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John McGrath
John McGrath
May Dunhill Chair in Cutaneous Medicine, King's College London
Verified email at kcl.ac.uk
Title
Cited by
Cited by
Year
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
JD Fine, RAJ Eady, EA Bauer, JW Bauer, L Bruckner-Tuderman, ...
Journal of the American Academy of Dermatology 58 (6), 931-950, 2008
12112008
Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification
JD Fine, L Bruckner-Tuderman, RAJ Eady, EA Bauer, JW Bauer, C Has, ...
Journal of the American Academy of Dermatology 70 (6), 1103-1126, 2014
10522014
Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations
PJ Pollard, JJ Briere, NA Alam, J Barwell, E Barclay, NC Wortham, T Hunt, ...
Human molecular genetics 14 (15), 2231-2239, 2005
10182005
Anatomy and organization of human skin
JA McGrath, RAJ Eady, FM Pope
Rook’s textbook of dermatology 1, 3.2-3.80, 2004
6132004
Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa
JD Fine, RAJ Eady, EA Bauer, RA Briggaman, L Bruckner-Tuderman, ...
Journal of the American Academy of Dermatology 42 (6), 1051-1066, 2000
5782000
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
C Has, JW Bauer, C Bodemer, MC Bolling, L Bruckner‐Tuderman, A Diem, ...
British Journal of Dermatology 183 (4), 614-627, 2020
5492020
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
4861997
Hay–Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
JA McGrath, PHG Duijf, V Doetsch, AD Irvine, R Waal, KRJ Vanmolkot, ...
Human molecular genetics 10 (3), 221-230, 2001
4582001
Bone marrow transplantation for recessive dystrophic epidermolysis bullosa
JE Wagner, A Ishida-Yamamoto, JA McGrath, M Hordinsky, DR Keene, ...
New England Journal of Medicine 363 (7), 629-639, 2010
4242010
Alopecia Universalis Associated with a Mutation in the Human hairless Gene
W Ahmad, M Faiyaz ul Haque, V Brancolini, HC Tsou, S Ul Haque, ...
Science 279 (5351), 720-724, 1998
4171998
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
4061995
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
4011996
Germline NLRP1 mutations cause skin inflammatory and cancer susceptibility syndromes via inflammasome activation
FL Zhong, O Mamaï, L Sborgi, L Boussofara, R Hopkins, K Robinson, ...
Cell 167 (1), 187-202. e17, 2016
3902016
Autoantibodies to extracellular matrix protein 1 in lichen sclerosus
N Oyama, I Chan, SM Neill, T Hamada, AP South, V Wessagowit, ...
The Lancet 362 (9378), 118-123, 2003
3902003
The role of fibroblasts in tissue engineering and regeneration
T Wong, JA McGrath, H Navsaria
British Journal of Dermatology 156 (6), 1149-1155, 2007
3822007
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin–extracellular-matrix linker protein UNC-112, causes Kindler syndrome
DH Siegel, GHS Ashton, HG Penagos, JV Lee, HS Feiler, KC Wilhelmsen, ...
The American Journal of Human Genetics 73 (1), 174-187, 2003
3822003
Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)
T Hamada, WHI McLean, M Ramsay, GHS Ashton, A Nanda, T Jenkins, ...
Human molecular genetics 11 (7), 833-840, 2002
3742002
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting
L Samuelov, O Sarig, RM Harmon, D Rapaport, A Ishida-Yamamoto, ...
Nature genetics 45 (10), 1244-1248, 2013
3432013
The filaggrin story: novel insights into skin-barrier function and disease
JA McGrath, J Uitto
Trends in molecular medicine 14 (1), 20-27, 2008
3302008
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
E Maestrini, AP Monaco, JA McGrath, A Ishida-Yamamoto, C Camisa, ...
Nature genetics 13 (1), 70-77, 1996
3191996
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