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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:

Canonical WNT Signaling Regulates the Pituitary Organizer and Pituitary Gland Formation
Allison M Osmundsen, Jessica L. Keisler, Makoto M. Taketo, et al.
Endocrinology (2017) Vol. 158, Iss. 10, pp. 3339-3353
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

Cell transcriptomic atlas of the non-human primate Macaca fascicularis
Lei Han, Xiaoyu Wei, Chuanyu Liu, et al.
Nature (2022) Vol. 604, Iss. 7907, pp. 723-731
Open Access | Times Cited: 142
Rathke’s cleft cyst: From history to molecular genetics
Ayşa Hacıoğlu, Halil Tekiner, Meric A. Altinöz, et al.
Reviews in Endocrine and Metabolic Disorders (2025)
Open Access | Times Cited: 1
All Together Now: Modeling the Interaction of Neural With Non-neural Systems Using Organoid Models
Evelyn Chukwurah, Allison M Osmundsen, Shannon W. Davis, et al.
Frontiers in Neuroscience (2019) Vol. 13
Open Access | Times Cited: 48
Pituitary stem cells produce paracrine WNT signals to control the expansion of their descendant progenitor cells
John P. Russell, Xinhong Lim, Alice Santambrogio, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 37
Pituitary stem cells: past, present and future perspectives
María Inés Pérez‐Millán, Leonard Cheung, María F. Mercogliano, et al.
Nature Reviews Endocrinology (2023) Vol. 20, Iss. 2, pp. 77-92
Open Access | Times Cited: 11
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
Biological pathways leading to septo-optic dysplasia: a review
Ludovica Pasca, Davide Politano, Federica Morelli, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Developmental Genes and Malformations in the Hypothalamus
Carmen Dı́az, Luis Puelles
Frontiers in Neuroanatomy (2020) Vol. 14
Open Access | Times Cited: 29
Stem Cells, Self-Renewal, and Lineage Commitment in the Endocrine System
Katia Mariniello, Gerard Ruiz‐Babot, Emily C. McGaugh, et al.
Frontiers in Endocrinology (2019) Vol. 10
Open Access | Times Cited: 28
Comparing Two Neurodevelopmental Disorders Linked to CK2: Okur-Chung Neurodevelopmental Syndrome and Poirier-Bienvenu Neurodevelopmental Syndrome—Two Sides of the Same Coin?
Demetra Ballardin, J. M. Cruz-Gamero, Thierry Bienvenu, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
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
Okur‐Chung neurodevelopmental syndrome in a patient from Spain
Antonio Federico Martínez‐Monseny, Dídac Casas‐Alba, César Arjona, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 1, pp. 20-24
Closed Access | Times Cited: 16
Regulation of Pituitary Progenitor Differentiation by β-Catenin
Julie L Youngblood, Tanner Coleman, Shannon W. Davis
Endocrinology (2018) Vol. 159, Iss. 9, pp. 3287-3305
Open Access | Times Cited: 16
Integrated analysis of Wnt signalling system component gene expression
Paula Murphy, Chris Armit, Bill Hill, et al.
Development (2022) Vol. 149, Iss. 16
Open Access | Times Cited: 8
Glycoprotein hormone subunit alpha 2 (GPHA2): A pituitary stem cell-expressed gene associated with NOTCH2 signaling
Xiyu Ge, Karen E. Weis, Lori T. Raetzman
Molecular and Cellular Endocrinology (2024) Vol. 586, pp. 112163-112163
Open Access | Times Cited: 1
Single-cell analysis of mesenchymal cells in permeable neural vasculature reveals novel diverse subpopulations of fibroblasts
William Edward Bastedo, R. Wilder Scott, Martin Arostegui, et al.
Fluids and Barriers of the CNS (2024) Vol. 21, Iss. 1
Open Access | Times Cited: 1
Molecular Mechanisms Governing Embryonic Differentiation of Pituitary Somatotropes
Buffy S. Ellsworth, Caitlin E Stallings
Trends in Endocrinology and Metabolism (2018) Vol. 29, Iss. 7, pp. 510-523
Closed Access | Times Cited: 10
Haploinsufficiency of <b><i>NKX2-1</i></b> in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction
Rathi Prasad, Adeline K. Nicholas, Nadia Schoenmakers, et al.
Hormone Research in Paediatrics (2019) Vol. 92, Iss. 5, pp. 340-344
Open Access | Times Cited: 10
Copy Number Variants Contributing to Combined Pituitary Hormone Deficiency
Bartłomiej Budny, Katarzyna Karmelita‐Katulska, Marek Stajgis, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 16, pp. 5757-5757
Open Access | Times Cited: 10
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
A severe case of Bosch–Boonstra–Schaaf optic atrophy syndrome with a novel description of coloboma and septo‐optic dysplasia, owing to a start codon variant in the NR2F1 gene
Gabriella Gazdagh, Rebecca Mawby, Jay Self, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 3, pp. 900-906
Open Access | Times Cited: 8
Hypothalamic β-Catenin Is Essential for FGF8-Mediated Anterior Pituitary Growth: Links to Human Disease
Sally A. Camper, Alexandre Z. Daly, Caitlin E Stallings, et al.
Endocrinology (2017) Vol. 158, Iss. 10, pp. 3322-3324
Open Access | Times Cited: 7
Pituitary Transcription Factor Mutations Leading to Hypopituitarism
Péter Gergics
Experientia supplementum (2019), pp. 263-298
Closed Access | Times Cited: 6
Compound heterozygous GLI3 variants in siblings with thyroid hemiagenesis
Ewelina Szczepanek‐Parulska, Bartłomiej Budny, Martyna Borowczyk, et al.
Endocrine (2020) Vol. 71, Iss. 2, pp. 514-519
Open Access | Times Cited: 5
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