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Research Outputs

  1. 2020
  2. Chiu, FPC, Salas-Alanis, JC, Amaya-Guerra, M, Cepeda-Valdes, R, McGrath, JA & Hsu, CK 2020, 'Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome', Clinical and Experimental Dermatology, vol. 45, no. 6, pp. 796-798. https://doi.org/10.1111/ced.14228
  3. Chiu, FPC, Wessagowit, V, Cakmak, MF, Doolan, BJ, Kootiratrakarn, T, Chaowalit, P, Bunnag, T, Simpson, MA, McGrath, JA & Onoufriadis, A 2020, 'Molecular basis and inheritance patterns of amyloidosis cutis dyschromica', Clinical and Experimental Dermatology, vol. 45, no. 5, pp. 650-653. https://doi.org/10.1111/ced.14183
  4. Takeichi, T, Suga, Y, Mizuno, T, Okuno, Y, Ichikawa, D, Kono, M, Lee, JYW, McGrath, JA & Akiyama, M 2020, 'Recurrent KRT10 variant in ichthyosis with confetti', Acta Dermato-Venereologica, vol. 100, no. 14, pp. 1-2. https://doi.org/10.2340/00015555-3570
  5. Deng, Q, Faghanimakrani, T & Aghvami, A-H 2020, GBDT-Based Modules for Force Prediction in a Model-Mediated Teleoperation System. in 2020 27th International Conference on Telecommunications (ICT) - Special Session on Machine Learning for Wireless Networks.
  6. Faghanimakrani, T, Aghvami, A-H, Shojaeifard, A & Wong, K-K 2020, Recurrent Neural Network Channel Estimation Using Measured Massive MIMO Data. in 2020 IEEE 31st Annual International Symposium on Personal, Indoor and Mobile Radio Communications (PIMRC).
  7. 2019
  8. 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
  9. 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
  10. Gouareb, R, Friderikos, V, Aghvami, AH & Tatipamula, M 2019, Joint reactive and proactive SDN controller assignment for load balancing. in 2019 IEEE Globecom Workshops, GC Wkshps 2019 - Proceedings., 9024555, 2019 IEEE Globecom Workshops, GC Wkshps 2019 - Proceedings, Institute of Electrical and Electronics Engineers Inc., 2019 IEEE Globecom Workshops, GC Wkshps 2019, Waikoloa, United States, 9/12/2019. https://doi.org/10.1109/GCWkshps45667.2019.9024555
  11. Hsu, CK, Yang, HS & McGrath, JA 2019, Genetics of scars and keloids. in Total Scar Management: From Lasers to Surgery for Scars, Keloids, and Scar Contractures. Springer Singapore, pp. 47-53. https://doi.org/10.1007/978-981-32-9791-3_4
  12. Faghani, T, Shojaeifard, A, Wong, KK & Aghvami, AH 2019, Deep Learning-Based Decision Region for MIMO Detection. in 2019 IEEE 30th Annual International Symposium on Personal, Indoor and Mobile Radio Communications, PIMRC 2019. vol. 2019-September, 8904346, Institute of Electrical and Electronics Engineers Inc., 30th IEEE Annual International Symposium on Personal, Indoor and Mobile Radio Communications, PIMRC 2019, Istanbul, Turkey, 8/09/2019. https://doi.org/10.1109/PIMRC.2019.8904346
  13. 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
  14. 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
  15. 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
  16. Faghanimakrani, T, Aghvami, A-H, Shojaeifard, A & Wong, K-K 2019, Deep Learning-Based Decision Region for MIMO Detection. in 2019 IEEE 30th Annual International Symposium on Personal, Indoor and Mobile Radio Communications (PIMRC).
  17. Hu, F, Babaei, A & Aghvami, AH 2019, Physical layer security in cellular network in the presence of terrains. in 2019 26th International Conference on Telecommunications, ICT 2019., 8798842, Institute of Electrical and Electronics Engineers Inc., pp. 16-20, 26th International Conference on Telecommunications, ICT 2019, Hanoi, Viet Nam, 8/04/2019. https://doi.org/10.1109/ICT.2019.8798842
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. Alsobhi, W & Aghvami, A-H 2019, QoS-Aware Resource Allocation of Two-tier HetNet: A Q-learning Approach. in 2019 26th International Conference on Telecommunications, ICT 2019., 8798829, IEEE Communications Society, pp. 330-334. https://doi.org/10.1109/ICT.2019.8798829
  24. Gouareb, R, Friderikos, V & Aghvami, AH 2019, Placement and Routing of VNFs for Horizontal Scaling. in 2019 26th International Conference on Telecommunications, ICT 2019., 8798780, Institute of Electrical and Electronics Engineers Inc., pp. 154-159, 26th International Conference on Telecommunications, ICT 2019, Hanoi, Viet Nam, 8/04/2019. https://doi.org/10.1109/ICT.2019.8798780
  25. 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
  26. 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.
  27. 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
  28. 2018
  29. 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
  30. 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
  31. Vahidnezhad, H, Youssefian, L, Saeidian, AH, Touati, A, Sotoudeh, S, Jazayeri, A, Guy, A, Lovell, PA, Liu, L, Kariminejad, A, McGrath, JA, Zeinali, S & Uitto, J 2018, 'Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa', Human Mutation, vol. 39, no. 10, pp. 1349-1354. https://doi.org/10.1002/humu.23592
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