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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:

Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosis
Michio Ozeki, Yoko Aoki, Akifumi Nozawa, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 62

Showing 26-50 of 62 citing articles:

The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms
Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza, Laura Florea, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12199-12199
Open Access | Times Cited: 11
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
Changes in cell morphology and function induced by the NRAS Q61R mutation in lymphatic endothelial cells
Shiho Yasue, Michio Ozeki, Akifumi Nozawa, et al.
PLoS ONE (2024) Vol. 19, Iss. 5, pp. e0289187-e0289187
Open Access | Times Cited: 2
Targeted therapies for vascular malformations
Gavin Kane, Israel Fernández‐Pineda
Frontiers in Medicine (2024) Vol. 11
Open 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
A high-throughput zebrafish screen identifies novel candidate treatments for Kaposiform Lymphangiomatosis (KLA)
Ivan Bassi, Amani Jabali, Naama Farag, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Multimodal therapeutic approach for a severe case of kaposiform lymphangiomatosis from procedural interventions to targeted therapies
Antoine Gourmel, Niina Kleiber, Victor Kokta, et al.
Pediatric Blood & Cancer (2024) Vol. 71, Iss. 8
Closed Access | Times Cited: 1
EML4::ALK fusions in complex lymphatic malformations
Beth Apsel Winger, W. Patrick Devine, Edward C. Hsiao, et al.
Pediatric Blood & Cancer (2023) Vol. 70, Iss. 9
Open Access | Times Cited: 2
Characterization of kaposiform lymphangiomatosis tissue‐derived cells
Akifumi Nozawa, Michio Ozeki, Shiho Yasue, et al.
Pediatric Blood & Cancer (2021) Vol. 68, Iss. 10
Closed Access | Times Cited: 4
Cell-free DNA from plasma as a promising alternative for detection of gene mutations in patients with Maffucci syndrome
Yi Sun, Xindong Fan, Yamin Rao, et al.
Hereditas (2022) Vol. 159, Iss. 1
Open Access | Times Cited: 3
Detection of NRAS Mutation in Kaposiform Lymphangiomatosis Using Cell-free DNA from Plasma
Fiona Lynch, Veronika Dvořáková, Alan D. Irvine
Journal of Vascular Anomalies (2023) Vol. 4, Iss. 1, pp. e062-e062
Open Access | Times Cited: 1
Klippel-Trenaunay Syndrome: To Be or Not to Be Afraid
Gautam N Vekariya, Sudhir Singh, Sabha Neazee, et al.
Cureus (2024)
Open Access
Disorders Affecting Cutaneous Vasculature
A. Dompmartin, Nicole Revençu, Laurence M. Boon, et al.
(2024), pp. 1-33
Closed Access
A multi-step approach to overcome challenges in the management of head and neck lymphatic malformations, and response to treatment
Valentina Trevisan, Eugenio De Corso, Germana Viscogliosi, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Vascular Malformations: Clinical Features, Molecular Genetics, and Modeling
M. D. Ceren Yilmaz, M. D. Ibrahim Vargel
(2024), pp. 67-96
Closed Access
Central Conducting Lymphatic Anomalies
Hui‐Qi Qu, Dong Li, Hákon Hákonarson
(2024), pp. 215-239
Closed Access
Molecular landscape and classification of vascular anomalies
Emmanuel Seront, Angela Queisser, Laurence M. Boon, et al.
Hematology (2024) Vol. 2024, Iss. 1, pp. 700-708
Closed Access
Klippel-Trenaunay Syndrome: A Case Study of Severe Anemia in a Rare Vascular Disorder
Usamah Al‐Anbagi, Ibrahim Elmakaty, Hadeel M Al-Zoubi, et al.
Cureus (2024)
Open Access
Troubles affectant la vascularisation cutanée : malformations vasculaires
J.-M. L’Orphelin, A. Dompmartin
EMC - Dermatologie (2024) Vol. 26, Iss. 4, pp. 1-13
Closed Access
Newcomers in Vascular Anomalies
Alyaa Al‐Ibraheemi
Surgical pathology clinics (2020) Vol. 13, Iss. 4, pp. 719-728
Closed Access | Times Cited: 2
Update December 2019
Francine Blei
Lymphatic Research and Biology (2019) Vol. 17, Iss. 6, pp. 680-695
Closed Access | Times Cited: 1
Lymphatic vascular anomalies and dysfunction
Christian El Amm, Federico Silva-Palacios, Xin Geng, et al.
Elsevier eBooks (2022), pp. 301-310
Closed Access | Times Cited: 1
A Case of Multifocal Lymphangioendotheliomatosis With Thrombocytopenia and Changes in Coagulopathy
D. Nagao, Michio Ozeki, Akifumi Nozawa, et al.
Journal of Pediatric Hematology/Oncology (2022) Vol. 45, Iss. 3, pp. e384-e388
Closed Access | Times Cited: 1

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