Mats Gåfvels

3.0k total citations
69 papers, 2.5k citations indexed

About

Mats Gåfvels is a scholar working on Surgery, Oncology and Molecular Biology. According to data from OpenAlex, Mats Gåfvels has authored 69 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Surgery, 21 papers in Oncology and 19 papers in Molecular Biology. Recurrent topics in Mats Gåfvels's work include Drug Transport and Resistance Mechanisms (19 papers), Cholesterol and Lipid Metabolism (18 papers) and Peroxisome Proliferator-Activated Receptors (13 papers). Mats Gåfvels is often cited by papers focused on Drug Transport and Resistance Mechanisms (19 papers), Cholesterol and Lipid Metabolism (18 papers) and Peroxisome Proliferator-Activated Receptors (13 papers). Mats Gåfvels collaborates with scholars based in Sweden, United States and Germany. Mats Gåfvels's co-authors include Gösta Eggertsen, Ingemar Björkhem, Jerome F. Strauss, Dudley K. Strickland, Jan Andersson, Gunnar Selstam, Maria Olin, David W. Russell, Gertrud U. Schuster and Erik Lund and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Mats Gåfvels

67 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mats Gåfvels Sweden 26 873 835 720 384 349 69 2.5k
Ying‐Hue Lee United States 16 1.3k 1.5× 766 0.9× 457 0.6× 287 0.7× 402 1.2× 24 2.6k
Oliver Tschopp Switzerland 20 1.5k 1.7× 500 0.6× 361 0.5× 225 0.6× 478 1.4× 47 2.7k
Katherine T. Landschulz United States 13 1.3k 1.5× 1.6k 1.9× 477 0.7× 536 1.4× 393 1.1× 17 3.3k
Anne M. Latour United States 15 1.5k 1.8× 493 0.6× 916 1.3× 153 0.4× 268 0.8× 20 3.6k
David H. Volle France 26 643 0.7× 700 0.8× 542 0.8× 192 0.5× 144 0.4× 64 1.8k
Ning Xu Sweden 28 1.0k 1.2× 809 1.0× 700 1.0× 358 0.9× 298 0.9× 97 2.6k
Laurent O. Martinez France 28 1.6k 1.8× 1.1k 1.3× 628 0.9× 398 1.0× 295 0.8× 81 3.2k
Elisabeth Fayard France 13 1.3k 1.4× 431 0.5× 545 0.8× 217 0.6× 169 0.5× 15 2.1k
Sungsoon Fang South Korea 25 1.3k 1.5× 587 0.7× 712 1.0× 270 0.7× 587 1.7× 69 2.9k
Hueng-Sik Choi South Korea 31 1.5k 1.7× 500 0.6× 406 0.6× 370 1.0× 397 1.1× 56 2.8k

Countries citing papers authored by Mats Gåfvels

Since Specialization
Citations

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

Fields of papers citing papers by Mats Gåfvels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mats Gåfvels

