Soledad Matus

6.8k total citations
11 papers, 662 citations indexed

About

Soledad Matus is a scholar working on Epidemiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Soledad Matus has authored 11 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Epidemiology, 6 papers in Cell Biology and 4 papers in Molecular Biology. Recurrent topics in Soledad Matus's work include Autophagy in Disease and Therapy (7 papers), Endoplasmic Reticulum Stress and Disease (5 papers) and Amyotrophic Lateral Sclerosis Research (4 papers). Soledad Matus is often cited by papers focused on Autophagy in Disease and Therapy (7 papers), Endoplasmic Reticulum Stress and Disease (5 papers) and Amyotrophic Lateral Sclerosis Research (4 papers). Soledad Matus collaborates with scholars based in Chile, United States and Belgium. Soledad Matus's co-authors include Claudio Hetz, Melissa Nassif, Felipe A. Court, Karen Castillo, Brigitte van Zundert, Fabiola Rojas, René L. Vidal, Vicente Valenzuela, Gabriela Mercado and Laurie H. Glimcher and has published in prestigious journals such as Scientific Reports, Brain Research and Trends in Pharmacological Sciences.

In The Last Decade

Soledad Matus

10 papers receiving 655 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 9 352 282 223 160 130 11 662
Vicente Valenzuela Chile 11 344 1.0× 351 1.2× 203 0.9× 238 1.5× 119 0.9× 13 724
M. Meroni Italy 10 315 0.9× 245 0.9× 382 1.7× 223 1.4× 126 1.0× 14 784
Christopher P Webster United Kingdom 10 163 0.5× 370 1.3× 221 1.0× 90 0.6× 108 0.8× 12 579
Vitaliy V. Bondar United States 9 222 0.6× 111 0.4× 292 1.3× 133 0.8× 134 1.0× 10 590
Mark A. Halloran Australia 6 116 0.3× 464 1.6× 250 1.1× 154 1.0× 125 1.0× 8 673
Geoffrey Parsons United States 8 275 0.8× 120 0.4× 231 1.0× 332 2.1× 122 0.9× 14 642
Tuancheng Feng United States 14 194 0.6× 280 1.0× 244 1.1× 168 1.1× 419 3.2× 18 770
Zongbing Hao China 12 141 0.4× 257 0.9× 228 1.0× 54 0.3× 96 0.7× 18 530
Rachel A.K. Atkinson Australia 10 109 0.3× 408 1.4× 236 1.1× 72 0.5× 166 1.3× 16 638
Alessandra Boncoraglio Italy 12 260 0.7× 274 1.0× 680 3.0× 360 2.3× 112 0.9× 12 971

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

11 of 11 papers shown
2.
Nassif, Melissa, Cristian Cortéz, Sergio Espinoza, et al.. (2019). Network approach identifies Pacer as an autophagy protein involved in ALS pathogenesis. Molecular Neurodegeneration. 14(1). 14–14. 25 indexed citations
3.
Barrera, María‐José, Sergio Aguilera, Patricia Carvajal, et al.. (2019). AB0158 DECREASED AUTOPHAGY IN SALIVARY GLANDS OF PRIMARY SJöGREN'S SYNDROME PATIENTS COULD BE ASSOCIATED WITH AN INCREASED EXPRESSION OF INFLAMMATORY MARKERS. Annals of the Rheumatic Diseases. 78. 1537–1537. 2 indexed citations
4.
Medinas, Danilo B., Francisca Martínez Traub, Pablo Rozas, et al.. (2017). Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43A315T ALS/FTD mouse model. Scientific Reports. 7(1). 14266–14266. 19 indexed citations
5.
Matamala, José Manuel, Raúl Arias‐Carrasco, Carolina Sánchez‐Rodríguez, et al.. (2017). Genome-wide circulating microRNA expression profiling reveals potential biomarkers for amyotrophic lateral sclerosis. Neurobiology of Aging. 64. 123–138. 52 indexed citations
6.
Hetz, Claudio, et al.. (2016). ERp57 in neurodegeneration and regeneration. Neural Regeneration Research. 11(2). 232–232. 14 indexed citations
7.
García-Huerta, Paula, et al.. (2016). ER chaperones in neurodegenerative disease: Folding and beyond. Brain Research. 1648(Pt B). 580–587. 8 indexed citations
8.
Vidal, René L., et al.. (2014). Targeting autophagy in neurodegenerative diseases. Trends in Pharmacological Sciences. 35(11). 583–591. 121 indexed citations
9.
Castillo, Karen, Soledad Matus, Melissa Nassif, et al.. (2013). Measurement of autophagy flux in the nervous system in vivo. Cell Death and Disease. 4(11). e917–e917. 95 indexed citations
10.
Castillo, Karen, Melissa Nassif, Vicente Valenzuela, et al.. (2013). Trehalose delays the progression of amyotrophic lateral sclerosis by enhancing autophagy in motoneurons. Autophagy. 9(9). 1308–1320. 291 indexed citations
11.
Matus, Soledad, Melissa Nassif, Laurie H. Glimcher, & Claudio Hetz. (2009). XBP-1 deficiency in the nervous system reveals a homeostatic switch to activate autophagy. Autophagy. 5(8). 1226–1228. 35 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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