Michiya Omi
5PUBLICATIONS
10CO-AUTHORS
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Publications (5)
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|Jun 23, 2025
The First Reported Japanese Case of PNPLA1-Nonsyndromic Epidermal Differentiation Disorder (PNPLA1-nEDD) Associated With an Unreported 92-Base-Pair Duplication Variant.Shiori Kato, Takuya Takeichi, Keisuke Jojima
|Oct 10, 2024
Comparing the severity of epidermolysis bullosa simplex harboring KRT5 variants with the AlphaMissense score.Michiya Omi, Takuya Takeichi, Takenori Yoshikawa
|Feb 16, 2024
Localized epidermolysis bullosa simplex caused by a previously unreported substitution in the linker 12 domain of keratin 14.Miyu Misaki, Takuya Takeichi, Michiya Omi
|Dec 19, 2023
Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations.Michiya Omi, Takuya Takeichi, Yasutoshi Ito
|Jul 04, 2023
An in-frame 18 bp deletion in linker domain L1 of KRT9 identified in a Japanese patient with epidermolytic palmoplantar keratoderma.Michiya Omi, Takuya Takeichi, Tomoko Chiba
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Frequent Collaborators
5 joint publications
Takuya Takeichi
5 joint publications
Yoshinao Muro
5 joint publications
Masashi Akiyama
2 joint publications
Yasutoshi Ito
1 joint publications
Takenori Yoshikawa
1 joint publications
Ryo Fukaura
1 joint publications
Keisuke Jojima
1 joint publications
Kana Tanahashi
1 joint publications
Atsushi Otsuka
1 joint publications
Akio Kihara
