King's College London

Research portal

Research Outputs

  1. 2020
  2. 2019
  3. Twaroski, K, Eide, C, Riddle, MJ, Xia, L, Lees, CJ, Chen, W, Mathews, W, Keene, DR, McGrath, JA & Tolar, J 2019, 'Revertant mosaic fibroblasts in recessive dystrophic epidermolysis bullosa', British Journal of Dermatology, vol. 181, no. 6, pp. 1247-1253. https://doi.org/10.1111/bjd.17943
  4. Onoufriadis, A, Hsu, CK, Eide, CR, Nanda, A, Orchard, GE, Tomita, K, Sheriff, A, Scott, W, Tierney, C, Lee, JYW, Gomaa, NS, Desomchoke, R, Lwin, SM, Tu, WT, Chen, LY, Huang, HY, Chao, SC, Yu-Yun Lee, J, Bare, Y, Hayday, T, Guy, AL, Liu, L, Lees, C, Hirdler, T, Lovell, P, Xia, L, Dayrit, JF, Calonje, E, Simpson, MA, Tolar, J, Parsons, M & McGrath, JA 2019, 'Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica', Journal of Investigative Dermatology, vol. 139, no. 12, pp. 2550-2554.e9. https://doi.org/10.1016/j.jid.2019.05.021
  5. Vahidnezhad, H, Youssefian, L, Daneshpazhooh, M, Mahmoudi, H, Kariminejad, A, Fischer, J, Christiansen, J, Schneider, H, Guy, A, Liu, L, McGrath, JA, Has, C & Uitto, J 2019, 'Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out”', Matrix Biology, vol. 83, pp. 48-59. https://doi.org/10.1016/j.matbio.2019.07.002
  6. Chasseuil, E, McGrath, JA, seo, A, Balguerie, X, Bodak, N, Chasseuill, H, Denis-Musquer, M, Goldenberg, A, Goussot, R, Irvine, AD, Khumalo, NP, King, MC, Kury, S, Lipsker, D, Mallet, S, Mayosi, BM, Nanda, A, Puzenat, E, Salort-Campana, E, Sidbury, R, Shimamura, A, Bezieau, S, Mercier, S & Barbarot, S 2019, 'Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients.', British Journal of Dermatology, vol. 181, no. 4, pp. 862-864. https://doi.org/10.1111/bjd.17996
  7. Di, WL, Lwin, SM, Petrova, A, Bernadis, C, Syed, F, Farzaneh, F, Moulding, D, Martinez, AE, Sebire, NJ, Rampling, D, Virasami, A, Zamiri, M, Wang, W, Hara, H, Kadiyirire, T, Abdul-Wahab, A, Martinez-Queipo, M, Harper, JI, McGrath, JA, Thrasher, AJ, Mellerio, JE & Qasim, W 2019, 'Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial', Human Gene Therapy, vol. 30, no. 9, pp. 1067-1078. https://doi.org/10.1089/hum.2019.049
  8. Elias, MS, Wright, SC, Remenyi, J, Abbott, JC, Bray, SE, Cole, C, Edwards, S, Gierlinski, M, Glok, M, McGrath, JA, Nicholson, WV, Paternoster, L, Prescott, AR, Have, ST, Whitfield, PD, Lamond, AI & Brown, SJ 2019, 'EMSY expression affects multiple components of the skin barrier with relevance to atopic dermatitis', Journal of Allergy and Clinical Immunology, vol. 144, no. 2, pp. 470-481. https://doi.org/10.1016/j.jaci.2019.05.024
  9. Atanasova, VS, Russell, RJ, Webster, TG, Cao, Q, Agarwal, P, Lim, YZ, Krishnan, S, Fuentes, I, Guttmann-Gruber, C, McGrath, JA, Salas-Alanis, JC, Fertala, A & South, AP 2019, 'Thrombospondin-1 Is a Major Activator of TGF-β Signaling in Recessive Dystrophic Epidermolysis Bullosa Fibroblasts', Journal of Investigative Dermatology, vol. 139, no. 7, pp. 1497-1505.e5. https://doi.org/10.1016/j.jid.2019.01.011
  10. Simpson, JK, Martinez-Quiepo, M, Onoufriadis, A, Tso, S, Glass, E, Liu, L, Higashino, T, Scott, W, Tierney, C, Simpson, MA, Desomchoke, R, Youssefian, L, SaeIdian, AH, Vahidnezhad, H, Bisquera, A, Ravenscroft, J, Moss, C, O'Toole, EA, Burrows, N, Leech, S, Jones, EA, Lim, D, Ilchyshyn, A, Goldstraw, N, Cork, MJ, Darne, S, Uitto, J, Martinez, AE, Mellerio, JE & McGrath, JA 2019, 'Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis', British Journal of Dermatology. https://doi.org/10.1111/bjd.18211
