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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The Hormone FGF21 Stimulates Water Drinking in Response to Ketogenic Diet and Alcohol
Parkyong Song, Christoph Zechner, Genaro Hernandez, et al.
Cell Metabolism (2018) Vol. 27, Iss. 6, pp. 1338-1347.e4
Open Access | Times Cited: 83

Showing 1-25 of 83 citing articles:

CD4 T cells mediate brain inflammation and neurodegeneration in a mouse model of Parkinson's disease
Gregory P. Williams, Aubrey M. Schonhoff, Asta Jurkuvenaite, et al.
Brain (2021) Vol. 144, Iss. 7, pp. 2047-2059
Open Access | Times Cited: 218
A Dozen Years of Discovery: Insights into the Physiology and Pharmacology of FGF21
Steven A. Kliewer, David J. Mangelsdorf
Cell Metabolism (2019) Vol. 29, Iss. 2, pp. 246-253
Open Access | Times Cited: 216
FGF21: An Emerging Therapeutic Target for Non-Alcoholic Steatohepatitis and Related Metabolic Diseases
Erik J. Tillman, Timothy P. Rolph
Frontiers in Endocrinology (2020) Vol. 11
Open Access | Times Cited: 162
New developments in the biology of fibroblast growth factors
David M. Ornitz, Nobuyuki Itoh
WIREs Mechanisms of Disease (2022) Vol. 14, Iss. 4
Open Access | Times Cited: 96
FGF-based drug discovery: advances and challenges
Gaozhi Chen, Lingfeng Chen, Xiaokun Li, et al.
Nature Reviews Drug Discovery (2025)
Closed Access | Times Cited: 4
Going Back to the Biology of FGF21: New Insights
Jo E. Lewis, Francis J. P. Ebling, Ricardo J. Samms, et al.
Trends in Endocrinology and Metabolism (2019) Vol. 30, Iss. 8, pp. 491-504
Open Access | Times Cited: 137
The FGF metabolic axis
Xiaokun Li
Frontiers of Medicine (2019) Vol. 13, Iss. 5, pp. 511-530
Open Access | Times Cited: 120
FGF21 Signals to Glutamatergic Neurons in the Ventromedial Hypothalamus to Suppress Carbohydrate Intake
Sharon O. Jensen-Cody, Kyle H. Flippo, Kristin E. Claflin, et al.
Cell Metabolism (2020) Vol. 32, Iss. 2, pp. 273-286.e6
Open Access | Times Cited: 110
FGF21 and the Physiological Regulation of Macronutrient Preference
Cristal M. Hill, Emily Qualls‐Creekmore, Hans‐Rudolf Berthoud, et al.
Endocrinology (2020) Vol. 161, Iss. 3
Open Access | Times Cited: 78
Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice
Susanne Keipert, Dominik Lutter, Bjoern O. Schroeder, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 73
FGF21 suppresses alcohol consumption through an amygdalo-striatal circuit
Kyle H. Flippo, Samuel A.J. Trammell, Matthew P. Gillum, et al.
Cell Metabolism (2022) Vol. 34, Iss. 2, pp. 317-328.e6
Open Access | Times Cited: 58
The Nuanced Metabolic Functions of Endogenous FGF21 Depend on the Nature of the Stimulus, Tissue Source, and Experimental Model
Redin A. Spann, Christopher D. Morrison, Laura J. den Hartigh
Frontiers in Endocrinology (2022) Vol. 12
Open Access | Times Cited: 44
FGF21 counteracts alcohol intoxication by activating the noradrenergic nervous system
Mihwa Choi, Marc Schneeberger, Wei Fan, et al.
Cell Metabolism (2023) Vol. 35, Iss. 3, pp. 429-437.e5
Open Access | Times Cited: 27
Biological and pharmacological functions of the FGF19- and FGF21-coreceptor beta klotho
Alexandra S. Aaldijk, Cristy R.C. Verzijl, Johan W. Jonker, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 26
FGF21 in obesity and cancer: New insights
Weiqin Lu, Xiaokun Li, Yongde Luo
Cancer Letters (2020) Vol. 499, pp. 5-13
Open Access | Times Cited: 63
Modulation of the Astrocyte-Neuron Lactate Shuttle System contributes to Neuroprotective action of Fibroblast Growth Factor 21
Yan Sun, Yue J. Wang, Suting Chen, et al.
Theranostics (2020) Vol. 10, Iss. 18, pp. 8430-8445
Open Access | Times Cited: 61
Circulating FGF21 Levels in Human Health and Metabolic Disease
Michaela Keuper, Hans‐Ulrich Häring, Harald Staiger
Experimental and Clinical Endocrinology & Diabetes (2019) Vol. 128, Iss. 11, pp. 752-770
Closed Access | Times Cited: 59
GDF15 is a major determinant of ketogenic diet-induced weight loss
Jun Lu, Mengqing Zhu, Bo Xia, et al.
Cell Metabolism (2023) Vol. 35, Iss. 12, pp. 2165-2182.e7
Open Access | Times Cited: 21
Role of liver FGF21-KLB signaling in ketogenic diet-induced amelioration of hepatic steatosis
Wanrong Guo, Huanyi Cao, Yunfeng Shen, et al.
Nutrition and Diabetes (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 7
Metabolic Effects of Ketogenic Diets: Exploring Whole-Body Metabolism in Connection with Adipose Tissue and Other Metabolic Organs
Yusra Ahmad, Dong Soo Seo, Younghoon Jang
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 13, pp. 7076-7076
Open Access | Times Cited: 7
Ketogenic diet but not free-sugar restriction alters glucose tolerance, lipid metabolism, peripheral tissue phenotype, and gut microbiome: RCT
Aaron Hengist, Russell G. Davies, Jean‐Philippe Walhin, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 8, pp. 101667-101667
Open Access | Times Cited: 7
Metabolic Crosstalk between Liver and Brain: From Diseases to Mechanisms
Xiaoyue Yang, Kangli Qiu, Yaoyao Jiang, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 14, pp. 7621-7621
Open Access | Times Cited: 6
Homeostatic sensing of dietary protein restriction: A case for FGF21
Cristal M. Hill, Hans‐Rudolf Berthoud, Heike Münzberg, et al.
Frontiers in Neuroendocrinology (2018) Vol. 51, pp. 125-131
Open Access | Times Cited: 57
Gut microbiota in non‐alcoholic fatty liver disease and alcohol‐related liver disease: Current concepts and perspectives
Juan Pablo Arab, Marco Arrese, Vijay H. Shah
Hepatology Research (2019) Vol. 50, Iss. 4, pp. 407-418
Open Access | Times Cited: 51
AIG1 and ADTRP are endogenous hydrolases of fatty acid esters of hydroxy fatty acids (FAHFAs) in mice
Meric Erikci Ertunc, Bernard P. Kok, William H. Parsons, et al.
Journal of Biological Chemistry (2020) Vol. 295, Iss. 18, pp. 5891-5905
Open Access | Times Cited: 37
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