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:

Refining critical regions in 15q24 microdeletion syndrome pertaining to autism
Yi Liu, Yanqing Zhang, Mehdi Zarrei, et al.
American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2020) Vol. 183, Iss. 4, pp. 217-226
Closed Access | Times Cited: 6

Showing 6 citing articles:

Gangliosides and Cholesterol: Dual Regulators of Neuronal Membrane Framework in Autism Spectrum Disorder
Borna Puljko, Marija Štracak, Svjetlana Kalanj Bognar, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 3, pp. 1322-1322
Open Access

Strabismus in Genetic Syndromes: A Review
Sara Şebnem Kılıç, Jordi Bové, Bethany Nahri So, et al.
Clinical and Experimental Ophthalmology (2025)
Open Access

The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling
Malek Bouassida, Denise Molina‐Gomes, F. Koraichi, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 4
Open Access | Times Cited: 2

Neuroplastin in Neuropsychiatric Diseases
Xiao Lin, Yi Chu Liang, Rodrigo Herrera‐Molina, et al.
Genes (2021) Vol. 12, Iss. 10, pp. 1507-1507
Open Access | Times Cited: 15

Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders
Yuanyuan Zhang, Xiaoliang Liu, Haiming Gao, et al.
Molecular Cytogenetics (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 5

Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities
Anaïk Previdi, Pénélope Jordan, Charles Egloff, et al.
Clinical Genetics (2024) Vol. 106, Iss. 5, pp. 537-544
Open Access

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