Naoya Morisada

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Topics

Intellectual Disability

Diffuse Large B Cell Lymphoma

Arterial Hypertension

Polycystic Kidney Disease

Top Venues

Human genome variation

Pediatrics international : official journal of the Japan Pediatric Society

Journal of human genetics

The journal of obstetrics and gynaecology research

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

Publications

Hiroaki Hanafusa, Hiroshi Yamaguchi, Naoya Morisada, Ming Juan Ye, Riki Matsumoto, Hiroaki Nagase, Kandai Nozu
End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy. Human genome variation 11 (1) (2024)
Hiroaki Hanafusa, Hiroshi Yamaguchi, Naoya Morisada, Ming Juan Ye, Riki Matsumoto, Hiroaki Nagase, Kandai Nozu
End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy. Human genome variation 11 (1) (2024)
Kana Hiromoto, Naoya Morisada, Shinya Tairaku, Kandai Nozu, Kazumoto Iijima, Toru Funakoshi
Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome. The journal of obstetrics and gynaecology research (2023)
Naoya Morisada, Yusuke Ishida, Shoichi Tokumoto, Azusa Maruyama, Kazumoto Iijima
Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation. Pediatrics international : official journal of the Japan Pediatric Society 63 (12) (2021)
Tomohiro Sameshima, Naoya Morisada, Tsuyoshi Egawa, Masaaki Kugo, Kazumoto Iijima
MPPH syndrome with aortic coarctation and macrosomia due to CCND2 mutations. Pediatrics international : official journal of the Japan Pediatric Society 62 (1) (2020)
Ayumi Shishido, Naoya Morisada, Kenta Tominaga, Hiroyasu Uemura, Akiko Haruna, Hiroaki Hanafusa, Kandai Nozu, Kazumoto Iijima
A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy. Human genome variation 7 (2020)
Shogo Minamikawa, Saori Miwa, Tetsuji Inagaki, Kei Nishiyama, Hiroshi Kaito, Takeshi Ninchoji, Tomohiko Yamamura, China Nagano, Nana Sakakibara, Shingo Ishimori, Shigeo Hara, Norishige Yoshikawa, Daishi Hirano, Ryoko Harada, Riku Hamada, Natsuki Matsunoshita, Michio Nagata, Yuko Shima, Koichi Nakanishi, Hiroaki Nagase, Hiroki Takeda, Naoya Morisada, Kazumoto Iijima, Kandai Nozu
Molecular mechanisms determining severity in patients with Pierson syndrome. Journal of human genetics 65 (4) (2020)
Rini Rossanti, Naoya Morisada, Kandai Nozu, Koichi Kamei, Tomoko Horinouchi, Tomohiko Yamamura, Shogo Minamikawa, Junya Fujimura, China Nagano, Nana Sakakibara, Takeshi Ninchoji, Hiroshi Kaito, Shuichi Ito, Ryojiro Tanaka, Kazumoto Iijima
Clinical and genetic variability of PAX2-related disorder in the Japanese population. Journal of human genetics 65 (6) (2020)
Takahisa Yoshikawa, Koichi Kamei, Hiroko Nagata, Ken Saida, Mai Sato, Masao Ogura, Shuichi Ito, Osamu Miyazaki, Maki Urushihara, Shuji Kondo, Noriko Sugawara, Kiyonobu Ishizuka, Yuko Hamasaki, Seiichiro Shishido, Naoya Morisada, Kazumoto Iijima, Michio Nagata, Takako Yoshioka, Kentaro Ogata, Kenji Ishikura
Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports. Nephrology (Carlton, Vic.) 22 (7) (2018)