| Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome JA McGrath, JR McMillan, CS Shemanko, SK Runswick, IM Leigh, ... Nature genetics 17 (2), 240-244, 1997 | 486 | 1997 |
| Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer M Akiyama, Y Sugiyama-Nakagiri, K Sakai, JR McMillan, M Goto, K Arita, ... The Journal of clinical investigation 115 (7), 1777-1784, 2005 | 479 | 2005 |
| Plectin deficiency results in muscular dystrophy with epidermolysis bullosa FJD Smith, RAJ Eady, IM Leigh, JR McMillan, EL Rugg, DP Kelsell, ... Nature genetics 13 (4), 450-457, 1996 | 458 | 1996 |
| Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa JA McGrath, B Gatalica, AM Christiano, K si, K Owaribe, JR McMillan, ... Nature genetics 11 (1), 83-86, 1995 | 406 | 1995 |
| Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. WH McLean, L Pulkkinen, FJ Smith, EL Rugg, EB Lane, F Bullrich, ... Genes & development 10 (14), 1724-1735, 1996 | 401 | 1996 |
| Humanization of autoantigen W Nishie, D Sawamura, M Goto, K Ito, A Shibaki, JR McMillan, K Sakai, ... Nature medicine 13 (3), 378-383, 2007 | 340 | 2007 |
| Hair follicle stem cells provide a functional niche for melanocyte stem cells S Tanimura, Y Tadokoro, K Inomata, NT Binh, W Nishie, S Yamazaki, ... Cell stem cell 8 (2), 177-187, 2011 | 316 | 2011 |
| Intercellular signaling and the polarization of body axes during Drosophila oogenesis 1711 RP Ray, T Schiipbach, WHI McLean, L Pulkkinen, FJD Smith, EL Rugg, ... DEVELOPMENT 10 (14), 1711-1844, 1996 | 254 | 1996 |
| A review of first aid treatments for burn injuries L Cuttle, J Pearn, JR McMillan, RM Kimble Burns 35 (6), 768-775, 2009 | 219 | 2009 |
| A functional" knockout" of human keratin 14. EL Rugg, WH McLean, EB Lane, R Pitera, JR McMillan, ... Genes & development 8 (21), 2563-2573, 1994 | 214 | 1994 |
| A homozygous nonsense mutation in the α3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa S Kivirikko, JA McGrath, C Baudoin, D Aberdam, S Ciatti, MGS Dunnill, ... Human molecular genetics 4 (5), 959-962, 1995 | 206 | 1995 |
| Epidermal basement membrane zone components: ultrastructural distribution and molecular interactions JR McMillan, M Akiyama, H Shimizu Journal of dermatological science 31 (3), 169-177, 2003 | 185 | 2003 |
| Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucida C Bedane, JR McMillan, SD Balding, P Bernard, C Prost, JM Bonnetblanc, ... Journal of investigative dermatology 108 (6), 901-907, 1997 | 185 | 1997 |
| Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress Swensson, Langbein, Mcmillan, Stevens, Leigh, Mclean, Lane, Eady British Journal of Dermatology 139 (5), 767-775, 1998 | 150 | 1998 |
| Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis … JA McGrath, B Gatalica, K Li, MG Dunnill, JR McMillan, AM Christiano, ... The American journal of pathology 148 (6), 1787, 1996 | 126 | 1996 |
| CTACK/CCL27 accelerates skin regeneration via accumulation of bone marrow‐derived keratinocytes D Inokuma, R Abe, Y Fujita, M Sasaki, A Shibaki, H Nakamura, ... Stem cells 24 (12), 2810-2816, 2006 | 122 | 2006 |
| Mutations in the rod 1A domain of keratins 1 and 10 in Bullous Congenital Ichthyosiform Erythoderma (BCIE) WHI McLean, RAJ Eady, PJC Dopping-Hepenstal, JR McMillan, IM Leigh, ... Journal of investigative dermatology 102 (1), 24-30, 1994 | 117 | 1994 |
| Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1 JA McGrath, PH Hoeger, AM Christiano, JR McMillan, JE Mellerio, ... British Journal of Dermatology 140 (2), 297-307, 1999 | 112 | 1999 |
| Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1) H Nakamura, D Sawamura, M Goto, H Nakamura, JR McMillan, S Park, ... The Journal of Molecular Diagnostics 7 (1), 28-35, 2005 | 107 | 2005 |
| Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations JA McGrath, GHS Ashton, JE Mellerio, JR McMillan, RAJ Eady, ... Journal of investigative dermatology 113 (3), 314-321, 1999 | 100 | 1999 |
John McGrathMay Dunhill Chair in Cutaneous Medicine, King's College LondonVerified email at kcl.ac.uk
