1. Chen, Shuting, Venkatesan, Anand, Lin, Yong Qi, Banerjee, Swati, Bhat, Manzoor A. 2022. Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 42, 7016-7030. doi:10.1523/JNEUROSCI.0442-22.2022. https://pubmed.ncbi.nlm.nih.gov/35944997/
2. Yu, Jing, Song, Hongyu, Wang, Hongfang, Liu, Zhenguo, Xu, Baohua. 2023. The MicroRNA Ame-Bantam-3p Controls Larval Pupal Development by Targeting the Multiple Epidermal Growth Factor-like Domains 8 Gene (megf8) in the Honeybee, Apis mellifera. In International journal of molecular sciences, 24, . doi:10.3390/ijms24065726. https://pubmed.ncbi.nlm.nih.gov/36982800/
3. Kong, Jennifer H, Young, Cullen B, Pusapati, Ganesh V, Lo, Cecilia W, Rohatgi, Rajat. 2020. A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. In Developmental cell, 55, 432-449.e12. doi:10.1016/j.devcel.2020.08.012. https://pubmed.ncbi.nlm.nih.gov/32966817/
4. Lloyd, Deborah L, Toegel, Markus, Fulga, Tudor A, Wilkie, Andrew O M. 2018. The Drosophila homologue of MEGF8 is essential for early development. In Scientific reports, 8, 8790. doi:10.1038/s41598-018-27076-y. https://pubmed.ncbi.nlm.nih.gov/29884872/
5. Zhang, Zhen, Alpert, Deanne, Francis, Richard, Pennacchio, Len A, Lo, Cecilia W. 2009. Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy. In Proceedings of the National Academy of Sciences of the United States of America, 106, 3219-24. doi:10.1073/pnas.0813400106. https://pubmed.ncbi.nlm.nih.gov/19218456/
6. Nakadate, Kazuhiko, Kawakami, Kiyoharu. 2023. Immunohistochemical and Immunoelectron Microscopical Distribution of MEGF8 in the Mouse Central Nervous System. In Cells, 13, . doi:10.3390/cells13010063. https://pubmed.ncbi.nlm.nih.gov/38201267/
7. Bilal, Muhammad, Haack, Tobias B, Buchert, Rebecca, Liaqat, Khurram, Ahmad, Wasim. 2023. Sequence Variants in MEGF8 and GJA1 Underlying Syndactyly. In Molecular syndromology, 14, 201-207. doi:10.1159/000528651. https://pubmed.ncbi.nlm.nih.gov/37323198/
8. Engelhard, Caitlin, Sarsfield, Sarah, Merte, Janna, Sucov, Henry M, Ginty, David D. 2013. MEGF8 is a modifier of BMP signaling in trigeminal sensory neurons. In eLife, 2, e01160. doi:10.7554/eLife.01160. https://pubmed.ncbi.nlm.nih.gov/24052814/
9. Watts, Laura M, Bertoli, Marta, Attie-Bitach, Tania, Twigg, Stephen R F, Wilkie, Andrew O M. 2024. The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients. In European journal of human genetics : EJHG, 32, 864-870. doi:10.1038/s41431-024-01624-9. https://pubmed.ncbi.nlm.nih.gov/38760421/
10. Wang, Wenfeng, Zheng, Xiaoling, Song, Hejie, Zhang, Min, Zhang, Zhen. 2020. Spatial and temporal deletion reveals a latent effect of Megf8 on the left-right patterning and heart development. In Differentiation; research in biological diversity, 113, 19-25. doi:10.1016/j.diff.2020.03.002. https://pubmed.ncbi.nlm.nih.gov/32203821/