Marion Korach-André

1.6k total citations
29 papers, 1.2k citations indexed

About

Marion Korach-André is a scholar working on Physiology, Surgery and Epidemiology. According to data from OpenAlex, Marion Korach-André has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Physiology, 10 papers in Surgery and 10 papers in Epidemiology. Recurrent topics in Marion Korach-André's work include Adipose Tissue and Metabolism (11 papers), Cholesterol and Lipid Metabolism (8 papers) and Adipokines, Inflammation, and Metabolic Diseases (8 papers). Marion Korach-André is often cited by papers focused on Adipose Tissue and Metabolism (11 papers), Cholesterol and Lipid Metabolism (8 papers) and Adipokines, Inflammation, and Metabolic Diseases (8 papers). Marion Korach-André collaborates with scholars based in Sweden, United States and Portugal. Marion Korach-André's co-authors include Jan-Ακε Gustafsson, Paolo Parini, Amena Archer, Joseph Rafter, Rodrigo P. A. Barros, Janet Håkansson, Jan-Åke Gustafsson, Ying Huang, Sven Pettersson and Velmurugesan Arulampalam and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and American Journal of Clinical Nutrition.

In The Last Decade

Marion Korach-André

29 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marion Korach-André Sweden 20 508 433 318 219 182 29 1.2k
Jan B. van Klinken Netherlands 24 501 1.0× 646 1.5× 274 0.9× 338 1.5× 165 0.9× 50 1.5k
Shailja Patel United States 22 628 1.2× 724 1.7× 325 1.0× 243 1.1× 95 0.5× 30 1.6k
Denise E. Lackey United States 12 678 1.3× 531 1.2× 170 0.5× 379 1.7× 120 0.7× 14 1.4k
Stephanie Pack United States 11 554 1.1× 551 1.3× 184 0.6× 417 1.9× 138 0.8× 12 1.3k
Bogna Grygiel‐Górniak Poland 14 658 1.3× 423 1.0× 136 0.4× 257 1.2× 103 0.6× 65 1.6k
Drew V. Tortoriello United States 18 520 1.0× 534 1.2× 130 0.4× 477 2.2× 154 0.8× 29 1.9k
Alberto O. Chávez United States 18 731 1.4× 539 1.2× 312 1.0× 281 1.3× 97 0.5× 26 1.6k
Arthur L. Castle United States 15 740 1.5× 653 1.5× 252 0.8× 285 1.3× 108 0.6× 17 1.5k
Luca Parrillo Italy 17 695 1.4× 746 1.7× 187 0.6× 556 2.5× 197 1.1× 28 1.8k
Maryam Rakhshandehroo Netherlands 13 973 1.9× 508 1.2× 190 0.6× 570 2.6× 109 0.6× 20 1.9k

Countries citing papers authored by Marion Korach-André

Since Specialization
Citations

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

Fields of papers citing papers by Marion Korach-André

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marion Korach-André. 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 Marion Korach-André. The network helps show where Marion Korach-André may publish in the future.

