1. Feng, Xin, Ye, Yongyu, Zhang, Jianan, Gao, Bo, Wu, Nan. 2024. Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2310283121. doi:10.1073/pnas.2310283121. https://pubmed.ncbi.nlm.nih.gov/38669183/
2. Cai, Chunquan, Shi, Ouyan, Wang, Baiqi, Wang, Fang, Shen, Changhong. 2014. Association between VANGL1 gene polymorphisms and neural tube defects. In Neuropediatrics, 45, 234-9. doi:10.1055/s-0033-1364103. https://pubmed.ncbi.nlm.nih.gov/24407469/
3. Andersen, Malene R, Farooq, Muhammad, Koefoed, Karen, Christensen, Søren T, Larsen, Lars A. . Mutation of the Planar Cell Polarity Gene VANGL1 in Adolescent Idiopathic Scoliosis. In Spine, 42, E702-E707. doi:10.1097/BRS.0000000000001927. https://pubmed.ncbi.nlm.nih.gov/27755493/
4. Fatima, Urooj, Khan, Shabnam, Riaz, Syeda Urooj, Iftikhar, Meesam, Fatima, Nida. . Myelomeningocele among Pakistani population. In JPMA. The Journal of the Pakistan Medical Association, 72, 874-877. doi:10.47391/JPMA.04-611. https://pubmed.ncbi.nlm.nih.gov/35713047/
5. Xu, Leilei, Sheng, Fei, Xia, Chao, Qiu, Yong, Zhu, Zezhang. . VANGL1 Is Not Associated With the Susceptibility of Adolescent Idiopathic Scoliosis in the Chinese Population. In Spine, 43, E580-E584. doi:10.1097/BRS.0000000000002497. https://pubmed.ncbi.nlm.nih.gov/29189642/
6. Bartsch, O, Kirmes, I, Thiede, A, Sabova, L, Horn, F. 2012. Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects. In Molecular syndromology, 3, 76-81. doi:10.1159/000339668. https://pubmed.ncbi.nlm.nih.gov/23326252/
7. Cheng, Chen, Zhao, Sheng, Zhu, Xia, Huang, Hui, Chen, Xinlin. 2021. The VANGL1 P384R variant cause both neural tube defect and Klippel-Feil syndrome. In Molecular genetics & genomic medicine, 9, e1710. doi:10.1002/mgg3.1710. https://pubmed.ncbi.nlm.nih.gov/34014041/
8. Jiang, Simon H, Mercan, Sevcan, Papa, Ilenia, Bahlo, Melanie, Vinuesa, Carola G. 2021. Deletions in VANGL1 are a risk factor for antibody-mediated kidney disease. In Cell reports. Medicine, 2, 100475. doi:10.1016/j.xcrm.2021.100475. https://pubmed.ncbi.nlm.nih.gov/35028616/