John A. McGrath
St John's Institute of Dermatology
King's College London (Guy's Campus)
London SE1 9RT
UK
Name/email consistency: high
- Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility. McGrath, J.A., Stone, K.L., Begum, R., Simpson, M.A., Dopping-Hepenstal, P.J., Liu, L., McMillan, J.R., South, A.P., Pourreyron, C., McLean, W.H., Martinez, A.E., Mellerio, J.E., Parsons, M. Am. J. Hum. Genet. (2012)
- Profilaggrin, dry skin, and atopic dermatitis risk: size matters. McGrath, J.A. J. Invest. Dermatol. (2012)
- Lethal acantholytic epidermolysis bullosa. McGrath, J.A., Bolling, M.C., Jonkman, M.F. Dermatol. Clin (2010)
- Ectodermal dysplasia-skin fragility syndrome. McGrath, J.A., Mellerio, J.E. Dermatol. Clin (2010)
- Filaggrin and the great epidermal barrier grief. McGrath, J.A. Australas. J. Dermatol. (2008)
- Second cite. McGrath, J.A. Clin. Exp. Dermatol. (2006)
- Inherited disorders of desmosomes. McGrath, J.A. Australas. J. Dermatol. (2005)
- Translational benefits from research on rare genodermatoses. McGrath, J.A. Australas. J. Dermatol. (2004)
- Recent advances in the molecular basis of inherited skin diseases. McGrath, J.A., Eady, R.A. Adv. Genet. (2001)
- Keratinocyte adhesion and the missing link: from Dowling-Meara to Hay-Wells. St John's Hospital Dermatological Society Annual Oration 2000. McGrath, J.A. Clin. Exp. Dermatol. (2001)
- Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations. McGrath, J.A., Ashton, G.H., Mellerio, J.E., Salas-Alanis, J.C., Swensson, O., McMillan, J.R., Eady, R.A. J. Invest. Dermatol. (1999)