1. Tadayoni Nia, Amin, Bazi, Zahra, Khosravi, Ayyoob, Oladnabi, Morteza. 2021. WDR81 Gene Silencing Can Reduce Exosome Levels in Human U87-MG Glioblastoma Cells. In Journal of molecular neuroscience : MN, 71, 1696-1702. doi:10.1007/s12031-021-01849-z. https://pubmed.ncbi.nlm.nih.gov/33954857/
2. Traka, Maria, Millen, Kathleen J, Collins, Devon, Gomez, Christopher M, Popko, Brian. . WDR81 is necessary for purkinje and photoreceptor cell survival. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 33, 6834-44. doi:10.1523/JNEUROSCI.2394-12.2013. https://pubmed.ncbi.nlm.nih.gov/23595742/
3. Doldur-Balli, Fusun, Ozel, Mehmet Neset, Gulsuner, Suleyman, Konu, Ozlen, Adams, Michelle M. 2015. Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). In BMC neuroscience, 16, 96. doi:10.1186/s12868-015-0229-4. https://pubmed.ncbi.nlm.nih.gov/27390838/
4. Rapiteanu, Radu, Davis, Luther J, Williamson, James C, Paul Luzio, J, Lehner, Paul J. 2016. A Genetic Screen Identifies a Critical Role for the WDR81-WDR91 Complex in the Trafficking and Degradation of Tetherin. In Traffic (Copenhagen, Denmark), 17, 940-58. doi:10.1111/tra.12409. https://pubmed.ncbi.nlm.nih.gov/27126989/
5. Cavallin, Mara, Rujano, Maria A, Bednarek, Nathalie, Thomas, Sophie, Bahi-Buisson, Nadia. . WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells. In Brain : a journal of neurology, 140, 2597-2609. doi:10.1093/brain/awx218. https://pubmed.ncbi.nlm.nih.gov/28969387/
6. Kalmár, Tibor, Szakszon, Katalin, Maróti, Zoltán, Bereczki, Csaba, Sztriha, László. 2020. A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia. In Journal of pediatric genetics, 10, 159-163. doi:10.1055/s-0040-1712916. https://pubmed.ncbi.nlm.nih.gov/33996189/
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