Naoto Nishimura

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 7

Top Topics

Attention Deficit Hyperactivity Disorder

Systemic Sclerosis

Top Venues

American journal of medical genetics. Part A

Congenital anomalies

Human genome variation

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

Publications

Minako Takagi, Shin Ono, Tatsuro Kumaki, Naoto Nishimura, Hiroaki Murakami, Yumi Enomoto, Takuya Naruto, Hideaki Ueda, Kenji Kurosawa
Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorder. American journal of medical genetics. Part A 191 (3) (2022)
Minako Takagi, Shin Ono, Tatsuro Kumaki, Naoto Nishimura, Hiroaki Murakami, Yumi Enomoto, Takuya Naruto, Hideaki Ueda, Kenji Kurosawa
Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorder. American journal of medical genetics. Part A 191 (3) (2022)
Minako Takagi, Shin Ono, Tatsuro Kumaki, Naoto Nishimura, Hiroaki Murakami, Yumi Enomoto, Takuya Naruto, Hideaki Ueda, Kenji Kurosawa
Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorder. American journal of medical genetics. Part A 191 (3) (2022)
Minako Takagi, Shin Ono, Tatsuro Kumaki, Naoto Nishimura, Hiroaki Murakami, Yumi Enomoto, Takuya Naruto, Hideaki Ueda, Kenji Kurosawa
Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorder. American journal of medical genetics. Part A (2022)
Naoto Nishimura, Hiroaki Murakami, Tomoko Hayashi, Hironobu Sato, Kenji Kurosawa
Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9. Congenital anomalies 60 (5) (2020)
Naoto Nishimura, Tatsuro Kumaki, Hiroaki Murakami, Yumi Enomoto, Kaoru Katsumata, Katsuaki Toyoshima, Kenji Kurosawa
Arthrogryposis multiplex congenita with polymicrogyria and infantile encephalopathy caused by a novel GRIN1 variant. Human genome variation 7 (2020)
Naoto Nishimura, Hiroaki Murakami, Toshiyuki Saito, Mitsuo Masuno, Kenji Kurosawa
Tumor predisposition in an individual with chromosomal rearrangements of 1q31.2-q41 encompassing cell division cycle protein 73. Congenital anomalies 60 (4) (2019)