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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:

Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group
Simone Hettmer, Guillaume Dachy, Guido Seitz, et al.
Familial Cancer (2020) Vol. 20, Iss. 4, pp. 327-336
Open Access | Times Cited: 21

Showing 21 citing articles:

Novel PDGFRB Gene Fusions in Two Cases of Infantile Myofibromatosis
Federica Boccia, Sabina Barresi, Silvia Vallese, et al.
Genes Chromosomes and Cancer (2025) Vol. 64, Iss. 1
Closed Access
Genetic susceptibility in children, adolescents, and young adults diagnosed with soft-tissue sarcomas
Julia Würtemberger, Tim Ripperger, Christian Vokuhl, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 5, pp. 104718-104718
Closed Access | Times Cited: 6
Novel COL4A1‐VEGFD gene fusion in myofibroma
Guillaume Dachy, S. Fraitag, Boutaina Boulouadnine, et al.
Journal of Cellular and Molecular Medicine (2021) Vol. 25, Iss. 9, pp. 4387-4394
Open Access | Times Cited: 11
A germline PDGFRB splice site variant associated with infantile myofibromatosis and resistance to imatinib
Boutaina Boulouadnine, Mathilde Filser, Camille Leducq, et al.
Genetics in Medicine (2024) Vol. 27, Iss. 2, pp. 101334-101334
Closed Access | Times Cited: 1
Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome–Based Resolution of Isoform Complexity
Anthony R. Miller, Saranga Wijeratne, Sean McGrath, et al.
Journal of Molecular Diagnostics (2022) Vol. 24, Iss. 12, pp. 1292-1306
Open Access | Times Cited: 7
Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
Monika Sparber‐Sauer, Christian Vokuhl, Guido Seitz, et al.
Pediatric Blood & Cancer (2021) Vol. 69, Iss. 3
Open Access | Times Cited: 9
A Unique Presentation of Multicentric Myofibromatosis in the Masseter Muscle of a Pediatric Patient
Elena P. Padilla, Katie Voelz, Tony L Kille
Ear Nose & Throat Journal (2022), pp. 014556132211259-014556132211259
Closed Access | Times Cited: 3
Aggressive infantile myofibromatosis with intestinal involvement
Tristan Römer, Norbert Wagner, Till Braunschweig, et al.
Molecular and Cellular Pediatrics (2021) Vol. 8, Iss. 1
Open Access | Times Cited: 4
Intramasseteric Solitary Myofibroma: A Case Report
Zakaria El Hafi, Eden Ayele Habte, khalil Hjaouj, et al.
Ear Nose & Throat Journal (2024)
Open Access
A Unique Presentation of Nodular Masses in Infancy
S.R. Velagala, Erica Heiden, Sean Lisse, et al.
NeoReviews (2024) Vol. 25, Iss. 6, pp. e370-e374
Closed Access
Autosomal Dominant Multicentric Infantile Myofibromatosis: A Case Report
Jessica Justus Kurian, M. Lyle
Pediatric Hematology Oncology Journal (2024) Vol. 9, Iss. 4, pp. 231-234
Open Access
Soft Tissue Neoplasms of the Head and Neck Region
Hana Saffar, Parisa Mokhles
Springer eBooks (2024), pp. 1-46
Closed Access
A Rare Case of Infantile Myofibromatosis With Intra Cranial Involvement
Fatima Zahrae El Mansoury, Zakia El Yousfi, Ayman El Farouki, et al.
Global Pediatric Health (2024) Vol. 11
Open Access
Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences
Alessio Conte, Damiana De Padova, S. Giglio, et al.
Journal of Pediatric Hematology/Oncology (2024) Vol. 46, Iss. 7, pp. e528-e530
Closed Access
Pneumothorax revealing late recurrence of infantile myofibromatosis
Clémence Yguel, J Vignaud, Angélica Tiotiu
Annals of Thoracic Medicine (2024) Vol. 19, Iss. 4, pp. 290-292
Open Access
Generalized Infantile Myofibromatosis with Extensive Small Bowel Involvement in a Neonate
Judit Pauline Schubert, Wilhelm Wößmann, Ingo Königs, et al.
Zeitschrift für Geburtshilfe und Neonatologie (2023) Vol. 227, Iss. 03, pp. 231-235
Closed Access | Times Cited: 1
True radial artery aneurysm in a patient with somatic mosaicism for a mutation in platelet-derived growth factor receptor β gene
Sherene Shalhub, Lisa Hysa, Peter H. Byers, et al.
Journal of Vascular Surgery Cases and Innovative Techniques (2021) Vol. 7, Iss. 3, pp. 567-571
Open Access | Times Cited: 2
Solitary cutaneous infantile myofibroma as a hallmark of myofibromatosis: Two cases and review of the literature
Mitchell Braun, Micah Pascual, Thaddeus W. Mully, et al.
Pediatric Dermatology (2022) Vol. 39, Iss. 3, pp. 438-442
Closed Access | Times Cited: 1
A review of paediatric maxillofacial bone pathology
Amrita Jay, Hannah Cottom, Reshma Agrawal
Diagnostic histopathology (2022) Vol. 28, Iss. 5, pp. 228-241
Closed Access | Times Cited: 1
Multicentric infantile myofibromatosis with extensive involvement limited to bone
María Luque-Cabal, Estíbaliz Obregón-Martínez, María Díez-Blanco, et al.
Skeletal Radiology (2021) Vol. 51, Iss. 7, pp. 1503-1510
Closed Access | Times Cited: 1
Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis
Kelly K. Barry, Jaclyn Schienda, James J. Morrow, et al.
Pediatric Blood & Cancer (2023) Vol. 70, Iss. 6
Closed Access
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