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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:

Novel therapeutic perspectives in Noonan syndrome and RASopathies
Céline Saint-Laurent, Laurène Mazeyrie, Armelle Yart, et al.
European Journal of Pediatrics (2023) Vol. 183, Iss. 3, pp. 1011-1019
Open Access | Times Cited: 18

Showing 18 citing articles:

Exploring New Drug Repurposing Opportunities for MEK Inhibitors in RASopathies: A Comprehensive Review of Safety, Efficacy, and Future Perspectives of Trametinib and Selumetinib
Andrea Gazzin, Federico Fornari, Simona Cardaropoli, et al.
Life (2024) Vol. 14, Iss. 6, pp. 731-731
Open Access | Times Cited: 6
Promising But Not Yet the Promised Land
Daphne T. Hsu
JACC Basic to Translational Science (2025) Vol. 10, Iss. 2, pp. 167-169
Open Access
[Growth and development patterns of Noonan syndrome and advances in the treatment of short stature].
Xin Li, Wen Tian, Biyun Feng, et al.
PubMed (2025) Vol. 27, Iss. 1, pp. 33-38
Closed Access
Noonan syndrome
Michael A. Patton
Elsevier eBooks (2025)
Closed Access
Growth hormone signaling and clinical implications: from molecular to therapeutic perspectives
Zahra Aghili, Golnoosh Khoshnevisan, Rezvan Mostoli, et al.
Molecular Biology Reports (2025) Vol. 52, Iss. 1
Closed Access
Trametinib as a targeted treatment in cardiac and lymphatic presentations of Noonan syndrome
Isabel De Brouchoven, Juan Lorand, Léon Bofferding, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
Impaired MC3T3-E1 osteoblast differentiation triggered by oncogenic HRAS is rescued by the farnesyltransferase inhibitor Tipifarnib
Yannik Andrasch, Moses Munene Ireri, Jean-Charles Gander, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B. Howell, Susan M. White, Amy McTague, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Noonan syndrome combined with juvenile xanthogranuloma in a newborn
D. M. Mushcherova, U. S. Severgina, A. P. Khokhlova, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2025) Vol. 70, Iss. 1, pp. 64-69
Open Access
The pathogenesis of Noonan syndrome is modulated by NOC2L, a novel interactor of LZTR1 leading to impaired p53 signalling
Sumana Chatterjee, Miho Ishida, Débora Romeo Bertola, et al.
Research Square (Research Square) (2025)
Closed Access
Functional and structural insights into RAS effector proteins
Alessandro M. Mozzarelli, Dhirendra K. Simanshu, Pau Castel
Molecular Cell (2024) Vol. 84, Iss. 15, pp. 2807-2821
Closed Access | Times Cited: 4
Reverse repurposing: Potential utility of cancer drugs in nonmalignant illnesses
Mina Nikanjam, Kaitlyn Wells, Shumei Kato, et al.
Med (2024) Vol. 5, Iss. 7, pp. 689-717
Closed Access | Times Cited: 3
Mapping the current status and outlook of research on noonan syndrome over the last 26 years: a bibliometric and visual analysis
Zhengjiu Cui, Yuanyuan Wang, Fei Luo, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 1
Impaired MC3T3-E1 osteoblast differentiation triggered by oncogenic HRAS is rescued by the farnesyltransferase inhibitor Tipifarnib
Yannik Andrasch, Moses Munene Ireri, Ann-Engelke Sabrina Timm, et al.
Research Square (Research Square) (2024)
Open Access
Computer-based facial recognition as an assisting diagnostic tool to identify children with Noonan syndrome
Yulu Huang, Haomiao Sun, Qinchang Chen, et al.
BMC Pediatrics (2024) Vol. 24, Iss. 1
Open Access
Biomarker Landscape in RASopathies
Noemi Ferrito, Juan Báez-Flores, Mario Rodríguez-Martín, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8563-8563
Open Access
Treatment of RAF1-Related Biventricular Hypertrophy and Double Chamber Right Ventricle by MEK Inhibition Using Trametinib
Staša Krasić, Ivana Đuric, Nikola Ilic, et al.
The Indian Journal of Pediatrics (2024) Vol. 92, Iss. 1, pp. 93-93
Open Access
Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation
Giulia Sbrini, Zaira Tomasoni, Maria Rosa Cutrì, et al.
Stem Cell Research (2023) Vol. 74, pp. 103293-103293
Open Access | Times Cited: 1
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