Akira Murakami

Incidence of Benign and Malignant Eyelid Tumors in Japan

N. Ebihara, S. Okisaka, H. Toshida, 2012 .

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing

K. Tsunoda, Makoto Nakamura, K. Yoshitake, 2022, Human mutation.

Gene expression profile study of corneal endothelium

N. Tachibana, T. Funaki, T. Fujimaki, 2002 .

LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells

K. Tsunoda, K. Yoshitake, T. Iwata, 2018, Journal of Human Genetics.

Hidden Genetic Variation in LCA9‐Associated Congenital Blindness Explained by 5′UTR Mutations and Copy‐Number Variations of NMNAT1

R. Veitia, M. De Bruyne, F. Coppieters, 2015, Human mutation.

Central retinal vein occlusion caused by human herpesvirus 6.

A. Mizota, T. Fujimaki, Minoru Tanaka, 2006, Journal of pediatric ophthalmology and strabismus.

Solitary intramuscular myofibroma in an adult: Case report and MR imaging findings.

P. Staziaki, Irene Dixe de Oliveira Santo, T. Sachs, 2020, Clinical imaging.

LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells

K. Tsunoda, K. Yoshitake, T. Iwata, 2018, Journal of Human Genetics.

Age-Related Changes in Spectral Transmittance of the Human Crystalline Lens in situ

K. Ohnuma, A. Mizota, Y. Sakanishi, 2012, Ophthalmologica.