2014 - 2017 The elucidation of the molecular biologic pathology in the Osteogenesis imperfecta and new molecular target treatment by the Wnt signal pathway.
2013 - 2016 Genetic analysis of HPMR syndrome
2009 - 2011 Analysis of phosphate metabolism and treatment for hereditary hypophosphatemic rickets
2009 - 2011 The elucidation of the genetic background of osteogenesis imperfecta : Deployment to the custom-made medical treatment by a genotype.
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Papers (87):
Junko Kanno, Akinobu Miura, Sayaka Kawashima, Hirohito Shima, Dai Suzuki, Miki Kamimura, Ikuma Fujiwara, Masayuki Kamimura, Mitsugu Uematsu, Masataka Kudo, et al. A case of 49,XXXYY followed-up from infancy to adulthood with review of literature. Endocrine journal. 2024
Hiroyuki Saitou, Taichi Kitaoka, Takuo Kubota, Junko Kanno, Hiroshi Mochizuki, Toshimi Michigami, Kosei Hasegawa, Ikuma Fujiwara, Takashi Hamajima, Daisuke Harada, et al. Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American journal of medical genetics. Part A. 2024. e63612