Yoshihiro Hotta
16PUBLICATIONS
34CO-AUTHORS
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Publications (16)
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|Sep 13, 2024
Ocular genetics in the Japanese population.Yoshihiro Hotta, Kaoruko Torii, Masakazu Takayama
|Sep 28, 2023
The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients.Kaoruko Torii, Sachiko Nishina, Hazuki Morikawa
|Mar 25, 2023
A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene.Hazuki Morikawa, Sachiko Nishina, Kaoruko Torii
|Nov 07, 2022
A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants.Akiko Hikoya, Katsuhiro Hosono, Kaoru Ono
|Mar 28, 2022
De novo heterozygous variants in KIF5B cause kyphomelic dysplasia.Toshiyuki Itai, Zheng Wang, Gen Nishimura
|Feb 25, 2022
Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa.Nobutaka Tachibana, Katsuhiro Hosono, Shuhei Nomura
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Frequent Collaborators
5 joint publications
Katsuhiro Hosono
5 joint publications
Kei Mizobuchi
5 joint publications
Maki Fukami
4 joint publications
Takaaki Hayashi
3 joint publications
Satoshi Katagiri
3 joint publications
Hirotomo Saitsu
2 joint publications
Tsutomu Ogata
2 joint publications
Masafumi Ohtsubo
2 joint publications
Nobutaka Tachibana
1 joint publications
Kentaro Kurata
