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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:

Successful treatment with MEK‐inhibitor in a patient with NRAS‐related cutaneous skeletal hypophosphatemia syndrome
Diana Carli, Simona Cardaropoli, Daniele Tessaris, et al.
Genes Chromosomes and Cancer (2022) Vol. 61, Iss. 12, pp. 740-746
Open Access | Times Cited: 21

Showing 21 citing articles:

Mosaic RASopathies concept: different skin lesions, same systemic manifestations?
Marie‐Anne Morren, Heidi Fodstad, Hilde Brems, et al.
Journal of Medical Genetics (2024), pp. jmg-109306
Closed Access | Times Cited: 6
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
Phosphaturic Mesenchymal Tumors with or without Phosphate Metabolism Derangements
Alberto Montanari, Maria Giulia Pirini, Ludovica Lotrecchiano, et al.
Current Oncology (2023) Vol. 30, Iss. 8, pp. 7478-7488
Open Access | Times Cited: 13
Neurofibromatosis type I (NF1) and bone involvement in a pediatric setting: insights from FGF23 levels
Giulia Rodari, Valeria Citterio, Masami Ikehata, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2025) Vol. 51, Iss. 1
Open Access
A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody
Jing Wu, Qiaoyu Cao, Wei Lü, et al.
Calcified Tissue International (2025) Vol. 116, Iss. 1
Open Access
Treatment of Refractory Epilepsy With MEK Inhibitor in Patients With RASopathy
Gianluca D’Onofrio, Marie‐Ange Delrue, Anne Lortie, et al.
Pediatric Neurology (2023) Vol. 148, pp. 148-151
Closed Access | Times Cited: 6
Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway
Diana Carli, Nicoletta Resta, Giovanni Battista Ferrero, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 520-529
Closed Access | Times Cited: 8
Molecular Basis and Diagnostic Approach to Isolated and Syndromic Lateralized Overgrowth in Childhood
Simone Bellucca, Diana Carli, Andrea Gazzin, et al.
The Journal of Pediatrics (2024) Vol. 274, pp. 114177-114177
Open Access | Times Cited: 1
Braf-mutant Schwann cells divert to a repair phenotype to induce congenital demyelinating neuropathy
Elise Maréchal, Patrice Quintana, Daniel Aldea, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
Unilateral verrucous facial skin lesions and amourosis in an infant
Marlies Wruhs, Esther Mzumara, Robert Feldmann, et al.
JDDG Journal der Deutschen Dermatologischen Gesellschaft (2024) Vol. 22, Iss. 8, pp. 1172-1174
Closed Access
Etiología de la hipofosfatemia en el adulto
Nuria Puente, Carmen Valero, José A. Riancho
Medicina Clínica (2024)
Closed Access
Einseitige faziale verruköse Hautveränderungen und Amaurose bei einem Säugling
Marlies Wruhs, Esther Mzumara, Robert Feldmann, et al.
JDDG Journal der Deutschen Dermatologischen Gesellschaft (2024) Vol. 22, Iss. 8, pp. 1172-1174
Closed Access
Neurofibromatosis Type I (NF1) and Bone Involvement in a pediatric setting: Insights from FGF23 Levels
Giulia Rodari, Valeria Citterio, Masami Ikehata, et al.
Research Square (Research Square) (2024)
Open Access
Mosaic RASopathies
Summer N. Meyer, Nick Love, Maija Kiuru
(2024), pp. 729-755
Closed Access
Ophthalmic Manifestations in RASopathies
Suma P. Shankar
(2024), pp. 679-706
Closed Access
Precision Medicine in RASopathies: Tailored Disease Management Through Enhanced Approaches, Disease Delineation, and Pathway-Specific Therapies
Vanina Taliercio, David Viskochil
(2024), pp. 319-328
Closed Access
Clinical Studies and Small Molecule Inhibitors for RASopathy Treatment
Andrea M. Gross, Marielle E. Yohe, Brigitte C. Widemann
(2024), pp. 895-908
Closed Access
Rickets: The Skeletal Disorders of Impaired Calcium or Phosphate Availability
Kaitlin Leopold, Peter J. Tebben
Pediatric Endocrinology (2024), pp. 527-556
Closed Access
Etiology of hypophosphatemia in adults
Nuria Puente, Carmen Valero, José A. Riancho
Medicina Clínica (English Edition) (2024)
Closed Access
Calcitriol/phosphates/trametinib

Reactions Weekly (2023) Vol. 1941, Iss. 1, pp. 115-115
Closed Access
Phacomatosis spilosebacea and cutaneous skeletal hypophosphatemia syndrome
Daniele Torchia
Bone (2022) Vol. 168, pp. 116649-116649
Closed Access
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