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A novel UBA1 gene mutation in a patient with infantile respiratory distress syndrome

Human Genome Variation
2025-01-06 | Journal article
Contributors: Masafumi Miyata; Arisa Kojima; Yuri Kawai; Hidetoshi Uchida; Hiroko Boda; Naoko Ishihara; Hidehito Inagaki; Tetsushi Yoshikawa; Hiroki Kurahashi
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Characterization of the MG828507 lncRNA Located Upstream of the FLT1 Gene as an Etiology for Pre-Eclampsia

Journal of Clinical Medicine
2022-08-07 | Journal article
Contributors: Hikari Yoshizawa; Haruki Nishizawa; Hidehito Inagaki; Keisuke Hitachi; Akiko Ohwaki; Yoshiko Sakabe; Mayuko Ito; Kunihiro Tsuchida; Takao Sekiya; Takuma Fujii et al.
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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes

Journal of Human Genetics
2022-06 | Journal article
Contributors: Tasuku Mariya; Takema Kato; Takeshi Sugimoto; Syunsuke Miyai; Hidehito Inagaki; Tamae Ohye; Eiji Sugihara; Yukako Muramatsu; Seiji Mizuno; Hiroki Kurahashi
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Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex

Human Genome Variation
2022-02-10 | Journal article
Contributors: Yoshinari Muto; Hitomi Sasaki; Makoto Sumitomo; Hidehito Inagaki; Maki Kato; Takema Kato; Shunsuke Miyai; Hiroki Kurahashi; Ryoichi Shiroki
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The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis

Nature Communications
2020-07-16 | Journal article
Contributors: Kentaro Tsukamoto; Naoaki Shinzawa; Akito Kawai; Masahiro Suzuki; Hiroyasu Kidoya; Nobuyuki Takakura; Hisateru Yamaguchi; Toshiki Kameyama; Hidehito Inagaki; Hiroki Kurahashi et al.
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Peer review (5 reviews for 2 publications/grants)

Review activity for Human genome variation. (2)
Review activity for Journal of human genetics. (3)