
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:
Molecular and clinical presentation of UBA1-mutated myelodysplastic syndromes
Maria Sirenko, Elsa Bernard, Maria Creignou, et al.
Blood (2024) Vol. 144, Iss. 11, pp. 1221-1229
Closed Access | Times Cited: 14
Maria Sirenko, Elsa Bernard, Maria Creignou, et al.
Blood (2024) Vol. 144, Iss. 11, pp. 1221-1229
Closed Access | Times Cited: 14
Showing 14 citing articles:
VEXAS associated Acute Disseminated Encephalo-Myelitis (ADEM)-like syndrome: a case report and review of the literature
Gregorio Maria Bergonzi, Corrado Campochiaro, Alessandro Tomelleri, et al.
Current Research in Translational Medicine (2025) Vol. 73, Iss. 3, pp. 103505-103505
Closed Access | Times Cited: 1
Gregorio Maria Bergonzi, Corrado Campochiaro, Alessandro Tomelleri, et al.
Current Research in Translational Medicine (2025) Vol. 73, Iss. 3, pp. 103505-103505
Closed Access | Times Cited: 1
Hypomethylating agents for patients with VEXAS without myelodysplastic syndrome: Clinical outcome and longitudinal follow‐up of vacuolization and UBA1 clonal dynamics
José Ramón Álamo Moreno, Lucía Mont‐de Torres, Sandra Castaño‐Díez, et al.
British Journal of Haematology (2025) Vol. 206, Iss. 2, pp. 565-575
Closed Access
José Ramón Álamo Moreno, Lucía Mont‐de Torres, Sandra Castaño‐Díez, et al.
British Journal of Haematology (2025) Vol. 206, Iss. 2, pp. 565-575
Closed Access
VEXAS Syndrome: A Perspective Focus on Genetics and Hematological Manifestations
Evdoxia Sapountzi, Genevieve M. Crane, Jane Whitney Gibson, et al.
Genetic Testing and Molecular Biomarkers (2025)
Closed Access
Evdoxia Sapountzi, Genevieve M. Crane, Jane Whitney Gibson, et al.
Genetic Testing and Molecular Biomarkers (2025)
Closed Access
UBA protein family: An emerging set of E1 ubiquitin ligases in cancer—A review
Huhu Zhang, Fulin Sun, Hongyu Cao, et al.
International Journal of Biological Macromolecules (2025), pp. 142277-142277
Closed Access
Huhu Zhang, Fulin Sun, Hongyu Cao, et al.
International Journal of Biological Macromolecules (2025), pp. 142277-142277
Closed Access
Germline UBA1 Variant With Somatic Amplification in a Woman With Inflammatory Diseases and Myelodysplastic Syndrome
Maria Creignou, Maria Sirenko, Pedro Luís Moura, et al.
Annals of Internal Medicine (2025)
Closed Access
Maria Creignou, Maria Sirenko, Pedro Luís Moura, et al.
Annals of Internal Medicine (2025)
Closed Access
Rapid screening and monitoring of UBA1 mutations in VEXAS syndrome.
Iván Martín, Elvira Mora, Rafael Hernani, et al.
Journal of Molecular Diagnostics (2025)
Closed Access
Iván Martín, Elvira Mora, Rafael Hernani, et al.
Journal of Molecular Diagnostics (2025)
Closed Access
Allogenic haematopoietic stem cell transplantation in VEXAS: A review of 33 patients
Syed Ali, Carmelo Gurnari
Clinical Rheumatology (2024)
Open Access | Times Cited: 3
Syed Ali, Carmelo Gurnari
Clinical Rheumatology (2024)
Open Access | Times Cited: 3
Role of allogeneic hematopoietic cell transplantation in VEXAS syndrome
Ajoy L. Dias, Emma M. Groarke, Dennis D. Hickstein, et al.
Annals of Hematology (2024) Vol. 103, Iss. 11, pp. 4427-4436
Open Access
Ajoy L. Dias, Emma M. Groarke, Dennis D. Hickstein, et al.
Annals of Hematology (2024) Vol. 103, Iss. 11, pp. 4427-4436
Open Access
UBA1 dysfunction in VEXAS and cancer
Maki Sakuma, Torsten Haferlach, Wencke Walter
Oncotarget (2024) Vol. 15, Iss. 1, pp. 644-658
Open Access
Maki Sakuma, Torsten Haferlach, Wencke Walter
Oncotarget (2024) Vol. 15, Iss. 1, pp. 644-658
Open Access
VEXAS syndrome: an adult-onset autoinflammatory disorder with underlying somatic mutation
Ina Kötter, Martin Krusche
Current Opinion in Rheumatology (2024) Vol. 37, Iss. 1, pp. 21-31
Closed Access
Ina Kötter, Martin Krusche
Current Opinion in Rheumatology (2024) Vol. 37, Iss. 1, pp. 21-31
Closed Access
Rapid growth of acquired UBA1 mutations predisposes male patients to low-risk MDS
Peng Li, Fnu Alnoor, Wei Xie, et al.
Leukemia (2024)
Closed Access
Peng Li, Fnu Alnoor, Wei Xie, et al.
Leukemia (2024)
Closed Access
Methodology and clinical utility of longitudinal UBA1 tracking in VEXAS syndrome
Carmelo Gurnari, Elisa Galossi, Eleonora Lumia, et al.
British Journal of Haematology (2024)
Open Access
Carmelo Gurnari, Elisa Galossi, Eleonora Lumia, et al.
British Journal of Haematology (2024)
Open Access
Understanding Myelodysplasia and Inflammation Through the Lense of VEXAS Syndrome: A Review
Louis Wolff, Leo Caratsch, Lin‐Pierre Zhao, et al.
Cells (2024) Vol. 13, Iss. 22, pp. 1890-1890
Open Access
Louis Wolff, Leo Caratsch, Lin‐Pierre Zhao, et al.
Cells (2024) Vol. 13, Iss. 22, pp. 1890-1890
Open Access
Expanding the VEXAS diagnostic workup: the role of peripheral blood cytological analysis
Chiara Baggio, Francesca Oliviero, Roberto Padoan, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access
Chiara Baggio, Francesca Oliviero, Roberto Padoan, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access