This figure shows the co-authorship network connecting the top 25 collaborators of Mats Gåfvels. A scholar is included among the top collaborators of Mats Gåfvels 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 Mats Gåfvels. Mats Gåfvels 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.
Gåfvels, Mats, et al.. (2025). Glycated Albumin Percentage is Correlated With HbA1c: Theoretic Marker in Patients With Altered Erythrocyte Turnover. Journal of Diabetes Science and Technology. 580993520–580993520.
2.
Axling, Ulrika, Michele Cavalera, Eva Degerman, et al.. (2020). Increased whole body energy expenditure and protection against diet-induced obesity in Cyp8b1-deficient mice is accompanied by altered adipose tissue features. Adipocyte. 9(1). 587–599. 8 indexed citations
3.
Gåfvels, Mats, et al.. (2015). A fast semi-quantitative LC–MS method for measurement of intact apolipoprotein A-I reveals novel proteoforms in serum. Clinica Chimica Acta. 442. 87–95. 18 indexed citations
4.
Kannisto, Kristina, Stefan Rehnmark, Paul Webb, et al.. (2014). The thyroid receptor β modulator GC-1 reduces atherosclerosis in ApoE deficient mice. Atherosclerosis. 237(2). 544–554. 17 indexed citations
5.
Hedman‐Lagerlöf, Erik, Mats Gåfvels, Gösta Eggertsen, et al.. (2013). Further characterization of human glucocorticoid receptor mutants, R477H and G679S, associated with primary generalized glucocorticoid resistance. Scandinavian Journal of Clinical and Laboratory Investigation. 73(3). 203–207. 2 indexed citations
6.
Anderlid, Britt‐Marie, et al.. (2012). [Lactose intolerance in children is an overdiagnosed condition. Risk of missing intestinal diseases such as IBD and celiac disease].. PubMed. 109(5). 218–21. 4 indexed citations
7.
Hu, Xiaoli, Knut R. Steffensen, Zhengyi Jiang, et al.. (2012). LXRβ activation increases intestinal cholesterol absorption, leading to an atherogenic lipoprotein profile. Journal of Internal Medicine. 272(5). 452–464. 23 indexed citations
8.
Thulin, Petra, Elisabeth Strandhagen, Ulf Lidberg, et al.. (2009). Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease. Journal of Lipid Research. 51(1). 103–111. 19 indexed citations
9.
Murray, Ann, et al.. (2007). Regulation by SREBP-2 defines a potential link between isoprenoid and adenosylcobalamin metabolism. Biochemical and Biophysical Research Communications. 355(2). 359–364. 19 indexed citations
10.
Gåfvels, Mats, et al.. (2006). Expression of iron regulatory genes in a rat model of hepatocellular carcinoma. Liver International. 26(8). 976–985. 39 indexed citations
11.
Gåfvels, Mats, et al.. (2005). Polymorphism in the coding part of the sterol 12α‐hydroxylase gene does not explain the marked differences in the ratio of cholic acid and chenodeoxycholic acid in human bile. Scandinavian Journal of Clinical and Laboratory Investigation. 65(7). 595–600. 6 indexed citations
12.
Hultcrantz, Rolf, Öjar Melefors, Per Stål, et al.. (2003). Structure and liver cell expression pattern of the HFE gene in the rat. Journal of Hepatology. 39(3). 308–314. 20 indexed citations
13.
Li-Hawkins, Jia, Mats Gåfvels, Maria Olin, et al.. (2002). Cholic acid mediates negative feedback regulation of bile acid synthesis in mice. Journal of Clinical Investigation. 110(8). 1191–1200. 194 indexed citations
14.
Andersson, Jan, Yizeng Yang, Ingemar Björkhem, et al.. (1999). Thyroid hormone suppresses hepatic sterol 12α-hydroxylase (CYP8B1) activity and messenger ribonucleic acid in rat liver: Failure to define known thyroid hormone response elements in the gene. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1438(2). 167–174. 37 indexed citations
15.
Magrané, Jordi, Manuel Reina, Roser Pagan, et al.. (1998). Bovine aortic endothelial cells express a variant of the very low density lipoprotein receptor that lacks the O-linked sugar domain. Journal of Lipid Research. 39(11). 2172–2181. 26 indexed citations
16.
Argraves, Kelley M., Frances D. Battey, Colin D. MacCalman, et al.. (1995). The Very Low Density Lipoprotein Receptor Mediates the Cellular Catabolism of Lipoprotein Lipase and Urokinase-Plasminogen Activator Inhibitor Type I Complexes. Journal of Biological Chemistry. 270(44). 26550–26557. 136 indexed citations
18.
Strauss, Jerome F., et al.. (1992). The cAMP signalling system and human trophoblast function. Placenta. 13(5). 389–403. 96 indexed citations
19.
Damber, Jan‐Erik, Stefan Cajander, Mats Gåfvels, & Gunnar Selstam. (1987). Blood Flow Changes and Vascular Appearance in Preovulatory Follicles and Corpora Lutea in Immature, Pregnant Mare’s Serum Gonadotropin-Treated Rats1. Biology of Reproduction. 37(3). 651–658. 14 indexed citations
20.
Selstam, Gunnar, Mats Gåfvels, Ensio Norjavaara, & J.‐E. Damber. (1985). Acute increase of noradrenaline on vascular resistance in the corpus luteum of the pseudopregnant rat. Reproduction. 75(2). 351–356. 24 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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