1. Abdelhafez, Nada, Aladsani, Amani, Alkharafi, Lateefa, Al-Bustan, Suzanne. 2024. Association of selected gene variants with nonsyndromic orofacial clefts in Kuwait. In Gene, 934, 149028. doi:10.1016/j.gene.2024.149028. https://pubmed.ncbi.nlm.nih.gov/39442823/
2. Shaw, Douglas M, Polikowsky, Hannah P, Pruett, Dillon G, Kraft, Shelly Jo, Below, Jennifer E. . Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. In American journal of human genetics, 108, 2271-2283. doi:10.1016/j.ajhg.2021.11.004. https://pubmed.ncbi.nlm.nih.gov/34861174/
3. Le, Anh Hoang, Yelland, Tamas, Paul, Nikki R, Ismail, Shehab, Machesky, Laura M. 2021. CYRI-A limits invasive migration through macropinosome formation and integrin uptake regulation. In The Journal of cell biology, 220, . doi:10.1083/jcb.202012114. https://pubmed.ncbi.nlm.nih.gov/34165494/
4. Chen, Chunyu, Guo, Qiang, Shi, Jinna, Hui, Xiang, Song, Tao. 2018. Genetic variants of MGMT, RHPN2, and FAM49A contributed to susceptibility of nonsyndromic orofacial clefts in a Chinese population. In Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 47, 796-801. doi:10.1111/jop.12758. https://pubmed.ncbi.nlm.nih.gov/29949196/
5. Azevedo, Camilla de Marchi Sanches, Machado, Renato Assis, Martelli-Júnior, Hercílio, Coletta, Ricardo D, Rangel, Ana Lúcia Carrinho Ayroza. 2019. Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of non-syndromic oral clefts in the Brazilian population. In Oral diseases, 26, 145-151. doi:10.1111/odi.13204. https://pubmed.ncbi.nlm.nih.gov/31564061/
智鼠故事 
