Research field (2)：
Cardiology
, Fetal medicine/Pediatrics
Research theme for competitive and other funds (4)：
2023 - 2027 小児循環器診療におけるゲノム医療の確立に関する試験研究事業
2019 - 2021 小児メタボリックシンドロームに対する新しい運動介入法に関する研究
2019 - 2020 家族性大動脈弁上狭窄症におけるエラスチン遺伝子変異の同定
2015 - 2018 Establishment of treatment strategies for early-onset inherited arrhythmias based on genotype-phenotype relationships
Papers (31)：
Ayumi Miyazaki, Masao Yoshinaga, Hiromitsu Ogata, Yoshiya Ito, Machiko Aoki, Toshihide Kubo, Masaki Shinomiya, Hitoshi Horigome, Masakuni Tokuda, Lisheng Lin, et al. An Alternative Approach to Determining Metabolic Syndrome Component Cutoffs in Children and Adolescents Using Segmental Regression Analysis. Circulation reports. 2024. 6. 4. 118-126
Sho Hosaka, Kazuo Imagawa, Yusuke Yano, Lisheng Lin, Junko Shiono, Miho Takahashi-Igari, Hideki Hara, Daisuke Hayashi, Hironori Imai, Atsushi Morita, et al. The CXCL10-CXCR3 axis plays an important role in Kawasaki Disease. Clinical and experimental immunology. 2023
Masaki T, Lisheng L, Yusuke Y, Junko S, Hitoshi H. Clinical features of pediatric acute myocarditis ~ A single institution experience ~. The Medical Journal of Ibaraki Prefectural Hospitals. 2023. 39. 2. 27-33
Masao Yoshinaga, Hideto Takahashi, Yoshiya Ito, Machiko Aoki, Ayumi Miyazaki, Toshihide Kubo, Masaki Shinomiya, Hitoshi Horigome, Masakuni Tokuda, Lisheng Lin, et al. Developmental trajectories at a high risk for childhood overweight/obesity. Pediatrics international : official journal of the Japan Pediatric Society. 2022. e15425
Masayuki Iijima, Lisheng Lin, Takashi Murakami, Junko Shiono, Hitoshi Horigome. A case of pulmonary atresia with total anomalous pulmonary venous connection. Pediatrics international : official journal of the Japan Pediatric Society. 2022. 64. 1. e15217
- 2015 Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan
1999 - 2005 Hamamatsu University of Medicine, Hamamatsu, Japan
Awards (1)：
2018/10 - The 11th Asia Pacific Heart Rhythm Society Scientific Session Best Poster Award A novel CACNA1C mutation(R860Q) in a family presented with QT prolongation and mild mental retardation without Timothy syndrome phenotype
Association Membership(s) (4)：
Japanese Society of Fetal Cardiology
, The Japanese Circulation Society
, JAPAN PEDIATRIC SOCIETY
, JAPANESE SOCIETY OF PEDIATRIC CARDIOLOGY AND CARDIAC SURGERY
