John A. McGrath

Research.com Recognitions

• 2026 - Research.com Biology and Biochemistry in United Kingdom Leader Award
• 2025 - Research.com Biology and Biochemistry in United Kingdom Leader Award

Overview

Best Publications

• Severity Scoring of Atopic Dermatitis: The SCORAD Index

  K.U. Schallreuter;Ch. Levenig;J. Berger;J. Umbert

  3046
  Citations

• 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

• Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations.

  P. J. Pollard;J. J. Briere;N. A. Alam;J. Barwell

  997
  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

• Prediction of Real-World Functional Disability in Chronic Mental Disorders: A Comparison of Schizophrenia and Bipolar Disorder

  Christopher R. Bowie;Colin Depp;John A. McGrath;Paula Wolyniec

  545
  Citations

• Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

  C. Has;J.W. Bauer;C. Bodemer;M.C. Bolling

  540
  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

• Hay–Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

  John A. McGrath;Pascal H.G. Duijf;Volker Doetsch;Alan D. Irvine

  461
  Citations

• Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation

  Franklin L. Zhong;Ons Mamaï;Lorenzo Sborgi;Lobna Boussofara

  423
  Citations

• Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa

  John E Wagner;Akemi Ishida-Yamamoto;John A McGrath;Maria Hordinsky

  419
  Citations

• Alopecia Universalis Associated with a Mutation in the Human hairless Gene

  Wasim Ahmad;Muhammad Faiyaz ul Haque;Valeria Brancolini;Hui C. Tsou

  408
  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

• Autoantibodies to extracellular matrix protein 1 in lichen sclerosus

  Noritaka Oyama;Ien Chan;Sallie M Neill;Takahiro Hamada

  389
  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

• The role of fibroblasts in tissue engineering and regeneration

  T Wong;J A McGrath;H Navsaria

  375
  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

• Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting

  Liat Samuelov;Ofer Sarig;Robert M Harmon;Debora Rapaport

  327
  Citations