1. Ahn, Byeong-Yun, Jeong, Yideul, Kim, Sunghee, Leem, Young-Eun, Kang, Jong-Sun. 2023. Cdon suppresses vascular smooth muscle calcification via repression of the Wnt/Runx2 Axis. In Experimental & molecular medicine, 55, 120-131. doi:10.1038/s12276-022-00909-7. https://pubmed.ncbi.nlm.nih.gov/36609601/
2. Obara-Moszyńska, Monika, Budny, Bartłomiej, Kałużna, Małgorzata, Ziemnicka, Katarzyna, Niedziela, Marek. 2021. CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy. In Journal of applied genetics, 62, 621-629. doi:10.1007/s13353-021-00649-w. https://pubmed.ncbi.nlm.nih.gov/34235642/
3. Kim, Sunghee, An, Subin, Lee, Jinwoo, Bae, Gyu-Un, Kang, Jong-Sun. 2023. Cdon ablation in motor neurons causes age-related motor neuron degeneration and impaired sciatic nerve repair. In Journal of cachexia, sarcopenia and muscle, 14, 2239-2252. doi:10.1002/jcsm.13308. https://pubmed.ncbi.nlm.nih.gov/37559423/
4. Chitsazan, Arash, Ferguson, Blake, Ram, Ramesh, Morahan, Grant, Walker, Graeme J. . A mutation in the Cdon gene potentiates congenital nevus development mediated by NRAS(Q61K). In Pigment cell & melanoma research, 29, 459-64. doi:10.1111/pcmr.12487. https://pubmed.ncbi.nlm.nih.gov/27155367/
5. Reis, Linda M, Basel, Donald, McCarrier, Julie, Weinberg, David V, Semina, Elena V. 2020. Compound heterozygous splicing CDON variants result in isolated ocular coloboma. In Clinical genetics, 98, 486-492. doi:10.1111/cge.13824. https://pubmed.ncbi.nlm.nih.gov/32729136/
6. Jeong, Myong-Ho, Kim, Hyun-Ji, Pyun, Jung-Hoon, Cho, Hana, Kang, Jong-Sun. 2017. Cdon deficiency causes cardiac remodeling through hyperactivation of WNT/β-catenin signaling. In Proceedings of the National Academy of Sciences of the United States of America, 114, E1345-E1354. doi:10.1073/pnas.1615105114. https://pubmed.ncbi.nlm.nih.gov/28154134/
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