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:

Secreted growth differentiation factor 15 as a potential biomarker for mitochondrial dysfunctions in aging and age-related disorders
Yasunori Fujita, Yu Taniguchi, Shoji Shinkai, et al.
Geriatrics and gerontology international/Geriatrics & gerontology international (2016) Vol. 16, Iss. S1, pp. 17-29
Open Access | Times Cited: 167

Showing 1-25 of 167 citing articles:

DNA methylation GrimAge strongly predicts lifespan and healthspan
Ake T. Lu, Austin Quach, James G. Wilson, et al.
Aging (2019) Vol. 11, Iss. 2, pp. 303-327
Open Access | Times Cited: 1662

Plasma proteomic signature of age in healthy humans
Toshiko Tanaka, Angélique Biancotto, Ruin Moaddel, et al.
Aging Cell (2018) Vol. 17, Iss. 5
Open Access | Times Cited: 429

Markers of inflammation and their association with muscle strength and mass: A systematic review and meta-analysis
Camilla S.L. Tuttle, Lachlan A. N. Thang, Andrea B. Maier
Ageing Research Reviews (2020) Vol. 64, pp. 101185-101185
Open Access | Times Cited: 422

Linking cellular stress responses to systemic homeostasis
Lorenzo Galluzzi, Takahiro Yamazaki, Guido Kroemer
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 11, pp. 731-745
Open Access | Times Cited: 414

Towards frailty biomarkers: Candidates from genes and pathways regulated in aging and age-related diseases
Ana L. Cardoso, Adelaide Fernandes, Juan Antonio Aguilar‐Pimentel, et al.
Ageing Research Reviews (2018) Vol. 47, pp. 214-277
Open Access | Times Cited: 396

GDF15 Provides an Endocrine Signal of Nutritional Stress in Mice and Humans
Satish Patel, Anna Álvarez-Guaita, Audrey Melvin, et al.
Cell Metabolism (2019) Vol. 29, Iss. 3, pp. 707-718.e8
Open Access | Times Cited: 384

The MIC-1/GDF15-GFRAL Pathway in Energy Homeostasis: Implications for Obesity, Cachexia, and Other Associated Diseases
Vicky Wang-Wei Tsai, Yasmin Husaini, Amanda Sainsbury, et al.
Cell Metabolism (2018) Vol. 28, Iss. 3, pp. 353-368
Open Access | Times Cited: 335

GDF15: emerging biology and therapeutic applications for obesity and cardiometabolic disease
Dongdong Wang, Emily A. Day, Logan K. Townsend, et al.
Nature Reviews Endocrinology (2021) Vol. 17, Iss. 10, pp. 592-607
Closed Access | Times Cited: 312

Advances and Utility of the Human Plasma Proteome
Eric W. Deutsch, Gilbert S. Omenn, Zhi Sun, et al.
Journal of Proteome Research (2021) Vol. 20, Iss. 12, pp. 5241-5263
Open Access | Times Cited: 142

GDF15, an emerging key player in human aging
Maria Conte, Cristina Giuliani, Antonio Chiariello, et al.
Ageing Research Reviews (2022) Vol. 75, pp. 101569-101569
Open Access | Times Cited: 89

Inflammaging as a target for healthy ageing
Ben Dugan, Jessica Conway, Niharika A. Duggal
Age and Ageing (2023) Vol. 52, Iss. 2
Closed Access | Times Cited: 55

Human Aging and Longevity Are Characterized by High Levels of Mitokines
Maria Conte, Rita Ostan, Cristina Fabbri, et al.
The Journals of Gerontology Series A (2018) Vol. 74, Iss. 5, pp. 600-607
Open Access | Times Cited: 155

Reduced oxidative capacity in macrophages results in systemic insulin resistance
Saet-Byel Jung, Min Jeong Choi, Dongryeol Ryu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 147

Mitohormesis, an Antiaging Paradigm
Clea Bárcena, Pablo Mayoral, Pedro M. Quirós
International review of cell and molecular biology (2018), pp. 35-77
Closed Access | Times Cited: 142

Insights Into Mechanisms of GDF15 and Receptor GFRAL: Therapeutic Targets
Luc Rochette, Marianne Zeller, Yves Cottin, et al.
Trends in Endocrinology and Metabolism (2020) Vol. 31, Iss. 12, pp. 939-951
Open Access | Times Cited: 116

International Workshop:
Michelangelo Mancuso, Robert McFarland, Thomas Klopstock, et al.
Neuromuscular Disorders (2017) Vol. 27, Iss. 12, pp. 1126-1137
Open Access | Times Cited: 115

Pharmacological but not physiological GDF15 suppresses feeding and the motivation to exercise
Anders B. Klein, Trine S. Nicolaisen, Niels Ørtenblad, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 103

GDF15, an update of the physiological and pathological roles it plays: a review
Artin Assadi, Azadeh Zahabi, Robert A. de J. Hart
Pflügers Archiv - European Journal of Physiology (2020) Vol. 472, Iss. 11, pp. 1535-1546
Closed Access | Times Cited: 102

Growth and differentiation factor 15 is secreted by skeletal muscle during exercise and promotes lipolysis in humans
Claire Laurens, Anisha Parmar, Enda Murphy, et al.
JCI Insight (2020) Vol. 5, Iss. 6
Open Access | Times Cited: 98

Dysregulation of mitophagy in carcinogenesis and tumor progression
Joon Young Chang, Hyon‐Seung Yi, Hyeon-Woo Kim, et al.
Biochimica et Biophysica Acta (BBA) - Bioenergetics (2016) Vol. 1858, Iss. 8, pp. 633-640
Closed Access | Times Cited: 97

GDF15 and Cardiac Cells: Current Concepts and New Insights
Luc Rochette, Geoffrey Dogon, Marianne Zeller, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8889-8889
Open Access | Times Cited: 97

REVISITING THE HALLMARKS OF AGING TO IDENTIFY MARKERS OF BIOLOGICAL AGE
Florent Guerville, Philipe de Souto Barreto, Isabelle Ader, et al.
The Journal of Prevention of Alzheimer s Disease (2019), pp. 1-9
Open Access | Times Cited: 96

Growth differentiation factor 15 ameliorates nonalcoholic steatohepatitis and related metabolic disorders in mice
Kook Hwan Kim, Seong‐Hun Kim, Dai Hoon Han, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 94

Growth differentiation factor 15 is positively associated with incidence of diabetes mellitus: the Malmö Diet and Cancer–Cardiovascular Cohort
Xue Bao, Yan Borné, Iram Faqir Muhammad, et al.
Diabetologia (2018) Vol. 62, Iss. 1, pp. 78-86
Open Access | Times Cited: 91

GDF15 Plasma Level Is Inversely Associated With Level of Physical Activity and Correlates With Markers of Inflammation and Muscle Weakness
Maria Conte, Morena Martucci, Giovanni Mosconi, et al.
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 91

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