Soledad Matus

2.1k total citations
21 papers, 1.5k citations indexed

About

Soledad Matus is a scholar working on Cell Biology, Molecular Biology and Epidemiology. According to data from OpenAlex, Soledad Matus has authored 21 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cell Biology, 10 papers in Molecular Biology and 9 papers in Epidemiology. Recurrent topics in Soledad Matus's work include Endoplasmic Reticulum Stress and Disease (11 papers), Autophagy in Disease and Therapy (9 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). Soledad Matus is often cited by papers focused on Endoplasmic Reticulum Stress and Disease (11 papers), Autophagy in Disease and Therapy (9 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). Soledad Matus collaborates with scholars based in Chile, United States and United Kingdom. Soledad Matus's co-authors include Claudio Hetz, Laurie H. Glimcher, Melissa Nassif, Peter Thielen, Vicente Valenzuela, Robert H. Brown, Gabriela Martínez, Roberta Kiffin, Ana María Cuervo and Felipe A. Court and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and Genes & Development.

In The Last Decade

Soledad Matus

20 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soledad Matus Chile 17 725 568 497 490 255 21 1.5k
Guy M. Lenk United States 23 620 0.9× 287 0.5× 616 1.2× 220 0.4× 339 1.3× 38 1.7k
Silvia Corrochano Spain 15 254 0.4× 581 1.0× 645 1.3× 573 1.2× 379 1.5× 24 1.5k
Aleksey Shatunov United Kingdom 26 402 0.6× 233 0.4× 972 2.0× 917 1.9× 325 1.3× 45 2.0k
Owen A. Brady United States 13 327 0.5× 489 0.9× 700 1.4× 666 1.4× 108 0.4× 14 1.7k
Natalia Rodríguez‐Muela Spain 17 286 0.4× 811 1.4× 840 1.7× 513 1.0× 253 1.0× 23 1.8k
Özlem Göker-Alpan United States 30 1.3k 1.7× 588 1.0× 709 1.4× 743 1.5× 166 0.7× 126 2.9k
Rodrigo A. Fuentealba Chile 11 259 0.4× 211 0.4× 801 1.6× 299 0.6× 336 1.3× 14 1.4k
Maurizio D’Antonio Italy 26 806 1.1× 224 0.4× 1.2k 2.5× 393 0.8× 1.5k 5.8× 47 2.6k
Hongfeng Wang China 25 289 0.4× 651 1.1× 1.0k 2.0× 727 1.5× 316 1.2× 48 1.8k

Countries citing papers authored by Soledad Matus

Since Specialization
Citations

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

Fields of papers citing papers by Soledad Matus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soledad Matus

