3.7k total citations
71 papers, 2.7k citations indexed

About

Jesús Pérez‐Losada is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Jesús Pérez‐Losada has authored 71 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 32 papers in Oncology and 15 papers in Cancer Research. Recurrent topics in Jesús Pérez‐Losada's work include Cancer Cells and Metastasis (12 papers), Cancer-related Molecular Pathways (12 papers) and Nonmelanoma Skin Cancer Studies (8 papers). Jesús Pérez‐Losada is often cited by papers focused on Cancer Cells and Metastasis (12 papers), Cancer-related Molecular Pathways (12 papers) and Nonmelanoma Skin Cancer Studies (8 papers). Jesús Pérez‐Losada collaborates with scholars based in Spain, United States and China. Jesús Pérez‐Losada's co-authors include Allan Balmain, Jian‐Hua Mao, Isidro Sánchez‐García, Javier Cañueto, Reyno Delrosario, Manuel Sánchez‐Martín, Roberto Corchado‐Cobos, Natalia García‐Sancha, T Flores and Rogelio González‐Sarmiento and has published in prestigious journals such as Nature, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Jesús Pérez‐Losada

68 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jesús Pérez‐Losada Spain 27 1.6k 1.1k 496 348 329 71 2.7k
P. Sivaramakrishna Rachakonda Germany 25 1.9k 1.2× 931 0.8× 577 1.2× 263 0.8× 317 1.0× 45 3.4k
Yoshiaki Kubo Japan 24 1.2k 0.7× 702 0.6× 410 0.8× 210 0.6× 573 1.7× 88 2.8k
Karine Lefort Switzerland 22 1.6k 1.0× 763 0.7× 510 1.0× 270 0.8× 299 0.9× 32 2.4k
Christine Jean France 24 1.5k 0.9× 793 0.7× 446 0.9× 550 1.6× 146 0.4× 52 2.9k
Claudia Wohlenberg Germany 12 983 0.6× 587 0.5× 340 0.7× 255 0.7× 185 0.6× 12 2.3k
Qingyun Liu China 18 2.1k 1.3× 1.7k 1.5× 996 2.0× 297 0.9× 153 0.5× 31 3.4k
Dany Nassar France 17 1.1k 0.7× 821 0.7× 519 1.0× 229 0.7× 126 0.4× 29 2.0k
Karin List United States 31 1.2k 0.8× 512 0.4× 761 1.5× 525 1.5× 97 0.3× 42 2.9k
Elisha Roberson United States 17 1.4k 0.9× 590 0.5× 282 0.6× 172 0.5× 226 0.7× 29 2.8k
Roslin Russell United Kingdom 22 1.5k 1.0× 977 0.9× 645 1.3× 207 0.6× 111 0.3× 30 2.7k

Countries citing papers authored by Jesús Pérez‐Losada

Since Specialization
Citations

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

Fields of papers citing papers by Jesús Pérez‐Losada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jesús Pérez‐Losada. 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 Jesús Pérez‐Losada. The network helps show where Jesús Pérez‐Losada may publish in the future.

