Robin A.J. Eady

Overview

Best Publications

• The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.

  Jo David Fine;Robin A J Eady;Eugene A. Bauer;Johann W. Bauer

  1191
  Citations

• Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

  Jo David Fine;Leena Bruckner-Tuderman;Robin A.J. Eady;Eugene A. Bauer

  1007
  Citations

• Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry.

  Jo-David Fine;Eugene A. Bauer;Robert A. Briggaman;D. Martin Carter

  682
  Citations

• Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa

  Jo David Fine;Robin A J Eady;Eugene A. Bauer;Robert A. Briggaman

  557
  Citations

• Anatomy and Organization of Human Skin

  J. A. McGrath;R. A. J. Eady;F. M. Pope

  483
  Citations

• Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome.

  J. A. McGrath;J. R. McMillan;Carrie S. Shemanko;S. K. Runswick

  480
  Citations

• A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering.

  E. B. Lane;E. L. Rugg;H. Navsaria;I. M. Leigh

  480
  Citations

• Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

  F.J.D. Smith;R.A.J. Eady;I.M. Leigh;J.R. McMillan

  453
  Citations

• Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

  W.H.I. McLean;E.L. Rugg;D.P. Lunny;S.M. Morley

  431
  Citations

• Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.

  David P. Kelsell;Elizabeth E. Norgett;Harriet Unsworth;Muy Teck Teh

  418
  Citations

• Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

  McGrath Ja;Gatalica B;Christiano Am;Li K

  397
  Citations

• Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.

  W. H. I. Mclean;L. Pulkkinen;F. J. D. Smith;E. L. Rugg

  392
  Citations

• Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome

  Dawn H. Siegel;Gabrielle H.S. Ashton;Homero G. Penagos;James V. Lee

  383
  Citations

• Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)

  Takahiro Hamada;W. H. Irwin McLean;Michele Ramsay;Gabrielle H. S. Ashton

  370
  Citations

• Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma.

  D. Keith B. Armstrong;Kevin E. McKenna;Patricia E. Purkis;Kathleen J. Green

  339
  Citations

• Evaluation of anchoring fibrils and other components of the dermal-epidermal junction in dystrophic epidermolysis bullosa by a quantitative ultrastructural technique.

  Michael J. Tidman;Robin A J Eady

  330
  Citations

• N-Terminal Deletion in a Desmosomal Cadherin Causes the Autosomal Dominant Skin Disease Striate Palmoplantar Keratoderma

  Lisa Rickman;Danijela Šimrak;Howard P. Stevens;Debbie M. Hunt

  278
  Citations

• Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14.

  Akemi Ishida-Yamamoto;John A. McGrath;Stephen J. Chapman;Irene M. Leigh

  271
  Citations

• Mast cell population density, blood vessel density and histamine content in normal human skin.

  R.A.J. Eady;T. Cowen;T.F. Marshall;Valerie Plummer

  231
  Citations

• Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis.

  A.H.M. Heagerty;A.R. Kennedy;I.M. Leigh;P. Purkis

  222
  Citations