Miranda Nabben

2.0k total citations
55 papers, 1.5k citations indexed

About

Miranda Nabben is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Physiology. According to data from OpenAlex, Miranda Nabben has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 22 papers in Cardiology and Cardiovascular Medicine and 22 papers in Physiology. Recurrent topics in Miranda Nabben's work include Adipose Tissue and Metabolism (20 papers), Cardiovascular Function and Risk Factors (19 papers) and Mitochondrial Function and Pathology (12 papers). Miranda Nabben is often cited by papers focused on Adipose Tissue and Metabolism (20 papers), Cardiovascular Function and Risk Factors (19 papers) and Mitochondrial Function and Pathology (12 papers). Miranda Nabben collaborates with scholars based in Netherlands, United States and Canada. Miranda Nabben's co-authors include Jan F. C. Glatz, Joost J.F.P. Luiken, Joris Hoeks, Dietbert Neumann, Patrick Schrauwen, Jeanine J. Prompers, Klaas Nicolay, Matthijs K. C. Hesselink, Desiree Abdurrachim and Dipanjan Chanda and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Miranda Nabben

53 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miranda Nabben Netherlands 25 787 540 463 191 146 55 1.5k
Danielle Murashige United States 7 891 1.1× 510 0.9× 263 0.6× 119 0.6× 154 1.1× 7 1.5k
Robert W. Schwenk Netherlands 24 918 1.2× 465 0.9× 317 0.7× 349 1.8× 145 1.0× 32 1.6k
Haipeng Sun China 24 1.5k 1.9× 684 1.3× 346 0.7× 169 0.9× 247 1.7× 67 2.2k
David J. Chess United States 19 547 0.7× 484 0.9× 486 1.0× 81 0.4× 79 0.5× 25 1.3k
Pei‐Ying Pai Taiwan 24 772 1.0× 238 0.4× 373 0.8× 167 0.9× 80 0.5× 68 1.6k
Venkatesh Rajapurohitam Canada 25 1.1k 1.4× 657 1.2× 575 1.2× 158 0.8× 111 0.8× 41 2.1k
Ángel Zarain‐Herzberg Mexico 26 1.4k 1.7× 237 0.4× 810 1.7× 243 1.3× 205 1.4× 57 2.1k
Carrie-Lynn M. Soltys Canada 15 864 1.1× 399 0.7× 275 0.6× 224 1.2× 54 0.4× 21 1.3k
Brian J. DeBosch United States 25 919 1.2× 496 0.9× 425 0.9× 299 1.6× 221 1.5× 52 2.1k
Gabriela Orasanu United States 14 822 1.0× 371 0.7× 220 0.5× 212 1.1× 61 0.4× 20 1.6k

