1. Bauwens, Miriam, Celik, Elifnaz, Zur, Dinah, De Baere, Elfride, Ben-Yosef, Tamar. 2024. Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction. In American journal of human genetics, 111, 393-402. doi:10.1016/j.ajhg.2024.01.001. https://pubmed.ncbi.nlm.nih.gov/38272031/
2. Omori, Yoshihiro, Kubo, Shun, Kon, Tetsuo, Nakagawa, Atsushi, Furukawa, Takahisa. 2017. Samd7 is a cell type-specific PRC1 component essential for establishing retinal rod photoreceptor identity. In Proceedings of the National Academy of Sciences of the United States of America, 114, E8264-E8273. doi:10.1073/pnas.1707021114. https://pubmed.ncbi.nlm.nih.gov/28900001/
3. Volkov, Leo I, Ogawa, Yohey, Somjee, Ramiz, Kefalov, Vladimir J, Corbo, Joseph C. 2024. Samd7 represses short-wavelength cone genes to preserve long-wavelength cone and rod photoreceptor identity. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2402121121. doi:10.1073/pnas.2402121121. https://pubmed.ncbi.nlm.nih.gov/39531499/
4. Hlawatsch, Julia, Karlstetter, Marcus, Aslanidis, Alexander, Böck, Julia, Langmann, Thomas. 2013. Sterile alpha motif containing 7 (samd7) is a novel crx-regulated transcriptional repressor in the retina. In PloS one, 8, e60633. doi:10.1371/journal.pone.0060633. https://pubmed.ncbi.nlm.nih.gov/23565263/
5. Huang, Gongchen, Sun, Yan, Li, Ruiqi, Liang, Qiulian, Yu, Xiangyuan. 2024. Functional genetic variants and susceptibility and prediction of gestational diabetes mellitus. In Scientific reports, 14, 18123. doi:10.1038/s41598-024-69079-y. https://pubmed.ncbi.nlm.nih.gov/39103437/