  11. Lwin, SM, Syed, F, Di, W, Kadiyirire, T, Liu, L, Guy, A, Petrova, A, Abdul-Wahab, A, Reid, F, Phillips, R, Elstad, M, Georgiadis, C, Aristodemou, S, Lovell, PA, Mcmillan, JR, Mee, J, Miskinyte, S, Titeux, M, Ozoemena, L, Pramanik, R, Serrano, S, Rowles, R, Maurin, C, Orrin, E, Martinez-Queipo, M, Rashidghamat, E, Tziotzios, C, Onoufriadis, A, Chen, M, Chan, L, Farzaneh, F, Del Rio, M, Tolar, J, Bauer, JW, Larcher, F, Antoniou, MN, Hovnanian, A, Thrasher, AJ, Mellerio, JE, Qasim, W & Mcgrath, JA 2019, 'Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa', JCI Insight, vol. 4, no. 11, :e126243. https://doi.org/10.1172/jci.insight.126243
  12. Atanasova, VS, Pourreyron, C, Farshchian, M, Lawler, M, Brown, CA, Watt, SA, Wright, S, Warkala, M, Guttmann-Gruber, C, Hofbauer, JP, Fuentes, I, Prisco, M, Rashidghamat, E, Has, C, Salas-Alanis, JC, Palisson, F, Hovnanian, A, McGrath, JA, Mellerio, JE, Bauer, JW & South, AP 2019, 'Identification of rigosertib for the treatment of recessive dystrophic epidermolysis bullosa–associated squamous cell carcinoma', Clinical Cancer Research, vol. 25, no. 11, pp. 3384-3391. https://doi.org/10.1158/1078-0432.CCR-18-2661
  13. Anzilotti, C, Swan, DJ, Boisson, B, Deobagkar-Lele, M, Oliveira, C, Chabosseau, P, Engelhardt, KR, Xu, X, Chen, R, Alvarez, L, Berlinguer-Palmini, R, Bull, KR, Cawthorne, E, Cribbs, AP, Crockford, TL, Dang, TS, Fearn, A, Fenech, EJ, de Jong, SJ, Lagerholm, BC, Ma, CS, Sims, D, van den Berg, B, Xu, Y, Cant, AJ, Kleiner, G, Leahy, TR, de la Morena, MT, Puck, JM, Shapiro, RS, van der Burg, M, Chapman, JR, Christianson, JC, Davies, B, McGrath, JA, Przyborski, S, Santibanez Koref, M, Tangye, SG, Werner, A, Rutter, GA, Padilla-Parra, S, Casanova, JL, Cornall, RJ, Conley, ME & Hambleton, S 2019, 'An essential role for the Zn 2+ transporter ZIP7 in B cell development', Nature Immunology, vol. 20, no. 3, pp. 350-361. https://doi.org/10.1038/s41590-018-0295-8
  14. Anzilotti, C, Swan, DJ, Boisson, B, Deobagkar-Lele, M, Oliveira, C, Chabosseau, P, Engelhardt, KR, Xu, X, Chen, R, Alvarez, L, Berlinguer-Palmini, R, Bull, KR, Cawthorne, E, Cribbs, AP, Crockford, AP, Dang, TS, Fearn, A, Fenech, EJ, de Jong, S, Lagerholm, BC, Ma, C, Sims, D, van den Berg, B, Xu, Y, Cant, AJ, Kleiner, G, Leahy, TR, McGrath, JA, Przyborski, S, Santibanez-Koref, M, Tangye, SG, Werner, A, Rutter, GA, Padilla Parra, S, Casanova, J, Cornall, R, Conley, ME & Hambleton, S 2019, 'An essential role for the Zn2+ transporter ZIP7 in B cell development', Nature Immunology, pp. 350-361.
  15. Tziotzios, C, Petridis, C, Dand, N, Ainali, C, Saklatvala, JR, Pullabhatla, V, Onoufriadis, A, Pramanik, R, Baudry, D, Lee, SH, Wood, K, Liu, L, Seegobin, S, Michelotti, GA, Lwin, SM, Christou, EAA, Curtis, CJ, de Rinaldis, E, Saxena, A, Holmes, S, Harries, M, Palamaras, I, Cunningham, F, Parkins, G, Kaur, M, Farrant, P, McDonagh, A, Messenger, A, Jones, J, Jolliffe, V, Ali, I, Ardern-Jones, M, Mitchell, C, Burrows, N, Atkar, R, Banfield, C, Alexandroff, A, Champagne, C, Cooper, HL, Vañó-Galván, S, Molina-Ruiz, AM, Perez, NO, Patel, GK, Macbeth, A, Page, M, Bryden, A, Mowbray, M, Wahie, S, Armstrong, K, Cooke, N, Goodfield, M, Man, I, de Berker, D, Dunnill, G, Takwale, A, Rao, A, Siah, T-W, Sinclair, R, Wade, MS, Dlova, NC, Setterfield, J, Lewis, F, Bhargava, K, Kirkpatrick, N, Estivill, X, Stefanato, CM, Flohr, C, Spector, T, Watt, FM, Smith, CH, Barker, JN, Fenton, DA, Simpson, MA & McGrath, JA 2019, 'Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02', Nature Communications, vol. 10, no. 1, 1150, pp. 1-9. https://doi.org/10.1038/s41467-019-09117-w
  16. 2018
