Yoshikazu Shimomura

Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene

Tomoya O. Akama, Kohji Nishida, Jun Nakayama et al. · Nature Genetics · 2000 · 296 citations

Ocular Disease, Ophthalmology, Corneal Dystrophy +6

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

Motokazu Tsujikawa, Hiroki Kurahashi, Toshihiro Tanaka et al. · Nature Genetics · 1999 · 209 citations

Ocular Disease, Ophthalmology, Corneal Dystrophy +4

Quantification of Metamorphopsia in Patients with Epiretinal Membranes

Chota Matsumoto, E. Arimura, Sachiko Okuyama et al. · Investigative Ophthalmology & Visual Science · 2003 · 171 citations

Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan

Yukihiko Mashima, Shuji Yamamoto, Yoshitsugu Inoue et al. · American Journal of Ophthalmology · 2000 · 140 citations

Ocular Disease, Mendelian Disorder, Ophthalmology +8

Isolation and Chromosomal Localization of a Cornea-Specific Human Keratin 12 Gene and Detection of Four Mutations in Meesmann Corneal Epithelial Dystrophy

Kohji Nishida, Yoichi Honma, Atsuyoshi Dota et al. · The American Journal of Human Genetics · 1997 · 130 citations · Full text

Ophthalmology, Corneal Dystrophy, Genetics +6