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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:

Genetic Disorders of Renal Electrolyte Transport
Steven J. Scheinman, Lisa M. Guay‐Woodford, Rajesh V. Thakker, et al.
New England Journal of Medicine (1999) Vol. 340, Iss. 15, pp. 1177-1187
Closed Access | Times Cited: 234

Showing 1-25 of 234 citing articles:

Potassium Channels: Molecular Defects, Diseases, and Therapeutic Opportunities
Char‐Chang Shieh, Michael J. Coghlan, James P. Sullivan, et al.
Pharmacological Reviews (2000) Vol. 52, Iss. 4, pp. 557-593
Closed Access | Times Cited: 509
Mammalian Distal Tubule: Physiology, Pathophysiology, and Molecular Anatomy
Robert F. Reilly, David H. Ellison
Physiological Reviews (2000) Vol. 80, Iss. 1, pp. 277-313
Closed Access | Times Cited: 342
Distribution of transcellular calcium and sodium transport pathways along mouse distal nephron
Johannes Loffing, Dominique Loffing‐Cueni, Víctor Valderrábano, et al.
AJP Renal Physiology (2001) Vol. 281, Iss. 6, pp. F1021-F1027
Closed Access | Times Cited: 340
Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules
Erik Christensen, Olivier Devuyst, Geert Dom, et al.
Proceedings of the National Academy of Sciences (2003) Vol. 100, Iss. 14, pp. 8472-8477
Open Access | Times Cited: 312
Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis
Sophia Wang
Human Molecular Genetics (2000) Vol. 9, Iss. 20, pp. 2937-2945
Open Access | Times Cited: 304
Localization of the Epithelial Ca2+ Channel in Rabbit Kidney and Intestine
Joost G.J. Hoenderop, Anita Hartog, Marchel Stuiver, et al.
Journal of the American Society of Nephrology (2000) Vol. 11, Iss. 7, pp. 1171-1178
Open Access | Times Cited: 219
Licorice abuse: time to send a warning message
Hesham R. Omar, Irina Komarova, Mohamed O. Elghonemi, et al.
Therapeutic Advances in Endocrinology and Metabolism (2012) Vol. 3, Iss. 4, pp. 125-138
Open Access | Times Cited: 209
Cytochrome P450 enzymes: Central players in cardiovascular health and disease
Reem H. Elbekai, Ayman O.S. El‐Kadi
Pharmacology & Therapeutics (2006) Vol. 112, Iss. 2, pp. 564-587
Closed Access | Times Cited: 177
Phenotype–genotype correlation in antenatal and neonatal variants of Bartter syndrome
Karine Brochard, Olivia Boyer, Anne Blanchard, et al.
Nephrology Dialysis Transplantation (2008) Vol. 24, Iss. 5, pp. 1455-1464
Closed Access | Times Cited: 157
Hypercalcemic Disorders in Children
Victoria Stokes, Morten Frost Nielsen, Fadil Hannan, et al.
Journal of Bone and Mineral Research (2017) Vol. 32, Iss. 11, pp. 2157-2170
Open Access | Times Cited: 112
Rickets and osteomalacia
Michael P. Whyte, Rajesh V. Thakker
Medicine (2013) Vol. 41, Iss. 10, pp. 594-599
Closed Access | Times Cited: 102
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes
Israel Zelikovic, Raymonde Szargel, Ali Hawash, et al.
Kidney International (2003) Vol. 63, Iss. 1, pp. 24-32
Open Access | Times Cited: 179
Physiological and pathophysiological role of magnesium in the cardiovascular system
Pascal Laurant, Rhian M. Touyz
Journal of Hypertension (2000) Vol. 18, Iss. 9, pp. 1177-1191
Closed Access | Times Cited: 171
Sodium and calcium transport pathways along the mammalian distal nephron: from rabbit to human
Johannes Loffing, Brigitte Kaissling
AJP Renal Physiology (2003) Vol. 284, Iss. 4, pp. F628-F643
Closed Access | Times Cited: 161
Human Cortical Distal Nephron
Helena Lagger Biner, Marie‐Pierre Arpin‐Bott, Johannes Loffing, et al.
Journal of the American Society of Nephrology (2002) Vol. 13, Iss. 4, pp. 836-847
Open Access | Times Cited: 153
Molecular Mechanisms of Primary Hypercalciuria
Kevin K. Frick, David A. Bushinsky
Journal of the American Society of Nephrology (2003) Vol. 14, Iss. 4, pp. 1082-1095
Open Access | Times Cited: 145
Functional Expression of Mutations in the Human NaCl Cotransporter
Joke C. de Jong, W A van der Vliet, Lambertus P. van den Heuvel, et al.
Journal of the American Society of Nephrology (2002) Vol. 13, Iss. 6, pp. 1442-1448
Open Access | Times Cited: 144
Bartter’s and Gitelman’s Syndromes: From Gene to Clinic
Maarten Naesens, Paul Steels, R. Verberckmoes, et al.
Nephron Physiology (2004) Vol. 96, Iss. 3, pp. p65-p78
Closed Access | Times Cited: 141
Inherited Primary Renal Tubular Hypokalemic Alkalosis: A Review of Gitelman and Bartter Syndromes
Andrea J. Shaer
The American Journal of the Medical Sciences (2001) Vol. 322, Iss. 6, pp. 316-332
Closed Access | Times Cited: 141
Bartter Syndromes and Other Salt-Losing Tubulopathies
Robert Kleta, Detlef Böckenhauer
Nephron Physiology (2006) Vol. 104, Iss. 2, pp. p73-p80
Open Access | Times Cited: 116
Functional modules, mutational load and human genetic disease
Norann A. Zaghloul, Nicholas Katsanis
Trends in Genetics (2010) Vol. 26, Iss. 4, pp. 168-176
Open Access | Times Cited: 100
Role of Proximal Tubules in the Pathogenesis of Kidney Disease
Nazih L. Nakhoul, Vecihi Batuman
Contributions to nephrology (2011), pp. 37-50
Closed Access | Times Cited: 85
A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome
Mahdi Salih, Ivan Gautschi, Miguel X. van Bemmelen, et al.
Journal of the American Society of Nephrology (2017) Vol. 28, Iss. 11, pp. 3291-3299
Open Access | Times Cited: 68
Integrative Physiology and Functional Genomics of Epithelial Function in a Genetic Model Organism
Julian A. T. Dow, Shireen A. Davies
Physiological Reviews (2003) Vol. 83, Iss. 3, pp. 687-729
Closed Access | Times Cited: 128
Divalent cation transport by the distal nephron: insights from Bartter's and Gitelman's syndromes
David H. Ellison
AJP Renal Physiology (2000) Vol. 279, Iss. 4, pp. F616-F625
Closed Access | Times Cited: 115
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