1. Sutani, Akito, Shima, Hirohito, Hijikata, Atsushi, Fukami, Maki, Kashimada, Kenichi. 2019. WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome. In European journal of medical genetics, 63, 103626. doi:10.1016/j.ejmg.2019.01.016. https://pubmed.ncbi.nlm.nih.gov/30711679/
2. Katoh, Masuko, Katoh, Masaru. . FGFR2 and WDR11 are neighboring oncogene and tumor suppressor gene on human chromosome 10q26. In International journal of oncology, 22, 1155-9. doi:. https://pubmed.ncbi.nlm.nih.gov/12684685/
3. Kim, Hyung-Goo, Layman, Lawrence C. 2011. The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. In Molecular and cellular endocrinology, 346, 74-83. doi:10.1016/j.mce.2011.07.013. https://pubmed.ncbi.nlm.nih.gov/21856375/
4. Chernova, O B, Hunyadi, A, Malaj, E, Roe, B, Cowell, J K. . A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells. In Oncogene, 20, 5378-92. doi:. https://pubmed.ncbi.nlm.nih.gov/11536051/
5. Kim, Yeon-Joo, Osborn, Daniel Ps, Lee, Ji-Young, Layman, Lawrence C, Kim, Soo-Hyun. 2017. WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome. In EMBO reports, 19, 269-289. doi:10.15252/embr.201744632. https://pubmed.ncbi.nlm.nih.gov/29263200/
6. Lee, Jiyoung, Kim, Yeonjoo, Ataliotis, Paris, Layman, Lawrence C, Kim, Soo-Hyun. 2023. Coordination of canonical and noncanonical Hedgehog signalling pathways mediated by WDR11 during primordial germ cell development. In Scientific reports, 13, 12309. doi:10.1038/s41598-023-38017-9. https://pubmed.ncbi.nlm.nih.gov/37516749/
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