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:

Pituitary stalk interruption syndrome
Antonis Voutetakis
Handbook of clinical neurology (2021), pp. 9-27
Closed Access | Times Cited: 11

Showing 11 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

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation
Michelle L. Brinkmeier, Leonard Cheung, Sean P. O’Connell, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation
Michelle L. Brinkmeier, Leonard Cheung, Sean P. O’Connell, et al.
Human Molecular Genetics (2025)
Open Access

The Fuzzy planar cell polarity protein (FUZ), necessary for primary cilium formation, is essential for pituitary development
Emily J. Lodge, William B. Barrell, Karen Liu, et al.
Journal of Anatomy (2023) Vol. 244, Iss. 2, pp. 358-367
Open Access | Times Cited: 7

Re-analysis of gene mutations found in pituitary stalk interruption syndrome and a new hypothesis on the etiology
Shengjie Wang, Qiaozhen Qin, Deyue Jiang, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 2

Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man
Hironori Bando, Michelle L. Brinkmeier, Frederic Castinetti, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 3, pp. 367-385
Open Access | Times Cited: 6

Lost Connection: A Case Report of Interrupted Pituitary Stalk Syndrome
Rana Bilal Idrees, Mariam Malik, Faisal Cheema, et al.
Cureus (2024)
Open Access

A rare case of pituitary stalk interruption syndrome (PSIS) presenting as short stature in an 8‐year‐old female
Kamana Sen, Kritick Bhandari, Suman Simkhada, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 8
Open Access

Fgf17: A regulator of the mid/hind brain boundary in mammals
Zane Oberholzer, Chiron Loubser, Natalya Nikitina
Differentiation (2024) Vol. 140, pp. 100813-100813
Open Access

Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease
Roberta Lattanzi, Rossella Miele
Life (2024) Vol. 14, Iss. 10, pp. 1254-1254
Open Access

The molecular basis of hypoprolactinaemia
Bryan Padraig Finn, Mehul Dattani
Reviews in Endocrine and Metabolic Disorders (2024)
Closed Access

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