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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:

SIRT5 is under the control of PGC‐1α and AMPK and is involved in regulation of mitochondrial energy metabolism
Marcin Buler, Sanna‐Mari Aatsinki, Valerio Izzi, et al.
The FASEB Journal (2014) Vol. 28, Iss. 7, pp. 3225-3237
Closed Access | Times Cited: 124

Showing 1-25 of 124 citing articles:

The Role of Sirtuins in Antioxidant and Redox Signaling
Chandra K. Singh, Gagan Chhabra, Mary A. Ndiaye, et al.
Antioxidants and Redox Signaling (2017) Vol. 28, Iss. 8, pp. 643-661
Open Access | Times Cited: 664
The role of sirtuins in cardiac disease
Shouji Matsushima, Junichi Sadoshima
AJP Heart and Circulatory Physiology (2015) Vol. 309, Iss. 9, pp. H1375-H1389
Open Access | Times Cited: 326
Mitochondria in health, disease, and aging
John S. Harrington, Stefan W. Ryter, Maria Plataki, et al.
Physiological Reviews (2023) Vol. 103, Iss. 4, pp. 2349-2422
Open Access | Times Cited: 266
Sirtuins and Their Roles in Brain Aging and Neurodegenerative Disorders
Henryk Jęśko, P.L. Wencel, Robert P. Strosznajder, et al.
Neurochemical Research (2016) Vol. 42, Iss. 3, pp. 876-890
Open Access | Times Cited: 235
Functions of the sirtuin deacylase SIRT5 in normal physiology and pathobiology
Surinder Kumar, David B. Lombard
Critical Reviews in Biochemistry and Molecular Biology (2018) Vol. 53, Iss. 3, pp. 311-334
Open Access | Times Cited: 220
The role of mitochondrial sirtuins in health and disease
Brenna Osborne, Nicholas L. Bentley, Magdalene K. Montgomery, et al.
Free Radical Biology and Medicine (2016) Vol. 100, pp. 164-174
Closed Access | Times Cited: 159
Mitochondrial Sirtuins and Their Relationships with Metabolic Disease and Cancer
Surinder Kumar, David B. Lombard
Antioxidants and Redox Signaling (2014) Vol. 22, Iss. 12, pp. 1060-1077
Open Access | Times Cited: 144
Metabolic Dysfunction in Parkinson’s Disease: Bioenergetics, Redox Homeostasis and Central Carbon Metabolism
Annadurai Anandhan, Maria S. Jacome, Shulei Lei, et al.
Brain Research Bulletin (2017) Vol. 133, pp. 12-30
Open Access | Times Cited: 138
PGC-1α, glucose metabolism and type 2 diabetes mellitus
Haijiang Wu, Xinna Deng, Yonghong Shi, et al.
Journal of Endocrinology (2016) Vol. 229, Iss. 3, pp. R99-R115
Open Access | Times Cited: 136
Obesity Is Associated With Low NAD+/SIRT Pathway Expression in Adipose Tissue of BMI-Discordant Monozygotic Twins
Sakari Jukarainen, Sini Heinonen, Joel Rämö, et al.
The Journal of Clinical Endocrinology & Metabolism (2015) Vol. 101, Iss. 1, pp. 275-283
Open Access | Times Cited: 133
Emerging Roles for SIRT5 in Metabolism and Cancer
Lauren Bringman-Rodenbarger, Angela H. Guo, Costas A. Lyssiotis, et al.
Antioxidants and Redox Signaling (2017) Vol. 28, Iss. 8, pp. 677-690
Open Access | Times Cited: 124
Alpha‐ketoglutarate dehydrogenase complex‐dependent succinylation of proteins in neurons and neuronal cell lines
Gary E. Gibson, Hui Xu, Huan‐Lian Chen, et al.
Journal of Neurochemistry (2015) Vol. 134, Iss. 1, pp. 86-96
Open Access | Times Cited: 119
Regulation of hepatic energy metabolism by the nuclear receptor PXR
Jukka Hakkola, Jaana Rysä, Janne Hukkanen
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2016) Vol. 1859, Iss. 9, pp. 1072-1082
Closed Access | Times Cited: 96
Therapeutic effects of baicalein on rotenone-induced Parkinson’s disease through protecting mitochondrial function and biogenesis
Xue Zhang, Li-Da Du, Wen Zhang, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 96
Role of CPS1 in Cell Growth, Metabolism, and Prognosis in LKB1-Inactivated Lung Adenocarcinoma
Müge Çeliktaş, Ichidai Tanaka, S. C. Tripathi, et al.
JNCI Journal of the National Cancer Institute (2016) Vol. 109, Iss. 3, pp. djw231-djw231
Open Access | Times Cited: 95
ERRα as a Bridge Between Transcription and Function: Role in Liver Metabolism and Disease
Hui Xia, Catherine R. Dufour, Vincent Giguère
Frontiers in Endocrinology (2019) Vol. 10
Open Access | Times Cited: 86
Progress in Nonalcoholic Fatty Liver Disease: SIRT Family Regulates Mitochondrial Biogenesis
Chuanfei Zeng, Mingkai Chen
Biomolecules (2022) Vol. 12, Iss. 8, pp. 1079-1079
Open Access | Times Cited: 48
Mitochondrial Sirtuins in Parkinson’s Disease
Ling He, Jihong Wang, Yazhi Yang, et al.
Neurochemical Research (2022) Vol. 47, Iss. 6, pp. 1491-1502
Closed Access | Times Cited: 40
The global succinylation of SARS-CoV-2–infected host cells reveals drug targets
Quan Liu, Heming Wang, Libin Chen, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 30
Open Access | Times Cited: 38
Emerging Roles of SIRT5 in Metabolism, Cancer, and SARS-CoV-2 Infection
Emanuele Fabbrizi, Francesco Fiorentino, Vincenzo Carafa, et al.
Cells (2023) Vol. 12, Iss. 6, pp. 852-852
Open Access | Times Cited: 35
Molecular mechanisms underlying the impact of muscle fiber types on meat quality in livestock and poultry
Meijie Mo, Zihao Zhang, Xiaotong Wang, et al.
Frontiers in Veterinary Science (2023) Vol. 10
Open Access | Times Cited: 29
Sirtuins at the Crossroads between Mitochondrial Quality Control and Neurodegenerative Diseases: Structure, Regulation, Modifications, and Modulators
Hui Xu, Yiyang Liu, Lin-Seng Li, et al.
Aging and Disease (2023) Vol. 14, Iss. 3, pp. 794-794
Open Access | Times Cited: 26
Gut microbial metabolites in MASLD: Implications of mitochondrial dysfunction in the pathogenesis and treatment
Ruhan Zhang, Zhaobo Yan, Huan Zhong, et al.
Hepatology Communications (2024) Vol. 8, Iss. 7
Open Access | Times Cited: 15
Sirtuins in kidney diseases: potential mechanism and therapeutic targets
Qi Jin, Fang Ma, Tong‐Tong Liu, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 11
The AKT2/SIRT5/TFEB pathway as a potential therapeutic target in non-neovascular AMD
Sayan Ghosh, Ruchi Sharma, Sridhar Bammidi, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
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