King's College London

Research portal

Research Outputs

  1. 2017
  2. Tissue and circulating microRNA co-expression analysis reveals potential involvement of miRNAs in the pathobiology of frontal fibrosing alopecia

    Tziotzios, C., Ainali, C., Holmes, S., Cunningham, F., Lwin, S. M., Palamaras, I., Bhargava, K., Rymer, J., Stefanato, C., Kirkpatrick, N., Vano-Galvan, S., Petridis, C., Fenton, D. A., Simpson, M. A., Onoufriadis, A. & McGrath, J. A., 31 Jul 2017, In : Journal of Investigative Dermatology. 137, 11, p. 2440-2443

    Research output: Contribution to journalLetter

  3. ATR gene mutations in HPV negative oropharyngeal cancer

    Jeannon, J. P., Tanaka, A., Thavaraj, S., Guerrero-Urbano, T., McGrath, J. A. & Tavassoli, M., 1 Feb 2017, In : ORAL ONCOLOGY. 65, p. 121-123 3 p.

    Research output: Contribution to journalLetter

  4. Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis by a homozygous deletion mutation in SDR9C7

    Takeichi, T., Nomura, T., Takama, H., Kono, M., Sugiura, K., Watanabe, D., Shimizu, H., Simpson, M. A., McGrath, J. A. & Akiyama, M., 23 Jan 2017, In : British Journal of Dermatology.

    Research output: Contribution to journalLetter

  5. Mutations in KLHL24 add to the molecular heterogeneity of epidermolysis bullosa simplex

    Lee, J. Y. W., Liu, L., Hsu, C-K., Aristodemou, S., Ozoemena, L., Ogboli, M., Moss, C., Martinez, A. E., Mellerio, J. E. & McGrath, J. A., 19 Jan 2017, In : Journal of Investigative Dermatology. 137, 6, p. 1378-1380

    Research output: Contribution to journalLetter

  6. Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing

    Saito, R., Boyce, A., Hsu, C., Rashidghamat, E., Hide, M., Wedgeworth, E. K., Flohr, C., Mellerio, J. E. & Mcgrath, J. A., 1 Jan 2017, In : British Journal of Dermatology. 176, 1, p. 249-251

    Research output: Contribution to journalLetter

  7. 2016
  8. Immune response to Mycobacterium tuberculosis in young contacts with discordant immunological test results

    Jeljeli, M., Guérin-El Khourouj, V., Hormi, M., Sterkers, G., Pommelet, V., Faye, A., Guilmin-Crepon, S. & Gressens, P., 31 Aug 2016, In : The Journal of infection.

    Research output: Contribution to journalLetter

  9. Ichthyosis Prematurity Syndrome: From Fetus to Adulthood

    Lwin, S. M., Hsu, C-K., McMillan, J. R., Mellerio, J. E. & McGrath, J. A., 25 May 2016, In : JAMA dermatology.

    Research output: Contribution to journalLetter

  10. Finasteride is of uncertain utility in treating frontal fibrosing alopecia

    Tziotzios, C., Fenton, D. A., Stefanato, C. M. & McGrath, J. A., Apr 2016, In : Journal of the American Academy of Dermatology. 74, 4, p. e73-e74

    Research output: Contribution to journalLetter

  11. 2015
  12. Potential of Systemic Allogeneic Mesenchymal Stromal Cell Therapy for Children with Recessive Dystrophic Epidermolysis Bullosa

    Petrof, G., Lwin, S. M., Martinez-Queipo, M., Abdul-Wahab, A., Tso, S., Mellerio, J. E., Slaper-Cortenbach, I., Boelens, J. J., Tolar, J., Veys, P., Ofuya, M., Peacock, J., Martinez, A. E. & McGrath, J. A., Sep 2015, In : Journal of Investigative Dermatology.

    Research output: Contribution to journalLetter

  13. Familial frontal fibrosing alopecia

    Tziotzios, C., Fenton, D. A., Stefanato, C. M. & McGrath, J. A., Jul 2015, In : Journal of the American Academy of Dermatology. 73, 1, p. e37

    Research output: Contribution to journalLetter

  14. Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

    Pohler, E., Cunningham, F., Sandilands, A., Cole, C., Digby, S., McMillan, J. R., Aristodemou, S., McGrath, J. A., Smith, F. J. D., McLean, W. H. I., Munro, C. S. & Zamiri, M., 12 May 2015, In : British Journal of Dermatology. 173, 5

    Research output: Contribution to journalLetter

  15. 2014
  16. The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome

    Has, C., Kiritsi, D., Mellerio, J. E., Franzke, C-W., Wedgeworth, E., Tantcheva-Poor, I., Kernland-Lang, K., Itin, P., Simpson, M. A., Dopping-Hepenstal, P. J., Fujimoto, W., McGrath, J. A. & Bruckner-Tuderman, L., Mar 2014, In : Journal of Investigative Dermatology. 134, 3, p. 845-849 5 p., N/A.

