2005 - 2006 Microarray analysis for cerebral aneurysm-by using the information of genome
第37回(平成21年度)三越医学研究助成
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Papers (68):
Satoshi Tanaka, Hiroyuki Akagawa, Kenkou Azuma, Sayaka Higuchi, Atsushi Ujiie, Koshi Hashimoto, Naoko Iwasaki. High prevalence of copy number variations in the Japanese participants with suspected MODY. Clinical Genetics. 2024
Tadashi Inoue, Ryuta Takase, Keiko Uchida, Kazuki Kodo, Kenji Suda, Yoriko Watanabe, Koh-Ichiro Yoshiura, Masaya Kunimatsu, Reina Ishizaki, Kenko Azuma, et al. Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease. Journal of human genetics. 2024. 69. 5. 223-223
Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, et al. Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association. 2024. e032872
Tadashi Inoue, Ryuta Takase, Keiko Uchida, Kazuki Kodo, Kenji Suda, Yoriko Watanabe, Koh-Ichiro Yoshiura, Masaya Kunimatsu, Reina Ishizaki, Kenko Azuma, et al. The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease. Journal of human genetics. 2024
Yusuke Ushio, Hiroshi Kataoka, Hiroyuki Akagawa, Masayo Sato, Shun Manabe, Keiko Kawachi, Shiho Makabe, Taro Akihisa, Momoko Seki, Atsuko Teraoka, et al. Factors associated with early-onset intracranial aneurysms in patients with autosomal dominant polycystic kidney disease. Journal of nephrology. 2024