1. Markenscoff-Papadimitriou, Eirene, Binyameen, Fadya, Whalen, Sean, State, Matthew W, Rubenstein, John L. . Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. In Cell reports, 37, 110089. doi:10.1016/j.celrep.2021.110089. https://pubmed.ncbi.nlm.nih.gov/34879283/
2. Ibaraki, Kyoko, Hamada, Nanako, Iwamoto, Ikuko, Tabata, Hidenori, Nagata, Koh-Ichi. 2019. Expression Analyses of POGZ, A Responsible Gene for Neurodevelopmental Disorders, during Mouse Brain Development. In Developmental neuroscience, 41, 139-148. doi:10.1159/000502128. https://pubmed.ncbi.nlm.nih.gov/31430754/
3. Sun, Xiaoyun, Zhang, Tianzhe, Tong, Bei, Jiang, Wei, Sun, Yuhua. 2023. POGZ suppresses 2C transcriptional program and retrotransposable elements. In Cell reports, 42, 112867. doi:10.1016/j.celrep.2023.112867. https://pubmed.ncbi.nlm.nih.gov/37494184/
4. . 2014. Large-scale discovery of novel genetic causes of developmental disorders. In Nature, 519, 223-8. doi:10.1038/nature14135. https://pubmed.ncbi.nlm.nih.gov/25533962/
5. Hamada, Nanako, Nishijo, Takuma, Iwamoto, Ikuko, Shifman, Sagiv, Nagata, Koh-Ichi. 2024. Analyses of Conditional Knockout Mice for Pogz, a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain. In Cells, 13, . doi:10.3390/cells13060540. https://pubmed.ncbi.nlm.nih.gov/38534384/
6. Wang, Tianyun, Guo, Hui, Xiong, Bo, Xia, Kun, Eichler, Evan E. 2016. De novo genic mutations among a Chinese autism spectrum disorder cohort. In Nature communications, 7, 13316. doi:10.1038/ncomms13316. https://pubmed.ncbi.nlm.nih.gov/27824329/
7. Tozkır, Jülide, Yıldırım, Gökberk, Demir, Selma, Görker, Işık, Gürkan, Hakan. 2024. Investigation of Pogz Gene Variants in Non-Syndromic Autism Spectrum Disorder. In Noro psikiyatri arsivi, 67, 208-212. doi:10.29399/npa.28625. https://pubmed.ncbi.nlm.nih.gov/39258134/
8. Nagy, Dóra, Verheyen, Sarah, Wigby, Kristen M, Duba, Hans-Christoph, Weis, Denisa. 2022. Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. In Genes, 13, . doi:10.3390/genes13010154. https://pubmed.ncbi.nlm.nih.gov/35052493/
9. Sun, Xiaoyun, Cheng, Linxi, Sun, Yuhua. 2022. Autism-associated protein POGZ controls ESCs and ESC neural induction by association with esBAF. In Molecular autism, 13, 24. doi:10.1186/s13229-022-00502-9. https://pubmed.ncbi.nlm.nih.gov/35650610/
10. Suliman-Lavie, Reut, Title, Ben, Cohen, Yahel, Yarom, Yosef, Shifman, Sagiv. 2020. Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice. In Nature communications, 11, 5836. doi:10.1038/s41467-020-19577-0. https://pubmed.ncbi.nlm.nih.gov/33203851/
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