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Items where Author is "Simpson, Michael A."

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Petridis, Christos and Navarini, Alexander A. and Dand, Nick and Saklatvala, Jake and Baudry, David and Duckworth, Michael and Allen, Michael H. and Curtis, Charles J. and Lee, Sang Hyuck and Burden, A. David and Layton, Alison and Bataille, Veronique and Pink, Andrew E. and Carlavan, Isabelle and Voegel, Johannes J. and Spector, Timothy D. and Trembath, Richard C. and McGrath, John A. and Smith, Catherine H. and Barker, Jonathan N. and Simpson, Michael A.. (2018) Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. Nature Communications, 9 (1). p. 5075.

Lichtenberger, Ramtin and Simpson, Michael A. and Smith, Catherine and Barker, Jonathan and Navarini, Alexander A.. (2017) Genetic architecture of acne vulgaris. Journal of the European Academy of Dermatology & Venereology : JEADV, 31 (12). pp. 1978-1990.

Navarini, Alexander A. and Simpson, Michael A. and Borradori, Luca and Yawalkar, Nikhil and Schlapbach, Christoph. (2015) Homozygous missense mutation in IL36RN in generalized pustular dermatosis with intraoral involvement compatible with both AGEP and generalized pustular psoriasis. JAMA dermatology, 151 (4). pp. 452-453.

Setta-Kaffetzi, Niovi and Simpson, Michael A. and Navarini, Alexander A. and Patel, Varsha M. and Lu, Hui-Chun and Allen, Michael H. and Duckworth, Michael and Bachelez, Hervé and Burden, A. David and Choon, Siew-Eng and Griffiths, Christopher E. M. and Kirby, Brian and Kolios, Antonios and Seyger, Marieke M. B. and Prins, Christa and Smahi, Asma and Trembath, Richard C. and Fraternali, Franca and Smith, Catherine H. and Barker, Jonathan N. and Capon, Francesca. (2014) AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 trafficking. American Journal of Human Genetics, 94 (5). pp. 790-797.

Recher, Mike and Karjalainen-Lindsberg, Marja-Liisa and Lindlof, Mikael and Soderlund-Venermo, Maria and Lanzi, Gaetana and Väisänen, Elina and Kumar, Arun and Sadeghi, Mohammadreza and Berger, Christoph T. and Alitalo, Tiina and Anttila, Pekka and Kolehmainen, Maija and Franssila, Rauli and Chen, Tingting and Siitonen, Sana and Delmonte, Ottavia M. and Walter, Jolan E. and Pessach, Itai and Hess, Christoph and Simpson, Michael A. and Navarini, Alexander A. and Giliani, Silvia and Hedman, Klaus and Seppänen, Mikko and Notarangelo, Luigi D.. (2014) Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotype. Journal Of Allergy And Clinical Immunology, 133 (5). pp. 1462-1465.

Navarini, Alexander A. and Simpson, Michael A. and Weale, Michael and Knight, Jo and Carlavan, Isabelle and Reiniche, Pascale and Burden, David A. and Layton, Alison and Bataille, Veronique and Allen, Michael and Pleass, Robert and Pink, Andrew and Creamer, Daniel and English, John and Munn, Stephanie and Walton, Shernaz and Acne Genetic Study Group, and Willis, Carolyn and Déret, Sophie and Voegel, Johannes J. and Spector, Tim and Smith, Catherine H. and Trembath, Richard C. and Barker, Jonathan N.. (2014) Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. Nature Communications, 5. p. 4020.

Has, Cristina and Kiritsi, Dimitra and Mellerio, Jemima E. and Franzke, Claus-Werner and Wedgeworth, Emma and Tantcheva-Poor, Iliana and Kernland-Lang, Kristin and Itin, Peter and Simpson, Michael A. and Dopping-Hepenstal, Patricia J. and Fujimoto, Wataru and McGrath, John A. and Bruckner-Tuderman, Leena. (2014) The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome. Journal of investigative dermatology, Vol. 134, H. 3. pp. 845-849.

This list was generated on Fri Mar 29 03:14:37 2024 CET.