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Yusuke Hattori, Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Takahito Inoue, Shinichi Hirose, Kimitoshi Nakamura. Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan. Molecular Genetics and Metabolism Reports. 2023. 37. 101003-101003
Jun Kido, Kimiyasu Egami, Yohei Misumi, Keishin Sugawara, Naomi Tsuchida, Naomichi Matsumoto, Mitsuharu Ueda, Kimitoshi Nakamura. X-linked intellectual disability related to a novel variant of KLHL15. Human genome variation. 2023. 10. 1. 21-21
Takaaki Sawada, Jun Kido, Yukako Yae, Kotaro Yuge, Keiko Nomura, Kentaro Okada, Natsumi Fujiyama, Shiro Ozasa, Kimitoshi Nakamura. Gene therapy for spinal muscular atrophy is considerably effective when administered as early as possible after birth. Molecular genetics and metabolism reports. 2023. 35. 100973-100973
Fusa Nagamatsu, Jun Kido, Yoshiko Suginohara, Toshiro Nakamura, Rie Nakamura, Nagisa Komatsu, Daisuke Miyamoto, Yasuyuki Hamada, Takafumi Kashiwagi, Shigeto Sugino, et al. Outcomes of pediatric obesity-related lifestyle disease screenings in Kumamoto. Pediatrics international : official journal of the Japan Pediatric Society. 2023. 65. 1. e15442
Takaaki Sawada, Jun Kido, Keishin Sugawara, Kimitoshi Nakamura. High-risk screening for fabry disease: A nationwide study in Japan and literature review. Diagnostics. 2021. 11. 10