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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:

Imagawa–Matsumoto syndrome: SUZ12‐related overgrowth disorder
Eri Imagawa, Rie Seyama, Hiromi Aoi, et al.
Clinical Genetics (2023) Vol. 103, Iss. 4, pp. 383-391
Closed Access | Times Cited: 12

Showing 12 citing articles:

Epigenetic and metabolic regulation of developmental timing in neocortex evolution
Matilde Aquilino, Nora Ditzer, Takashi Namba, et al.
Trends in Neurosciences (2025)
Open Access
Growth disorders caused by variants in epigenetic regulators: progress and prospects
Julian C. Lui
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 2
May the force be with you: Nuclear condensates function beyond transcription control
Maria Luce Negri, Sarah D’Annunzio, Giulia Vitali, et al.
BioEssays (2023) Vol. 45, Iss. 10
Open Access | Times Cited: 6
A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition
Christine W. Gao, Wanying Lin, Ryan C. Riddle, et al.
JCI Insight (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 6
Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition
Christine W. Gao, Wanying Lin, Ryan C. Riddle, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
BAP1 is required prenatally for differentiation and maintenance of postnatal murine enteric nervous system
Sabine Schneider, Jessica B. Anderson, Rebecca P Bradley, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 9
Open Access | Times Cited: 1
Droplet Digital PCR for Fast and Accurate Characterization of NF1 Locus Deletions
Laurence Pacot, Manuela Ye, Juliette Nectoux, et al.
Journal of Molecular Diagnostics (2023) Vol. 26, Iss. 2, pp. 150-157
Open Access | Times Cited: 3
Identification of an NF1 Microdeletion with Optical Genome Mapping
Gergely Büki, Anna Bekő, Csaba Bödör, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 17, pp. 13580-13580
Open Access | Times Cited: 2
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and review
Laurence Pacot, Milind Girish, Samantha J.L. Knight, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access
Biallelic loss‐of‐function variants of EZH1 cause a novel developmental disorder with central precocious puberty
Nobuhiko Okamoto, Sayaka Yoshida, Ayako Ogitani, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 10
Closed Access
Fetal and postnatal neuroimaging of SUZ12-related overgrowth: Imagawa-matsumoto syndrome
Onur Simsek, Arastoo Vossough
Journal of Neuroradiology (2024) Vol. 51, Iss. 5, pp. 101210-101210
Closed Access
Overgrowth syndromes, diagnosis and management
Steven D. Klein, Alex F. Nisbet, Jennifer M. Kalish
Current Opinion in Pediatrics (2023) Vol. 35, Iss. 6, pp. 620-630
Closed Access
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