1. Gadad, Bharathi S, Raj, Prithvi, Jha, Manish K, Wakeland, Edward K, Trivedi, Madhukar H. 2018. Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial. In Molecular neuropsychiatry, 4, 7-19. doi:10.1159/000487321. https://pubmed.ncbi.nlm.nih.gov/29998114/
2. Lan, Yu, Wu, Zhaoming, Liu, Han, Jiang, Rulang. 2024. Lineage-specific requirements of Alx4 function in craniofacial and hair development. In Developmental dynamics : an official publication of the American Association of Anatomists, 253, 940-948. doi:10.1002/dvdy.705. https://pubmed.ncbi.nlm.nih.gov/38481039/
3. Buitkamp, Johannes, Semmer, Jördis, Schmaußer, Michael, Schade, Benjamin. 2022. A case of tibial hemimelia in a German Galloway calf is associated with a novel mutation in the ALX4 gene. In Animal genetics, 54, 220-221. doi:10.1111/age.13290. https://pubmed.ncbi.nlm.nih.gov/36585373/
4. Salehi, Rasoul, Atapour, Norollah, Vatandoust, Nasimeh, Ahangari, Fatemeh, Salehi, Ahmad Reza. 2015. Methylation pattern of ALX4 gene promoter as a potential biomarker for blood-based early detection of colorectal cancer. In Advanced biomedical research, 4, 252. doi:10.4103/2277-9175.170677. https://pubmed.ncbi.nlm.nih.gov/26918234/
5. Zilla, Megan L, Korentzelos, Dimitrios, Lebamoff, Jacob, Naous, Rana, John, Ivy. 2024. ALX4::NCOA2 rearranged round and spindle cell sarcoma. In Histopathology, 85, 201-204. doi:10.1111/his.15189. https://pubmed.ncbi.nlm.nih.gov/38566331/
6. Wu, Y Q, Badano, J L, McCaskill, C, Potocki, L, Shaffer, L G. 2000. Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. In American journal of human genetics, 67, 1327-32. doi:. https://pubmed.ncbi.nlm.nih.gov/11017806/
智鼠故事 