Countries citing papers authored by Miranda Nabben

Since Specialization
Citations

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

Fields of papers citing papers by Miranda Nabben

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miranda Nabben

This figure shows the co-authorship network connecting the top 25 collaborators of Miranda Nabben. A scholar is included among the top collaborators of Miranda Nabben 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 Miranda Nabben. Miranda Nabben 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.
Michel, Lauriane Y. M., Hrag Esfahani, Jérôme Ambroise, et al.. (2025). An NRF2/β3-Adrenoreceptor Axis Drives a Sustained Antioxidant and Metabolic Rewiring Through the Pentose-Phosphate Pathway to Alleviate Cardiac Stress. Circulation. 151(18). 1312–1328. 3 indexed citations
2.
Neumann, Dietbert, et al.. (2024). Specific Compounds Derived from Traditional Chinese Medicine Ameliorate Lipid-Induced Contractile Dysfunction in Cardiomyocytes. International Journal of Molecular Sciences. 25(15). 8131–8131.
3.
Wang, Shujin, Mengqian Hou, Dietbert Neumann, et al.. (2024). Glycolysis-Mediated Activation of v-ATPase by Nicotinamide Mononucleotide Ameliorates Lipid-Induced Cardiomyopathy by Repressing the CD36-TLR4 Axis. Circulation Research. 134(5). 505–525. 16 indexed citations
4.
Lunde, Ida G., Debby M.E.I. Hellebrekers, Godelieve R.F. Claes, et al.. (2023). Prevalence and Clinical Consequences of Multiple Pathogenic Variants in Dilated Cardiomyopathy. Circulation Genomic and Precision Medicine. 16(2). e003788–e003788. 10 indexed citations
5.
Wang, Shujin, Dietbert Neumann, B. Daan Westenbrink, et al.. (2022). Ketone Body Exposure of Cardiomyocytes Impairs Insulin Sensitivity and Contractile Function through Vacuolar-Type H+-ATPase Disassembly—Rescue by Specific Amino Acid Supplementation. International Journal of Molecular Sciences. 23(21). 12909–12909. 4 indexed citations
6.
Wang, Shujin, et al.. (2022). Endosomal v-ATPase as a Sensor Determining Myocardial Substrate Preference. Metabolites. 12(7). 579–579. 7 indexed citations
7.
Wang, Shujin, Dietbert Neumann, Aomin Sun, et al.. (2021). Specific amino acid supplementation rescues the heart from lipid overload-induced insulin resistance and contractile dysfunction by targeting the endosomal mTOR–v-ATPase axis. Molecular Metabolism. 53. 101293–101293. 28 indexed citations
8.
Wang, Shujin, Dietbert Neumann, Yilin Liu, et al.. (2020). Augmenting Vacuolar H+-ATPase Function Prevents Cardiomyocytes from Lipid-Overload Induced Dysfunction. International Journal of Molecular Sciences. 21(4). 1520–1520. 19 indexed citations
9.
Glatz, Jan F. C., et al.. (2020). Putative Role of Protein Palmitoylation in Cardiac Lipid-Induced Insulin Resistance. International Journal of Molecular Sciences. 21(24). 9438–9438. 16 indexed citations
10.
Luiken, Joost J.F.P., Miranda Nabben, Dietbert Neumann, & Jan F. C. Glatz. (2020). Understanding the distinct subcellular trafficking of CD36 and GLUT4 during the development of myocardial insulin resistance. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(7). 165775–165775. 30 indexed citations
11.
Zhong, Xi, Zhongwei Zhang, Shujin Wang, et al.. (2019). Microbial-Driven Butyrate Regulates Jejunal Homeostasis in Piglets During the Weaning Stage. Frontiers in Microbiology. 9. 3335–3335. 45 indexed citations
12.
Sun, Aomin, et al.. (2018). Acute and Chronic Effects of Protein Kinase-D Signaling on Cardiac Energy Metabolism. Frontiers in Cardiovascular Medicine. 5. 65–65. 16 indexed citations
13.
Leenders, Geert J. van, Mirjam B. Smeets, Miranda Nabben, et al.. (2017). Statins Promote Cardiac Infarct Healing by Modulating Endothelial Barrier Function Revealed by Contrast-Enhanced Magnetic Resonance Imaging. Arteriosclerosis Thrombosis and Vascular Biology. 38(1). 186–194. 24 indexed citations
14.
Chanda, Dipanjan, Yvonne Oligschlaeger, Xiaoqing Zhu, et al.. (2017). 2-Arachidonoylglycerol ameliorates inflammatory stress-induced insulin resistance in cardiomyocytes. Journal of Biological Chemistry. 292(17). 7105–7114. 31 indexed citations
15.
Chanda, Dipanjan, Florence H. J. van Tienen, Arthur van den Wijngaard, et al.. (2017). Human embryonic stem cell-derived cardiomyocytes as an in vitro model to study cardiac insulin resistance. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(5). 1960–1967. 16 indexed citations
16.
Choi, Yong Seon, Dan Shao, Tao Li, et al.. (2016). Preservation of myocardial fatty acid oxidation prevents diastolic dysfunction in mice subjected to angiotensin II infusion. Journal of Molecular and Cellular Cardiology. 100. 64–71. 68 indexed citations
17.
Lenaers, Ellen, Miranda Nabben, Jacob J. Briedé, et al.. (2016). A genistein-enriched diet neither improves skeletal muscle oxidative capacity nor prevents the transition towards advanced insulin resistance in ZDF rats. Scientific Reports. 6(1). 22854–22854. 9 indexed citations
18.
Nabben, Miranda, Ellen Lenaers, Joris Hoeks, et al.. (2014). Lack of UCP3 does not affect skeletal muscle mitochondrial function under lipid-challenged conditions, but leads to sudden cardiac death. Basic Research in Cardiology. 109(6). 447–447. 15 indexed citations
19.
Abdurrachim, Desiree, Jolita Čiapaitė, Bart Wessels, et al.. (2014). Cardiac diastolic dysfunction in high-fat diet fed mice is associated with lipotoxicity without impairment of cardiac energetics in vivo. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1841(10). 1525–1537. 56 indexed citations
20.
Nabben, Miranda, Joris Hoeks, Jacob J. Briedé, et al.. (2008). The effect of UCP3 overexpression on mitochondrial ROS production in skeletal muscle of young versus aged mice. FEBS Letters. 582(30). 4147–4152. 68 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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