業績
論文2022年
- Aihara, Y., Shirota, M., Kikuchi, A., Katata, Y., Abe, Y., Niihori, T., Funayama, R., Nakayama, K., Aoki, Y., Kure, S. A novel variant in the transmembrane 4 domain of ANO3 identified in a two-year-old girl with developmental delay and tremor. J Hum Genet 68, 51-54 (2023).
- Iemura, K., Anzawa, H., Funayama, R., Iwakami, R., Nakayama, K., Kinoshita, K., Tanaka, K. High levels of chromosomal instability facilitate the tumor growth and sphere formation. Cancer Sci 113, 2727-2737 (2022).
- Kanno, M., Suzuki, M., Tanikawa, K., Numakura, C., Matsuzawa, S.I., Niihori, T., Aoki, Y., Matsubara, Y., Makino, S., Tamiya, G., Nakano, S., Funayama, R., Shirota, M., Nakayama, K., Mitsui, T., Hayasaka, K. Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct. J Hum Genet67, 393-397 (2022).
- Yu, Z., Ueno, K., Funayama, R., Sakai, M., Nariai, N., Kojima, K., Kikuchi, Y., Li, X., Ono, C., Kanatani, J., Ono, J., Iwamoto, K., Hashimoto, K., Kinoshita, K., Nakayama, K., Nagasaki, M., Tomita, H. Sex-Specific Differences in the Transcriptome of the Human Dorsolateral Prefrontal Cortex in Schizophrenia. Mol Neurobiol 60, 1083-1098 (2023).
- Nakagawa, T., Hattori, S., Hosoi, T., Nakayama, K. Neurobehavioral characteristics of mice with SETD5 mutations as models of IDD23 and KBG syndromes. Front Genet,13,1022339 (2022).