Research field (2)：
Fetal medicine/Pediatrics
, Hematology and oncology
Research theme for competitive and other funds (3)：
2023 - 2027 思春期がん患者の自己理解と自己表現スキルを促進する復学支援ツールの開発
2015 - 2018 Pathomechanism of neonatal hyperbilirubinemia: the relationship between genetics and nutrition
2013 - 2015 Pathomechanism of neonatal hyperbilirubinemia: the relationship between genetics and nutrition
Papers (4)：
Tetsuo Mitsui, Satoshi Makino, Gen Tamiya, Hiroko Sato, Yuki Kawakami, Yoshitaka Takahashi, Toru Meguro, Hiroko Izumino, Yosuke Sudo, Ikuo Norota, et al. ALOX12 mutation in a family with dominantly inherited bleeding diathesis. Journal of Human Genetics. 2021. 66. 8. 753-759
Hiroko Sato, Naomi Kawasaki, Motoi Kawasaki, Yu Abiko, Toru Meguro, Noriyuki Takahashi, Hiroko Izumino, Miyako Kanno, Chikahiko Numakura, Ayako Sasaki, et al. Three Consecutive Cases of Familial Hemophagocytic Lymphohistiocytosis, Including a Case Due to Maternal Uniparental Disomy. Journal of Pediatric Hematology/Oncology. 2020. 42. 8. e819-e821
Hiroko Sato, Toshihiko Uchida, Kentaro Toyota, Tomohiro Nakamura, Gen Tamiya, Miyako Kanno, Taeko Hashimoto, Masashi Watanabe, Kuraaki Aoki, Kiyoshi Hayasaka. Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms. Journal of Human Genetics. 2015. 60. 1. 35-40
Hiroko Sato, Toshihiko Uchida, Kentaro Toyota, Miyako Kanno, Taeko Hashimoto, Masashi Watanabe, Tomohiro Nakamura, Gen Tamiya, Kuraaki Aoki, Kiyoshi Hayasaka. Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding. Journal of Human Genetics. 2013. 58. 1. 7-10
