Yuji Takahashi, Hidetoshi Date, Hideki Oi, Takeya Adachi, Noriaki Imanishi, En Kimura, Hotake Takizawa, Shinji Kosugi, Naomichi Matsumoto, Kenjiro Kosaki, et al. Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures. Journal of Human Genetics. 2022
Hitomi Nishizawa, Mitsuo Motobayashi, Miwa Akahane, Keiko Wakui, Noritaka Kitazawa, Yuji Inaba, Yoshimitsu Fukushima, Tomoki Kosho. Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder. Brain & development. 2022. 44. 3. 229-233
中込さと子, 村上裕美, 佐藤智佳, 玉置知子, 玉置知子, 大川恵, 佐々木規子, 浦野真理, 山下浩美, 渡邊淳, et al. The first educational seminar on basic medical genetics and genomics held by the Committee of Genetic Nursing of the Japanese Society for Genetic Counseling. 日本遺伝カウンセリング学会誌. 2021. 42. 2. 118-118
Hiroaki Hanafusa, Yoshihiko Hidaka, Tomomi Yamaguchi, Hisashi Shimojo, Takanori Tsukahara, Tsubasa Murase, Daisuke Matsuoka, Nao Chiba, Shun Shimada, Hirokazu Morokawa, et al. Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis. American journal of medical genetics. Part A. 2021
2017/11 - The Japan Society of Human Genetics Award for distinguished contribution to the Japan Society of Human Genetics
Association Membership(s) (5)：
日本学術会議臨床医学委員会臨床ゲノム医学分科会
, The National Liaison Council for Clinical Sections of Medical Genetics
, THE JAPANESE SOCIETY OF GENETIC DIAGNOSIS AND TREATMENT
, THE JAPANESE SOCIETY FOR GENETIC COUNSELING
, THE JAPAN SOCIETY OF HUMAN GENETICS
