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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:

Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
Hironori Bando, Shin Urai, Keitaro Kanie, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 10

Showing 10 citing articles:

Knockout mice with pituitary malformations help identify human cases of hypopituitarism
Julian Martinez-Mayer, Michelle L. Brinkmeier, Sean P. O’Connell, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 4
Identification of POU1F1 Variants in Vietnamese Patients with Combined Pituitary Hormone Deficiency
Ha Thu Nguyen, Khanh Ngoc Nguyen, Tran Minh Dien, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2406-2406
Open Access
Next-generation therapeutics for rare genetic disorders
A. A. Sankar, Ravi Kumar Y.S, Anjali Singh, et al.
Mutagenesis (2024) Vol. 39, Iss. 3, pp. 157-171
Closed Access | Times Cited: 3
Hypopituitarism in Sox3 null mutants correlates with altered NG2-glia in the median eminence and is influenced by aspirin and gut microbiota
Christophe Galichet, Karine Rizzoti, Robin Lovell‐Badge
PLoS Genetics (2024) Vol. 20, Iss. 9, pp. e1011395-e1011395
Open Access | Times Cited: 1
Genetic Disorders of the Pituitary Gland
Reed E. Pyeritz
Elsevier eBooks (2024), pp. 455-493
Closed Access | Times Cited: 1
Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study
Yoonha Lee, Young Ah Lee, Jung Min Ko, et al.
Annals of Pediatric Endocrinology & Metabolism (2024) Vol. 29, Iss. 6, pp. 379-386
Closed Access | Times Cited: 1
Revisitando o gene HESX1 na busca de variantes sinônimas
Renata Kertsz
(2024)
Open Access
Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene
Lukáš Plachý, Petra Dušátková, Klára Maratová, et al.
Endocrine Connections (2024) Vol. 13, Iss. 10
Open Access
A Rare Case of Severe Jaundice in a Panhypopituitarism Patient
Jennifer Wiese, Abdel Wahap El Ghezewi, Mujtaba Mohamed, et al.
Journal of Medical Cases (2023) Vol. 14, Iss. 6, pp. 204-207
Open Access
Sox3-null hypopituitarism depends on median eminence NG2-glia and is influenced by aspirin and gut microbiota
Christophe Galichet, Karine Rizzoti, Robin Lovell‐Badge
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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