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Y. Shimomura · SciRah

Researcher profile · Semantic Scholar

Y. Shimomura

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Y. Shimomura — researcher profile on SciRah

h-index: 32
Works: 188
Citations: 4,063

Most-cited papers

Guidelines for the diagnosis and treatment of male‐pattern and female‐pattern hair loss, 2017 version
M. Manabe, R. Tsuboi, S. Itami, S. Osada +13 more
2018Journal of dermatology (Print)75 citations Open access
Semantic Scholar
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis
Y. Shigehara, S. Okuda, G. Nemer, A. Chedraoui +10 more
201754 citations Open access
Semantic Scholar
Linagliptin‐associated bullous pemphigoid that was most likely caused by IgG autoantibodies against the midportion of BP180
A. Sakai, Y. Shimomura, O. Ansai, Y. Saito +6 more
2017British Journal of Dermatology36 citations
Semantic Scholar
Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles.
N. Zernov, M. Skoblov, A. Marakhonov, Y. Shimomura +4 more
2016Journal of Investigative Dermatology32 citations Open access
Semantic Scholar
SLURP‐1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
C. Bergqvist, H. Kadara, L. Hamie, G. Nemer +9 more
2018International Journal of Dermatology26 citations
Semantic Scholar
Functional studies for a dominant mutation in the EDAR gene responsible for hypohidrotic ectodermal dysplasia
T. Okita, Nobuyuki Asano, S. Yasuno, Y. Shimomura
2019Journal of dermatology (Print)22 citations
Semantic Scholar
An autosomal recessive mutation of DSG4 causes monilethrix through the ER stress response.
Madoka Kato, A. Shimizu, Y. Yokoyama, K. Kaira +5 more
2015Journal of Investigative Dermatology22 citations Open access
Semantic Scholar
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans
G. Nemer, N. El-Hachem, E. Eid, L. Hamie +8 more
2020Clinical Genetics20 citations
Semantic Scholar
Update of recent findings in genetic hair disorders
R. Hayashi, Y. Shimomura
2021Journal of dermatology (Print)19 citations
Semantic Scholar
Analysis of unique mutations in the LPAR6 gene identified in a Japanese family with autosomal recessive woolly hair/hypotrichosis: Establishment of a useful assay system for LPA6.
R. Hayashi, A. Inoue, Y. Suga, J. Aoki +1 more
2015Journal of dermatological science (Amsterdam)18 citations Open access
Semantic Scholar
Two cases of severe congenital hypotrichosis caused by compound heterozygous mutations in the LSS gene
Mami Murata, R. Hayashi, Yoshio Kawakami, S. Morizane +1 more
2020Journal of dermatology (Print)16 citations
Semantic Scholar
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis.
Y. Shigehara, S. Okuda, G. Nemer, A. Chedraoui +10 more
2016Human Molecular Genetics16 citations
Semantic Scholar
Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia
Nobuyuki Asano, S. Yasuno, R. Hayashi, Y. Shimomura
2021Journal of dermatology (Print)15 citations
Semantic Scholar
Understanding the phenotypic similarities between IFAP and Olmsted syndrome from a molecular perspective: the interaction of MBTPS2 and TRPV3
G. Nemer, R. Safi, F. Kreidieh, J. Usta +8 more
2017Archives of Dermatological Research15 citations
Semantic Scholar
Journey toward unraveling the molecular basis of hereditary hair disorders.
Y. Shimomura
2016Journal of dermatological science (Amsterdam)15 citations
Semantic Scholar
Cutaneous vasculitis induced by osimertinib.
K. Hamada, K. Oishi, T. Okita, A. Chikumoto +12 more
2019Journal of Thoracic Oncology12 citations Open access
Semantic Scholar
Panniculitis as the initial manifestation of dermatomyositis with anti‐MDA5 antibody
A. Hasegawa, Y. Shimomura, Natsuko Kibune, J. Koshio +2 more
