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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:

Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome
Fang Zhong, Hao Ying, Wangping Jia, et al.
Journal of Endocrinological Investigation (2018) Vol. 42, Iss. 6, pp. 653-665
Open Access | Times Cited: 15

Showing 15 citing articles:

Functional evaluation of novel compound heterozygous variants in SLC12A3 of Gitelman syndrome
Na Wang, Yuanxing Yang, Xiong Tian, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access | Times Cited: 1
Case Report: Familial hypocalciuric hypercalcemia type 1 with a novel mutation combined with Gitelman syndrome and a review of the literature
Tianxiang He, Xinyu Li, Guosheng Li, et al.
Frontiers in Endocrinology (2025) Vol. 16
Open Access
Gitelman syndrome with Graves’ disease leading to rhabdomyolysis: a case report and literature review
Jing Xu, Juan He, Shujing Xu, et al.
BMC Nephrology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 7
A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature
Oguzhan Koca, Mustafa Tarık Alay, Ahmet Murt, et al.
CEN Case Reports (2024) Vol. 13, Iss. 5, pp. 330-338
Closed Access | Times Cited: 1
Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia
Guangyu He, Xiaokun Gang, Zhonghua Sun, et al.
Medicine (2020) Vol. 99, Iss. 29, pp. e21123-e21123
Open Access | Times Cited: 11
Multi‐centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children
Qian Shen, Jiemei Chen, Minghui Yu, et al.
Clinical Genetics (2020) Vol. 99, Iss. 4, pp. 558-564
Closed Access | Times Cited: 10
R158Q and G212S, novel pathogenic compound heterozygous variants in SLC12A3 of Gitelman syndrome
Zongyue Li, Huixiao Wu, Shuoshuo Wei, et al.
Frontiers of Medicine (2022) Vol. 16, Iss. 6, pp. 932-945
Closed Access | Times Cited: 3
Gitelman syndrome with primary hyperparathyroidism: A case report
Shanshen Yu, Jia Sun, Lijun Mou
Medicine (2024) Vol. 103, Iss. 34, pp. e39447-e39447
Open Access
Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene
Sahoko Kamejima, Izumi Yamamoto, Akiko Tajiri, et al.
Internal Medicine (2020) Vol. 60, Iss. 10, pp. 1567-1572
Open Access | Times Cited: 2
Generation of a human induced pluripotent stem cell line (WMUi021-A) from a Gitelman syndrome patient carrying a SLC12A3 gene mutation (c.179C > T)
Xiaoling Guo, Rengchen Qian, Xiaoou Shan, et al.
Stem Cell Research (2021) Vol. 53, pp. 102280-102280
Open Access | Times Cited: 2
Gitelman syndrome diagnosed in the first trimester of pregnancy: a case report and literature review
Yang Cao, Dan Hu, Yun Peng, et al.
Case Reports in Perinatal Medicine (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 1
Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome
Ying Qiao, Zhinan Ye, Wei Zhang, et al.
Clinical Endocrinology (2022) Vol. 99, Iss. 5, pp. 474-480
Closed Access | Times Cited: 1
Novel mutations of the SLC12A3 gene in patients with Gitelman syndrome
Feng Wang, Manli Guo, Jing Li, et al.
Scandinavian Journal of Clinical and Laboratory Investigation (2021) Vol. 81, Iss. 8, pp. 629-633
Closed Access | Times Cited: 1
Hypokalemia: Early marker of autosomal recessive tubulopathy (Gitelman's syndrome): Case report
Milica Petrović, Vlastimir Vlatković, Dejan Pilčević, et al.
Medicinski casopis (2023) Vol. 57, Iss. 1, pp. 34-39
Open Access
Whole-exome sequencing in diagnosing 2 cases of Gitelman syndrome.
Rongrong Xie, Ping Jin, Youbo Yang, et al.
PubMed (2022) Vol. 47, Iss. 3, pp. 401-406
Closed Access
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