Yoshiyuki Furutani

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 9

Top Topics

Molecular Docking

Chemotherapy Induced

Top Venues

Journal of the American Heart Association

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, Utano Tomaru, Yoshiyuki Furutani, Tatsuya Kato, Gen Harada, Kei Inai, Toshio Nakanishi, Atsushi Manabe, Atsuhito Takeda, Zhi-Cheng Jing
Identification of Prostaglandin I 2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association 13 (9) (2024)
Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, Utano Tomaru, Yoshiyuki Furutani, Tatsuya Kato, Gen Harada, Kei Inai, Toshio Nakanishi, Atsushi Manabe, Atsuhito Takeda, Zhi-Cheng Jing
Identification of Prostaglandin I 2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association 13 (9) (2024)
Shuhei Morita, Shunsuke Nomura, Kenko Azuma, Ayako Chida-Nagai, Yoshiyuki Furutani, Kei Inai, Tatsuya Inoue, Yasunari Niimi, Yuo Iizuka, Yoshiyuki Tsutsumi, Reina Ishizaki, Hiroyuki Yamagishi, Takakazu Kawamata, Hiroyuki Akagawa
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia. Clinical genetics 105 (5) (2024)
Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, Utano Tomaru, Yoshiyuki Furutani, Tatsuya Kato, Gen Harada, Kei Inai, Toshio Nakanishi, Atsushi Manabe, Atsuhito Takeda, Zhi-Cheng Jing
Identification of Prostaglandin I 2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association 13 (9) (2024)
Shuhei Morita, Shunsuke Nomura, Kenko Azuma, Ayako Chida-Nagai, Yoshiyuki Furutani, Kei Inai, Tatsuya Inoue, Yasunari Niimi, Yuo Iizuka, Yoshiyuki Tsutsumi, Reina Ishizaki, Hiroyuki Yamagishi, Takakazu Kawamata, Hiroyuki Akagawa
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia. Clinical genetics (2024)
Shuhei Morita, Shunsuke Nomura, Kenko Azuma, Ayako Chida-Nagai, Yoshiyuki Furutani, Kei Inai, Tatsuya Inoue, Yasunari Niimi, Yuo Iizuka, Yoshiyuki Tsutsumi, Reina Ishizaki, Hiroyuki Yamagishi, Takakazu Kawamata, Hiroyuki Akagawa
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia. Clinical genetics 105 (5) (2024)
Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, Utano Tomaru, Yoshiyuki Furutani, Tatsuya Kato, Gen Harada, Kei Inai, Toshio Nakanishi, Atsushi Manabe, Atsuhito Takeda, Zhi-Cheng Jing
Identification of Prostaglandin I 2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association (2024)
Shuhei Morita, Shunsuke Nomura, Kenko Azuma, Ayako Chida-Nagai, Yoshiyuki Furutani, Kei Inai, Tatsuya Inoue, Yasunari Niimi, Yuo Iizuka, Yoshiyuki Tsutsumi, Reina Ishizaki, Hiroyuki Yamagishi, Takakazu Kawamata, Hiroyuki Akagawa
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia. Clinical genetics 105 (5) (2024)
Emiko Hayama, Yoshiyuki Furutani, Nanako Kawaguchi, Akiko Seki, Yoji Nagashima, Keisuke Okita, Daiji Takeuchi, Rumiko Matsuoka, Kei Inai, Nobuhisa Hagiwara, Toshio Nakanishi
Induced Pluripotent Stem Cell-Derived Cardiomyocytes with SCN5A R1623Q Mutation Associated with Severe Long QT Syndrome in Fetuses and Neonates Recapitulates Pathophysiological Phenotypes. Biology 10 (10) (2021)