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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:

SLC4A11 Prevents Osmotic Imbalance Leading to Corneal Endothelial Dystrophy, Deafness, and Polyuria
Nicole Gröger, Henning Fröhlich, H. Maier, et al.
Journal of Biological Chemistry (2010) Vol. 285, Iss. 19, pp. 14467-14474
Open Access | Times Cited: 68

Showing 1-25 of 68 citing articles:

The SLC4 family of bicarbonate transporters
Michael F. Romero, An‐Ping Chen, Mark D. Parker, et al.
Molecular Aspects of Medicine (2013) Vol. 34, Iss. 2-3, pp. 159-182
Open Access | Times Cited: 291
The Divergence, Actions, Roles, and Relatives of Sodium-Coupled Bicarbonate Transporters
Mark D. Parker, Walter F. Boron
Physiological Reviews (2013) Vol. 93, Iss. 2, pp. 803-959
Open Access | Times Cited: 265
Fuchs endothelial corneal dystrophy: The vicious cycle of Fuchs pathogenesis
Stephan Ong Tone, Viridiana Kocaba, Myriam Böhm, et al.
Progress in Retinal and Eye Research (2020) Vol. 80, pp. 100863-100863
Open Access | Times Cited: 170
Molecular bases of corneal endothelial dystrophies
Thore Schmedt, Mariana Mazzini Silva, Alireza Ziaei, et al.
Experimental Eye Research (2011) Vol. 95, Iss. 1, pp. 24-34
Open Access | Times Cited: 114
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases
Gonzalo L. Vilas, Sampath K. Loganathan, Jun Liu, et al.
Human Molecular Genetics (2013) Vol. 22, Iss. 22, pp. 4579-4590
Open Access | Times Cited: 94
Human SLC4A11 Is a Novel NH3/H+ Co-transporter
Wenlin Zhang, Diego G. Ogando, Joseph A. Bonanno, et al.
Journal of Biological Chemistry (2015) Vol. 290, Iss. 27, pp. 16894-16905
Open Access | Times Cited: 73
Ion Transport Function of SLC4A11 in Corneal Endothelium
Supriya S. Jalimarada, Diego G. Ogando, Eranga N. Vithana, et al.
Investigative Ophthalmology & Visual Science (2013) Vol. 54, Iss. 6, pp. 4330-4330
Open Access | Times Cited: 72
SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy
Sangita P. Patel, Mark D. Parker
BioMed Research International (2015) Vol. 2015, pp. 1-7
Open Access | Times Cited: 59
Mice With a Targeted Disruption ofSlc4a11Model the Progressive Corneal Changes of Congenital Hereditary Endothelial Dystrophy
Sang Beom Han, Heng-Pei Ang, Rebekah Poh, et al.
Investigative Ophthalmology & Visual Science (2013) Vol. 54, Iss. 9, pp. 6179-6179
Closed Access | Times Cited: 59
Structure, Function, and Trafficking of SLC4 and SLC26 Anion Transporters
Emmanuelle Cordat, Reinhart A.F. Reithmeier
Current topics in membranes (2014), pp. 1-67
Closed Access | Times Cited: 57
SLC4A11 is an EIPA-sensitive Na+ permeable pHi regulator
Diego G. Ogando, Supriya S. Jalimarada, Wenlin Zhang, et al.
AJP Cell Physiology (2013) Vol. 305, Iss. 7, pp. C716-C727
Open Access | Times Cited: 56
Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome
Salina Siddiqui, Juan Carlos Zenteno, Aine Rice, et al.
Cornea (2013) Vol. 33, Iss. 3, pp. 247-251
Open Access | Times Cited: 52
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies
Sampath K. Loganathan, Hans-Peter Schneider, Patricio E. Morgan, et al.
AJP Cell Physiology (2016) Vol. 311, Iss. 5, pp. C735-C748
Open Access | Times Cited: 44
Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants
Liyo Kao, Rustam Azimov, Xuesi M. Shao, et al.
AJP Cell Physiology (2016) Vol. 311, Iss. 5, pp. C820-C830
Open Access | Times Cited: 43
Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH− conductance pathway that is stimulated by rises in intracellular and extracellular pH
Evan J. Myers, Anikó Marshall, Michael L. Jennings, et al.
AJP Cell Physiology (2016) Vol. 311, Iss. 6, pp. C945-C959
Open Access | Times Cited: 40
The Molecular Basis of Fuchs’ Endothelial Corneal Dystrophy
Jie Zhang, Charles N. J. McGhee, Dipika V. Patel
Molecular Diagnosis & Therapy (2019) Vol. 23, Iss. 1, pp. 97-112
Closed Access | Times Cited: 38
A Biochemical Framework for SLC4A11, the Plasma Membrane Protein Defective in Corneal Dystrophies
Gonzalo L. Vilas, Patricio E. Morgan, Sampath K. Loganathan, et al.
Biochemistry (2011) Vol. 50, Iss. 12, pp. 2157-2169
Open Access | Times Cited: 44
Depletion ofSLC4A11Causes Cell Death by Apoptosis in an Immortalized Human Corneal Endothelial Cell Line
Jun Liu, Li‐Fong Seet, Li Wei Koh, et al.
Investigative Ophthalmology & Visual Science (2012) Vol. 53, Iss. 7, pp. 3270-3270
Open Access | Times Cited: 40
Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy
Sampath K. Loganathan, Joseph R. Casey
Human Mutation (2014) Vol. 35, Iss. 9, pp. 1082-1091
Open Access | Times Cited: 36
High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy–Causing Mutants of SLC4A11
Anthony M. Chiu, Jake Mandziuk, Sampath K. Loganathan, et al.
Investigative Ophthalmology & Visual Science (2015) Vol. 56, Iss. 13, pp. 7739-7739
Open Access | Times Cited: 29
Defective cell adhesion function of solute transporter, SLC4A11, in endothelial corneal dystrophies
Darpan Malhotra, Martin Jung, Claudia Fecher‐Trost, et al.
Human Molecular Genetics (2019)
Closed Access | Times Cited: 26
The H+ Transporter SLC4A11: Roles in Metabolism, Oxidative Stress and Mitochondrial Uncoupling
Joseph A. Bonanno, Rajalekshmy Shyam, Moonjung Choi, et al.
Cells (2022) Vol. 11, Iss. 2, pp. 197-197
Open Access | Times Cited: 15
Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation
Kumari Alka, Joseph R. Casey
Investigative Ophthalmology & Visual Science (2018) Vol. 59, Iss. 10, pp. 4258-4258
Open Access | Times Cited: 24
Corneal dystrophies and genetics in the International Committee for Classification of Corneal Dystrophies era: a review
Andrea L. Vincent
Clinical and Experimental Ophthalmology (2013) Vol. 42, Iss. 1, pp. 4-12
Open Access | Times Cited: 26
Early Hearing Loss upon Disruption of Slc4a10 in C57BL/6 Mice
Antje K. Huebner, H. Maier, Alena Maul, et al.
Journal of the Association for Research in Otolaryngology (2019) Vol. 20, Iss. 3, pp. 233-245
Open Access | Times Cited: 21
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