OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Showing 11 citing articles:

A clinical approach to tubulopathies in children and young adults
Rachael Kermond, Andrew Mallett, Hugh J. McCarthy
Pediatric Nephrology (2022) Vol. 38, Iss. 3, pp. 651-662
Open Access | Times Cited: 19

Distinct cell types along thick ascending limb express pathways for monovalent and divalent cation transport
Hasan Demirci, Jessica Paola Bahena-López, Alina Smorodchenko, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
Laura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 13

Magnesium Homeostasis
Aubrey R. Morrison
Clinical Journal of the American Society of Nephrology (2023) Vol. 18, Iss. 7, pp. 969-978
Closed Access | Times Cited: 4

Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea
Naye Choi, Seong Heon Kim, Eun Hui Bae, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 4

Impact of claudin‐10 deficiency on amelogenesis: Lesson from a HELIX tooth
Nicolas Obtel, Adeline Le Cabec, Thè Nghia Nguyen, et al.
Annals of the New York Academy of Sciences (2022) Vol. 1516, Iss. 1, pp. 197-211
Open Access | Times Cited: 5

Clinical and molecular features of four families with CLDN10-related HELIX syndrome
Ahmad Qudair, Maged H. Hussein, Mohammed Al‐Owain, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 12, pp. 104886-104886
Closed Access | Times Cited: 2

HELIX Syndrome, a Claudinopathy with Relevant Dermatological Manifestations: Report of Two New Cases
María Carmen Martínez-Romero, M.E. Hernández-Contreras, Juan Antonio Bafalliu-Vidal, et al.
Genes (2024) Vol. 15, Iss. 6, pp. 687-687
Open Access

Tubulopathies with hypokalemic alkalosis: Bartter and HELIX syndromes in children
Ж. Г. Левиашвили, Н. Д. Савенкова, M. О. Amiryan
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2023) Vol. 68, Iss. 3, pp. 12-20
Open Access

New Insights into the Pivotal Roles of Claudins in Proximal Tubule Electrolyte Reabsorption
Peter S. Aronson
Journal of the American Society of Nephrology (2022) Vol. 33, Iss. 4, pp. 659-661
Open Access

Bartter Syndrome: Perspectives of a Pediatric Nephrologist
Naye Choi, Hee Gyung Kang
Electrolytes & Blood Pressure (2022) Vol. 20, Iss. 2, pp. 49-49
Open Access

Page 1

Scroll to top