1. Puente, Xose S, Beà, Silvia, Valdés-Mas, Rafael, López-Otín, Carlos, Campo, Elías. 2015. Non-coding recurrent mutations in chronic lymphocytic leukaemia. In Nature, 526, 519-24. doi:10.1038/nature14666. https://pubmed.ncbi.nlm.nih.gov/26200345/
2. Hu, Xiangjing, Shen, Bin, Liao, Shangying, Huang, Xingxu, Han, Chunsheng. 2017. Gene knockout of Zmym3 in mice arrests spermatogenesis at meiotic metaphase with defects in spindle assembly checkpoint. In Cell death & disease, 8, e2910. doi:10.1038/cddis.2017.228. https://pubmed.ncbi.nlm.nih.gov/28661483/
3. Malcher, Agnieszka, Stokowy, Tomasz, Berman, Andrea, Yatsenko, Alexander N, Kurpisz, Maciej K. 2022. Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia. In Andrology, 10, 1605-1624. doi:10.1111/andr.13269. https://pubmed.ncbi.nlm.nih.gov/36017582/
4. Tirode, Franck, Surdez, Didier, Ma, Xiaotu, Zhang, Jinghui, Delattre, Olivier. 2014. Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. In Cancer discovery, 4, 1342-53. doi:10.1158/2159-8290.CD-14-0622. https://pubmed.ncbi.nlm.nih.gov/25223734/
5. Hiatt, Susan M, Trajkova, Slavica, Sebastiano, Matteo Rossi, Myers, Richard M, Cooper, Gregory M. 2022. Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. In American journal of human genetics, 110, 215-227. doi:10.1016/j.ajhg.2022.12.007. https://pubmed.ncbi.nlm.nih.gov/36586412/
6. Afshar, H, Khamse, S, Alizadeh, F, Kowsari, A, Ohadi, M. 2020. Evolving evidence on a link between the ZMYM3 exceptionally long GA-STR and human cognition. In Scientific reports, 10, 19454. doi:10.1038/s41598-020-76461-z. https://pubmed.ncbi.nlm.nih.gov/33173136/
7. Alizadeh, F, Bozorgmehr, A, Tavakkoly-Bazzaz, J, Ohadi, M. 2018. Skewing of the genetic architecture at the ZMYM3 human-specific 5' UTR short tandem repeat in schizophrenia. In Molecular genetics and genomics : MGG, 293, 747-752. doi:10.1007/s00438-018-1415-8. https://pubmed.ncbi.nlm.nih.gov/29332164/