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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.

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Showing 9 citing articles:

A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy
Hane Lee, Debra A. Moon, Rin Khang, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 1
Open Access
Clinical and Molecular Features of Patients With Congenital Disorders of Glycosylation in Japan
Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada
JIMD Reports (2025) Vol. 66, Iss. 3
Open Access
First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations
Siyu Zhao, Fengyu Che, Le Yang, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 8
Whole paternal uniparental disomy of chromosome 4 with a novel homozygous IDUA splicing variant, c.159‐9T>A, in a Chinese patient with mucopolysaccharidosis type I
Lulu Yan, Shuxia Ding, Yan He, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 8
Open Access | Times Cited: 1
A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene
Hazuki Morikawa, Sachiko Nishina, Kaoruko Torii, et al.
Human Genome Variation (2023) Vol. 10, Iss. 1
Open Access | Times Cited: 3
The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients
Kaoruko Torii, Sachiko Nishina, Hazuki Morikawa, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 13678-13678
Open Access | Times Cited: 3
Ocular genetics in the Japanese population
Yoshihiro Hotta, Kaoruko Torii, Masakazu Takayama
Japanese Journal of Ophthalmology (2024)
Open Access
Uniparental Disomy of Chromosome 4: A Case of Whole Chromosome UPD Presenting with LRBA Deficiency
Bilgesu Ak, Erhan Parıltay, Reyhan Gümüşburun, et al.
Journal of Clinical Immunology (2024) Vol. 45, Iss. 1
Closed Access
A rare case ofSRD5A3‐CDGin a patient with ataxia and telangiectasia: A case report
Seyed Hesamedin Nabavizadeh, Rafat Noeiaghdam, Leila Johari, et al.
Clinical Case Reports (2022) Vol. 10, Iss. 11
Open Access | Times Cited: 2
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