Rchr
J-GLOBAL ID:201801016800162671   Update date: Feb. 12, 2024

KEIKO MATSUBARA

Matsubara Keiko | KEIKO MATSUBARA
Affiliation and department:
Research field  (3): Cell biology ,  Molecular biology ,  Fetal medicine/Pediatrics
Research keywords  (6): clinical sequencing ,  assisted reproductive technologies ,  advanced maternal age ,  DNA methylation ,  Prader-Willi syndrome ,  imprinting disorders
Research theme for competitive and other funds  (10):
  • 2022 - 2025 Creation of treatment strategies for imprinting disorders through hydroxymethylation profiling
  • 2020 - 2022 網羅的遺伝子・エピゲノム解析による性成熟疾患の病因の解明
  • 2019 - 2022 The role of hydroxymethylation in imprinting diseases caused by abnormal methylation
  • 2016 - 2019 Pathologic clarification and development of new medicine for imprinting disorders in terms of hydroxymethylation
  • 2015 - 2018 Elucidation of the onset mechanism of human imprinting disorders using the method of methylation analysis with high-density DNA methylation arrays
Show all
Papers (112):
  • Tatsuki Urakawa, Shinichiro Sano, Sayaka Kawashima, Akie Nakamura, Hirohito Shima, Motoki Ohta, Yuki Yamada, Ai Nishida, Hiromune Narusawa, Yoshiaki Ohtsu, et al. (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B. European journal of endocrinology. 2023
  • Tomoko Yoshida, Keiko Matsubara, Hiroko Ogata-Kawata, Mami Miyado, Keisuke Ishiwata, Kazuhiko Nakabayashi, Kenichiro Hata, Ikuko Kageyama, Satoshi Tamaoka, Yukiko Shimada, et al. Variations in gender identity and sexual orientation of university students. Sexual medicine. 2023. 11. 5. qfad057
  • Satoshi Tamaoka, Akinari Fukuda, Kazuhiko Nakabayashi, Keiko Matsubara, Hiroko Ogata-Kawata, Yuki Muranishi, Kenichiro Hata, Yuko Kato-Fukui, Seisuke Sakamoto, Mureo Kasahara, et al. Rare sequence variants associated with the risk of non-syndromic biliary atresia. Hepatology research : the official journal of the Japan Society of Hepatology. 2023
  • Kaori Hara-Isono, Keiko Matsubara, Akie Nakamura, Shinichiro Sano, Takanobu Inoue, Sayaka Kawashima, Tomoko Fuke, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, et al. Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes. Clinical epigenetics. 2023. 15. 1. 78-78
  • 鈴木 江莉奈, 宮戸 真美, 松原 圭子, 黒木 陽子, 川嶋 明香, 原 香織, 鏡 雅代, 緒方 勤, 深見 真紀. 低ゴナドトロピン性性腺機能低下症における疾患特異的メチル化異常の探索. 日本内分泌学会雑誌. 2023. 98. 5. 1481-1481
more...
MISC (40):
  • 青砥早希, 松原圭子, 松原圭子, 山澤一樹, 秦健一郎, 秦健一郎, 鏡雅代, 中林一彦. Development of a reference database and toolkit for rare undiagnosed disease-specific epivariant analysis. 日本分子生物学会年会プログラム・要旨集(Web). 2023. 46th
  • 高橋 路子, 蟹江 慶太郎, 坂東 弘教, 山本 雅昭, 福岡 秀規, 井口 元三, 山田 倫子, 森貞 直哉, 松原 圭子, 鏡 雅代, et al. 肥満のゲノムサイエンス 減量外来受診後にパイロシークエンス法によって診断し得たPrader-Willi症候群の一例. 肥満研究. 2022. 27. Suppl. 176-176
  • 高橋 路子, 蟹江 慶太郎, 坂東 弘教, 山本 雅昭, 福岡 秀規, 井口 元三, 山田 倫子, 森貞 直哉, 松原 圭子, 鏡 雅代, et al. 肥満のゲノムサイエンス 減量外来受診後にパイロシークエンス法によって診断し得たPrader-Willi症候群の一例. 肥満研究. 2022. 27. Suppl. 176-176
  • 鏡雅代, 福家智子, 中村明枝, 中村明枝, 井上毅信, 川嶋明香, 原香織, 松原圭子, 佐野伸一朗, 佐野伸一朗, et al. Silver-Russell症候群の臨床診断基準を満たした173名における遺伝学的原因および遺伝学的原因別臨床像の検討. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
  • 山澤一樹, 中嶋萌子, 久保井徹, 横田一郎, 杉野典子, 小川昌宏, 盆野元紀, 曳野俊治, 佐藤和夫, 中嶋敏紀, et al. SGA児309例の包括的メチル化解析によるインプリンティング疾患の探索. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
more...
Education (1):
  • 1996 - 2002 Hamamatsu University School of Medicine Faculty of Medicine School of Medicine
Work history (4):
  • 2023/07 - 現在 National Center for Child Health and Development Division of Diversity Research chief
  • 2022/05 - 現在 National Center for Child Health and Development
  • 2021/10 - 現在 National Center for Child Health and Development
  • 2008/04 - 現在 National Center for Child Health and Development Department of molecular endocrinology
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page