{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T11:59:00Z","timestamp":1791115140095,"version":"4.1.0"},"reference-count":134,"publisher":"MDPI AG","issue":"3","license":[{"start":{"date-parts":[[2014,8,4]],"date-time":"2014-08-04T00:00:00Z","timestamp":1407110400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Genes"],"abstract":"<jats:p>The last decade has seen considerable advances in our understanding of the genetic basis of skin disease, as a consequence of high throughput sequencing technologies including next generation sequencing and whole exome sequencing. We have now determined the genes underlying several monogenic diseases, such as harlequin ichthyosis, Olmsted syndrome, and exfoliative ichthyosis, which have provided unique insights into the structure and function of the skin. In addition, through genome wide association studies we now have an understanding of how low penetrance variants contribute to inflammatory skin diseases such as psoriasis vulgaris and atopic dermatitis, and how they contribute to underlying pathophysiological disease processes. In this review we discuss strategies used to unravel the genes underlying both monogenic and complex trait skin diseases in the last 10 years and the implications on mechanistic studies, diagnostics, and therapeutics.<\/jats:p>","DOI":"10.3390\/genes5030615","type":"journal-article","created":{"date-parts":[[2014,8,5]],"date-time":"2014-08-05T10:59:37Z","timestamp":1407236377000},"page":"615-634","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":14,"title":["Discovery in Genetic Skin Disease: The Impact of High Throughput Genetic Technologies"],"prefix":"10.3390","volume":"5","author":[{"given":"Thiviyani","family":"Maruthappu","sequence":"first","affiliation":[{"name":"Centre for Cutaneous Research, Blizard Institute, Barts and The London School of Medicine  and Dentistry, Queen Mary University of London, 4 Newark Street, London E1 2AT, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claire","family":"Scott","sequence":"additional","affiliation":[{"name":"Centre for Cutaneous Research, Blizard Institute, Barts and The London School of Medicine  and Dentistry, Queen Mary University of London, 4 Newark Street, London E1 2AT, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Kelsell","sequence":"additional","affiliation":[{"name":"Centre for Cutaneous Research, Blizard Institute, Barts and The London School of Medicine  and Dentistry, Queen Mary University of London, 4 Newark Street, London E1 2AT, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2014,8,4]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"1131","DOI":"10.1093\/hmg\/9.7.1131","article-title":"Hailey-hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump","volume":"9","author":"Sudbrak","year":"2000","journal-title":"Hum. 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