References

Basso-Valentina, Francesca, Alessandro Donada, Vladimir T Manchev, et al. 2023. “ANKRD26 Is a New Regulator of Type i Cytokine Receptor Signaling in Normal and Pathological Hematopoiesis.” Haematologica 108 (8): 2130–45. https://doi.org/10.3324/haematol.2022.282049.

Bluteau, Dominique, Alessandra Balduini, Nathalie Balayn, et al. 2014. “Thrombocytopenia-Associated Mutations in the ANKRD26 Regulatory Region Induce MAPK Hyperactivation.” Journal of Clinical Investigation 124 (2): 580–91. https://doi.org/10.1172/jci71861.

Creignou, Maria, Maria Sirenko, Pedro L. Moura, et al. 2025. “Germline UBA1 Variant with Somatic Amplification in a Woman with Inflammatory Diseases and Myelodysplastic Syndrome.” Annals of Internal Medicine 178 (2): 300–304. https://doi.org/10.7326/l24-0125.

Deuitch, Natalie T., Lylach Haizler-Cohen, Amra Kajdic, et al. 2025. “Pregnancy and Delivery Outcomes in Individuals with RUNX1-Familial Platelet Disorder.” British Journal of Haematology, ahead of print, May 29. https://doi.org/10.1111/bjh.20194.

Knuth, Donald E. 1984. “Literate Programming.” Comput. J. (USA) 27 (2): 97–111. https://doi.org/10.1093/comjnl/27.2.97.

Noris, Patrizia, Silverio Perrotta, Marco Seri, et al. 2011. “Mutations in ANKRD26 Are Responsible for a Frequent Form of Inherited Thrombocytopenia: Analysis of 78 Patients from 21 Families.” Blood 117 (24): 6673–80. https://doi.org/10.1182/blood-2011-02-336537.

Wahlster, Lara, Lucy A Godley, Jason X Cheng, et al. 2025. “ANKRD26-Related Thrombocytopenia 2 with a Baseline Increase in Blasts: Implications for Clinical Surveillance.” Blood Journal, ahead of print, May 7. https://doi.org/10.1182/blood.2024027368.

Wahlster, Lara, Jeffrey M. Verboon, Leif S. Ludwig, et al. 2021. “Familial Thrombocytopenia Due to a Complex Structural Variant Resulting in a WAC-ANKRD26 Fusion Transcript.” Journal of Experimental Medicine 218 (6). https://doi.org/10.1084/jem.20210444.