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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:

αKlotho and Chronic Kidney Disease
Javier A. Neyra, Mengwen Hu
Vitamins and hormones (2016), pp. 257-310
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Inflammation and renal fibrosis: Recent developments on key signaling molecules as potential therapeutic targets
Wenshan Lv, George W. Booz, Yangang Wang, et al.
European Journal of Pharmacology (2017) Vol. 820, pp. 65-76
Open Access | Times Cited: 271
Klotho in Clinical Nephrology
Javier A. Neyra, Ming Chang Hu, Orson W. Moe
Clinical Journal of the American Society of Nephrology (2020) Vol. 16, Iss. 1, pp. 162-176
Open Access | Times Cited: 129
Uremic Toxins, Oxidative Stress, Atherosclerosis in Chronic Kidney Disease, and Kidney Transplantation
Ewa Wojtaszek, Urszula Ołdakowska‐Jedynak, Marlena Kwiatkowska, et al.
Oxidative Medicine and Cellular Longevity (2021) Vol. 2021, Iss. 1
Open Access | Times Cited: 63
Klotho exerts protection in chronic kidney disease associated with regulating inflammatory response and lipid metabolism
Junhui Liu, Huaicheng Wang, Qinyu Liu, et al.
Cell & Bioscience (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Fibroblast Growth Factor 23 and Klotho in AKI
Marta Christov, Javier A. Neyra, Sanjeev Gupta, et al.
Seminars in Nephrology (2018) Vol. 39, Iss. 1, pp. 57-75
Closed Access | Times Cited: 67
FGF23 activates injury-primed renal fibroblasts via FGFR4-dependent signalling and enhancement of TGF-β autoinduction
Edward R. Smith, S. Holt, Tim D. Hewitson
The International Journal of Biochemistry & Cell Biology (2017) Vol. 92, pp. 63-78
Open Access | Times Cited: 62
Association between serum soluble α-klotho and bone mineral density (BMD) in middle-aged and older adults in the United States: a population-based cross-sectional study
Zhang Yang, Changtai Zhao, Hanyong Zhang, et al.
Aging Clinical and Experimental Research (2023) Vol. 35, Iss. 10, pp. 2039-2049
Closed Access | Times Cited: 19
Soluble Klotho, a Potential Biomarker of Chronic Kidney Disease–Mineral Bone Disorders Involved in Healthy Ageing: Lights and Shadows
Julia Martín-Vírgala, Beatriz Martín-Carro, Sara Fernández-Villabrille, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1843-1843
Open Access | Times Cited: 8
Association of cognitive impairment with the interaction between chronic kidney disease and depression: findings from NHANES 2011–2014
Tong Zhou, Jiayu Zhao, Yimei Ma, et al.
BMC Psychiatry (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 8
Performance of soluble Klotho assays in clinical samples of kidney disease
Javier A. Neyra, Orson W. Moe, Johanne Pastor, et al.
Clinical Kidney Journal (2019) Vol. 13, Iss. 2, pp. 235-244
Open Access | Times Cited: 54
Long noncoding RNA NEAT1 is involved in the protective effect of Klotho on renal tubular epithelial cells in diabetic kidney disease through the ERK1/2 signaling pathway
Yanlin Yang, Meng Xue, Yijie Jia, et al.
Experimental & Molecular Medicine (2020) Vol. 52, Iss. 2, pp. 266-280
Open Access | Times Cited: 50
Effect of essential amino acid кetoanalogues and protein restriction diet on morphogenetic proteins (FGF-23 and Кlotho) in 3b–4 stages chronic кidney disease patients: a randomized pilot study
Lyudmila Milovanova, В. В. Фомин, Sergey Moiseev, et al.
Clinical and Experimental Nephrology (2018) Vol. 22, Iss. 6, pp. 1351-1359
Closed Access | Times Cited: 35
Blocking the histone lysine 79 methyltransferase DOT1L alleviates renal fibrosis through inhibition of renal fibroblast activation and epithelial‐mesenchymal transition
Lirong Liu, Jianan Zou, Yingjie Guan, et al.
The FASEB Journal (2019) Vol. 33, Iss. 11, pp. 11941-11958
Open Access | Times Cited: 30
Soluble Klotho and Incident Hypertension
David A. Drew, Ronit Katz, Stephen B. Kritchevsky, et al.
Clinical Journal of the American Society of Nephrology (2021) Vol. 16, Iss. 10, pp. 1502-1511
Open Access | Times Cited: 26
Relationship of Soluble Klotho and Early Stage of Diabetic Nephropathy: A Systematic Review and Meta-Analysis
Caihong Xin, Xin Sun, Zheng Li, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 17
αKlotho–FGF23 interactions and their role in kidney disease: a molecular insight
Edward R. Smith, S. Holt, Tim D. Hewitson
Cellular and Molecular Life Sciences (2019) Vol. 76, Iss. 23, pp. 4705-4724
Closed Access | Times Cited: 28
Defective Skeletal Mineralization in Pediatric CKD
Katherine Wesseling‐Perry
Current Osteoporosis Reports (2015) Vol. 13, Iss. 2, pp. 98-105
Closed Access | Times Cited: 23
Serum Klotho in Living Kidney Donors and Kidney Transplant Recipients: A Meta-Analysis
Charat Thongprayoon, Javier A. Neyra, Panupong Hansrivijit, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 6, pp. 1834-1834
Open Access | Times Cited: 20
Histone deacetylase 3 (HDAC3) as an important epigenetic regulator of kidney diseases
Lijun Zhang, Wangsen Cao
Journal of Molecular Medicine (2021) Vol. 100, Iss. 1, pp. 43-51
Closed Access | Times Cited: 17
Klotho and Mesenchymal Stem Cells: A Review on Cell and Gene Therapy for Chronic Kidney Disease and Acute Kidney Disease
Marcella Liciani Franco, Stephany Beyerstedt, Érika Bevilaqua Rangel
Pharmaceutics (2021) Vol. 14, Iss. 1, pp. 11-11
Open Access | Times Cited: 17
Relationship of Serum Soluble Klotho Levels and Echocardiographic Parameters in Patients on Maintenance Hemodialysis
Aihua Zhang, Weikang Guo, Ling Yu, et al.
Kidney & Blood Pressure Research (2019) Vol. 44, Iss. 3, pp. 396-404
Open Access | Times Cited: 14
Calcification of coronary arteries and aortic valve and circulating a-klotho levels in patients with chronic kidney disease
Panagiotis Savvoulidis, Andreas P. Kalogeropoulos, Vasileios Raptis, et al.
Journal of Thoracic Disease (2020) Vol. 12, Iss. 3, pp. 431-437
Open Access | Times Cited: 13
Cardiovascular remodeling as a result of fibroblast growth factor-23 (FGF-23)/Klotho imbalance in patients with CKD
Ludmilа Milоvаnоvа, Marina Taranova, Svetlana Milоvаnova, et al.
International Urology and Nephrology (2021) Vol. 54, Iss. 7, pp. 1613-1621
Closed Access | Times Cited: 12
The Role of Alterations in Alpha-Klotho and FGF-23 in Kidney Transplantation and Kidney Donation
Meera Gupta, Gabriel Orozco, Madhumati Rao, et al.
Frontiers in Medicine (2022) Vol. 9
Open Access | Times Cited: 9
Anti-aging factor, serum alpha-Klotho, as a marker of acute physiological stress, and a predictor of ICU mortality, in patients with septic shock
Peter A. Abdelmalik, Robert D. Stevens, Sarabdeep Singh, et al.
Journal of Critical Care (2017) Vol. 44, pp. 323-330
Closed Access | Times Cited: 12
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