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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:

Vaptans or voluntary increased hydration to protect the kidney: how do they compare?
Lise Bankir, Dominique Guerrot, Daniel G. Bichet
Nephrology Dialysis Transplantation (2021) Vol. 38, Iss. 3, pp. 562-574
Open Access | Times Cited: 10

Showing 10 citing articles:

Aquaporin-2 in the early stages of the adenine-induced chronic kidney disease model
Lucas H. Oronel, M. Clara Ortíz, Carolina A. Yarza, et al.
PLoS ONE (2025) Vol. 20, Iss. 1, pp. e0314827-e0314827
Open Access
Development and validation of the thirst distress scale for patients with autosomal dominant polycystic kidney disease
Şeyda Gül Özcan, Sibel Gökçay Bek, Necmi Eren, et al.
Journal of Nephrology (2025)
Open Access
Mechanistic insights into the primary and secondary alterations of renal ion and water transport in the distal nephron
Nahid Tabibzadeh, Gilles Crambert
Journal of Internal Medicine (2022) Vol. 293, Iss. 1, pp. 4-22
Open Access | Times Cited: 15
Pharmacological Interventions for Cirrhotic Ascites: From Challenges to Emerging Therapeutic Horizons
Yuan Gao, Xin Liu, Yunyi Gao, et al.
Gut and Liver (2024) Vol. 18, Iss. 6, pp. 934-948
Open Access | Times Cited: 2
The role of urinary supersaturations for lithogenic salts in the progression of autosomal dominant polycystic kidney disease
Pietro Manuel Ferraro, Matteo Bargagli, Nicolas Faller, et al.
Journal of Nephrology (2022) Vol. 36, Iss. 4, pp. 1011-1018
Closed Access | Times Cited: 3
The SLC6A18 transporter is most likely a Na-dependent glycine/urea antiporter responsible for urea secretion in the proximal straight tubule. Influence of this urea secretion on GFR
Lise Bankir, Gilles Crambert, Rosa Vargas‐Poussou
˜The œNephron journals/Nephron journals (2024), pp. 1-27
Open Access
Can Additional Water a Day Keep the Cysts Away, in Patients with Polycystic Kidney Disease?
Louise Moist
NEJM Evidence (2021) Vol. 1, Iss. 1
Closed Access | Times Cited: 3
Apelin is altered in subjects with autosomal dominant polycystic kidney disease and preserved kidney function
Peter Janssens, Wilfried Cools, Nadia De Mota, et al.
Nephrology Dialysis Transplantation (2023) Vol. 38, Iss. 8, pp. 1907-1911
Open Access
Development and Validation of the Thirst Distress Scale for Patients with Autosomal Dominant Polycystic Kidney Disease
Şeyda Gül Özcan, Sibel Gökçay Bek, Necmi Eren, et al.
Research Square (Research Square) (2022)
Open Access
Az autoszomális domináns policisztás vesebetegség és a tolvaptankezelés
Nóra Garam, András Tislér
Hypertonia és Nephrologia (2022) Vol. 26, Iss. 5, pp. 237-244
Open Access
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