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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:

Pharmacological Correction of Trafficking Defects in ATP-sensitive Potassium Channels Caused by Sulfonylurea Receptor 1 Mutations
Gregory Martin, Emily A. Rex, Prasanna K. Devaraneni, et al.
Journal of Biological Chemistry (2016) Vol. 291, Iss. 42, pp. 21971-21983
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

Cryo-EM structure of the ATP-sensitive potassium channel illuminates mechanisms of assembly and gating
Gregory M. Martin, Craig Yoshioka, Emily A. Rex, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 193
ATP‐Sensitive Potassium Channels and Their Physiological and Pathophysiological Roles
Andrew Tinker, Qadeer Aziz, Yiwen Li, et al.
Comprehensive physiology (2018), pp. 1463-1511
Open Access | Times Cited: 124
Mechanism of pharmacochaperoning in a mammalian KATP channel revealed by cryo-EM
Gregory M. Martin, Min Woo Sung, Zhongying Yang, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 80
Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension
Michael S. Bohnen, Lijiang Ma, Na Zhu, et al.
Circulation Genomic and Precision Medicine (2018) Vol. 11, Iss. 10
Open Access | Times Cited: 69
Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management
María Güemes, Sofia Rahman, Ritika R. Kapoor, et al.
Reviews in Endocrine and Metabolic Disorders (2020) Vol. 21, Iss. 4, pp. 577-597
Open Access | Times Cited: 69
Small molecule SWELL1 complex induction improves glycemic control and nonalcoholic fatty liver disease in murine Type 2 diabetes
Susheel K. Gunasekar, Litao Xie, Ashutosh Kumar, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 32
KATP channel mutations in congenital hyperinsulinism: Progress and challenges towards mechanism-based therapies
Assmaa ElSheikh, Show‐Ling Shyng
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 15
Non-radioactive Rb+ Efflux Assay for Screening KATP Channel Modulators
Assmaa ElSheikh, Camden Driggers, Show‐Ling Shyng
Methods in molecular biology (2024), pp. 191-210
Closed Access | Times Cited: 5
Targeted pharmacotherapies for defective ABC transporters
Virginie Vauthier, Chantal Housset, Thomas Falguières
Biochemical Pharmacology (2017) Vol. 136, pp. 1-11
Open Access | Times Cited: 40
Genetic characteristics of patients with congenital hyperinsulinism
Mary Ellen Vajravelu, Diva D. De León
Current Opinion in Pediatrics (2018) Vol. 30, Iss. 4, pp. 568-575
Open Access | Times Cited: 40
Gating modules of the AMPA receptor pore domain revealed by unnatural amino acid mutagenesis
Mette H. Poulsen, Anahita Poshtiban, Viktoria Klippenstein, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 27, pp. 13358-13367
Open Access | Times Cited: 39
AI-Based Discovery and CryoEM Structural Elucidation of a KATP Channel Pharmacochaperone
Assmaa ElSheikh, Camden Driggers, Ha H. Truong, et al.
(2025)
Open Access
Pharmacological chaperones of ATP-sensitive potassium channels: Mechanistic insight from cryoEM structures
Gregory Martin, Min Woo Sung, Show‐Ling Shyng
Molecular and Cellular Endocrinology (2019) Vol. 502, pp. 110667-110667
Open Access | Times Cited: 32
AI-based discovery and cryoEM structural elucidation of a KATP channel pharmacochaperone
Assmaa ElSheikh, Camden Driggers, Ha H. Truong, et al.
eLife (2025) Vol. 13
Open Access
Morphine Efficacy, Tolerance, and Hypersensitivity Are Altered After Modulation of SUR1 Subtype KATP Channel Activity in Mice
Cole Fisher, Kayla Johnson, Travis Okerman, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 29
Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology
Hüseyin Demirbilek, Sofia Rahman, Gönül Büyükyılmaz, et al.
International Journal of Pediatric Endocrinology (2017) Vol. 2017, Iss. 1
Open Access | Times Cited: 27
Subcellular trafficking and endocytic recycling of KATP channels
Hua-Qian Yang, Fabio A. Echeverry, Assmaa ElSheikh, et al.
AJP Cell Physiology (2022) Vol. 322, Iss. 6, pp. C1230-C1247
Open Access | Times Cited: 14
High-throughput characterization of photocrosslinker-bearing ion channel variants to map residues critical for function and pharmacology
Nina Braun, Søren Friis, Christian Ihling, et al.
PLoS Biology (2021) Vol. 19, Iss. 9, pp. e3001321-e3001321
Open Access | Times Cited: 16
The current chemical biology tool box for studying ion channels
Nina Braun, Zeshan P. Sheikh, Stephan A. Pless
The Journal of Physiology (2020) Vol. 598, Iss. 20, pp. 4455-4471
Open Access | Times Cited: 18
Maturity-Onset Diabetes of the Young: Mutations, Physiological Consequences, and Treatment Options
Hazar Younis, Se Eun Ha, Brian G. Jorgensen, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 11, pp. 1762-1762
Open Access | Times Cited: 10
Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties
Arianna Maiorana, Carlo Dionisi‐Vici
Journal of Inherited Metabolic Disease (2017) Vol. 40, Iss. 4, pp. 531-542
Closed Access | Times Cited: 18
Functional characterization of activating mutations in the sulfonylurea receptor 1 ( ABCC8 ) causing neonatal diabetes mellitus in Asian Indian children
Kandasamy Balamurugan, B Kavitha, Zhongying Yang, et al.
Pediatric Diabetes (2019) Vol. 20, Iss. 4, pp. 397-407
Open Access | Times Cited: 17
Novel dominant KATP channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotyping
Kara E. Boodhansingh, Balamurugan Kandasamy, Lauren Mitteer, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 11, pp. 2214-2227
Open Access | Times Cited: 17
Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young‐onset diabetes with exome sequencing
Norihiko Matsutani, Hiroto Furuta, Shohei Matsuno, et al.
Journal of Diabetes Investigation (2019) Vol. 11, Iss. 2, pp. 333-336
Open Access | Times Cited: 12
Production and purification of ATP-sensitive potassium channel particles for cryo-electron microscopy
Camden Driggers, Show‐Ling Shyng
Methods in enzymology on CD-ROM/Methods in enzymology (2021), pp. 121-150
Open Access | Times Cited: 11
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