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.

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Showing 1-25 of 289 citing articles:

Molecular Structure and Physiological Function of Chloride Channels
Thomas J. Jentsch, Valentin Stein, Frank Weinreich, et al.
Physiological Reviews (2002) Vol. 82, Iss. 2, pp. 503-568
Closed Access | Times Cited: 1247

ClC-5 Cl--channel disruption impairs endocytosis in a mouse model for Dent's disease
Nils Piwon, W. C. Gunther, Michael Schwake, et al.
Nature (2000) Vol. 408, Iss. 6810, pp. 369-373
Closed Access | Times Cited: 534

Renal Vacuolar H+-ATPase
Carsten A. Wagner, Karin E. Finberg, Sylvie Breton, et al.
Physiological Reviews (2004) Vol. 84, Iss. 4, pp. 1263-1314
Closed Access | Times Cited: 442

CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease
Thomas J. Jentsch, Michael Pusch
Physiological Reviews (2018) Vol. 98, Iss. 3, pp. 1493-1590
Open Access | Times Cited: 392

CLC Chloride Channels and Transporters: From Genes to Protein Structure, Pathology and Physiology
Thomas J. Jentsch
Critical Reviews in Biochemistry and Molecular Biology (2008) Vol. 43, Iss. 1, pp. 3-36
Closed Access | Times Cited: 383

Boron based anion receptors as sensors
Ewan Galbraith, Tony D. James
Chemical Society Reviews (2010) Vol. 39, Iss. 10, pp. 3831-3831
Closed Access | Times Cited: 365

Hereditary causes of kidney stones and chronic kidney disease
Viðar Ö. Eðvarðsson, David S. Goldfarb, John C. Lieske, et al.
Pediatric Nephrology (2013) Vol. 28, Iss. 10, pp. 1923-1942
Open Access | Times Cited: 252

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

The CLC chloride channel family
Thomas J. Jentsch, Thomas Friedrich, Antje M. Schriever, et al.
Pflügers Archiv - European Journal of Physiology (1999) Vol. 437, Iss. 6, pp. 783-795
Closed Access | Times Cited: 326

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

RENAL TUBULE ALBUMIN TRANSPORT
Michael Gekle
Annual Review of Physiology (2004) Vol. 67, Iss. 1, pp. 573-594
Closed Access | Times Cited: 263

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

Strapped and other topographically nonplanar calixpyrrole analogues. Improved anion receptors
Chang‐Hee Lee, Hidekazu Miyaji, Dae-Wi Yoon, et al.
Chemical Communications (2007), Iss. 1, pp. 24-34
Closed Access | Times Cited: 231

PHYSIOLOGICAL FUNCTIONS OF CLC ClCHANNELS GLEANED FROM HUMAN GENETIC DISEASE AND MOUSE MODELS
Thomas J. Jentsch, Mallorie Poët, Jens C. Fuhrmann, et al.
Annual Review of Physiology (2005) Vol. 67, Iss. 1, pp. 779-807
Closed Access | Times Cited: 227

Ion channel diseases
Christian A. Hübner
Human Molecular Genetics (2002) Vol. 11, Iss. 20, pp. 2435-2445
Closed Access | Times Cited: 226

Dent's disease
Olivier Devuyst, Rajesh V. Thakker
Orphanet Journal of Rare Diseases (2010) Vol. 5, Iss. 1, pp. 28-28
Open Access | Times Cited: 226

Polycystin-1, the Gene Product of PKD1 , Induces Resistance to Apoptosis and Spontaneous Tubulogenesis in MDCK Cells
Alessandra Boletta, Feng Qian, Luiz F. Onuchic, et al.
Molecular Cell (2000) Vol. 6, Iss. 5, pp. 1267-1273
Open Access | Times Cited: 221

A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy with Abnormal Expression of Uromodulin
Karin Dahan, Olivier Devuyst, Michèle Smaers, et al.
Journal of the American Society of Nephrology (2003) Vol. 14, Iss. 11, pp. 2883-2893
Open Access | Times Cited: 214

Chloride in Vesicular Trafficking and Function
Tobias Stauber, Thomas J. Jentsch
Annual Review of Physiology (2012) Vol. 75, Iss. 1, pp. 453-477
Closed Access | Times Cited: 206

The ClC-5 chloride channel knock-out mouse – an animal model for Dent's disease
W. C. Gunther, Nils Piwon, Thomas J. Jentsch
Pflügers Archiv - European Journal of Physiology (2003) Vol. 445, Iss. 4, pp. 456-462
Closed Access | Times Cited: 197

Regulated acid–base transport in the collecting duct
Carsten A. Wagner, Olivier Devuyst, Soline Bourgeois, et al.
Pflügers Archiv - European Journal of Physiology (2009) Vol. 458, Iss. 1, pp. 137-156
Closed Access | Times Cited: 163

A primary culture of mouse proximal tubular cells, established on collagen-coated membranes
Sara Terryn, François Jouret, Frank Vandenabeele, et al.
AJP Renal Physiology (2007) Vol. 293, Iss. 2, pp. F476-F485
Open Access | Times Cited: 158

Cell Biology and Physiology of CLC Chloride Channels and Transporters
Tobias Stauber, Stefanie Weinert, Thomas J. Jentsch
Comprehensive physiology (2012), pp. 1701-1744
Closed Access | Times Cited: 141

From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes
Haifa Hichri, John Rendu, Nicole Monnier, et al.
Human Mutation (2010) Vol. 32, Iss. 4, pp. 379-388
Open Access | Times Cited: 128

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