Rosa Puertollano

25.0k total citations · 4 hit papers
106 papers, 9.6k citations indexed

About

Rosa Puertollano is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Rosa Puertollano has authored 106 papers receiving a total of 9.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 47 papers in Cell Biology and 36 papers in Physiology. Recurrent topics in Rosa Puertollano's work include Cellular transport and secretion (38 papers), Calcium signaling and nucleotide metabolism (35 papers) and Autophagy in Disease and Therapy (30 papers). Rosa Puertollano is often cited by papers focused on Cellular transport and secretion (38 papers), Calcium signaling and nucleotide metabolism (35 papers) and Autophagy in Disease and Therapy (30 papers). Rosa Puertollano collaborates with scholars based in United States, Spain and Italy. Rosa Puertollano's co-authors include José A. Martina, Juan S. Bonifacino, Nina Raben, Yong Chen, Marjan Guček, Andrea Ballabio, Silvia Vergarajauregui, Heba I. Diab, Miguel A. Alonso and Nina Raben and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Rosa Puertollano

103 papers receiving 9.5k citations

Hit Papers

MTORC1 functions as a tra... 2011 2026 2016 2021 2012 2011 2014 2018 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rosa Puertollano United States 51 4.8k 3.7k 3.4k 2.4k 2.2k 106 9.6k
Marco Sardiello United States 31 3.9k 0.8× 2.0k 0.5× 4.5k 1.3× 1.7k 0.7× 2.4k 1.1× 47 8.9k
José A. Martina United States 33 2.8k 0.6× 1.9k 0.5× 2.2k 0.6× 1.1k 0.5× 1.0k 0.5× 53 5.5k
Yasemin Sancak United States 23 9.2k 1.9× 2.4k 0.6× 2.0k 0.6× 755 0.3× 1.5k 0.7× 42 11.7k
Michela Palmieri United States 30 2.5k 0.5× 1.3k 0.3× 2.5k 0.7× 1.0k 0.4× 1.4k 0.6× 53 6.1k
Tuong Huynh United States 19 3.7k 0.8× 1.2k 0.3× 3.8k 1.1× 937 0.4× 1.2k 0.5× 19 6.7k
Gregory A. Grabowski United States 63 5.7k 1.2× 5.1k 1.4× 2.6k 0.8× 990 0.4× 9.2k 4.2× 261 13.6k
Liron Bar‐Peled United States 21 6.3k 1.3× 2.4k 0.6× 2.1k 0.6× 965 0.4× 1.1k 0.5× 31 9.0k
György Csordás United States 40 6.9k 1.4× 1.7k 0.5× 1.2k 0.4× 389 0.2× 1.2k 0.6× 72 8.4k
Fiona M. Menzies United Kingdom 36 4.3k 0.9× 2.6k 0.7× 5.6k 1.6× 965 0.4× 1.8k 0.8× 42 9.6k
Shamshad Cockcroft United Kingdom 64 8.4k 1.8× 4.9k 1.3× 460 0.1× 1.5k 0.6× 2.0k 0.9× 190 11.9k

Countries citing papers authored by Rosa Puertollano

Since Specialization
Citations

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

Fields of papers citing papers by Rosa Puertollano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rosa Puertollano

