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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:

A somatic activating KRAS variant identified in an affected lesion of a patient with Gorham–Stout disease
Akifumi Nozawa, Michio Ozeki, Tetsuya Niihori, et al.
Journal of Human Genetics (2020) Vol. 65, Iss. 11, pp. 995-1001
Closed Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

Lymphatic Malformations: Genetics, Mechanisms and Therapeutic Strategies
Taija Mäkinen, Laurence M. Boon, Miikka Vikkula, et al.
Circulation Research (2021) Vol. 129, Iss. 1, pp. 136-154
Open Access | Times Cited: 153
Primary lymphoedema
Pascal Brouillard, Marlys H. Witte, Robert P. Erickson, et al.
Nature Reviews Disease Primers (2021) Vol. 7, Iss. 1
Closed Access | Times Cited: 62
KRAS-driven model of Gorham-Stout disease effectively treated with trametinib
Nassim Homayun Sepehr, Anna McCarter, Raphaël Helaers, et al.
JCI Insight (2021)
Open Access | Times Cited: 58
Genomic profiling informs diagnoses and treatment in vascular anomalies
Dong Li, Sarah E. Sheppard, Michael March, et al.
Nature Medicine (2023) Vol. 29, Iss. 6, pp. 1530-1539
Open Access | Times Cited: 32
Lymphatic malformations: mechanistic insights and evolving therapeutic frontiers
Milena Petkova, Ingvar Ferby, Taija Mäkinen
Journal of Clinical Investigation (2024) Vol. 134, Iss. 6
Open Access | Times Cited: 9
Homeostatic maintenance of the lymphatic vasculature
Simon Stritt, Katarzyna Koltowska, Taija Mäkinen
Trends in Molecular Medicine (2021) Vol. 27, Iss. 10, pp. 955-970
Open Access | Times Cited: 55
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
Sarah E. Sheppard, Michael March, Christoph Seiler, et al.
JCI Insight (2023) Vol. 8, Iss. 9
Open Access | Times Cited: 19
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype–Phenotype Correlations
Vanessa F. Schmidt, Friedrich Kapp, Constantin Goldann, et al.
Journal of the American Heart Association (2024) Vol. 13, Iss. 8
Open Access | Times Cited: 7
Lymphatic Anomalies in Children: Update on Imaging Diagnosis, Genetics, and Treatment
Elizabeth Snyder, Asha Sarma, Alexandra J. Borst, et al.
American Journal of Roentgenology (2022) Vol. 218, Iss. 6, pp. 1089-1101
Closed Access | Times Cited: 28
Dysregulation of Lymphatic Endothelial VEGFR3 Signaling in Disease
Kevin Kuonqui, Adana-Christine Campbell, Ananta Sarker, et al.
Cells (2023) Vol. 13, Iss. 1, pp. 68-68
Open Access | Times Cited: 16
Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants
Caitlin A. Chang, Renée Perrier, Kyle C. Kurek, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 9, pp. 2829-2845
Closed Access | Times Cited: 31
Vascular malformations: An overview of their molecular pathways, detection of mutational profiles and subsequent targets for drug therapy
Ann Mansur, Ivan Radovanovic
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 11
Trastornos que afectan a la vascularización cutánea: malformaciones vasculares
J.-M. L’Orphelin, A. Dompmartin
EMC - Dermatología (2025) Vol. 59, Iss. 1, pp. 1-13
Closed Access
RAS Pathway Mutations and Therapeutics in Vascular Anomalies
Sara Alharbi, Svatava Merkle, Adrienne M. Hammill, et al.
Pediatric Blood & Cancer (2025)
Open Access
Association of Somatic KRAS Variants with Osteolysis in Arteriovenous Malformations
María San Basilio, Lara Rodríguez‐Laguna, Paloma Triana, et al.
European Journal of Pediatric Surgery (2025)
Closed Access
The role of key biomarkers in lymphatic malformation: An updated review
Mohammad-Hadi Saeed Modaghegh, Hamid Tanzadehpanah, Mohammad Mahdi Kamyar, et al.
The Journal of Gene Medicine (2024) Vol. 26, Iss. 2
Closed Access | Times Cited: 3
How we approach genetics in the diagnosis and management of vascular anomalies
Bhuvana A. Setty, Katie Wusik, Adrienne M. Hammill
Pediatric Blood & Cancer (2022) Vol. 69, Iss. S3
Closed Access | Times Cited: 12
Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function
Lorenzo M. Fernandes, Jeffrey D. Tresemer, Jing Zhang, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 7
Complex lymphatic anomalies: Molecular landscape and medical management
Alexandra J. Borst, Allison Britt, Denise M. Adams
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151422-151422
Closed Access | Times Cited: 2
Complex Lymphatic Anomalies: Report on a Patient Registry Using the Latest Diagnostic Guidelines
Themis‐Areti A. Andreoti, Sebastian Berg, Annegret Holm, et al.
Lymphatic Research and Biology (2023)
Closed Access | Times Cited: 6
Lymphatic endothelial cell-specific NRAS p.Q61R mutant embryos show abnormal lymphatic vessel morphogenesis
Akifumi Nozawa, Taiki Abe, Tetsuya Niihori, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 16, pp. 1420-1428
Closed Access | Times Cited: 2
Molecular pathways and possible therapies for head and neck vascular anomalies
Julien Coulie, Laurence M. Boon, Miikka Vikkula
Journal of Oral Pathology and Medicine (2022) Vol. 51, Iss. 10, pp. 878-887
Closed Access | Times Cited: 9
Osteopathy in Complex Lymphatic Anomalies
Ernesto Solorzano, Andrew L Alejo, Hope C. Ball, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8258-8258
Open Access | Times Cited: 8
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
破骨细胞中信号素3A表达的减少导致小鼠GSD模型中淋巴管扩张
Dongfang Zhang, Hao Xu, Chi Qin, et al.
Journal of Zhejiang University SCIENCE B (2024) Vol. 25, Iss. 1, pp. 38-50
Open Access | Times Cited: 1
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