1. Kim, Jihye, Kwon, Jun Tae, Jeong, Juri, Eddy, Edward M, Cho, Chunghee. 2018. SPATC1L maintains the integrity of the sperm head-tail junction. In EMBO reports, 19, . doi:10.15252/embr.201845991. https://pubmed.ncbi.nlm.nih.gov/30026308/
2. Morgan, Anna, Vuckovic, Dragana, Krishnamoorthy, Navaneethakrishnan, Gasparini, Paolo, Girotto, Giorgia. 2018. Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. In European journal of human genetics : EJHG, 27, 70-79. doi:10.1038/s41431-018-0229-9. https://pubmed.ncbi.nlm.nih.gov/30177775/
3. Katrinli, Seyma, Zheng, Yuanchao, Gautam, Aarti, Ressler, Kerry J, Smith, Alicia K. 2020. PTSD is associated with increased DNA methylation across regions of HLA-DPB1 and SPATC1L. In Brain, behavior, and immunity, 91, 429-436. doi:10.1016/j.bbi.2020.10.023. https://pubmed.ncbi.nlm.nih.gov/33152445/
4. Li, You-Zhu, Li, Na, Liu, Wen-Sheng, Lu, Zhong-Xian, Zhang, Fu-Xing. . Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility. In Asian journal of andrology, 24, 67-72. doi:10.4103/aja.aja_56_21. https://pubmed.ncbi.nlm.nih.gov/34213489/
5. Yamada, Yoshiji, Sakuma, Jun, Takeuchi, Ichiro, Arai, Tomio, Tanaka, Masashi. 2017. Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies. In International journal of molecular medicine, 39, 1091-1100. doi:10.3892/ijmm.2017.2927. https://pubmed.ncbi.nlm.nih.gov/28339009/
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