2017Clincal and Experimental Dermatology12 citations
Semantic Scholar
Segmental lichen aureus in infancy
Y. Saito, Y. Shimomura, M. Orime, N. Kariya +1 more
2017Clincal and Experimental Dermatology12 citations
Semantic Scholar
Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
Y. Mizukami, R. Hayashi, D. Tsuruta, Y. Shimomura +1 more
2018Journal of dermatology (Print)11 citations
Semantic Scholar
Case of generalized pustular psoriasis that might have progressed from terbinafine‐induced acute generalized exanthematous pustulosis
S. Yasuno, Michiya Yamaguchi, A. Tanaka, K. Umehara +4 more
2018Journal of dermatology (Print)11 citations
Semantic Scholar
A novel heterozygous mutation in desmoplakin gene in a Lebanese patient with Carvajal syndrome and tooth agenesis
F. Bitar, T. Najjar, R. Hayashi, Georges Nemer +6 more
2016Journal of the European Academy of Dermatology and Venereology11 citations
Semantic Scholar
Perivascular Hedgehog responsive cells play a critical role in peripheral nerve regeneration via controlling angiogenesis.
Yurie Yamada, J. Nihara, Supaluk Trakanant, T. Kudo +8 more
2021Neurosciences research10 citations Open access
Semantic Scholar
Case of pemphigus herpetiformis with immunoglobulin G autoantibodies against desmocollin‐3
O. Ansai, Y. Shimomura, A. Fujimoto, A. Sakai +5 more
2017Journal of dermatology (Print)10 citations
Semantic Scholar
PLCD1 and Pilar Cysts.
Y. Shimomura, R. O'Shaughnessy, N. Rajan
2019Journal of Investigative Dermatology9 citations Open access
Semantic Scholar
First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24.
R. Hayashi, K. Yoshida, R. Abe, H. Niizeki +1 more
2017Journal of dermatological science (Amsterdam)9 citations
Semantic Scholar
Novel heterozygous deletion mutation c.821delC in the AAA domain of BCS1L underlies Björnstad syndrome
Y. Shigematsu, R. Hayashi, K. Yoshida, A. Shimizu +4 more
2017Journal of dermatology (Print)9 citations
Semantic Scholar
A novel mutation in the RSPO4 gene in a patient with autosomal recessive anonychia
S. Khalil, R. Hayashi, L. Daou, S. A. Staiteieh +5 more
2017Clincal and Experimental Dermatology9 citations
Semantic Scholar
Identification of a novel mutation in the LOR gene in an Iraqi patient with loricrin keratoderma resembling epidermolytic hyperkeratosis
S. Khalil, L. Daou, R. Hayashi, O. Abbas +4 more
2017Journal of the European Academy of Dermatology and Venereology8 citations
Semantic Scholar
Novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
Y. Matsuo, A. Tanaka, Y. Shimomura, M. Hide
2016Journal of dermatology (Print)8 citations
Semantic Scholar
Evidence for a dominant‐negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I
S. Yasuno, O. Ansai, R. Hayashi, Sawako Nakamura +1 more
2021Journal of dermatology (Print)6 citations
Semantic Scholar
Case of autosomal recessive woolly hair/hypotrichosis with atopic dermatitis
E. Itoh, T. Nakahara, M. Furumura, M. Furue +1 more
2017Journal of dermatology (Print)6 citations
Semantic Scholar
Erythropoietic protoporphyria a clinical and molecular study from Lebanon: Ferrochelatase a potential tumor suppressor gene in colon cancer
H. Kadara, G. Nemer, R. Safi, N. Rebeiz +9 more
2017Clinical Genetics6 citations
Semantic Scholar
Epidermolysis Bullosa Acquisita Develops in Dominant Dystrophic Epidermolysis Bullosa.
R. Hayashi, K. Natsuga, M. Watanabe, H. Iwata +5 more
2016Journal of Investigative Dermatology6 citations Open access
Semantic Scholar
Novel splice site mutation in the fumarate hydratase (FH) gene is associated with multiple cutaneous leiomyomas in a Japanese patient
Yukina Yoshinaga, H. Nakai, R. Hayashi, A. Ito +3 more
2016Journal of dermatology (Print)6 citations
Semantic Scholar
