F
Fenella Wojnarowska
Researcher at University of Oxford
Publications - 273
Citations - 13201
Fenella Wojnarowska is an academic researcher from University of Oxford. The author has contributed to research in topics: Bullous pemphigoid & Lichen sclerosus. The author has an hindex of 62, co-authored 273 publications receiving 12416 citations. Previous affiliations of Fenella Wojnarowska include James Cook University Hospital & Churchill Hospital.
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Journal ArticleDOI
The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators.
Lawrence S. Chan,A. Razzaque Ahmed,Grant J. Anhalt,Wolfgang Bernauer,Kevin D. Cooper,Mark J Elder,Jo-David Fine,C. Stephen Foster,Reza F. Ghohestani,Takashi Hashimoto,Thanh Hoang-Xuan,Gudula Kirtschig,Neil J. Korman,Susan Lightman,Francina Lozada-Nur,M. Peter Marinkovich,M. Peter Marinkovich,Bartly J. Mondino,Catherine Prost-Squarcioni,Roy S. Rogers,Jane Setterfield,Dennis P. West,Fenella Wojnarowska,David T. Woodley,Kim B. Yancey,Detlef Zillikens,John J. Zone +26 more
TL;DR: Specific consensus-based recommendations were made regarding the definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators for mucous membrane pemphigoid.
Journal ArticleDOI
Epitope spreading : Lessons from autoimmune skin diseases
Lawrence S. Chan,Carol J. Vanderlugt,Takashi Hashimoto,Takeji Nishikawa,John J. Zone,Martin M. Black,Fenella Wojnarowska,Seth R. Stevens,Mei Chen,Janet A. Fairley,David T. Woodley,Stephen D. Miller,Kenneth B. Gordon +12 more
TL;DR: The current concepts in animal models of autoimmune diseases are reviewed in order to define the "epitope spreading" phenomenon, and how this phenomenon might play a significant role in the development and the course of autoimmune skin diseases are proposed.
Journal ArticleDOI
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
Dawn H. Siegel,G H S Ashton,Homero Penagos,James V. Lee,Heidi S. Feiler,Kirk C. Wilhelmsen,Andrew P. South,Frances J.D. Smith,Alan R. Prescott,V Wessagowit,Noritaka Oyama,Masashi Akiyama,Daifullah Al Aboud,Khalid A Al Aboud,Ahmad Al Githami,Khalid Al Hawsawi,Abla Al Ismaily,Raouf Al-Suwaid,David J. Atherton,Ruggero Caputo,Jo David Fine,Ilona J. Frieden,Elaine Fuchs,Richard M. Haber,Takashi Harada,Yasuo Kitajima,Susan B. Mallory,Hideoki Ogawa,Sedef Şahin,Hiroshi Shimizu,Yasushi Suga,Gianluca Tadini,Kikuo Tsuchiya,Colin Wiebe,Fenella Wojnarowska,Adel B. Zaghloul,Takahiro Hamada,R. Mallipeddi,Robin A.J. Eady,W.H. Irwin McLean,John A. McGrath,Ervin H. Epstein +41 more
TL;DR: Kindler syndrome is, to the authors' knowledge, the first skin fragility disorder caused by a defect in actin-ECM linkage, rather than keratin- ECM linkage.
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Chronic bullous disease of childhood, childhood cicatricial pemphigoid, and linear IgA disease of adults. A comparative study demonstrating clinical and immunopathologic overlap.
TL;DR: It is suggested that adult linear IgA disease, chronic bullous disease of childhood, and childhood cicatricial pemphigoid are the same disease, with childhood cICatrician bullous diseases being a more severe form of chronic Bullous Disease of childhood.
Journal Article
A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer.
Samantha Winsey,Neil A. Haldar,Howard P. Marsh,Michael Bunce,Sara E. Marshall,Adrian L. Harris,Fenella Wojnarowska,Ken I. Welsh +7 more
TL;DR: The presence of a T allele in exon 7 (position 18067) of the XRCC3 gene was significantly associated with melanoma development, and may provide further insights into the pathogenesis and the mechanism of UV-radiation induced carcinogenesis as well as having a role in prevention.