1. Aoki-Suzuki, Mika, Yamada, Kazuo, Meerabux, Joanne, Nishikawa, Toru, Yoshikawa, Takeo. . A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia. In Biological psychiatry, 57, 382-93. doi:. https://pubmed.ncbi.nlm.nih.gov/15705354/
2. Liu, Dong, Nanclares, Carmen, Simbriger, Konstanze, Gkogkas, Christos G, Cao, Ruifeng. 2022. Autistic-like behavior and cerebellar dysfunction in Bmal1 mutant mice ameliorated by mTORC1 inhibition. In Molecular psychiatry, 28, 3727-3738. doi:10.1038/s41380-022-01499-6. https://pubmed.ncbi.nlm.nih.gov/35301425/
3. Yaguchi, Kunio, Nishimura-Akiyoshi, Sachiko, Kuroki, Satoshi, Onodera, Takashi, Itohara, Shigeyoshi. 2014. Identification of transcriptional regulatory elements for Ntng1 and Ntng2 genes in mice. In Molecular brain, 7, 19. doi:10.1186/1756-6606-7-19. https://pubmed.ncbi.nlm.nih.gov/24642214/
4. Heimer, Gali, van Woerden, Geeske M, Barel, Ortal, Kushner, Steven A, Ben Zeev, Bruria. 2019. Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia. In Human mutation, 41, 476-486. doi:10.1002/humu.23945. https://pubmed.ncbi.nlm.nih.gov/31692205/