1. Seth, Abhishek, Rivera, Armando, Chahdi, Ahmed, Jorgez, Carolina, Lamb, Dolores J. . Gene dosage changes in KCTD13 result in penile and testicular anomalies via diminished androgen receptor function. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 36, e22567. doi:10.1096/fj.202200558R. https://pubmed.ncbi.nlm.nih.gov/36196997/
2. Escamilla, Christine Ochoa, Filonova, Irina, Walker, Angela K, Speed, Haley E, Powell, Craig M. 2017. Kctd13 deletion reduces synaptic transmission via increased RhoA. In Nature, 551, 227-231. doi:10.1038/nature24470. https://pubmed.ncbi.nlm.nih.gov/29088697/
3. Kizner, Valeria, Naujock, Maximilian, Fischer, Sandra, Dorner-Ciossek, Cornelia, Gillardon, Frank. 2019. CRISPR/Cas9-mediated Knockout of the Neuropsychiatric Risk Gene KCTD13 Causes Developmental Deficits in Human Cortical Neurons Derived from Induced Pluripotent Stem Cells. In Molecular neurobiology, 57, 616-634. doi:10.1007/s12035-019-01727-1. https://pubmed.ncbi.nlm.nih.gov/31402430/
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5. Taniue, Kenzui, Sugawara, Anzu, Zeng, Chao, Hamada, Michiaki, Akimitsu, Nobuyoshi. 2024. The MTR4/hnRNPK complex surveils aberrant polyadenylated RNAs with multiple exons. In Nature communications, 15, 8684. doi:10.1038/s41467-024-51981-8. https://pubmed.ncbi.nlm.nih.gov/39419981/
6. Madison, Jon M, Duong, Karen, Vieux, Ellen F, Scolnick, Edward M, Cottrell, Jeffrey R. 2020. Regulation of purine metabolism connects KCTD13 to a metabolic disorder with autistic features. In iScience, 24, 101935. doi:10.1016/j.isci.2020.101935. https://pubmed.ncbi.nlm.nih.gov/33409479/
7. Chahdi, Ahmed, Jorgez, Carolina, Rosenfeld, Jill A, Neetu, Neetu, Seth, Abhishek. . Androgen receptor ubiquitination links KCTD13 to genitourinary tract defects. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 39, e70406. doi:10.1096/fj.202402072RR. https://pubmed.ncbi.nlm.nih.gov/39968753/
8. Arbogast, Thomas, Razaz, Parisa, Ellegood, Jacob, Golzio, Christelle, Katsanis, Nicholas. . Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions. In Human molecular genetics, 28, 1474-1486. doi:10.1093/hmg/ddy436. https://pubmed.ncbi.nlm.nih.gov/30590535/
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