Identification of a novel mutation, c.686delAins18 (p.Asp229Glyfs*22), in the LIPH gene as a compound heterozygote with c.736T>A (p.Cys246Ser) in autosomal recessive woolly hair/hypotrichosis
T. Ito, Y. Shimomura, R. Hayashi, Y. Tokura
2015Journal of dermatology (Print)6 citations
Semantic Scholar
Novel compound heterozygous mutations in the PLEC gene in a neonate with epidermolysis bullosa simplex with pyloric atresia
Hidenobu Kaneyasu, Kazumasa Takahashi, N. Ohta, Seigo Okada +11 more
2022Journal of dermatology (Print)5 citations
Semantic Scholar
An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases
Minako Inazawa-Terada, T. Namiki, Chika Omigawa, Tomoko Fujimoto +9 more
2021Journal of dermatology (Print)5 citations
Semantic Scholar
Identification of a novel splice site mutation in the LIPH gene in a Japanese family with autosomal recessive woolly hair
Nobuyuki Asano, T. Okita, S. Yasuno, Michiya Yamaguchi +3 more
2018Journal of dermatology (Print)5 citations
Semantic Scholar
Identification of a recurrent mitochondrial mutation in a Japanese family with palmoplantar keratoderma, nail dystrophy, and deafness
R. Hayashi, H. Fujiwara, M. Morishita, Masaaki Ito +1 more
2015EJD. European journal of dermatology5 citations
Semantic Scholar
Waardenburg syndrome type IIE in a Japanese patient caused by a novel non‐frame‐shift duplication mutation in the SOX10 gene
Ami Hemmi, K. Okamura, R. Tazawa, Y. Abe +6 more
2018Journal of dermatology (Print)4 citations
Semantic Scholar
Hypohidrotic ectodermal dysplasia with strabismus
Aoi Okubo, K. Fujii, A. Arimura, Hiromi Katsue +3 more
2018Journal of dermatology (Print)4 citations
Semantic Scholar
A heterozygous mutation in the SAM domain of p63 underlies a mild form of ectodermal dysplasia.
T. Kawai, R. Hayashi, H. Nakai, Y. Shimomura +5 more
2018Journal of dermatological science (Amsterdam)4 citations Open access
Semantic Scholar
Structural behavior of keratin-associated protein 8.1 in human hair as revealed by a monoclonal antibody.
H. Akiba, Emina Ikeuchi, J. Ganbat, H. Fujikawa +6 more
2018Journal of Structural Biology4 citations
Semantic Scholar
Photodynamic therapy with intradermal application of 5‐aminolevulinic acid successfully improved tumor lesions of mycosis fungoides
Y. Kabata, Y. Shimomura, Yoshie Matsuo, H. Fujiwara +1 more
2017International Journal of Dermatology4 citations
Semantic Scholar
Case of infantile digital fibromatosis: Observation of its dermoscopic features
K. Tomii, Y. Shimomura, H. Fujikawa, N. Kariya +1 more
2017Journal of dermatology (Print)4 citations
Semantic Scholar
Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family
K. Yoshida, R. Hayashi, Y. Shimomura, H. Niizeki
2017Journal of dermatology (Print)4 citations
Semantic Scholar
Expression studies of nectin-1 in human hair follicles and identification of a p63-responsive element in the NECTIN1 promoter.
R. Hayashi, R. Abe, Y. Shimomura
2016Journal of dermatological science (Amsterdam)4 citations
Semantic Scholar
Case of unilateral epidermal nevi without extracutaneous anomalies
N. Kitayama, A. Otsuka, Y. Kaku, Y. Matsumura +5 more
2016Journal of dermatology (Print)4 citations
Semantic Scholar
Two-way Revascularization to Manage Celiac Artery Stenosis during Pancreaticoduodenectomy: A Case Report
Hiroyuki Takasu, Yasuyo Kuramoto, S. Yokoyama, H. Ota +4 more
2021Plastic and Reconstructive Surgery, Global Open3 citations Open access
Semantic Scholar
Alopecia areata and psoriasis vulgaris associated with Turner syndrome
R. Yokoyama, R. Hayashi, O. Ansai, A. Hasegawa +3 more
2021Australasian Journal of Dermatology3 citations
Semantic Scholar

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