Robin A.J. Eady

Robin A.J. Eady publication distribution in Biology and Biochemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Biology and Biochemistry in 2026. The highlighted bar marks where Robin A.J. Eady sits on this spectrum.

Robin A.J. Eady D-index placement in Biology and Biochemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Biology and Biochemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Robin A.J. Eady sits on this spectrum.

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