Marı́a Isabel Sánchez-Reus

757 total citations
16 papers, 655 citations indexed

About

Marı́a Isabel Sánchez-Reus is a scholar working on Molecular Biology, Plant Science and Nutrition and Dietetics. According to data from OpenAlex, Marı́a Isabel Sánchez-Reus has authored 16 papers receiving a total of 655 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Plant Science and 4 papers in Nutrition and Dietetics. Recurrent topics in Marı́a Isabel Sánchez-Reus's work include Alzheimer's disease research and treatments (3 papers), Seaweed-derived Bioactive Compounds (3 papers) and Drug-Induced Hepatotoxicity and Protection (3 papers). Marı́a Isabel Sánchez-Reus is often cited by papers focused on Alzheimer's disease research and treatments (3 papers), Seaweed-derived Bioactive Compounds (3 papers) and Drug-Induced Hepatotoxicity and Protection (3 papers). Marı́a Isabel Sánchez-Reus collaborates with scholars based in Spain and Mexico. Marı́a Isabel Sánchez-Reus's co-authors include Juana Benedı́, Marı́a Cascales, Irene Iglesias Peinado, Francisco J. Sánchez‐Muniz, David Aguinaga, Sagrario Martín‐Aragón, Beatriz de las Heras, María José González‐Muñoz, Sara Bastida and Karla Slowing and has published in prestigious journals such as Brain Research, Food Chemistry and International Journal of Molecular Sciences.

In The Last Decade

Marı́a Isabel Sánchez-Reus

16 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marı́a Isabel Sánchez-Reus Spain 13 229 161 88 87 78 16 655
S Sethupathy India 17 191 0.8× 270 1.7× 101 1.1× 104 1.2× 100 1.3× 35 839
Heros Horst Brazil 13 188 0.8× 172 1.1× 127 1.4× 106 1.2× 59 0.8× 20 609
Thangaiyan Radhiga India 16 261 1.1× 93 0.6× 132 1.5× 134 1.5× 63 0.8× 24 705
Ken-ichi Miyamoto Japan 12 301 1.3× 102 0.6× 115 1.3× 60 0.7× 69 0.9× 22 903
Chukwuemeka R. Nwokocha Jamaica 19 226 1.0× 193 1.2× 75 0.9× 96 1.1× 53 0.7× 76 980
Feng-Lin Hsu Taiwan 16 323 1.4× 101 0.6× 73 0.8× 72 0.8× 59 0.8× 21 662
Lingyuan Xu China 12 225 1.0× 77 0.5× 64 0.7× 79 0.9× 39 0.5× 16 689
Lalit Kishore India 13 153 0.7× 99 0.6× 125 1.4× 100 1.1× 108 1.4× 34 873
Vijaya Juturu Türkiye 13 217 0.9× 113 0.7× 70 0.8× 65 0.7× 36 0.5× 34 638

Countries citing papers authored by Marı́a Isabel Sánchez-Reus

Since Specialization
Citations

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

Fields of papers citing papers by Marı́a Isabel Sánchez-Reus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marı́a Isabel Sánchez-Reus. 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 Marı́a Isabel Sánchez-Reus. The network helps show where Marı́a Isabel Sánchez-Reus may publish in the future.

