Yutaka Shimomura

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 22

Top Topics

Intellectual Disability

Angiotensin Converting Enzyme

Genome Wide Identification

Top Venues

The Journal of dermatology

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

Publications

Yuki Aoki, Hiroko Sugimoto, Kenta Sentoku, Takafumi Hisamoto, Yutaka Shimomura
Case of familial trichilemmal cyst caused by a recurrent monoallelic mutational mechanism in the PLCD1 gene. The Journal of dermatology (2024)
Naoko Shimomura, Hiroko Sugimoto, Ayana Nakayama, Kensaku Katsuki, Hidekazu Tanaka, Yutaka Shimomura
Case of mycosis fungoides palmaris et plantaris possibly associated with nail psoriasis. The Journal of dermatology (2023)
Toshihiko Aranishi, Taisuke Ito, Masahiro Fukuyama, Yoshitaka Isaka, deMauri S Mackie, Kristen King-Concialdi, Steven S Senglaub, Dena H Jaffe, Yutaka Shimomura, Manabu Ohyama
Prevalence of alopecia areata in Japan: Estimates from a nationally representative sample. The Journal of dermatology (2022)
Mami Onitsuka, Muhammad Farooq, Muhammad Nasir Iqbal, Shuichiro Yasuno, Yutaka Shimomura
A homozygous loss-of-function variant in the MPO gene is associated with generalized pustular psoriasis. The Journal of dermatology (2022)
Hidenobu Kaneyasu, Kazumasa Takahashi, Naoki Ohta, Seigo Okada, Sasagu Kimura, Shuichiro Yasuno, Susumu Murata, Shunsaku Katsura, Naoyuki Yamada, Koji Shiraishi, Junko Tsuda, Shunsuke Miyai, Hiroki Kurahashi, Shunji Hasegawa, Yutaka Shimomura
Novel compound heterozygous mutations in the PLEC gene in a neonate with epidermolysis bullosa simplex with pyloric atresia. The Journal of dermatology (2022)
Yutaka Shimomura
Welcome to the hair world! The Journal of dermatology 49 (1) (2022)
Sasagu Yagi, Shuichiro Yasuno, Osamu Ansai, Ryota Hayashi, Yutaka Shimomura
Different degree of loss-of-function among four missense mutations in the EDAR gene responsible for autosomal recessive hypohidrotic ectodermal dysplasia may be associated with the phenotypic severity. The Journal of dermatology (2022)
Minako Inazawa-Terada, Takeshi Namiki, Chika Omigawa, Tomoko Fujimoto, Takichi Munetsugu, Tsukasa Ugajin, Yutaka Shimomura, Yuichiro Ohshima, Kazue Yoshida, Hironori Niizeki, Ryota Hayashi, Hajime Nakano, Hiroo Yokozeki
An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases. The Journal of dermatology 49 (4) (2021)
Nobuyuki Asano, Shuichiro Yasuno, Ryota Hayashi, Yutaka Shimomura
Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia. The Journal of dermatology 48 (10) (2021)
Akito Hasegawa, Ryota Hayashi, Yutaka Shimomura, Masanori Hirashima, Riichiro Abe
Only plantar lesion of punctate palmoplantar keratoderma with a novel missense mutation in the AAGAB gene: Two Japanese familial case reports and review of reported mutations. The Journal of dermatology 48 (12) (2021)
Ryota Hayashi, Yutaka Shimomura
Update of recent findings in genetic hair disorders. The Journal of dermatology (2021)
Shuichiro Yasuno, Osamu Ansai, Ryota Hayashi, Sawako Nakamura, Yutaka Shimomura
Evidence for a dominant-negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I. The Journal of dermatology 48 (8) (2021)
Mami Onitsuka, Takahiro Yamada, Masahiko Muto, Anna Hirano, Yutaka Shimomura
Subcutaneous Trichophyton rubrum abscesses in an immunocompromised patient. The Journal of dermatology 47 (3) (2020)
Mami Onitsuka, Ryota Hayashi, Yoshio Kawakami, Shin Morizane, Yutaka Shimomura
Two cases of severe congenital hypotrichosis caused by compound heterozygous mutations in the LSS gene. The Journal of dermatology 48 (3) (2020)
Tomoko Okita, Nobuyuki Asano, Shuichiro Yasuno, Yutaka Shimomura
Functional studies for a dominant mutation in the EDAR gene responsible for hypohidrotic ectodermal dysplasia. The Journal of dermatology 46 (8) (2019)
Tomoko Okita, Michiya Yamaguchi, Nobuyuki Asano, Shuichiro Yasuno, Keisuke Kashiwagi, Yutaka Shimomura
Two Japanese families with hypohidrotic ectodermal dysplasia: Phenotypic differences between affected individuals. The Journal of dermatology 46 (3) (2018)
Nobuyuki Asano, Tomoko Okita, Shuichiro Yasuno, Michiya Yamaguchi, Keisuke Kashiwagi, Takuro Kanekura, Yutaka Shimomura
Identification of a novel splice site mutation in the LIPH gene in a Japanese family with autosomal recessive woolly hair. The Journal of dermatology 46 (1) (2018)
Motomu Manabe, Ryoji Tsuboi, Satoshi Itami, Shin-Ichi Osada, Yasuyuki Amoh, Taisuke Ito, Shigeki Inui, Rie Ueki, Manabu Ohyama, Sotaro Kurata, Takeshi Kono, Norimitsu Saito, Akio Sato, Yutaka Shimomura, Motonobu Nakamura, Hiroshi Narusawa, Masashi Yamazaki, null null
Guidelines for the diagnosis and treatment of male-pattern and female-pattern hair loss, 2017 version. The Journal of dermatology 45 (9) (2018)
Mami Nakajima, Ryota Hayashi, Satoru Shinkuma, Mio Watanabe, Yohya Shigehara, Yutaka Shimomura, Riichiro Abe
Two cases of hypohidrotic ectodermal dysplasia caused by novel deletion mutations in the EDA gene. The Journal of dermatology 46 (1) (2018)
Yukari Mizukami, Ryota Hayashi, Daisuke Tsuruta, Yutaka Shimomura, Koji Sugawara
Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review. The Journal of dermatology 45 (5) (2018)
Shuichiro Yasuno, Michiya Yamaguchi, Akemi Tanaka, Kaori Umehara, Tomoko Okita, Nobuyuki Asano, Keisuke Kashiwagi, Yutaka Shimomura
Case of generalized pustular psoriasis that might have progressed from terbinafine-induced acute generalized exanthematous pustulosis. The Journal of dermatology 45 (12) (2018)
Ami Hemmi, Ken Okamura, Ryushi Tazawa, Yuko Abe, Masahiro Hayashi, Shuji Izumi, Jun Tohyama, Yutaka Shimomura, Yutaka Hozumi, Tamio Suzuki
Waardenburg syndrome type IIE in a Japanese patient caused by a novel non-frame-shift duplication mutation in the SOX10 gene. The Journal of dermatology 45 (5) (2017)