東京科学大学 · 医歯学総合研究科

研究キーワードshort root anomaly・craniofacial microsomia・SATB2-associated syndrome・PUF60 variants・oculo-facio-cardio-dental syndrome・cleft lip and palate・dental genetics・alveolar bone grafting・oral habits

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• Ukita N, Ogawa T, Yamada M, Takeuchi C, Kosaki K, Moriyama K. Functional Analyses of SATB2 Variants Reveal Pathogenicity Mechanisms Linked With SATB2-Associated Syndrome. American Journal of Medical Genetics, Part A. 2025.06; 197 (6): e64005. ( PubMed , DOI )2025
• Ikeda-Sagawa Y, Ogawa T, Sudo T, Nagata Y, Tanaka T, Moriyama K. Protocadherin alpha gene cluster variants are potentially associated with short root anomaly in Japanese European Journal of Orthodontics. 2025.09; 47 (5): cjaf065.2025
• Uezono M, Okubo S, Ogawa T, Moriyama K. Association Between the Vertical Position of the Inferior Turbinate and Alveolar Bone Bridge Morphology After Secondary Alveolar Bone Grafting in Patients with Unilateral Cleft Lip and Palate: A Retrospective Study Seminars in Orthodontics. 2025.12; 31 (5): 675-680.2025
• Ogawa T, Xue J, Guo L, Inoue-Arai MS, Vendramini-Pittoli S, Zechi-Ceide RM, Candido-Souza RM, Tonello C, Brandão MM, Okada Ozawa T, Porto Peixoto A, Ruiz DMCF, Nakashima T, Ikegawa S, Moriyama K, Kokitsu-Nakata NM. Identification of a de novo PUF60 variant associated with craniofacial microsomia. American Journal of Medical Genetics Part A. 2024.09; 194 (9): e63631. ( PubMed , DOI )2024

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