Martín Gotteland

8.3k total citations · 2 hit papers
112 papers, 6.1k citations indexed

About

Martín Gotteland is a scholar working on Nutrition and Dietetics, Molecular Biology and Physiology. According to data from OpenAlex, Martín Gotteland has authored 112 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Nutrition and Dietetics, 36 papers in Molecular Biology and 28 papers in Physiology. Recurrent topics in Martín Gotteland's work include Diet and metabolism studies (23 papers), Gut microbiota and health (23 papers) and Probiotics and Fermented Foods (16 papers). Martín Gotteland is often cited by papers focused on Diet and metabolism studies (23 papers), Gut microbiota and health (23 papers) and Probiotics and Fermented Foods (16 papers). Martín Gotteland collaborates with scholars based in Chile, France and Australia. Martín Gotteland's co-authors include Fabien Magne, Paola Navarrete, Catalina Carrasco‐Pozo, Alejandra Zazueta, Susana Pesoa, Léa Gauthier, Balamurugan Ramadass, Sylvia Cruchet, Oscar Brunser and Hernán Speisky and has published in prestigious journals such as PLoS ONE, Hepatology and Journal of Agricultural and Food Chemistry.

In The Last Decade

Martín Gotteland

108 papers receiving 5.9k citations

Hit Papers

The Firmicutes/Bacteroidetes Ratio: A Relevant Marker of ... 2020 2026 2022 2024 2020 2021 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martín Gotteland Chile 39 3.2k 1.4k 1.3k 1.1k 723 112 6.1k
Michael A. Conlon Australia 41 3.9k 1.2× 1.4k 1.0× 1.3k 1.0× 1.2k 1.0× 417 0.6× 84 6.5k
Muriel Thomas France 39 3.6k 1.1× 1.2k 0.9× 995 0.8× 1.2k 1.0× 441 0.6× 138 6.0k
Francesca Fava Italy 27 3.8k 1.2× 2.3k 1.6× 1.0k 0.8× 879 0.8× 483 0.7× 50 6.1k
Jianxin Zhao China 39 4.0k 1.3× 1.2k 0.9× 1.1k 0.9× 1.7k 1.5× 408 0.6× 222 6.3k
Göran Molin Sweden 41 3.4k 1.1× 1.1k 0.8× 1.0k 0.8× 2.1k 1.9× 424 0.6× 114 5.9k
Ara Koh South Korea 15 4.6k 1.5× 2.1k 1.5× 846 0.7× 875 0.8× 421 0.6× 43 6.4k
Nuria Salazar Spain 38 4.4k 1.4× 2.0k 1.4× 1.9k 1.5× 1.8k 1.6× 323 0.4× 85 6.6k
Andreas Schwiertz Germany 29 4.5k 1.4× 2.5k 1.8× 907 0.7× 919 0.8× 352 0.5× 61 6.8k
Jin‐zhong Xiao Japan 48 4.6k 1.5× 1.9k 1.4× 1.6k 1.2× 2.2k 1.9× 388 0.5× 150 7.1k
Volker Mai United States 42 2.8k 0.9× 781 0.6× 1.8k 1.4× 683 0.6× 547 0.8× 104 6.4k