Co-authorship network of co-authors of Jesús Pérez‐Losada

This figure shows the co-authorship network connecting the top 25 collaborators of Jesús Pérez‐Losada. A scholar is included among the top collaborators of Jesús Pérez‐Losada 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 Jesús Pérez‐Losada. Jesús Pérez‐Losada 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.
García‐Sancha, Natalia, Roberto Corchado‐Cobos, & Jesús Pérez‐Losada. (2025). Understanding Susceptibility to Breast Cancer: From Risk Factors to Prevention Strategies. International Journal of Molecular Sciences. 26(7). 2993–2993. 8 indexed citations
2.
Yang, Hui, Xinzhi Wang, Adrián Blanco‐Gómez, et al.. (2024). A susceptibility gene signature for ERBB2-driven mammary tumour development and metastasis in collaborative cross mice. EBioMedicine. 106. 105260–105260. 2 indexed citations
3.
Pérez‐Losada, Jesús, et al.. (2023). The Role of GAB1 in Cancer. Cancers. 15(16). 4179–4179. 8 indexed citations
4.
García‐Sancha, Natalia, Roberto Corchado‐Cobos, Adrián Blanco‐Gómez, et al.. (2022). Evolutionary Origins of Metabolic Reprogramming in Cancer. International Journal of Molecular Sciences. 23(20). 12063–12063. 1 indexed citations
5.
San‐Segundo, Laura, et al.. (2022). Chloroquine-Induced DNA Damage Synergizes with Nonhomologous End Joining Inhibition to Cause Ovarian Cancer Cell Cytotoxicity. International Journal of Molecular Sciences. 23(14). 7518–7518. 8 indexed citations
6.
Corchado‐Cobos, Roberto, Natalia García‐Sancha, Marina Holgado-Madruga, et al.. (2022). Pathophysiological Integration of Metabolic Reprogramming in Breast Cancer. Cancers. 14(2). 322–322. 16 indexed citations
7.
Chang, Hang, Yang Xu, Xiaoping Liu, et al.. (2022). From Mouse to Human: Cellular Morphometric Subtype Learned From Mouse Mammary Tumors Provides Prognostic Value in Human Breast Cancer. Frontiers in Oncology. 11. 819565–819565. 7 indexed citations
8.
García‐Sancha, Natalia, Roberto Corchado‐Cobos, Concepción Román‐Curto, et al.. (2021). Overcoming Resistance to Immunotherapy in Advanced Cutaneous Squamous Cell Carcinoma. Cancers. 13(20). 5134–5134. 12 indexed citations
9.
Blanco‐Gómez, Adrián, Sonia Castillo‐Lluva, María Isidoro‐García, et al.. (2018). The biological age linked to oxidative stress modifies breast cancer aggressiveness. Free Radical Biology and Medicine. 120. 133–146. 17 indexed citations
10.
Mao, Jian‐Hua, P. J. van Diest, Jesús Pérez‐Losada, & Antoine M. Snijders. (2017). Revisiting the impact of age and molecular subtype on overall survival after radiotherapy in breast cancer patients. Scientific Reports. 7(1). 12587–12587. 20 indexed citations
11.
Lü, Jing, Mingxin Wen, Yurong Huang, et al.. (2013). C2ORF40suppresses breast cancer cell proliferation and invasion through modulating expression of M phase cell cycle genes. Epigenetics. 8(6). 571–583. 40 indexed citations
12.
Kim, Il-Jin, Di Wu, Jing Lü, et al.. (2012). Pten Regulates Aurora-A and Cooperates with Fbxw7 in Modulating Radiation-Induced Tumor Development. Molecular Cancer Research. 10(6). 834–844. 57 indexed citations
13.
Ridd, Katie, Elise F. Saunier, Frederic F. Clermont, et al.. (2009). Elevated Cutaneous Smad Activation Associates with Enhanced Skin Tumor Susceptibility in Organ Transplant Recipients. Clinical Cancer Research. 15(16). 5101–5107. 12 indexed citations
14.
Quigley, David A., Minh D. To, Jesús Pérez‐Losada, et al.. (2009). Genetic architecture of mouse skin inflammation and tumour susceptibility. Nature. 458(7237). 505–508. 99 indexed citations
15.
To, Minh D., Jesús Pérez‐Losada, Jian‐Hua Mao, et al.. (2006). A functional switch from lung cancer resistance to susceptibility at the Pas1 locus in Kras2LA2 mice. Nature Genetics. 38(8). 926–930. 60 indexed citations
16.
Mao, Jian‐Hua, Jiangzhen Li, Tao Jiang, et al.. (2005). Genomic instability in radiation-induced mouse lymphoma from p53 heterozygous mice. Oncogene. 24(53). 7924–7934. 24 indexed citations
17.
Mao, Jian‐Hua, Minh D. To, Jesús Pérez‐Losada, et al.. (2004). Mutually exclusive mutations of the Pten and ras pathways in skin tumor progression. Genes & Development. 18(15). 1800–1805. 55 indexed citations
18.
Pérez‐Losada, Jesús, et al.. (2001). Philadelphia-Positive B-Cell Acute Lymphoblastic Leukemia Is Initiated in an Uncommitted Progenitor Cell. Leukemia & lymphoma. 42(4). 569–576. 11 indexed citations
19.
Pérez‐Losada, Jesús, Belén Pintado, Alfonso Gutiérrez‐Adán, et al.. (2000). The chimeric FUS/TLS-CHOP fusion protein specifically induces liposarcomas in transgenic mice. Oncogene. 19(20). 2413–2422. 118 indexed citations
20.
Pérez‐Losada, Jesús, Manuel Sánchez‐Martín, Belén Pintado, et al.. (2000). Liposarcoma initiated by FUS/TLS-CHOP: the FUS/TLS domain plays a critical role in the pathogenesis of liposarcoma. Oncogene. 19(52). 6015–6022. 67 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by P. Sivaramakrishna Rachakonda Breakdown of academic impact, for papers by Yoshiaki Kubo Breakdown of academic impact, for papers by Karine Lefort Breakdown of academic impact, for papers by Christine Jean Breakdown of academic impact, for papers by Claudia Wohlenberg Breakdown of academic impact, for papers by Qingyun Liu Breakdown of academic impact, for papers by Dany Nassar Breakdown of academic impact, for papers by Karin List Breakdown of academic impact, for papers by Elisha Roberson Breakdown of academic impact, for papers by Roslin Russell
Rankless by CCL
2026