Co-authorship network of co-authors of Marı́a Isabel Sánchez-Reus

This figure shows the co-authorship network connecting the top 25 collaborators of Marı́a Isabel Sánchez-Reus. A scholar is included among the top collaborators of Marı́a Isabel Sánchez-Reus 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 Marı́a Isabel Sánchez-Reus. Marı́a Isabel Sánchez-Reus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
González-Torres, Laura, Sara Bastida, Juana Benedı́, et al.. (2014). Liver oxidation and inflammation in Fa/Fa rats fed glucomannan/spirulina-surimi. Food Chemistry. 159. 215–221. 18 indexed citations
2.
Garcimartín, Alba, José Joaquín Merino, Marı́a Isabel Sánchez-Reus, et al.. (2014). Organic silicon protects human neuroblastoma SH-SY5Y cells against hydrogen peroxide effects. BMC Complementary and Alternative Medicine. 14(1). 384–384. 31 indexed citations
3.
Sánchez-Reus, Marı́a Isabel, Irene Iglesias Peinado, Miguel A. Pozo, et al.. (2013). Neuroprotective Properties of Standardized Extracts of Hypericum perforatum on Rotenone Model of Parkinson’s Disease. CNS & Neurological Disorders - Drug Targets. 12(5). 665–679. 41 indexed citations
4.
García‐Fernández, Rosa A., Aránzazu Bocanegra, María Teresa Méndez Picazo, et al.. (2013). Effects of seaweed-restructured pork diets enriched or not with cholesterol on rat cholesterolaemia and liver damage. Food and Chemical Toxicology. 56. 223–230. 13 indexed citations
5.
Bautista, Mirandeli, David Aguinaga, Marı́a Cascales, et al.. (2011). Role of Kupffer Cells in Thioacetamide-Induced Cell Cycle Dysfunction. Molecules. 16(10). 8319–8331. 6 indexed citations
6.
González-Torres, Laura, Sara Bastida, Juana Benedı́, et al.. (2011). Effects of Nori- and Wakame-enriched meats with or without supplementary cholesterol on arylesterase activity, lipaemia and lipoproteinaemia in growing Wistar rats. British Journal Of Nutrition. 106(10). 1476–1486. 33 indexed citations
7.
8.
Bautista, Mirandeli, David Aguinaga, Marı́a Cascales, José A. Morales‐González, & Marı́a Isabel Sánchez-Reus. (2010). Effect of Gadolinium Chloride on Liver Regeneration Following Thioacetamide-Induced Necrosis in Rats. International Journal of Molecular Sciences. 11(11). 4426–4440. 12 indexed citations
9.
Oliver, R., Mirandeli Bautista, María José González‐Muñoz, et al.. (2008). Moderate ingestion of beer reduces inflammatory and oxidative brain events induced by aluminium in mice. Proceedings of The Nutrition Society. 67(OCE1). 1 indexed citations
10.
González‐Muñoz, María José, et al.. (2007). Beer consumption reduces cerebral oxidation caused by aluminum toxicity by normalizing gene expression of tumor necrotic factor alpha and several antioxidant enzymes. Food and Chemical Toxicology. 46(3). 1111–1118. 59 indexed citations
11.
Sánchez-Reus, Marı́a Isabel, et al.. (2006). Standardized Hypericum perforatum reduces oxidative stress and increases gene expression of antioxidant enzymes on rotenone-exposed rats. Neuropharmacology. 52(2). 606–616. 72 indexed citations
12.
Sánchez-Reus, Marı́a Isabel, et al.. (2005). Fraxetin prevents rotenone-induced apoptosis by induction of endogenous glutathione in human neuroblastoma cells. Neuroscience Research. 53(1). 48–56. 47 indexed citations
13.
Sánchez-Reus, Marı́a Isabel, et al.. (2005). Effect of fraxetin on antioxidant defense and stress proteins in human neuroblastoma cell model of rotenone neurotoxicity. Comparative study with myricetin and N-acetylcysteine. Toxicology and Applied Pharmacology. 209(3). 214–225. 46 indexed citations
14.
Sánchez-Reus, Marı́a Isabel, et al.. (2004). Neuroprotective effect of fraxetin and myricetin against rotenone-induced apoptosis in neuroblastoma cells. Brain Research. 1009(1-2). 9–16. 104 indexed citations
15.
Sánchez-Reus, Marı́a Isabel, et al.. (2003). Effect of fraxetin and myricetin on rotenone-induced cytotoxicity in SH-SY5Y cells: comparison with N-acetylcysteine. European Journal of Pharmacology. 472(1-2). 81–87. 64 indexed citations
16.
Martín‐Aragón, Sagrario, Beatriz de las Heras, Marı́a Isabel Sánchez-Reus, & Juana Benedı́. (2001). Pharmacological modification of endogenous antioxidant enzymes by ursolic acid on tetrachloride-induced liver damagein rats and primary cultures of rat hepatocytes. Experimental and Toxicologic Pathology. 53(2-3). 199–206. 80 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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