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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:

Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome
Sarah R. Poll, Renan Paulo Martin, Elizabeth Wohler, et al.
PLoS Genetics (2022) Vol. 18, Iss. 12, pp. e1010504-e1010504
Open Access | Times Cited: 11

Showing 11 citing articles:

Hypoxic Conditions Modulate Chondrogenesis through the Circadian Clock: The Role of Hypoxia-Inducible Factor-1α
Krisztián Z. Juhász, Tibor Hajdú, Patrik Kovács, et al.
Cells (2024) Vol. 13, Iss. 6, pp. 512-512
Open Access | Times Cited: 6
Using existing pediatric cancer data from the Gabriella Miller Kids First Data Resource Program
Alexandra Hudson, Marcia V. Fournier, James N. Coulombe, et al.
JNCI Cancer Spectrum (2023) Vol. 7, Iss. 6
Open Access | Times Cited: 7
Clinical and radiological response of Maffucci related enchondromas to mutant IDH1 inhibitor Ivosidenib
Thomas Funck‐Brentano, Martine Cohen‐Solal, François Ducray, et al.
Bone (2024) Vol. 188, pp. 117221-117221
Open Access | Times Cited: 1
Maffucci Syndrome May Be a Heritable Thoracic Aortic Disease and a Cause of Aortic Dissection
Scott Eisenberg, Kim D. Thompson, Muhammad Waqas Naeem, et al.
JACC Case Reports (2024) Vol. 29, Iss. 17, pp. 102496-102496
Open Access | Times Cited: 1
Cartilage Forming Tumors of the Skeleton
Julio A. Díaz-Pérez, Andrew E. Rosenberg
Advances in Anatomic Pathology (2024)
Closed Access | Times Cited: 1
Update on cancer screening in children with syndromes of bone lesions, hereditary leiomyoma and renal cell carcinoma syndrome, and other rare syndromes
Orli Michaeli, Sun Young Kim, Sarah G. Mitchell, et al.
Clinical Cancer Research (2024) Vol. 31, Iss. 3, pp. 457-465
Closed Access | Times Cited: 1
A Rare Ovarian Mixed Sex Cord Stromal Tumor in a Patient with Ollier Disease: A Case Report
Kyle M. Devins, Allan M. Goldstein, Amanda French
Journal of Pediatric and Adolescent Gynecology (2024) Vol. 37, Iss. 6, pp. 629-631
Closed Access
Treatment of a patient with Ollier’s disease
T. I. Aleksandrov, В. М. Прохоренко, E. N. Simonova
The Scientific Notes of the Pavlov University (2024) Vol. 31, Iss. 2, pp. 73-82
Open Access
Abnormalities of Bone Structure
Reed E. Pyeritz
Elsevier eBooks (2024), pp. 617-631
Closed Access
Spectrum of IDH-mutant tumors in Ollier-Maffucci disease: the triple interaction theory
Emmanuel Mandonnet, Thomas Funck‐Brentano, Jean‐Philippe Hugnot, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Osteocytic oxygen sensing: Distinct impacts of VHL and HIF-2ΑLPHA on bone integrity
Sarah V. Mendoza, Kristina V Wells, Deepa K. Murugesh, et al.
Bone (2024) Vol. 192, pp. 117339-117339
Open Access
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