  17. The Acne Genetic Study Group, Petridis, C, Navarini, AA, Dand, N, Saklatvala, J, Baudry, D, Duckworth, M, Allen, MH, Curtis, CJ, Lee, SH, Burden, AD, Layton, A, Bataille, V, Pink, AE, Alexandroff, A, Anstey, A, Azad, J, Aziz, O, Burrows, N, Butt, A, Cartwright, P, Chapman, A, Clayton, TH, Cliff, S, Cutler, T, Daly, B, Darvay, A, DeGiovanni, C, Downs, A, Dwyer, C, English, J, Ferguson, A, Fleming, C, Fraser-Andrews, E, Goodfield, M, Grattan, CE, Hempel, H, Hood, S, Hughes, B, Ladoyanni, E, Lyon, C, Mahmud, A, Malik, M, Mallon, E, Meggitt, S, Messenger, A, Moosa, Y, Munn, S, Ormerod, A, Rallan, D, Ross, J, McGrath, JA, Barker, JNWN, Smith, CH, Spector, TD, Smith, CH, Barker, JN & Simpson, MA 2018, 'Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne', Nature Communications, vol. 9, no. 1, 5075. https://doi.org/10.1038/s41467-018-07459-5
  18. Vahidnezhad, H, Youssefian, L, Saeidian, AH, Touati, A, Pajouhanfar, S, Baghdadi, T, Shadmehri, AA, Giunta, C, Kraenzlin, M, Syx, D, Malfait, F, Has, C, Lwin, SM, Karamzadeh, R, Liu, L, Guy, A, Hamid, M, Kariminejad, A, Zeinali, S, McGrath, JA & Uitto, J 2018, 'Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency', Matrix Biology. https://doi.org/10.1016/j.matbio.2018.11.006
  19. Cho, RJ, Alexandrov, LB, Den Breems, NY, Atanasova, VS, Farshchian, M, Purdom, E, Nguyen, TN, Coarfa, C, Rajapakshe, K, Prisco, M, Sahu, J, Tassone, P, Greenawalt, EJ, Collisson, EA, Wu, W, Yao, H, Su, X, Guttmann-Gruber, C, Hofbauer, JP, Hashmi, R, Fuentes, I, Benz, SC, Golovato, J, Ehli, EA, Davis, CM, Davies, GE, Covington, KR, Murrell, DF, Salas-Alanis, JC, Palisson, F, Bruckner, AL, Robinson, W, Has, C, Bruckner-Tuderman, L, Titeux, M, Jonkman, MF, Rashidghamat, E, Lwin, SM, Mellerio, JE, McGrath, JA, Bauer, JW, Hovnanian, A, Tsai, KY & South, AP 2018, 'APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa', Science Translational Medicine, vol. 10, no. 455, eaas9668. https://doi.org/10.1126/scitranslmed.aas9668
  20. Liao, Y, Ivanova, L, Sivalenka, R, Plumer, T, Zhu, H, Zhang, X, Christiano, AM, McGrath, JA, Gurney, JP & Cairo, MS 2018, 'Efficacy of human placental-derived stem cells in collagen VII knockout (Recessive dystrophic epidermolysis bullosa) animal model', Stem cells translational medicine, vol. 7, no. 7, pp. 530-542. https://doi.org/10.1002/sctm.17-0182
  21. Mohamad, J, Samuelov, L, Malchin, N, Tiaber, S, Rabinowitz, T, Bitterman-Deutsch, O, Molho-Pessach, V, Cohen-Barak, E, Bach, G, Garty, B, Bergman, R, Harel, A, Nanda, A, Lestringant, G, McGrath, J, Shalev, S, Shomron, N, Mashiach, J, Eskin-Schwartz, M, Sarig, O & Sprecher, E 2018, '283 Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a middle eastern population: International Investigative Dermatology (IID) 2018 Meeting Abstract SupplementInternational Investigative Dermatology (IID) 2018', Journal of Investigative Dermatology, vol. 138, no. 5, Supplement, pp. S48. https://doi.org/10.1016/j.jid.2018.03.289
  22. 2017
  23. Vahidnezhad, H, Youssefian, L, Saeidian, AH, Mahmoudi, H, Touati, A, Abiri, M, Kajbafzadeh, AM, Aristodemou, S, Liu, L, McGrath, JA, Ertel, A, Londin, E, Kariminejad, A, Zeinali, S, Fortina, P & Uitto, J 2017, 'Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy', Matrix Biology. https://doi.org/10.1016/j.matbio.2017.11.003
Previous 1 2 3 4 5 6 7 8 ...12 Next

Export:RIS BibTex Word PDF - will at most contain 500 items

Refine results Clear filters

Language

Language

Publication year

Publication year

Full text

Full text

Meeting and poster abstracts

Authors

© 2018 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454