• 788 Citations
  • 14 h-Index
20042019
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Fingerprint Dive into the research topics where Neil Wilson is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 9 Similar Profiles
Mutation Medicine & Life Sciences
Palmoplantar Keratoderma Medicine & Life Sciences
Pachyonychia Congenita Medicine & Life Sciences
Desmoglein 1 Medicine & Life Sciences
Keratins Medicine & Life Sciences
Desmoplakins Medicine & Life Sciences
Genes Medicine & Life Sciences
Skin Medicine & Life Sciences

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Research Output 2004 2019

  • 788 Citations
  • 14 h-Index
  • 25 Article
  • 13 Letter
  • 4 Meeting abstract
  • 2 Book/Film/Article review

Novel mutations in desmoglein 1: Focal palmoplantar keratoderma in milder phenotypes

Zamiri, M., Wilson, N. J., O'Toole, E. A. & Smith, F. J. D., 1 Sep 2019, In : British Journal of Dermatology. 181, 3, p. 618-620 3 p.

Research output: Contribution to journalLetter

Desmoglein 1
Keratin-16
Keratin-1
Desmoplakins
Palmoplantar Keratoderma
1 Citation (Scopus)

Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma

Smith, F. J. D., Kreuser-Genis, I. M., Jury, C. S., Wilson, N. J., Terron-Kwiatowski, A. & Zamiri, M., 4 Oct 2018, In : Clinical and Experimental Dermatology. 7 p.

Research output: Contribution to journalArticle

Keratoderma, Palmoplantar, Epidermolytic
Epidermolytic Hyperkeratosis
Keratin-1
Palmoplantar Keratoderma
Mutation
1 Citation (Scopus)

Painful punctate palmoplantar keratoderma due to heterozygous mutations in AAGAB

Zamiri, M., Wilson, N. J., Mackenzie, A., Sobey, G., Leitch, C. & Smith, F. J. D., 19 Nov 2018, In : The British journal of dermatology. 7 p.

Research output: Contribution to journalLetter

Palmoplantar Keratoderma
Mutation
Genes
Weight-Bearing
Carrier Proteins

Skin fragility, woolly hair syndrome with a desmoplakin mutation – a case from India

Peter, D. C. V., Thomas, M., Wilson, N. J. & Smith, F. J. D., Sep 2018, In : International Journal of Dermatology. 57, 9, p. e73-e75 3 p.

Research output: Contribution to journalLetter

First Report of Pachyonychia Congenita Type PC-K6a in the Romanian Population

Chiriac, A., Rusu, C., Murgu, A., Chiriac, A. E., Wilson, N. J. & Smith, F. J. D., Jun 2017, In : Maedica. 12, 2, p. 123-126 4 p.

Research output: Contribution to journalArticle

Pachyonychia Congenita
Population
Nails
Natal Teeth
Follicular Cyst

Press / Media

Rare skin disease gene discovered

Elizabeth Pohler, Alan Irvine, Toshifumi Nomura, John A. McGrath, W. H. Irwin McLean, Neil Wilson, Frances J. D. Smith, Aileen Sandilands, Christian Cole, Alan Evans, Sara J. Brown & David R. Goudie

15/10/12

1 item of Media coverage

Press/Media: Research