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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:

Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy
Jianbo Mao, Yijing Chen, Yuyan Fang, et al.
Annals of Medicine (2022) Vol. 54, Iss. 1, pp. 3285-3297
Open Access | Times Cited: 11

Showing 11 citing articles:

Genetic Characteristics and Clinical Manifestations of Foveal Hypoplasia in Familial Exudative Vitreoretinopathy
Yuqiao Ju, Lili Zhang, Feng‐Juan Gao, et al.
American Journal of Ophthalmology (2024) Vol. 262, pp. 73-85
Closed Access | Times Cited: 4
LRP5, Bone Mass Polymorphisms and Skeletal Disorders
Jake Littman, Wentian Yang, Jon Olansen, et al.
Genes (2023) Vol. 14, Iss. 10, pp. 1846-1846
Open Access | Times Cited: 5
Mutations in TSPAN12 gene causing familial exudative vitreoretinopathy
Yuqiao Ju, Tianhui Chen, Lu Ruan, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 1
Retinoic acid signaling pathway perturbation impacts mesodermal-tissue development in the zebrafish embryo: Biomarker candidate identification using transcriptomics.
Laura M.M. Samrani, Florent Dumont, Nina Hallmark, et al.
Reproductive Toxicology (2023) Vol. 119, pp. 108404-108404
Open Access | Times Cited: 3
Osteoporosis, Fractures, and Blindness Due to a Missense Mutation in the LRP5 Receptor
Jake Littman, Chanika Phornphutkul, Céline Saade, et al.
Orthopedic Research and Reviews (2023) Vol. Volume 15, pp. 39-45
Open Access | Times Cited: 2
Optical Coherence Tomography and Optical Coherence Tomography Angiography in Pediatric Retinal Diseases
Chung-Ting Wang, Yin‐Hsi Chang, Gavin Tan, et al.
Diagnostics (2023) Vol. 13, Iss. 8, pp. 1461-1461
Open Access | Times Cited: 2
Early onset high myopia and severe anisometropia associated with familial exudative vitreoretinopathy of irregular dominant inheritance in 12 Chinese families：analysis of refraction features and pathogenic variations
Wanyu Cheng, Weining Rong, Huiping Li, et al.
Research Square (Research Square) (2024)
Open Access
Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations
Erkuan Dai, Min Liu, Shujin Li, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 4, pp. 1-1
Open Access
FEVR combined with macular heterotopia in children presenting as pseudo-exotropia: a case report and literature review
Yujie Zhang, Shuimiao Chen, Yanghui Xiu
Frontiers in Medicine (2024) Vol. 11
Open Access
Identification of biomarkers of the retinoic acid signaling pathway in the zebrafish embryo model to predict human developmental toxicants
Laura M.M. Samrani
(2023)
Open Access
De novel heterozygous copy number deletion on 7q31.31-7q31.32 involving TSPAN12 gene with familial exudative vitreoretinopathy in a Chinese family
Shuang Zhang, Gang Zou, Mei-Jiao Ma, et al.
International Journal of Ophthalmology (2023) Vol. 16, Iss. 12, pp. 1952-1961
Open Access
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