    Research output: Contribution to journalLetter

  17. 2013
  18. Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

    Samuelov, L., Sarig, O., Harmon, R. M., Rapaport, D., Ishida-Yamamoto, A., Isakov, O., Koetsier, J. L., Gat, A., Goldberg, I., Bergman, R., Spiegel, R., Eytan, O., Geller, S., Peleg, S., Shomron, N., Goh, C. S. M., Wilson, N. J., Smith, F. J. D., Pohler, E., Simpson, M. A. & 6 others, McLean, W. H. I., Irvine, A. D., Horowitz, M., McGrath, J. A., Green, K. J. & Sprecher, E., Oct 2013, In : Nature Genetics. 45, 10, p. 1244-1248 6 p., N/A.

    Research output: Contribution to journalLetter

  19. 2012
  20. Case of Kindler syndrome resulting from mutation in the FERMT1 gene

    Wada, M., Masuda, K., Tsuruta, D., Tamai, K., Lai-Cheong, J. E., McGrath, J. A. & Katoh, N., Dec 2012, In : The Australasian journal of dermatology. 39, 12, p. 1057-1058 2 p., N/A.

    Research output: Contribution to journalLetter

  21. Twenty top tips to triumph in dermatology

    Finlay, A. Y., Griffiths, C. E. M. & McGrath, J. A., Aug 2012, In : British Journal of Dermatology. 167, 2, p. 445-446 3 p.

    Research output: Contribution to journalLetter

  22. Inhaled NO protects cerebral white matter in neonatal rats with combined brain and lung injury

    Pham, H., Vottier, G., Pansiot, J., Dalous, J., Gallego, J., Gressens, P., Duong-Quy, S., Dinh-Xuan, A-T., Mercier, J-C., Biran, V., Charriaut-Marlangue, C. & Baud, O., 15 Apr 2012, In : American Journal of Respiratory and Critical Care Medicine. 185, 8, p. 897-899 3 p., N/A.

    Research output: Contribution to journalLetter

  23. Compound heterozygous mutations in desmoplakin cause skin fragility and woolly hair

    Smith, F. J. D., Wilson, N. J., Moss, C., Dopping-Hepenstal, P. & McGrath, J., Apr 2012, In : British Journal of Dermatology. 166, 4, p. 894 - 896 3 p.

    Research output: Contribution to journalLetter

  24. Autosomal Recessive Epidermolysis Bullosa Simplex Due to Loss of BPAG1-e Expression

    Liu, L., Dopping-Hepenstal, P. J., Lovell, P. A., Michael, M., Horn, H., Fong, K., Lai-Cheong, J. E., Mellerio, J. E., Parsons, M. & McGrath, J. A., Mar 2012, In : Journal of Investigative Dermatology. 132, 3, p. 742 - 744 3 p.

    Research output: Contribution to journalLetter

  25. Revertant Mosaicism in Kindler Syndrome

    Lai-Cheong, J. E., Moss, C., Parsons, M., Almaani, N. & McGrath, J. A., Mar 2012, In : Journal of Investigative Dermatology. 132, 3, p. 730 - 732 3 p.

    Research output: Contribution to journalLetter

  26. Novel and recurrent COL7A1 mutations in Chilean patients with dystrophic epidermolysis bullosa

    Rodríguez, F. A., Gana, M. J., Yubero, M. J., Zillmann, G., Krämer, S. M., Catalán, J., Rubio-Astudillo, J., González, S., Liu, L., Ozoemena, L., Mellerio, J. E., Mellerio, J. M., McGrath, J. A., Palisson, F. & Conget, P., Feb 2012, In : Journal of Dermatological Science. 65, 2, p. 149-152 4 p., N/A.

    Research output: Contribution to journalLetter

  27. 2011
  28. Extracellular matrix protein 1 autoantibodies in male genital lichen sclerosus

    Edmonds, E. V. J., Oyama, N., Chan, I., Francis, N., McGrath, J. A. & Bunker, C. B., Jul 2011, In : British Journal of Dermatology. 165, 1, p. 218 - 219 2 p., N/A.

    Research output: Contribution to journalLetter

  29. Intra-familial Variability of Ectodermal Defects Associated with WNT10A Mutations

    Wedgeworth, E. K., Nagy, N., White, J. M. L., Pembroke, A. C. & McGrath, J. A., May 2011, In : Acta Dermato-Venereologica. 91, 3, p. 346 - 347 2 p.

    Research output: Contribution to journalLetter

  30. 2010
  31. Revertant Mosaicism in Recessive Dystrophic Epidermolysis Bullosa

    Almaani, N., Nagy, N., Liu, L., Dopping-Hepenstal, P. J. C., Lai-Cheong, J. E., Clements, S. E., Techanukul, T., Tanaka, A., Mellerio, J. E. & McGrath, J. A., Jul 2010, In : Journal of Investigative Dermatology. 130, 7, p. 1937 - 1940 4 p.

    Research output: Contribution to journalLetter

  32. Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis

    El-Kamah, G. Y., Fong, K., El-Ruby, M., Affifi, H. H., Clements, S. E., Lai-Cheong, J. E., Amr, K., El-Darouti, M. & McGrath, J. A., Jul 2010, In : British Journal of Dermatology. 163, 1, p. 213 - 215 3 p.

