1. Nagai, Masayoshi, Iemura, Kenji, Kikkawa, Takako, Osumi, Noriko, Tanaka, Kozo. 2022. Deficiency of CHAMP1, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioural phenotype. In Brain communications, 4, fcac220. doi:10.1093/braincomms/fcac220. https://pubmed.ncbi.nlm.nih.gov/36106092/
2. Isidor, Bertrand, Küry, Sébastien, Rosenfeld, Jill A, Tanaka, Kozo, Bézieau, Stéphane. 2016. De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability. In Human mutation, 37, 354-8. doi:10.1002/humu.22952. https://pubmed.ncbi.nlm.nih.gov/26751395/
3. Garrity, Madison, Kavus, Haluk, Rojas-Vasquez, Marta, Isidor, Bertrand, Chung, Wendy K. 2021. Neurodevelopmental phenotypes in individuals with pathogenic variants in CHAMP1. In Cold Spring Harbor molecular case studies, 7, . doi:10.1101/mcs.a006092. https://pubmed.ncbi.nlm.nih.gov/34021018/
4. Yoshizaki, Yujiro, Ouchi, Yunosuke, Kurniawan, Dicky, Iemura, Kenji, Tanaka, Kozo. 2024. CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency. In Scientific reports, 14, 31904. doi:10.1038/s41598-024-83435-y. https://pubmed.ncbi.nlm.nih.gov/39738383/
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