Research theme for competitive and other funds (2):
2020 - 2022 相互転座保因者の遺伝カウンセリングに有用なアプリケーションの開発とその運用
2010 - 2012 羊水染色体検査の限界をMLPA法、DNAアレイ法はどこまで克服できるか。
Papers (52):
Yo Niida, Mika Inoue, Mamoru Ozaki, Etsuko Takase. Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model. Cytogenetic and Genome Research. 2018. 153. 2. 56-65
Yo Niida, Ayano Yokoi, Mondo Kuroda, Yusuke Mitani, Hiroyasu Nakagawa, Mamoru Ozaki. Reply to: Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1. BRAIN & DEVELOPMENT. 2017. 39. 2. 184-185