This figure shows the co-authorship network connecting the top 25 collaborators of Soledad Matus. A scholar is included among the top collaborators of Soledad Matus 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 Soledad Matus. Soledad Matus 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.
Martínez, Nicolás W., et al.. (2025). GCN2-Mediated eIF2α Phosphorylation Is Required for Central Nervous System Remyelination. International Journal of Molecular Sciences. 26(4). 1626–1626. 2 indexed citations
2.
Carvajal, Patricia, Sergio Aguilera, María‐José Barrera, et al.. (2024). Giantin mediates Golgi localization of Gal3-O-sulfotransferases and affects salivary mucin sulfation in patients with Sjögren’s disease. JCI Insight. 9(22).
3.
Carvajal, Patricia, V. Bahamondes, Daniela Jara, et al.. (2023). The integrated stress response is activated in the salivary glands of Sjögren’s syndrome patients. Frontiers in Medicine. 10. 1118703–1118703. 3 indexed citations
4.
Martínez, Nicolás W., et al.. (2021). The Potential Role of Protein Kinase R as a Regulator of Age-Related Neurodegeneration. Frontiers in Aging Neuroscience. 13. 638208–638208. 21 indexed citations
5.
Barrera, María‐José, Sergio Aguilera, Isabel Castro, et al.. (2020). Tofacitinib counteracts IL-6 overexpression induced by deficient autophagy: implications in Sjögren’s syndrome. Lara D. Veeken. 60(4). 1951–1962. 36 indexed citations
6.
Matus, Soledad, et al.. (2019). Nutrient Sensing and Redox Balance: GCN2 as a New Integrator in Aging. Oxidative Medicine and Cellular Longevity. 2019. 1–9. 16 indexed citations
7.
Elgueta, Daniela, et al.. (2019). Dopamine receptor D3 signalling in astrocytes promotes neuroinflammation. Journal of Neuroinflammation. 16(1). 258–258. 64 indexed citations
8.
Torres, Mauricio, Danilo B. Medinas, José Manuel Matamala, et al.. (2015). The Protein-disulfide Isomerase ERp57 Regulates the Steady-state Levels of the Prion Protein. Journal of Biological Chemistry. 290(39). 23631–23645. 44 indexed citations
9.
Nassif, Melissa, Vicente Valenzuela, Diego Rojas‐Rivera, et al.. (2014). Pathogenic role of BECN1/Beclin 1 in the development of amyotrophic lateral sclerosis. Autophagy. 10(7). 1256–1271. 86 indexed citations
10.
Matus, Soledad, Vicente Valenzuela, & Claudio Hetz. (2014). A new method to measure autophagy flux in the nervous system. Autophagy. 10(4). 710–714. 23 indexed citations
11.
Matus, Soledad, Daryl A. Bosco, & Claudio Hetz. (2014). Autophagy meets fused in sarcoma-positive stress granules. Neurobiology of Aging. 35(12). 2832–2835. 13 indexed citations
12.
Matus, Soledad, Danilo B. Medinas, & Claudio Hetz. (2014). Common Ground: Stem Cell Approaches Find Shared Pathways Underlying ALS. Cell stem cell. 14(6). 697–699. 17 indexed citations
13.
Matus, Soledad, et al.. (2013). Functional Contribution of the Transcription Factor ATF4 to the Pathogenesis of Amyotrophic Lateral Sclerosis. PLoS ONE. 8(7). e66672–e66672. 77 indexed citations
14.
Matus, Soledad, Karen Castillo, & Claudio Hetz. (2012). Hormesis. Autophagy. 8(6). 997–1001. 61 indexed citations
15.
Gupta, Sanjeev, Danielle E. Read, Ayswaria Deepti, et al.. (2012). Perk-dependent repression of miR-106b-25 cluster is required for ER stress-induced apoptosis. Cell Death and Disease. 3(6). e333–e333. 82 indexed citations
16.
Matus, Soledad, Laurie H. Glimcher, & Claudio Hetz. (2011). Protein folding stress in neurodegenerative diseases: a glimpse into the ER. Current Opinion in Cell Biology. 23(2). 239–252. 189 indexed citations
17.
Nassif, Melissa, Soledad Matus, Karen Castillo, & Claudio Hetz. (2010). Amyotrophic Lateral Sclerosis Pathogenesis: A Journey Through the Secretory Pathway. Antioxidants and Redox Signaling. 13(12). 1955–1989. 53 indexed citations
18.
Hetz, Claudio, Peter Thielen, Soledad Matus, et al.. (2009). XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagy. Genes & Development. 23(19). 2294–2306. 436 indexed citations
19.
Matus, Soledad, et al.. (2008). The Stress Rheostat: An Interplay Between the Unfolded Protein Response (UPR) and Autophagy in Neurodegeneration. Current Molecular Medicine. 8(3). 157–172. 107 indexed citations
20.
Matus, Soledad, Patricia V. Burgos, Marcela Bravo‐Zehnder, et al.. (2007). Antiribosomal-P autoantibodies from psychiatric lupus target a novel neuronal surface protein causing calcium influx and apoptosis. The Journal of Experimental Medicine. 204(13). 3221–3234. 137 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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