1. Faul, Thomas, Gawlik, Micha, Bauer, Martin, Knapp, Michael, Stöber, Gerald. 2005. ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies. In BMC psychiatry, 5, 35. doi:. https://pubmed.ncbi.nlm.nih.gov/16225675/
2. Mukai, Jun, Liu, Hui, Burt, Rachel A, Karayiorgou, Maria, Gogos, Joseph A. 2004. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. In Nature genetics, 36, 725-31. doi:. https://pubmed.ncbi.nlm.nih.gov/15184899/
3. Xu, Mingqing, St Clair, David, He, Lin. . Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets. In American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 153B, 1266-75. doi:10.1002/ajmg.b.31096. https://pubmed.ncbi.nlm.nih.gov/20661937/
4. Chen, Wu-Yan, Shi, Yong-Yong, Zheng, Yong-Lan, Yang, Pei-Di, He, Lin. 2004. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. In Human molecular genetics, 13, 2991-5. doi:. https://pubmed.ncbi.nlm.nih.gov/15489219/
5. Qin, Xianzheng, Chen, Jiang, Zhou, Tian. . 22q11.2 deletion syndrome and schizophrenia. In Acta biochimica et biophysica Sinica, 52, 1181-1190. doi:10.1093/abbs/gmaa113. https://pubmed.ncbi.nlm.nih.gov/33098288/
6. Shin, Hyoung Doo, Park, Byung Lae, Bae, Joon Seol, Shin, Tae-Min, Woo, Sung-Il. . Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality. In American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 153B, 1167-72. doi:10.1002/ajmg.b.31083. https://pubmed.ncbi.nlm.nih.gov/20468065/
7. Nunes, Natalia, Carvalho Nunes, Beatriz, Zamariolli, Malú, Ae Kim, Chong, Melaragno, Maria Isabel. 2024. Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion Syndrome. In Genetics research, 2024, 5549592. doi:10.1155/2024/5549592. https://pubmed.ncbi.nlm.nih.gov/38586596/