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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. 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

  9. 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

  10. 2015
  11. 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

  12. 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

  13. 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

  14. 2014
  15. 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

  16. 2013
  17. 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

  18. 2012
  19. 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

  20. 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

  21. 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

  22. 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

  23. 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

  24. 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

  25. Antibodies to GP2, the major zymogen granule membrane glycoprotein, in inflammatory bowel diseases reply

    Roggenbuck, D., Reinhold, D., Wex, T., von Arnim, U., Malfertheiner, P., Sturm, A., Werner, L., Bogdanos, D. P., Laass, M. W. & Conrad, K., Jan 2012, In : Gut. 61, 1, p. 164 - 165 2 p.

    Research output: Contribution to journalLetter

  26. 2011
  27. 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

  28. Antibodies to glycoprotein 2 (GP2) in patients with inflammatory bowel diseases from UK

    Pavlidis, P., Forbes, A. & Bogdanos, D. P., 12 May 2011, In : Clinica Chimica Acta. 412, 11-12, p. 1163 - 1164 2 p.

    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. Primary biliary cirrhosis-specific autoantibodies in patients with systemic sclerosis

    Mytilinaiou, M. G. & Bogdanos, D. P., Dec 2009, In : DIGESTIVE AND LIVER DISEASE. 41, 12, p. 916 - 916 1 p.

    Research output: Contribution to journalLetter

  37. Anti-Helicobacter pylori antibody responses specific for VacA do not trigger primary biliary cirrhosis-specific antimitochondrial antibodies

    Koutsoumpas, A., Mytilinaiou, M., Polymeros, D., Dalekos, G. N. & Bogdanos, D. P., Oct 2009, In : European Journal of Gastroenterology and Hepatology. 21, 10, p. 1220 - 1220 1 p.

    Research output: Contribution to journalLetter

  38. 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

  39. 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

  40. 2008
  41. LKM1-positive type 2 autoimmune hepatitis following allogenic hematopoietic stem-cell transplantation

    Granito, A., Stanzani, M., Muratori, L., Bogdanos, D. P., Muratori, P., Pappas, G., Quarneti, C., Lenzi, M., Vergani, D. & Bianchi, F. B., May 2008, In : American Journal of Gastroenterology. 103, 5, p. 1313 - 1314 2 p.

    Research output: Contribution to journalLetter

  42. Disease-specific autoantibodies in patients with acute liver failure: The King's College London experience

    Bernal, W., Meda, F., Ma, Y., Bogdanos, D. P. & Vercani, D., Mar 2008, In : Hepatology. 47, 3, p. 1096 - 1097 2 p.

    Research output: Contribution to journalLetter

  43. 2007
  44. 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

  45. 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

  46. Anti-gp210 antibody mirrors disease severity in primary biliary cirrhosis

    Bogdanos, D. P., Liaskos, C., Pares, A., Norman, G., Rigopoulou, E. I., Caballeria, L., Dalekos, G. N., Rodes, J. & Vergani, D., Jun 2007, In : Hepatology. 45, 6, p. 1583 - 1583 1 p.

    Research output: Contribution to journalLetter

  47. 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

  48. Diagnostic relevance of anti-filamentous actin antibodies in autoimmune hepatitis

    Liaskos, C., Bogdanos, D. P., Davies, E. T. & Dalekos, G. N., Jan 2007, In : Journal of Clinical Pathology. 60, 1, p. 107 - 108 2 p.

    Research output: Contribution to journalLetter

  49. 2006
  50. Anti-mitochondrial antibodies in patients with systemic lupus erythematosus: Revealing the unforeseen

    Bogdanos, D. P., Liaskos, C., Rigopoulou, E. I., Liaskos, C. & Dalekos, G. N., Nov 2006, In : Clinica Chimica Acta. 373, 1-2, p. 183 - 184 2 p.

    Research output: Contribution to journalLetter

  51. Cytochrome P450 1A2 is a target antigen in hepatitic graft-versus-host disease

    Mullighan, C. G., Bogdanos, D. P., Vergani, D. & Bardy, P. G., Nov 2006, In : Bone Marrow Transplantation. 38, 10, p. 703 - 705 3 p.

    Research output: Contribution to journalLetter

  52. Borrelia Burgdorferi: a new self-mimicking trigger in primary biliary cirrhosis

    Bogdanos, D. P., Koutsoumpas, A., Baum, H. & Vergani, D., Oct 2006, In : DIGESTIVE AND LIVER DISEASE. 38, 10, p. 781 - 782 2 p.

    Research output: Contribution to journalLetter

  53. 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

  54. Self-mimicking autoimmune domains of hepatitis C virus core antigen

    Bogdanos, D. P. & Rigopoulou, E. I., 11 Sep 2006, In : Vaccine. 24, 37-39, p. 6173 - 6174 2 p.

    Research output: Contribution to journalLetter

  55. 2005
  56. 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

  57. 2004
  58. 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

  59. 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

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