Countries citing papers authored by Martín Gotteland

Since Specialization
Citations

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

Fields of papers citing papers by Martín Gotteland

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martín Gotteland

This figure shows the co-authorship network connecting the top 25 collaborators of Martín Gotteland. A scholar is included among the top collaborators of Martín Gotteland 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 Martín Gotteland. Martín Gotteland 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.
Gotteland, Martín, et al.. (2025). Gut microbiota in patients with metabolic, dysfunction-associated steatotic liver disease. Current Opinion in Clinical Nutrition & Metabolic Care. 28(4). 307–315. 2 indexed citations
2.
Zazueta, Alejandra, et al.. (2024). Alteration of Gut Microbiota Composition in the Progression of Liver Damage in Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD). International Journal of Molecular Sciences. 25(8). 4387–4387. 26 indexed citations
5.
Gotteland, Martín, Alejandra Zazueta, Juana Codoceo, et al.. (2023). Modulation of Postprandial Plasma Concentrations of Digestive Hormones and Gut Microbiota by Foods Containing Oat ß-Glucans in Healthy Volunteers. Foods. 12(4). 700–700. 7 indexed citations
6.
Gasaly, Naschla, Guillermo Orellana, Marco A. Vega, et al.. (2022). Metabolic Modeling and Bidirectional Culturing of Two Gut Microbes Reveal Cross-Feeding Interactions and Protective Effects on Intestinal Cells. mSystems. 7(5). e0064622–e0064622. 24 indexed citations
8.
Gasaly, Naschla, et al.. (2021). Polyphenols and their anti-obesity role mediated by the gut microbiota: a comprehensive review. Reviews in Endocrine and Metabolic Disorders. 22(2). 367–388. 44 indexed citations
9.
Magne, Fabien, Martín Gotteland, Léa Gauthier, et al.. (2020). The Firmicutes/Bacteroidetes Ratio: A Relevant Marker of Gut Dysbiosis in Obese Patients?. Nutrients. 12(5). 1474–1474. 1564 indexed citations breakdown →
10.
Carrasco‐Pozo, Catalina, Marı́a José Cires, & Martín Gotteland. (2019). Quercetin and Epigallocatechin Gallate in the Prevention and Treatment of Obesity: From Molecular to Clinical Studies. Journal of Medicinal Food. 22(8). 753–770. 61 indexed citations
11.
Thomson, Pamela, et al.. (2018). Anti-inflammatory effect of microbial consortia during the utilization of dietary polysaccharides. Food Research International. 109. 14–23. 44 indexed citations
12.
Gotteland, Martín, Marı́a José Cires, Natalia Vega, et al.. (2014). Probiotic Screening and Safety Evaluation of Lactobacillus Strains from Plants, Artisanal Goat Cheese, Human Stools, and Breast Milk. Journal of Medicinal Food. 17(4). 487–495. 27 indexed citations
13.
Carrasco‐Pozo, Catalina, et al.. (2012). Stimulation of cytosolic and mitochondrial calcium mobilization by indomethacin in Caco-2 cells: Modulation by the polyphenols quercetin, resveratrol and rutin. Biochimica et Biophysica Acta (BBA) - General Subjects. 1820(12). 2052–2061. 40 indexed citations
14.
Carrasco‐Pozo, Catalina, Hernán Speisky, Oscar Brunser, Edgar Pastene, & Martín Gotteland. (2011). Apple Peel Polyphenols Protect against Gastrointestinal Mucosa Alterations Induced by Indomethacin in Rats. Journal of Agricultural and Food Chemistry. 59(12). 6459–6466. 44 indexed citations
15.
Brignardello, Jerusa, Pamela Morales, Erik Díaz-Bautista, et al.. (2010). Pilot study: alterations of intestinal microbiota in obese humans are not associated with colonic inflammation or disturbances of barrier function. Alimentary Pharmacology & Therapeutics. 32(11-12). 1307–1314. 78 indexed citations
16.
Vega, Natalia, et al.. (2010). Effects of Lactobacillus rhamnosus HN001 on acute respiratory infections and intestinal secretory IgA in children.. Journal of Pediatric Infectious Diseases. 5(4). 353–362. 23 indexed citations
17.
Haschke‐Becher, Elisabeth, Oscar Brunser, Sylvia Cruchet, et al.. (2008). Urinary <i>D</i>-Lactate Excretion in Infants Receiving <i>Lactobacillus johnsonii</i> with Formula. Annals of Nutrition and Metabolism. 53(3-4). 240–244. 19 indexed citations
18.
19.
Gotteland, Martín, et al.. (2001). Effect ofLactobacillusingestion on the gastrointestinal mucosal barrier alterations induced by indometacin in humans. Alimentary Pharmacology & Therapeutics. 15(1). 11–17. 135 indexed citations
20.
Hirsch, Sandra, et al.. (1997). [Intestinal permeability in alcoholic patients without liver damage].. PubMed. 125(6). 653–8. 5 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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