Atsumi Tsuji-Hosokawa

ResearcherID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Metabolic Syndrome

Top Venues

Human molecular genetics

The Journal of clinical endocrinology and metabolism

The Journal of physiology

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

Publications

Eriko Adachi, Ryuichi Nakagawa, Atsumi Tsuji-Hosokawa, Maki Gau, Shizuka Kirino, Analia Yogi, Hisae Nakatani, Kei Takasawa, Tomomi Yamaguchi, Tomoki Kosho, Masanori Murakami, Toshihiro Tajima, Tomonobu Hasegawa, Tetsuya Yamada, Tomohiro Morio, Osamu Ohara, Kenichi Kashimada
A MinION-Based Long-Read Sequencing Application with One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency. The Journal of clinical endocrinology and metabolism (2023)
Chieko Takizawa, Hisae Nakatani, Yoko Saito, Atsumi Tsuji-Hosokawa, Eriko Kikuchi, Masuhiro Shimoda, Kei Takasawa
A hypercalcemic episode in an adolescent with autosomal dominant hypocalcemia. Pediatrics international : official journal of the Japan Pediatric Society 65 (1) (2023)
Yuya Ogawa, Miho Terao, Atsumi Tsuji-Hosokawa, Iku Tsuchiya, Midori Hasegawa, Shuji Takada
SOX9 and SRY binding sites on mouse mXYSRa/Enh13 enhancer redundantly regulate Sox9 expression to varying degrees. Human molecular genetics (2022)
Kazuhiro Watanabe, Atsumi Tsuji-Hosokawa, Atsuko Hashimoto, Kaoru Konishi, Nobuyuki Ishige, Harumi Yajima, Akito Sutani, Hisae Nakatani, Maki Gau, Kei Takasawa, Toshihiro Tajima, Tomonobu Hasegawa, Tomohiro Morio, Kenichi Kashimada
The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency. The Journal of clinical endocrinology and metabolism 107 (12) (2022)
Ryuichi Nakagawa, Kei Takasawa, Maki Gau, Atsumi Tsuji-Hosokawa, Hideya Kawaji, Yasuhiro Murakawa, Shuji Takada, Masashi Mikami, Satoshi Narumi, Maki Fukami, Rajini Sreenivasan, Tetsuo Maruyama, Elena J Tucker, Liang Zhao, Josephine Bowles, Andrew Sinclair, Peter Koopman, Yoshihide Hayashizaki, Tomohiro Morio, Kenichi Kashimada
Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency. Human molecular genetics 31 (13) (2022)
Atsumi Tsuji-Hosokawa, Yuya Ogawa, Iku Tsuchiya, Miho Terao, Shuji Takada
Human SRY Expression at the Sex-determining Period is Insufficient to Drive Testis Development in Mice. Endocrinology 163 (1) (2021)
Atsumi Tsuji-Hosokawa, Kenichi Kashimada
Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan. International journal of neonatal screening 7 (3) (2021)
Conor Willson, Makiko Watanabe, Atsumi Tsuji-Hosokawa, Ayako Makino
Pulmonary vascular dysfunction in metabolic syndrome. The Journal of physiology 597 (4) (2018)