    Research output: Contribution to journalLetter

  33. Identification of a Homozygous Deletion Mutation in C16orf57 in a Family With Clericuzio-Type Poikiloderma With Neutropenia

    Tanaka, A., Morice-Picard, F., Lacombe, D., Nagy, N., Hide, M., Taieb, A. & McGrath, J., Jun 2010, In : American Journal of Medical Genetics. Part A. 152A, 6, p. 1347 - 1348 2 p.

    Research output: Contribution to journalLetter

  34. Schopf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

    Nagy, N., Wedgeworth, E., Hamada, T., White, J. M., Hashimoto, T. & McGrath, J. A., Jun 2010, In : Journal of Dermatological Science. 58, 3, p. 220 - 222 3 p.

    Research output: Contribution to journalLetter

  35. 2009
  36. Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema

    Nagy, N., Greaves, M. W., Tanaka, A., McGrath, J. A. & Grattan, C. E., Oct 2009, In : Journal of Dermatological Science. 56, 1, p. 62 - 64 3 p.

    Research output: Contribution to journalLetter

  37. A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family

    Arita, K., Abe, R., Baba, K., McGrath, J. A., Akiyama, M. & Shimizu, H., Jul 2009, In : Journal of Dermatological Science. 55, 1, p. 64 - 65 2 p.

    Research output: Contribution to journalLetter

  38. 2007
  39. Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome

    Martignago, B. C. F., Lai-Cheong, J. E., Liu, L., McGrath, J. A. & Cestari, T. F., Dec 2007, In : British Journal of Dermatology. 157, 6, p. 1281 - 1284 4 p.

    Research output: Contribution to journalLetter

  40. Five new homozygous mutations in the KIND1 gene in Kindler syndrome

    Lai-Cheong, J. E., Liu, L., Sethuraman, G., Kumar, R., Sharma, V. K., Reddy, S. R., Vahlquist, A., Pather, S., Arita, K., Wessagowit, V. & McGrath, J. A., Sep 2007, In : Journal of Investigative Dermatology. 127, 9, p. 2268 - 2270 3 p.

    Research output: Contribution to journalLetter

  41. The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1

    Arita, K., Jacyk, W. K., Wessagowit, V., van Rensburg, E. J., Chaplin, T., Mein, C. A., Akiyama, M., Shimizu, H., Happle, R. & McGrath, J. A., Feb 2007, In : Journal of Investigative Dermatology. 127, 2, p. 490 - 493 4 p.

    Research output: Contribution to journalLetter

  42. 2006
  43. Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: Implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa

    Liu, L., Choy, Y. S., Wessagowit, V., Ozoemena, L., Dopping-Hepenstal, P. J. C., Fassihi, H. & McGrath, J. A., Oct 2006, In : Journal of Dermatological Science. 44, 1, p. 48 - 51 4 p.

    Research output: Contribution to journalLetter

  44. 2005
  45. Infantile acquired zinc deficiency resembling acrodermatitis enteropathica.

    Chew, A. L., Chan, I., McGrath, J. A. & Atherton, D. J., Sep 2005, In : Clinical and Experimental Dermatology. 30, 5, p. 594 - 595 2 p.

    Research output: Contribution to journalLetter

  46. 2004
  47. An Indian child with lipoid proteinosis resulting from a recurrent frameshift mutation (507delT) in the extracellular matrix protein 1 gene

    Chan, I., Bingewar, G., Patil, K., Nayak, C., Wadhwa, S. L. & McGrath, J. A., Sep 2004, In : British Journal of Dermatology. 151, 3, p. 726 - 727 2 p.

    Research output: Contribution to journalLetter

  48. Molecular basis of lipoid proteinosis in two Indian siblings

    Chan, I., Sethuraman, G., Sharma, V. K., Bruning, E., Hamada, T. & McGrath, J. A., Sep 2004, In : Journal of Dermatology. 31, 9, p. 764 - 766 3 p.

    Research output: Contribution to journalLetter

  49. Rapid diagnosis of lipoid proteinosis using an anti-extracelluar matrix protein 1 (ECM1) antibody

    Chan, I., South, A. P., McGrath, J. A., Oyama, N., Bhogal, B. S., Black, M. M. & Hamada, T., 2004, In : Journal of Dermatological Science. 35, 2, p. 151 - 153 3 p.

    Research output: Contribution to journalLetter

  50. 2002
  51. 2000
  52. A homozygous missense mutation in the cytoplasmic tail of beta 4 integrin, G931D, that disrupts hemidesmosome assembly nd underlies non-Herlitz junctional epidermolysis bullosa without pyloric atresia?

    Inoue, M., Tamai, K., Shimizu, H., Owaribe, K., Nakama, T., Hashimoto, T. & McGrath, J. A., 2000, In : Journal of Investigative Dermatology. 114, 5, p. 1061 - 1064 4 p.

    Research output: Contribution to journalLetter

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