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2. Bayat, Allan, Liu, Zhenjiang, Luo, Sheng, Liao, Weiping, Ren, Dejian. 2023. A new neurodevelopmental disorder linked to heterozygous variants in UNC79. In Genetics in medicine : official journal of the American College of Medical Genetics, 25, 100894. doi:10.1016/j.gim.2023.100894. https://pubmed.ncbi.nlm.nih.gov/37183800/
3. Chen, Hui-Wen, Ma, Chung-Pei, Chin, En, Huang, Po-Jung, Tan, Bertrand Chin-Ming. 2024. Imbalance in Unc80 RNA Editing Disrupts Dynamic Neuronal Activity and Olfactory Perception. In International journal of molecular sciences, 25, . doi:10.3390/ijms25115985. https://pubmed.ncbi.nlm.nih.gov/38892173/
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5. Heczko, Lucie, Liška, Václav, Vyčítal, Ondřej, Hlaváč, Viktor, Souček, Pavel. 2024. Targeted panel sequencing of pharmacogenes and oncodrivers in colorectal cancer patients reveals genes with prognostic significance. In Human genomics, 18, 83. doi:10.1186/s40246-024-00644-2. https://pubmed.ncbi.nlm.nih.gov/39030589/
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7. Lear, Bridget C, Darrah, Eric J, Aldrich, Benjamin T, Nash, Howard A, Allada, Ravi. 2013. UNC79 and UNC80, putative auxiliary subunits of the NARROW ABDOMEN ion channel, are indispensable for robust circadian locomotor rhythms in Drosophila. In PloS one, 8, e78147. doi:10.1371/journal.pone.0078147. https://pubmed.ncbi.nlm.nih.gov/24223770/
8. Stray-Pedersen, Asbjørg, Cobben, Jan-Maarten, Prescott, Trine E, Ren, Dejian, Yoon, Grace. 2015. Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. In American journal of human genetics, 98, 202-9. doi:10.1016/j.ajhg.2015.11.004. https://pubmed.ncbi.nlm.nih.gov/26708751/
9. Wie, Jinhong, Bharthur, Apoorva, Wolfgang, Morgan, Zhou, Yandong, Ren, Dejian. 2020. Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex. In Nature communications, 11, 3351. doi:10.1038/s41467-020-17105-8. https://pubmed.ncbi.nlm.nih.gov/32620897/
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