Co-authorship network of co-authors of Marion Korach-André

This figure shows the co-authorship network connecting the top 25 collaborators of Marion Korach-André. A scholar is included among the top collaborators of Marion Korach-André 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 Marion Korach-André. Marion Korach-André 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.
Sommerauer, Christian, Linnea Hases, Madeleine Birgersson, et al.. (2024). Estrogen receptor activation remodels TEAD1 gene expression to alleviate hepatic steatosis. Molecular Systems Biology. 20(4). 374–402. 5 indexed citations
2.
Helguero, Luísa A., Marcela González‐Granillo, Tânia Melo, et al.. (2022). Molecular programming modulates hepatic lipid metabolism and adult metabolic risk in the offspring of obese mothers in a sex-specific manner. Communications Biology. 5(1). 1057–1057. 9 indexed citations
3.
Helguero, Luísa A., Marcela González‐Granillo, Tânia Melo, et al.. (2022). Maternal high-fat diet programs white and brown adipose tissue lipidome and transcriptome in offspring in a sex- and tissue-dependent manner in mice. International Journal of Obesity. 46(4). 831–842. 21 indexed citations
4.
Helguero, Luísa A., Marcela González‐Granillo, Daniela Couto, et al.. (2021). Obese mother offspring have hepatic lipidic modulation that contributes to sex-dependent metabolic adaptation later in life. Communications Biology. 4(1). 14–14. 13 indexed citations
5.
Hases, Linnea, et al.. (2020). High-fat diet and estrogen impacts the colon and its transcriptome in a sex-dependent manner. Scientific Reports. 10(1). 16160–16160. 29 indexed citations
6.
González‐Granillo, Marcela, Luísa A. Helguero, Eliana Alves, et al.. (2019). Sex-specific lipid molecular signatures in obesity-associated metabolic dysfunctions revealed by lipidomic characterization in ob/ob mouse. Biology of Sex Differences. 10(1). 11–11. 27 indexed citations
7.
González‐Granillo, Marcela, et al.. (2019). Selective estrogen receptor (ER)β activation provokes a redistribution of fat mass and modifies hepatic triglyceride composition in obese male mice. Molecular and Cellular Endocrinology. 502. 110672–110672. 20 indexed citations
8.
González‐Granillo, Marcela, Xidan Li, Mark Fitch, et al.. (2018). ERβ activation in obesity improves whole body metabolism via adipose tissue function and enhanced mitochondria biogenesis. Molecular and Cellular Endocrinology. 479. 147–158. 30 indexed citations
9.
Bryzgalova, Galyna, Ismael Valladolid‐Acebes, Marion Korach-André, et al.. (2016). 17β-Estradiol suppresses visceral adipogenesis and activates brown adipose tissue-specific gene expression. Hormone Molecular Biology and Clinical Investigation. 29(1). 13–26. 19 indexed citations
10.
Korach-André, Marion & Jan-Ακε Gustafsson. (2015). Liver X receptors as regulators of metabolism. BioMolecular Concepts. 6(3). 177–190. 32 indexed citations
11.
Archer, Amena, Émilie Stolarczyk, M. Luísa Dória, et al.. (2013). LXR activation by GW3965 alters fat tissue distribution and adipose tissue inflammation in ob/ob female mice. Journal of Lipid Research. 54(5). 1300–1311. 38 indexed citations
12.
González‐Granillo, Marcela, Knut R. Steffensen, Omar Granados, et al.. (2012). Soy protein isoflavones differentially regulate liver X receptor isoforms to modulate lipid metabolism and cholesterol transport in the liver and intestine in mice. Diabetologia. 55(9). 2469–2478. 41 indexed citations
13.
Korach-André, Marion, Amena Archer, Chiara Gabbi, et al.. (2011). Liver X receptors regulate de novo lipogenesis in a tissue-specific manner in C57BL/6 female mice. American Journal of Physiology-Endocrinology and Metabolism. 301(1). E210–E222. 40 indexed citations
14.
Gabbi, Chiara, Hyun‐Jin Kim, Rodrigo P. A. Barros, et al.. (2010). Estrogen-dependent gallbladder carcinogenesis in LXRβ −/− female mice. Proceedings of the National Academy of Sciences. 107(33). 14763–14768. 49 indexed citations
15.
Aronsson, Linda, Ying Huang, Paolo Parini, et al.. (2010). Decreased Fat Storage by Lactobacillus Paracasei Is Associated with Increased Levels of Angiopoietin-Like 4 Protein (ANGPTL4). PLoS ONE. 5(9). e13087–e13087. 235 indexed citations
16.
Korach-André, Marion, John Gounarides, Richard Deacon, et al.. (2005). Age and muscle-type modulated role of intramyocellular lipids in the progression of insulin resistance in nondiabetic Zucker rats. Metabolism. 54(4). 522–528. 18 indexed citations
17.
Korach-André, Marion, Hubert Roth, D. Barn�oud, et al.. (2004). Glucose appearance in the peripheral circulation and liver glucose output in men after a large 13C starch meal. American Journal of Clinical Nutrition. 80(4). 881–886. 40 indexed citations
18.
Korach-André, Marion, Pascale Leclercq, François Péronnet, & Xavier Leverve. (2002). Metabolic response to a 13C-glucose load in human immunodeficiency virus patients before and after antiprotease therapy. Metabolism. 51(3). 307–313. 3 indexed citations
19.
Korach-André, Marion, Yan Burelle, François Péronnet, et al.. (2002). Differential metabolic fate of the carbon skeleton and amino-N of [13C]alanine and [15N]alanine ingested during prolonged exercise. Journal of Applied Physiology. 93(2). 499–504. 7 indexed citations
20.
Korach-André, Marion, Tarek Sharshar, Irène Jarrin, et al.. (2001). Cardiac variability in critically ill adults: Influence of sepsis. Critical Care Medicine. 29(7). 1380–1385. 122 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026