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa Puertollano. A scholar is included among the top collaborators of Rosa Puertollano 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 Rosa Puertollano. Rosa Puertollano 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.
Rissone, Alberto, Martina La Spina, Erica Bresciani, et al.. (2025). The transcription factors Tfeb and Tfe3 are required for survival and embryonic development of pancreas and liver in zebrafish. PLoS Genetics. 21(6). e1011754–e1011754.
2.
López‐Haber, Cynthia, et al.. (2025). The lysosomal carrier SLC29A3 supports antibacterial signaling, and promotes autophagy by activating TRPML1 in murine dendritic cells. Proceedings of the National Academy of Sciences. 122(48). e2511539122–e2511539122.
3.
Gómez‐Orte, Eva, Xavier González, José A. Martina, et al.. (2024). Regulation of Caenorhabditis elegans HLH-30 subcellular localization dynamics: Evidence for a redox-dependent mechanism. Free Radical Biology and Medicine. 223. 369–383. 2 indexed citations
4.
Willett, Rose, et al.. (2024). TMEM55B links autophagy flux, lysosomal repair, and TFE3 activation in response to oxidative stress. Nature Communications. 15(1). 93–93. 8 indexed citations
5.
Machado-Oliveira, Gisela, Cristiano Ramos, José S. Ramalho, et al.. (2023). Cholesteryl Hemiazelate Present in Cardiovascular Disease Patients Causes Lysosome Dysfunction in Murine Fibroblasts. Cells. 12(24). 2826–2826. 2 indexed citations
6.
Contreras, Pablo S., et al.. (2023). Beta-coronaviruses exploit cellular stress responses by modulating TFEB and TFE3 activity. iScience. 26(3). 106169–106169. 8 indexed citations
7.
Martina, José A., et al.. (2022). The FACT complex facilitates expression of lysosomal and antioxidant genes through binding to TFEB and TFE3. Autophagy. 18(10). 2333–2349. 19 indexed citations
8.
Liu, Hui‐Ying, Naresh Kumar Meena, Chao Li, et al.. (2021). Chemoenzymatic glycan-selective remodeling of a therapeutic lysosomal enzyme with high-affinity M6P-glycan ligands. Enzyme substrate specificity is the name of the game. Chemical Science. 12(37). 12451–12462. 7 indexed citations
9.
Martina, José A., Nina Raben, & Rosa Puertollano. (2020). SnapShot: Lysosomal Storage Diseases. Cell. 180(3). 602–602.e1. 28 indexed citations
10.
Martina, José A., Eva Gómez‐Orte, José Antonio Bárcena, et al.. (2020). A conserved cysteine‐based redox mechanism sustains TFEB/HLH‐30 activity under persistent stress. The EMBO Journal. 40(3). e105793–e105793. 31 indexed citations
11.
Choy, Christopher H., Matthew Gray, Callen T. Wallace, et al.. (2018). Lysosome enlargement during inhibition of the lipid kinase PIKfyve proceeds through lysosome coalescence. Journal of Cell Science. 131(10). 96 indexed citations
12.
Puertollano, Rosa, Shawn M. Ferguson, James Brugarolas, & Andrea Ballabio. (2018). The complex relationship between TFEB transcription factor phosphorylation and subcellular localization. The EMBO Journal. 37(11). 381 indexed citations breakdown →
13.
Chen, Cheng‐Chang, Elisabeth Butz, Anna Scotto Rosato, et al.. (2018). Selective agonist of TRPML2 reveals direct role in chemokine release from innate immune cells. eLife. 7. 77 indexed citations
14.
Martina, José A., Heba I. Diab, Owen A. Brady, & Rosa Puertollano. (2016). TFEB and TFE 3 are novel components of the integrated stress response. The EMBO Journal. 35(5). 479–495. 231 indexed citations
15.
Ai, Teng, Rose Willett, J.M. Williams, et al.. (2016). N-(1-Benzyl-3,5-dimethyl-1H-pyrazol-4-yl)benzamides: Antiproliferative Activity and Effects on mTORC1 and Autophagy. ACS Medicinal Chemistry Letters. 8(1). 90–95. 12 indexed citations
16.
Wada, Shogo, Michael D. Neinast, Cholsoon Jang, et al.. (2016). The tumor suppressor FLCN mediates an alternate mTOR pathway to regulate browning of adipose tissue. Genes & Development. 30(22). 2551–2564. 91 indexed citations
17.
Spampanato, Carmine, Erin Feeney, Lishu Li, et al.. (2013). Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease. EMBO Molecular Medicine. 5(5). 691–706. 262 indexed citations
18.
Vergarajauregui, Silvia, José A. Martina, & Rosa Puertollano. (2011). LAPTMs regulate lysosomal function and interact with mucolipin 1: new clues for understanding mucolipidosis type IV. Journal of Cell Science. 124(3). 459–468. 44 indexed citations
19.
Rismanchi, Neggy, Rosa Puertollano, & Craig Blackstone. (2008). STAM Adaptor Proteins Interact with COPII Complexes and Function in ER‐to‐Golgi Trafficking. Traffic. 10(2). 201–217. 20 indexed citations
20.
Puertollano, Rosa & Miguel A. Alonso. (1999). MAL, an Integral Element of the Apical Sorting Machinery, Is an Itinerant Protein That Cycles between theTrans-Golgi Network and the Plasma Membrane. Molecular Biology of the Cell. 10(10). 3435–3447. 83 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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