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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. Increased expression of PLS3 correlates with better outcome in Sézary syndrome

    Boonk, S. E., Zoutman, W. H., Putter, H., Ram-Wolff, C., Felcht, M., Klemke, C. D., Ranki, A., Quaglino, P., Whittaker, S., Bagot, M., Willemze, R. & Vermeer, M. H., 28 Oct 2016, In : Journal of Investigative Dermatology.

    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. Roth Spots in Infective Endocarditis

    Mahroo, O. & Graham, E. M., 19 Jun 2014, In : New England Journal of Medicine. 370, 25, 1 p., e38.

    Research output: Contribution to journalLetter

  17. 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

  18. 'Dilatation' and 'dilation': trends in use on both sides of the Atlantic

    Mahroo, O. A., Shalchi, Z. & Hammond, C. J., 2014, In : The British journal of ophthalmology. N/A, N/A, p. N/A 2 p., N/A.

    Research output: Contribution to journalLetter

  19. Re: Abegg et al.: Microcystic Macular Edema: Retrograde Maculopathy Caused by Optic Neuropathy (Ophthalmology 2014;121:142-9)

    Mahroo, O., Shalchi, Z., Kisimbi, J., Sanyiwa, A. J., Mohamed, M. D. & Plant, G. T., 2014, In : Ophthalmology. 1 p.

    Research output: Contribution to journalLetter

  20. 2013
  21. Using cyanoacrylate glue for corneal perforations: caution with use of a needle and syringe

    Gavin, E. A., Mahroo, O. A., Lim, R. & de Benito-Llopis, L., Dec 2013, In : Cornea. 32, 12, p. e193-e193 1 p., N/A.

    Research output: Contribution to journalLetter

  22. 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

  23. Potential effect of 'cut-off intensity' on correlation between light meter measurements and time outdoors

    Mahroo, O. A., Gavin, E. A., Williams, K. M., De Smit, E., Hammond, C. J. & Morrison, D. A., Aug 2013, In : Eye. 27, 8, p. 990-991 2 p.

    Research output: Contribution to journalLetter

  24. Potential effects of laterality and learning on misalignment in marking horizontal meridian

    Mahroo, O. A. & Zuberbuhler, B., Jun 2013, In : Journal of Cataract and Refractive Surgery. 39, 6, p. 966-966 1 p., N/A.

    Research output: Contribution to journalLetter

  25. 2012
  26. 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

  27. Limbus vs. fornix-based trabeculectomy results

    Gavin, E. A., Mahroo, O. A. & Lim, K. S., Oct 2012, In : Ophthalmology. 119, 10, p. 2196-2196 1 p., N/A.

    Research output: Contribution to journalLetter

  28. 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

  29. Choice of analytic approach for eye-specific outcomes: one eye or two?

    Mahroo, O. A. R., Hammond, C. J. & Williamson, T. H., Apr 2012, In : American Journal of Ophthalmology. 153, 4, p. 781-2; author reply 782

    Research output: Contribution to journalLetter

  30. 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

  31. 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

  32. 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

  33. 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

  34. 2011
  35. 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

  36. 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

  37. 2010
  38. Selecting tomorrow's doctors: Money, motivation, and medicine

    Mahroo, O. A. R., 30 Nov 2010, In : BMJ. 341, c6830.

    Research output: Contribution to journalLetter

  39. Were the groups in the trabeculectomy versus Ahmed valve study really comparable?

    Mahroo, O. A. R., Stanbury, R. & Lim, K. S., Nov 2010, In : The British journal of ophthalmology. 94, 11, p. 1551-1552 2 p.

    Research output: Contribution to journalLetter

  40. 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

  41. 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

  42. 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

  43. 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

  44. 2009
  45. 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

  46. 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

  47. 2007
  48. 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

  49. Central nervous system involvement in stage 1b mycosis fungoides.

    Lally, A., Hollowood, K., Whittaker, S. & Turner, R., Oct 2007, In : British Journal of Dermatology. 157, 4, p. 815 - 816 2 p.

    Research output: Contribution to journalLetter

  50. 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

  51. Graft versus lymphoma effect early relapse following reduced-intensity allogenic stem cell transplantation for relapsed cytotoxic variant of mycosis fungoides.

    Gabriel, IH., Olavarria, E., Jones, RR., Whittaker, S., Chaideos, A. & Apperley, JF., 2 Aug 2007, In : Bone Marrow Transplantation. 40, 4, p. 401 - 403 3 p.

    Research output: Contribution to journalLetter

  52. Palliative care in patients with primary cutaneous lymphoma: symptom burden and characteristics of hospital palliative care team input.

    Lebon, B., Beynon, TA. & Whittaker, SJ., Mar 2007, In : Archives of Dermatology. 143, 3, p. 423 - 424 2 p.

    Research output: Contribution to journalLetter

  53. 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

  54. 2006
  55. 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

  56. Cytomegalovaris seroprevalence is not higher in patients with mycosis fungoides/Sezary syndrome.

    Gupta, R. K., Ramble, J., Tong, C. Y., Whittaker, S. & MacMahon, E., 2006, In : Blood. 107, 3, p. 1241 - 1242 2 p.

    Research output: Contribution to journalLetter

  57. 2005
  58. 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

  59. 2004
  60. 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

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